Domains are the structural, functional and evolutionary units of proteins. They combine to form multidomain proteins. The evolutionary history of this molecular combinatorics has been studied with phylogenomic methods. Here, we construct networks of domain organization and explore their evolution. A time series of networks revealed two ancient waves of structural novelty arising from ancient ‘p-loop’ and ‘winged helix’ domains and a massive ‘big bang’ of domain organization. The evolutionary recruitment of domains was highly modular, hierarchical and ongoing. Domain rearrangements elicited non-random and scale-free network structure. Comparative analyses of preferential attachment, randomness and modularity showed yin-and-yang complementary transition and biphasic patterns along the structural chronology. Remarkably, the evolving networks highlighted a central evolutionary role of cofactor-supporting structures of non-ribosomal peptide synthesis pathways, likely crucial to the early development of the genetic code. Some highly modular domains featured dual response regulation in two-component signal transduction systems with DNA-binding activity linked to transcriptional regulation of responses to environmental change. Interestingly, hub domains across the evolving networks shared the historical role of DNA binding and editing, an ancient protein function in molecular evolution. Our investigation unfolds historical source-sink patterns of evolutionary recruitment that further our understanding of protein architectures and functions.
The biological functions of genes manifest through the proteins or functional RNA molecules they encode. In evolution, novel functions appear when genes produce new genes by duplication, mutation, recombination, fusion and fission, or when genes are generated de novo. Research has attempted to quantitatively describe the origins of these processes of molecular diversification and how they increase molecular complexity over the course of evolution, for instance through pathways of protein domain organization1,2. Protein domains are structural and functional units of evolution that make up proteins3,4,5, sometimes in unusually complex arrangements6,7. They fold into compact 3-dimensional (3D) atomic structures that arrange alpha-helical and beta-sheet structure elements into tightly packed conformations of the polypeptide chain8. The Structural Classification of Proteins (SCOP)9 and its extended version SCOPe10 are popular taxonomy gold standards of domain structure. SCOP definitions can be used to scan genome sequences for motifs of domains and study how they combine in proteins6. In SCOP, the structure of domains exhibiting similar 3D arrangements of secondary structures and thus identical topologies have been classified as folds (F)9. Within folds, protein domains whose structure and functional features indicate a common evolutionary origin are further grouped into fold superfamilies (FSF). These FSFs sometimes hold multiple evolutionarily related families, which unify domains with pairwise amino acid identities of more than 30% (Supplementary Fig. S1A). As of March 9, 2021, 276,231 annotated SCOPe domains populate the 175,282 protein structures of the Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB-PDB). We note that the cornerstone of the SCOP domain hierarchy is common ancestry, i.e. the existence of shared-and-derived features in domain sequence, structure and function. Homology is also central to many other domain taxonomies, including CATH11, CDD12, ProDom13, Pfam14, and the meta-database InterPro15. Most databases benefit from machine learning. For example, SCOP and Pfam depend on the identification of conserved regions in protein sequences through sequence alignment and background knowledge, which are then used to build probabilistic hidden Markov models (HMMs) of linear sequence analysis. For example, SCOP uses HMMs of structural recognition to recurrently enrich the database16 in a framework that increases alignment-quality and stability of family and superfamily relationships. A similar framework drives the Pfam database but focuses exclusively on sequence information. One difficulty is that not all domains fold into discrete structural entities within the space of possible folds17. Some popular domains overlap within a continuum. This ‘gregariousness’ complicates domain classification, demanding the exploration of super-secondary structural motifs as candidate lower-level units of structure, function and evolution18.
Domain structures appear repeatedly in the protein molecules, singly or in combination with other domains7. More than two-thirds of protein sequences are longer than an average domain length, a vast majority of which are multidomain proteins19. A study of protein structures in 749 genomes showed that the lengths of orthologous protein families in Eukarya were almost double the lengths found in Bacteria and Archaea20. This variance among lengths results from shorter prokaryotic nondomain sequences that link domains to each other in proteins and have evolved reductively in prokaryotes but not in eukaryotes. The arrangement of domains along the sequence of multimeric proteins is referred to as ‘domain organization.’ Both the structure and organization of domains, which have been collectively termed protein domain ‘architecture’, are considered far more evolutionarily conserved than protein sequence7,21,22,23. In addition, some domain combinations make up functional units that recur in different protein contexts24. They have been termed supradomains (Supplementary Fig. S1B). Thus, domains and supradomains behave as modules, parts that interact more often with each other than with other parts or modules of the system.
Comparative genomic approaches allow to study the modular landscape of domain organization. For example, the evolutionary placement of domains in multiple architectural contexts can be quantified by counting distinct neighbors25, domain adjacencies26, or consecutive domain triplets27 in proteins. These measures of ‘versatility’, ‘promiscuity’ or ‘mobility’ (reuse) of domain building blocks depend on both domain size and abundance. Smaller domains are more likely to be used in multidomain proteins and are therefore more mobile27,28, an observation supported by a Menzerath-Altmann’s law of domain organization driven by an economy of scale29. Similarly, highly abundant domains appear more versatile, prompting abundance-based normalization of domain versatility measurements when studying intrinsic combinatorial properties and variation across lineages and biological functions30,31,32.
In order to retrace past events in architectural evolution, statements of history (phylogenies) proposed directly from genomic data must be used to build chronologies of first evolutionary appearance of domains and domain architectures. Unfortunately, protein sequence has limited power in deep retrodictive exploration7,21,22,23. Furthermore, while structure is conserved over longer evolutionary timescales, a general metric for global pairwise comparison of structures does not yet exist33. Thus, the systematic classification of protein structure has been unable to unify the widely divergent folded structures at any level of abstraction (e.g. FSFs in a ‘galaxy’ of folds34), likely because different neighborhoods in protein sequence space contain different structures and functions35. Construction of a ‘periodic table’ of idealized structural representations of folds36 has not alleviated this difficulty due to an absence of rules of structural transformation that would explain the comparative framework. Numerous efforts to dissect the evolution of domain architectures have recently been reviewed37. To overcome limitations and produce global evolutionary views of the protein world, the focus shifted from molecules to proteomes. Trees of proteomes were first reconstructed from a proteomic census of structural domains (beginning with ref.38), and were later used to trace character-state changes along their branches to establish possible domain origins39,40. This approach, however, was restricted to domain structures and architectures appearing after the common ancestor of the proteomes surveyed in the trees. A much more effective way to create truly global chronologies of the protein world was the reconstruction of phylogenomic trees of domain organization (beginning with ref.41). These phylogenies take advantage of powerful serial homologies defined by the proteomic abundance of domains42 or architectures7,43 defined at F and FSF levels. Phylogenomic trees of domain structures helped uncover the natural history of biocatalysis by tracing chemical mechanisms in enzymatic reactions44, analyze the optimization and increase of protein folding speed derived from a flexibility-correlated factor known as contact order (the average relative distance of amino acid contacts in the tertiary structure of proteins)45, and study the history of an ‘elementary functionome’ with a bipartite network of elementary functional loop sequences and structural domains of proteins46. This last study revealed two initial waves of functional innovation involving founder ‘p-loop’ and ‘winged helix’ domain structures, and the emergence of hierarchical modularity and power law behavior in network evolution. Phylogenomic trees of domain architectures and their associated chronologies of molecular accretion showed that architectural diversification evolved through gradual accumulation of domains (singly occurring domains), domain pairs (two different domains), multidomains (numerous domains, with occasional repetition) and domain repeats (domains of one type that are repeated)7. The diversification began with a few single-domain architectures earlier in the timeline, followed by an increasing rate of accretion that culminated in a massive “big bang” of domain organization. The accumulation of architectures continued to date but with a decreasing rate7,46.
Here, we explore the evolving interactome of protein domain organization. We generate a chronology that captures the historical development of domain and multidomain interactions with a graph theoretical approach6 of time-varying (evolving) network structure. The chronology was calibrated with a molecular clock of protein structures, which transforms times of origin of domain architectures into geological timescales of billions of years (Gy)47. Five distinct composition- and topology-based ‘operative’ criteria of connectivity defined nodes and links of the evolving networks. This strategy identified connectivity distributions in a series of 169 growing networks, hubs of evolutionary recruitment acting as donors and acceptors, and structural adaptations of evolving networks to modular, random and scale-free properties. In particular, we discover a pattern of connectivity driven by fusions and fissions, respectively, with densely linked older and younger architectures from the evolutionary timeline sandwiching a period of sparse connectivity. This supports a biphasic or hourglass pattern previously observed in protein evolution48 and follows a model of module emergence49. We thus reveal remarkable patterns of emergence of hierarchy, modularity and structural cooption in evolving networks.
Results and discussion
Construction of evolving networks
We build a time series of networks of domain organization embedding evolutionary information derived from the sequence and structure of millions of protein sequences encoded in hundreds of genomes. The goal is to unfold the history of how single-domain and multidomain proteins share domain make-up and how recruitment processes shape protein evolution. An ‘entity set’ of domains, supradomains, and multidomains were first extracted from the genomic census of fold structure and domain organization. This set of component parts of proteins, mostly recurrent, defined the nodes of the networks, which were labeled with concise classification strings (ccs) describing SCOP domain constituents (Fig. 1A). We define supradomains as sub-combinations of domains that appear in the census and are often used as evolutionary building blocks of multidomains. The definition is more inclusive than that of ref24.
The growing interactions among contemporary architectures are constrained by domain make up and domain arrangement in the protein chain. These evolving interactions were captured with five different operative criteria for timed network generation defined by composition, pairwise occurrence, adjacency, and splicing of domain parts in a protein molecule, where: (1) composition describes makeup (component parts) of the molecular whole; (2) pairwise occurrence describes appearance of parts in sets of two; (3) adjacency refers to their geometrical or spatial arrangement (topology); and (4) splicing refers to the rearrangement of parts by operations of joining and excision that decompose structures (Fig. 1B). The Composition Network (CX) linked domain and supradomain to multidomain nodes (in a partially bimodal fashion) when proteins shared compositional makeup. The Pairwise Network (PX) connected domain to supradomain nodes when components occurred in pairs in a protein. The Pairwise Adjacency Network (PAX) connected domain to supradomain nodes when components occurred in pairs that were adjacent. The Spliced Pairwise Network (SPX) linked domain nodes to each other when their pairs were present in domain-spliced proteins. Lastly, the Spliced Pairwise Adjacency Network (SPAX) linked domain nodes to each other when their adjacent pairs were present in the domain-spliced proteins (Fig. 2).
Finally, we mapped the time or origin (age) of individual architectures onto the nodes of networks built using these five operative criteria (Supplementary Fig. S2). We did so for each of the 169 time-events of the timeline. Network construction has been illustrated with connectivity details of the most ancient domains (Supplementary Fig. S3) and further described in Sect. 1 of Supplementary Text. Networks showcased time directionality, connectivity distributions, and network layouts:
Time Directionality Mapping ages onto networks helped follow their evolutionary growth, as nodes and links accumulated over time since the origin of proteins to the present. The timeline of networks imposed a time directionality on network links, making them arcs (directed edges with arrows pointing from older to younger nodes) of directed graphs (Fig. 1C). The ages of arcs were borrowed from the youngest of the component nodes involved in a link (Supplementary Fig. S3B).
Degree Distributions The number of links connected to a node define that node’s ‘degree’. The degree distribution is a ‘composability’ attribute of a network and the entity set represented by its nodes, a design principle describing the inter-relationship of components of a system. In network evolution, the appearance of a new node may trigger establishment of one or more arcs from existing (older) nodes. Furthermore, outdegree describes the number of outward links and indegree the number of inward links from a node. As the timeline progresses, older nodes gain higher outdegrees as compared to the higher indegrees of recent nodes (Fig. 1C), polarizing the network with arcs depicting ‘arrows of time’ (Supplementary Figs. S2 and S3). The chronological appearance of architectures (domains, supradomains and multidomains) as network connectivity expands along the timeline causes degree to accumulate in the evolving networks (Fig. 2). Multiple interactions of nodes along the timeline diversified connectivity, a feature captured and quantified by weighted degree. Interestingly, box-and-whisker’s plots of weighted outdegree and indegree demonstrate bimodal degree distributions typical of biological systems49,50 (Supplementary Fig. S4). The yin-yang patterns of contractions and expansions of architectural innovation are evident from the distributions of modern outdegrees and indegrees (Supplementary Fig. S5). In particular, the cumulative outdegree and indegree scattergrams demonstrate an hourglass (or bimodal) pattern of linkage development unfolding in evolution (Supplementary Fig. S6).
Time Event-based ‘Radial’ and ‘Waterfall’ Layouts The growth of a network evolving at discrete temporal intervals can be modeled with Discrete Event Simulation (DES) tools51,52,53. Borrowing the DES rationale, we modeled the evolution of directed networks of domain organization with time flowing from one event to another as discrete evolutionary ‘time steps’, typical of a step function. The progression of events was visualized with two types of layouts, a vertical representation we coined ‘waterfall’ layout that had nodes arranged top-down by age and a concentric ‘radial’ representation of growing networks that unfolded time-events of protein evolution from center to periphery (Fig. 1C). Network clusters comprising of hubs and their cohesive neighbors were segregated to improve differentiation along the horizontal axis. The waterfall and radial layouts made evolutionary recruitment evident as time events progressed downward or outward, respectively (Figs. 2 and 3).
Early history of modern domain organization
The accumulation of links connecting domain, supradomain and multidomain proteins in evolving CX, PX, PAX, SPX and SPAX networks played back the complicated history of domain recruitments that drive the evolution of domain organization. Figure 2 shows networks in radial layout at representative time-events defining boundaries of the three epochs of the evolving protein world (‘architectural diversification’, ‘superkingdom specification’ and ‘organismal diversification’, sensu7,42). Networks grew in time and became increasingly complicated tangles, massively expanding after a “big bang” of domain combinations during the organismal diversification epoch. Movies described the evolutionary growth of these networks (Supplementary Video 1).
To illustrate the versatility of the waterfall visualization strategy, we dissected the early origin of proteins with the SPX network. Two major waves of structural innovation arising from ancient ‘p-loop’ and ‘winged helix’ domains were observed in the waterfall diagrams of a highly connected (reduced) subnetwork visualization of the SPX network (Fig. 3), matching similar recruitment waves observed in the study of evolutionary networks of elementary functionomes46 and metabolites54. Waves originated in primordial α/β/α-layered sandwich, β-barrel and helical bundle structures identified in an earlier structural phylogenomic study as part of the most ancient 54 protein domain families55. However, most of the connectivity of these major pathways was established during the organismal diversification epoch less than 1.5 Gy ago (nd ≥ 0.6) and hence was fully developed relatively recently in evolution. The ‘p-loop’ and ‘winged helix’ waves embedded the major gateways of enzymatic recruitment we previously reported for metabolism54. The first gateway was mediated by the c.37 P-loop hydrolase fold and originated in the energy interconversion pathways of the purine metabolism subnetwork. The second pathway was mediated by the a.4 winged helix fold and originated in the biosynthesis of cofactors and the metabolic subnetwork of porphyrin and chlorophyll54,56,57. The congruent realization of these evolutionary patterns with data sources of different types is remarkable (Supplementary Video 2). It strongly supports the historical statements we propose. Further information can be found in Sect. 2 of Supplementary Text.
Network analysis of cooption mechanisms of recruitment
The networks of domains (SPX and SPAX) elicited 161 unique time-events along the evolutionary timeline, out of a total 169 events expected for networks of domains, supradomains and domain combinations (CX, PX and PAX) (Supplementary Tables 1–5). The node and connectivity distributions among the time-event bins of the evolving networks highlight the widespread, growing and recurrent combinatorial recruitment process that incorporates domains and their combinations into protein scaffolds and drives structural evolution (Fig. 2). Indeed, the largest hubs representing the most popular domains in the highly connected SPX subnetwork appeared not only early in evolution but also in the modern protein world (Fig. 3). Similar to the evolution of elementary functions46, domain innovation also developed early during the first ~ 1.8 Gy of protein history (Fig. 3). The combinatorial recruitment process however spanned the entire timeline (Supplementary Fig. S2). In terms of origins, the first donor and acceptor composition event occurred in protein evolution with the appearance of a link in the CX network connecting domain c.2.1 to domain combination c.2.1|a.100.1, ~ 3.54 Gya (nd = 0.069). The first donor and acceptor pair occurred in the pairwise PX and SPX networks ~ 3.12 Gya (nd = 0.179), ~ 0.42 Gy later (Δnd = 0.11). The pairing event involved domains c.37.1 and d.14.1. The first adjacent donor and acceptor pair of the adjacency-based PAX and SPAX networks appeared ~ 2.90 Gya (nd = 0.237), ~ 0.22 Gy later (Δnd = 0.06). The adjacently paired nodes were domains c.37.1 and c.23.16. These observations highlight a remarkable tendency of domain organization to gradually but recurrently constrain pairwise occurrences in multidomain proteins. The evolutionary history of donors and acceptors of domain organization is hence associated with a highly optimized process of cooption. To explore this combinatorics, we first dissected the network connectivity with bar plots that describe the chronological accumulation of links along the evolutionary timeline (Supplementary Fig. S7). This made general patterns quantitative and source-sink relationships explicit. Second, we analyzed the per unit donor/acceptor ratio in the evolving networks to highlight pairwise cooption and composability, respectively (Supplementary Fig. S8). Specifically, domain acceptors (represented by network indegree) of SPX increased in number to a global average of 8.63 (± 0.15) sinks per domain in evolution. Domain donors (represented by network outdegree) of SPX reached a higher global average of 9.7 (± 0.56) sources per domain, indicating significant reutilization of relatively ancient domains. In contrast, the average number of donors and acceptors in the evolving CX network plateaued at 3.41 ± 0.34 sources and 3.43 ± 0.05 sinks per domain/multidomain, respectively. This showed uniform source/sink evolutionary rates as proteins acquired higher composability with time. Third, an inferential analysis of cooption-based source-sink relationships maturing at modern times revealed an independence of patterns from the selected network generation criteria (Supplementary Fig. S9). Primarily, the composition events yielding source domains and supradomains were dominant, with the number of events almost doubling in the CX network from the origin to the organismal diversification epoch ~ 1.5 Gya (nd = 0.6). However, the pairwise cooption events of the SPX domain network, e.g., doubled in number and reached relatively comparable levels in evolution only after delays of ~ 0.6 Gy (Δnd = 0.15) and ~ 2.1 Gya (nd = 0.75), respectively. Moreover, the number of cooption events yielding sink domains in SPX almost tripled by the beginning of the organismal diversification epoch. In contrast, the number of CX sinks reached that level only halfway along that evolutionary epoch. These divergent patterns indicate a frustrated dynamics of network growth. The early adoption of composability of domains and supradomains in multidomains seems to have preceded the pairwise cooption of domains in protein history, leading to the numerous recruitment pathways of the modern protein world. A discussion on the source-sink relationships impacted by domain fusion and fission processes can be found in Sect. 3 of Supplementary Text.
Hubs in network evolution
Network hubs are at the heart of network connectivity and could chaperone network evolution26. We ranked modern domains and domain combinations of age nd = 1 as hubs based on the 99.9th percentile of indegree and outdegree. Hubs were annotated with domain organization attributes, including SCOP domain descriptions, age, fusional/fissional information, and GO terms. We also associated hubs with age ranks reflecting their order of evolutionary appearance in the timeline.
The most notable donor hubs for all networks types were the carrier protein domains e.23.1, a.28.1 and c.69.1, which are involved in Non-Ribosomal Peptide Synthesis (NRPS), whether directly or indirectly through other pathways (Table 1). These domains diversified later in evolution yielding cofactor-binding molecular switches and barrel structures55. Ancient NRPS pathways of domain accretion have been associated with a model that not only described stabilization and decoration of membranes by primordial alpha-helical bundles and beta-sheets, but also explained primordial protein synthesis and genetic code specificity chaperoned by ancient forms of aminoacyl-tRNA synthetase (aaRS) catalytic domains and NRPS modules. NRPS even preceded the emergence of the ribosome, acting as scaffold for nucleic acids and the modern translation function. In particular, the PX and PAX networks highlight the central evolutionary role of these novel emerging cofactor structures in the NRPS pathways. Thus, our findings made explicit that our connectivity criteria of generating networks of domain organization were at the cornerstone of the early development of genetic code and supported the evolutionary model of early biochemistry based on phylogenomic information and network structure.
Domains c.30.1, b.1.1, d.142.1 and g.3.11 (0.723 < nd < 0.977) were the most prominent acceptor hubs (Table 2). These structures are integral parts of two-component signal transduction systems that are common in microbes. The highly modular domains feature dual response regulator proteins involved in the two-component signal transduction system comprising of an N-terminal response regulator receiver domain and a variable C-terminal effector domain with DNA-binding activity. These proteins are transcriptional regulators in bacteria and some protozoa, detecting and responding to environmental changes, e.g. nitrogen fixation. These evolving interactions of microbes with the environment mediated by two-component systems have apparently influenced the evolutionary process of cooption. Three acceptor hubs that were significant in PX with indegree > 250 (following behind the 99.9th percentile in other networks) were Nucleotide cyclase (d.58.29), Spermadhesin, CUB domain (b.23.1), and Fibronectin type III (b.1.2) (nd = 0.723–0.809). See Sect. 4 of Supplementary Text for additional donor/acceptor hub information, and Sect. 5 for cooption events occurring during the ‘big bang’ of domain organization.
Emergence of preferential attachment in network evolution
Genomic-centric processes such as duplication, recombination, fusion and fission shape patterns of molecular complexity2. Many of these patterns can be explained with large ‘scale-free’ networks that grow by following the preferential attachment principle58. These self-organizing and highly inhomogeneous networks attach links to highly connected hub-like nodes in a ‘rich-get-richer’ fashion, lacking a characteristic scale, irrespective of the properties of individual nodes or systems59. This pattern of network expansion, which is remarkably popular in biology60, is sharply distinct from that of the Erdős–Rényi random network model61,62. In a scale-free network, the probability P(k) of nodes connecting with neighboring k nodes (i.e. the ratio of nodes with k links) decays as a power law, P(k) ~ k–γ, with γ defined as the exponent of power law decay. The frequency distributions of node-connectivity in biomolecular networks have γ typically ranging 2.1–2.463. Thus, scale-free properties drive degree distributions with heavy tails, where very few nodes have high degree values.
Our statistical analyses of the featured indegree distributions along the timeline of growing networks uncovered interesting patterns of power law dynamics (Fig. 4). The scale-free patterns were established early on in protein evolution, primarily evident in the CX composition network. These patterns were remarkably divergent from evolving networks connected at random (RVN p value > 0.05). While power law behavior generally declined as the networks evolved (KS p-value < 0.05, α < 2.5), it somewhat sustained after the ‘big bang’ but only in CX and not in the pairwise networks (KS fit and γ closer to 0 and 2 in CX, respectively). A log linear regression model of CX produced the highest absolute value for γ of 3.81 among the five networks, which was achieved early along the evolutionary timeline (nd ~ 0.25). This value of γ was much higher than values reported for metabolic networks (γ ~ 2.2)60. Remarkably, the γ was maintained at ~ 3 before and after the ‘big bang’, while remaining at ~ 2 until modern times with a minimum value of 1.7. The other four networks generated primarily with the pairwise criterion apparently deviated from the power-law behavior, especially after the ‘big bang’. For instance, the γ of PX and PAX peaked at 2.4 (nd ~ 0.35) and 3.2 (nd ~ 0.38), respectively, slightly later than CX. We also noted a transition in γ from 2.1 in PX and 2.7 in PAX prior to the ‘big bang’ to 1.6 in both after the big bang, plateauing at ~ 1 until the present. In the SPX and SPAX networks, γ reached a peak even later in time than PX and PAX with values of 2.8 (nd ~ 0.54) and 3.4 (nd ~ 0.66), respectively. These values transitioned from 2.4 in SPX and 2.8 in SPAX from before the big bang to 1.6 and 1.7 after the big bang, respectively, plateauing at ~ 1 in both the networks. As expected, the average γ based on less representative outdegree of each of the five networks remained low (1 ± 0.05).
We noticed biphasic patterns when -γ was plotted over network connectivity, with two minima at nd ~ 0.37 and ~ 0.67. Moreover, the scale-free tendency of adjacency networks seemed comparatively higher than that of networks lacking the adjacency restriction. For instance, the average values of γ for the PAX and SPAX networks (1.87 ± 0.06 and 2.13 ± 0.07, respectively) were relatively higher than those for the corresponding parent PX and SPX networks (1.61 ± 0.05 and 1.89 ± 0.06, respectively). This suggests that proximity in amino acid sequence plays a major role in rendering the power-law behavior of evolving networks of domain organization. Overall, the average γ of CX (2.56 ± 0.06) remained the highest along the evolutionary timeline, indicating that composition strongly elicits the preferential attachment property. A complementary transition from random to non-random behavior (RVN p value: 1 → 0) in ancient networks (nd ~ 0.3) implies deviation from randomness as biological networks evolve. Remarkably, this transition event coincides with the origin of a processive ribosome. Such biphasic patterns are common in biology and have explained the emergence of biological modules49 in metabolic networks of Escherichia coli50, networks of elementary functionomes46, and molecular ancestry networks of enzymes64. Section 6 of Supplementary Text further discusses scale-freeness and randomness of networks.
Emergence of hierarchical modularity
Modular networks embed sets of communities (closely-knit modules) that establish links preferentially within themselves and do so sparsely with the rest65. Network modularity usually offsets the power-law behavior of biological networks by distributing node degrees within communities66,67,68. However, both scale-free properties and modular structure may co-exist in a network when modules coalesce hierarchically60. A primary index of modularity is the average clustering coefficient (C), defined as a node-averaged ratio of triangles (graph cycles of length 3) to triads (the connected graph triples) of the network, not taking into account the weights or direction of the node-links60,69,70 (Fig. 5). The adjacency PAX and SPAX networks both showed the lowest C (averaged over nd) with a value of 0.09 ± 0.009. The composition CX network had a relatively higher C of 0.2 ± 0.009. However, the non-adjacency pairwise PX and SPX networks had the highest C values of 0.5 ± 0.02 and 0.32 ± 0.014, respectively. These values were still lower than those reported for metabolic networks (C = ~ 0.6)60,68,71. Hence, the networks supposedly evolved more random smaller modules connected by various inter-modular links, rather than stronger larger modules with few interconnections. Also, the evolution of modular structure appeared better consolidated by pairwise (PX and SPX) and to a lesser degree composability (CX) constraints rather than by adjacency (PAX and SPAX). Comparing patterns of modularity of evolving networks to those of randomness (given by RVNp value) indicated complementary transitions between the two behaviors over the evolutionary timeline (Figs. 4 and 5).
In order to dissect the modular behavior of evolving networks, we studied the regression patterns of C against network size N and evolutionary age nd. For typical scale-free models, C declines sharply with increasing N (C ~ N-coefficient), while the coefficients are as high as 0.7572. Instead, highly modular networks are typically independent of N60. In our networks, C regressed by N with very low coefficients (CX, 0.000036; PX, 0.00007; PAX, 0.000035; SPX, 0.00016; SPAX, 0.00016). In contrast, the regression of C with age (C ~ nd-coefficient) produced significantly higher coefficients (CX, 0.39; PX, 0.85; PAX, 0.39; SPX, 0.35; SPAX, 0.41) (Fig. 5). As expected73, the reference power-law (Barabási) networks that were used as control showed a C of zero. Our data strongly suggests the existence of a highly modular structure that is independent of network growth but is strongly constrained by history, especially when considering the pairwise interactions of the PX network. The rise of the modularity index with emerging power-law degree distribution during certain periods of network evolution indicated a parallel formation of complex hierarchical module clusters with scale-free properties, not distinct from those present in metabolic networks60. Our networks of domain organization showed a slight lag between an onset of scale-free organization (measured with KS fit and γ indegree statistics) and a delayed emergence of modular behavior (measured with C), occurring during early protein evolution. This was followed by intermittent periods of hierarchical modularity spanning across the middle of the evolutionary timeline. Remarkably, the evolving networks showed again a prominent biphasic pattern of hierarchical modularity involving two peaks of modularity (higher statistic C) coinciding with increased power-law behavior (valleys of KS fit and -γ curves), at nd ~ 0.37 and nd ~ 0.67, respectively (Figs. 4 and 5). The modularity heatmaps and dendrograms of select phases of network evolution confirm these biphasic patterns (Fig. 6), which were markedly distinct from the long-tailed clustering patterns of preferential attachment (Supplementary Fig. S10). As identified earlier46, the timing of this switch coincides with the early development of genetic code specificity in the emerging ribosomal aaRS catalytic domains, which was facilitated by the OB-fold structure74. These counteracting and delicately balanced trends of modularity and preferential attachment suggest that the emergence of scale-free behavior of the partial bipartite CX network must have impacted the hierarchical modular structure of the modern pairwise networks of domain organization (PX, PAX, SPX, SPAX) (Supplementary Video 3). A detailed account of our testing and verification of this conjecture is explained in Sect. 7 of Supplementary Text.
We here present for the first time an evolutionary chronology of networks of domain organization. Tracing the time events of origination of protein domain architectures in these growing networks revealed major evolutionary pathways of molecular recruitment of domains and functions. Two prominent ancestral waves of structural novelty involved ancient domain innovations and founder ‘p-loop’ and ‘winged helix’ domain structures. We found that evolutionary recruitment in proteins is ongoing and highly modular. Remarkably, the networks highlighted the role of cofactor-supporting structures of NRPS pathways, which were backbone to the early evolution of the genetic code. The evolving domain rearrangements featured multitier evolutionary episodes of scale-free network structure, hierarchy and modular behavior. Remarkably, our analyses support biphasic patterns of diversification and module emergence that we have observed earlier46,49. In an initial phase, at the cusp of architectural diversification, the modular components of emerging domain organization associated through weak linkages of recruitment. The second phase was massive and prolonged, with a multitude of modules appearing after the ‘big bang’ of the protein world, supporting the onset of organismal diversification. Such biphasic patterns are prevalent in biology and impact size, dipeptide makeup, and loop-mediated flexibility of proteins, possibly due to their intrinsic disorder45,74. We propose that biphasic patterns in evolving networks are integral to module emergence in biological history. We prompt further study of their structure and origin.
Phylogenomic analysis of the entity set of protein domain architectures
We explore the evolution of networks describing how structural domains combine and split to form single domain and multidomain proteins, i.e. the domain organization of proteins. The definition of protein domain structures followed the FSF level of SCOP version 1.759 (Fig. 1). Domain interactions were studied along an evolutionary timeline of structural and architectural innovation directly derived from a phylogenomic tree of architectures reconstructed from an HMM-based census of structural domain organization of 1,730 FSF structures from ~ 3 million protein sequences encoded in 749 genomes of 52 archaeal, 478 bacterial and 219 eukaryal organisms (dataset A749)20 (Supplementary Fig. S1). The percentage of proteins with structural assignments was 62.2 ± 0.09(SD)% (see Table S1 and discussion in ref.20). The tree was generated using maximum parsimony as the optimality criterion in PAUP* following the parsimony ratchet search strategy described in ref.7. Data matrix and tree files are provided as Supplementary Files 1–3 at https://github.com/gcalab/SciRep. The phylogeny represents reconstruction of the “natural history” of proteins that is supported by a model of protein structural growth75 and is carefully indexed with various evolutionary epochs of the protein world7.
Calculation of the ages of domain organization
The ages of domains and domain combinations were calculated as node distance (nd) values, which were derived directly from the rooted phylogenomic tree of protein domain organization7. nd values describe relative ages (in a relative 0–1 scale) of first appearances of 6,162 domains and domain combinations (multidomains) defined at SCOP FSF level (the extant ‘entity set’ sampled by our study; Fig. 2) Collectively, ages defined an evolutionary timeline embodying architectural transformations and molecular transitions mediated by fusion and fission processes in the form of 169 unique ‘time events’ (age groups or time slivers) (Supplementary Fig. S2). A Python script was used to count the number of nodes from the root (base) of the tree to each leaf node and present the distance matrix of nodes in a relative zero-to-one scale46. The script utilized the high imbalance of phylogenomic trees as a fundamental feature to derive the relative ages of domain organization7. The tree imbalance resulted from the accumulation of structures and their combinations in proteins and proteomes and not from node density, thus representing a true evolutionary process47.
The timeline was calibrated with a molecular clock of FSF structures (t = –3.831nd + 3.628) used to calculate geological age in Gy through calibration points of FSF domains associated with microfossil, fossil and biogeochemical evidence, biomarkers, and first-appearance of clade-specific domains47. The RSCB–PDB count was determined by following the hyperlink associated to the number of entries or structures (which is updated weekly) and selecting “Customizable Table” from the ’Reports’ menu above the results section. Subsequently, SCOP, CATH, and PFAM ID options were selected as domain information under the ’Domain Details’ section and domain counts data were exported as a comma separated value (.csv) file report. Supplementary Tables 1–5 provide an exhaustive summary of various connectivity categories of evolving networks based on this ‘entity set’ of domain organization. The extraction pipeline of SPX/SPAX domain units from the original data set can be found in Supplementary Table 6.
Indexing domain attributes
Domain ages and assignment of fusional/fissional properties followed ref.7. SCOP concise classification strings (ccs) of domain descriptions9 were downloaded from http://scop.mrc-lmb.cam.ac.uk/scop/parse/index.html for SCOP version 1.75 as the file dir_des_scop_txt_1_75.txt. Available descriptions for 2,223 single domains were obtained from SCOP unique identifiers (sunID). The Gene Ontology (GO) specifications were recorded from the Superfamily Database (SUPFAM) available at http://supfam.cs.bris.ac.uk/SUPERFAMILY/GO.html. High-coverage domain-centric GO annotations that were supported only by all UniProts (including multidomain UniProts) were downloaded as the file Domain2GO_supported_only_by_all.txt. High-quality truly domain-centric GO annotations that were supported by both single domain UniProts and all UniProts (including multidomain UniProts) were downloaded as the file Domain2GO_supported_by_both.txt. We reported only the GO annotations ‘by all’ to capture higher coverage. Also, the GO terms were reported only for the 2223 single domains with descriptions available. Specialized GO annotations from two levels of hierarchy downstream were taken from files Domain2GO-Hie-Dist1.csv and Domain2GO-Hie-Dist2.csv. Structural domains functional ontology (SDFO) that mapped information from a theoretic analysis of Domain2GO annotation profiles were reported from the file SDFO.txt.
Network construction, visualization and analysis
Mathematical definitions for construction of networks can be found in Supplementary Materials and Methods. The social network analysis tool Pajek76 and the statistical test bench R’s igraph package77 were used to visualize and analyze the networks, respectively. The collective impact of events was made explicit by Pajek’s Visualization of Similarity (VOS) clustering method78,79. VOS helped reveal communities and design layouts of networks with nodes separated into network modules, where high modularity indices ranged from 94–95%. Number of clusters varied over networks (CX, 691; PX, 3,886; PAX, 4,126; SPX, 607; SPAX, 620). Network clusters were visually compacted to hubs and their cohesive neighbors with the energy-optimizing Kamada-Kawai ‘separate components’ algorithm80. Pajek allowed to proportionally reduce the size of highly connected nodes by some scaling factor for optimally uncluttered visualization. Waterfall and radial network layouts were designed with node-size scaled down by factors of 0.1 and 0.25, respectively. R packages equipped with specialized code constructs to draw graphs and derive statistics were used to analyze network properties81,82. We also used Pre-Hypertext Processing language (PHP) to write custom scripts that generated radial visualizations of the networks and helped conduct housekeeping data management83. The PHP scripts were executed in the command line. Results of these scripts were input into Pajek’s and R’s analytical procedures. We used the open-source software ImageMagick (www.imagemagick.org) for batch conversion, captioning, and appending of network images (to represent legends and scales). A detailed description of partition and data files, list of network data analysis functions, charting and graphing procedures, methods to generate power law statistics, modularity indices and randomness checks, and the method pipeline used to achieve waterfall diagrams can be found in Supplementary Materials and Methods.
Scale-free network behavior
Linear regression models of P(k) given k (i.e. the probability of having k-neighbors) were used to derive the γ coefficient of the power law distribution and the determination coefficient, R2. The value of γ represents an absolute slope of the log linear model of P(k) versus k. The slope is usually ≤ 0. γ >> 1 indicates strong tendency towards preferential attachment. R2 indicates the percentage of data that fits the linear model. High values of both γ and R2 suggest strong scale-free behavior. Additional power law statistics were calculated as: (1) the exponent of the fitted power law distribution, α, with an assumption that P(X = x) is proportional to x–α; (2) KS fit statistic to compare the input degree distribution with that of fitted power-law; and (3) the KS p-value of a statistical test, with the null hypothesis that data is being drawn from a power law distribution84,85. α >> 1, 0 < KS fit scores << 1, and KS p-values ≥ 0.05 suggest that degree data was derived from a fitted power law distribution. Maximum log likelihood of the fitted scale-free parameters was also determined. Control networks were included for reference that were generated with ‘Barabási’ methods58 of the igraph package from R77. These controls simulated basic and extended age-dependent power law graph models given varying sizes of the evolving networks.
We investigated modularity using six indices: (1) The VOS Quality index (VQ) was determined using the Pajek VOS algorithm by considering the number or weights of the links (arcs) between the nodes as similarities. Clusters or communities that were deemed ‘similar’ were iteratively drawn closer to each other until a final layout was achieved with least crossings and closest clusters. The quality index VQ was thus calculated for this final layout as ∑i=1 c, j=i+1 c (eij − ai2), where c is the number of communities; eij is the fraction of edges with one node v in the community i (ci) and the other node w in the community j (cj), defined as ∑vw (Avw/2 m) where v ϵ ci, w ϵ cj, m is the sum of weights in the graph and Avw is the weighted value or 0, indicating presence or absence of edge between nodes v and w in the adjacency matrix A of the network; and ai is the fraction of weighted k neighbors attached to the nodes in community i, i.e. ki/2m78,79. (2) The Clustering Ratio (C-ratio) is the ratio of the number of network clusters to the count of the connected nodes in the network. (3) The average Clustering Coefficient (C) is defined as the ratio of the triangles impingent on a node to the connected triples, determined as a global average over all nodes in a simplified (undirected/unweighted) network60,69,70. C is not meaningful for strictly bipartite or scale-free graphs73. We also report coefficients of linear regression of C over the age and size of the networks of domain organization. (4) The Fast-Greedy Community (FGC) agglomerative hierarchical algorithm detects community structure for networks with m edges, n nodes, and a depth d of the dendrogram describing the community structure, given an optimized linear running time of O(m × d × logn) ~ O(n × log2n)86. The Newman-Girvan algorithm index (NG) was computed with two different input partitions, the first (5) defined by age (NGage) and the second (6) defined by VOS clustering (NGvos). NG calculates the modularity of a network given a predefined division or partition to measure the influence of the partition in separating the different node types. This indicates either assortative (positive) or disassortative (negative) mixing across modules65. The NG algorithm computes an index as 1/(2 m)∑ij(Aij − 1/(2m)kikj × ∆(ci,cj)), where m is the sum total of weights in the graph and Aij are weighted entries in the adjacency matrix of the network; ki | kj and ci | cj are the weighted degrees and the components (numeric partitions) of the nodes i and j, respectively; finally, ∆(x,y) equals 1 if x = y and 0 otherwise65. The VQ, C-ratio, C and FGC indices each range from 0 to 1, while the NG indices range from − 1 to 1. In all cases, higher values represent strong modularity of the network at an event of evolutionary history. Heatmaps of modularity were constructed using log10-scaled modularity matrices, with each map element given as (Aij − kikj/(2m))Mnd, where Aij, ki, kj and m were the same as defined for NG65, while Mnd was the network’s modularity index at event nd. Cladistic representations of modularity were visualized with dendrograms whose metrics were calculated from squared Euclidean distance matrices, which indicate dissimilarities between cluster means87. The dissimilarity or distance matrices were clustered hierarchically using the Ward's minimum variance method that seeks compact and spherical clusters88.
Quantifying randomness in networks
The Bartels rank test of randomness, which primarily offers a rank version of von Neumann's Ratio Test for Randomness89, was used to measure random network behavior. The resultant test statistic RVN is defined as ∑i=1→n−1 (Ri−Ri+1)2/∑i=1→n (Ri – (n + 1)/2)2, where Ri = rank (Xi) with i = 1…n, (RVN − 2)/σ is the asymptotically standard normal, and σ2 = [4(n − 2)(5n2 − 2n − 9)]/[5n(n + 1)(n − 1)2]. The null hypothesis of this method was randomness, which was tested against the alternate hypothesis of non-randomness, given a trend of RVN values. A p value is computed from a two-sided beta distribution approximation test. Random graph controls were created by following the Erdős–Rényi graph model6190.
Chothia, C. & Gough, J. Genomic and structural aspects of protein evolution. Biochem. J. 419, 15–28 (2009).
Chothia, C., Gough, J., Vogel, C. & Teichmann, S. A. Evolution of the protein repertoire. Science 300, 1701 (2003).
Wetlaufer, D. B. Nucleation, rapid folding, and globular intrachain regions in proteins. Proc. Natl. Acad. Sci. USA 70, 697–701 (1973).
Janin, J. & Wodak, S. J. Structural domains in proteins and their role in the dynamics of protein function. Prog. Biophys. Mol. Biol. 42, 21–78 (1983).
Han, J. H., Batey, S., Nickson, A. A., Teichmann, S. A. & Clarke, J. The folding and evolution of multidomain proteins. Nat. Rev. Mol. Cell Biol. 8, 319–330 (2007).
Apic, G., Gough, J. & Teichmann, S. A. Domain combinations in archaeal, eubacterial and eukaryotic proteomes. J. Mol. Biol. 310, 311–325 (2001).
Wang, M. & Caetano-Anollés, G. The evolutionary mechanics of domain organization in proteomes and the rise of modularity in the protein world. Structure 17, 66–78 (2009).
Caetano-Anollés, G., Wang, M., Caetano-Anollés, D. & Mittenthal, J. E. The origin, evolution and structure of the protein world. Biochem. J. 417, 621–637 (2009).
Murzin, A. G. et al. SCOP: a structural classification of proteins database for the investigation of sequences and structures. J. Mol. Biol. 247, 536–540 (1995).
Chandonia, J. M., Fox, N. K. & Brenner, S. E. SCOPe: manual curation and artifact removal in the structural classification of proteins—extended database. J. Mol. Biol. 429, 348–355 (2017).
Dawson, N. L. et al. CATH: an expanded resource to predict protein function through structure and sequence. Nucleic Acids Res. 45, D289–D295 (2017).
Marchler-Bauer, A. et al. CDD: NCBI’s conserved domain database. Nucleic Acids Res. 43, D222–D226 (2015).
Bru, C. et al. The ProDom database of protein domain families: more emphasis on 3D. Nucleic Acids Res. 33, D212–D215 (2005).
Finn, R. D. et al. The Pfam protein families database. Nucleic Acids Res. 36, D281–D288 (2008).
Finn, R. D. et al. InterPro in 2017—beyond protein family and domain annotations. Nucleic Acids Res. 45, D190–D199 (2017)
Wilson, D. et al. SUPERFAMILY—sophisticated comparative genomics, data mining, visualization and phylogeny. Nucleic Acids Res. 37, D380–D386 (2009).
Harrison, A., Pearl, F., Mott, R., Thornton, J. & Orengo, C. Quantifying the similarities within fold space. J. Mol. Biol. 323, 909–926 (2002).
Berezovsky, I. N., Guarnera, E. & Zheng, Z. Basic units of protein structure, folding, and function. Prog. Biophys. Mol. Biol. 128, 85–99 (2017).
Gerstein, M. How representative are the known structures of the proteins in a complete genome? A comprehensive structural census. Fold. Des. 3, 497–512 (1998).
Wang, M., Kurland, C. G. & Caetano-Anollés, G. Reductive evolution of proteomes and protein structures. Proc. Natl. Acad. Sci. USA 108, 11954–11958 (2011).
Illergård, K., Ardell, D. H. & Elofsson, A. Structure is three to ten times more conserved than sequence—a study of structural response in protein cores. Proteins Struct. Funct. Bioinforma. 77, 499–508 (2009).
Bashton, M. & Chothia, C. The geometry of domain combination in proteins1. J. Mol. Biol. 315, 927–939 (2002).
Chothia, C. & Lesk, A. M. The relation between the divergence of sequence and structure in proteins. EMBO J. 5, 823–826 (1986).
Vogel, C., Berzuini, C., Bashton, M., Gough, J. & Teichmann, S. A. Supra-domains: evolutionary units larger than single protein domains. J. Mol. Biol. 336, 809–823 (2004).
Wuchty, S. Scale-free behavior in protein domain networks. Mol. Biol. Evol. 18, 1694–1702 (2001).
Apic, G., Huber, W. & Teichmann, S. A. Multi-domain protein families and domain pairs: comparison with known structures and a random model of domain recombination. J. Struct. Funct. Genom. 4, 67–78 (2003).
Tordai, H., Nagy, A., Farkas, K., Bányai, L. & Patthy, L. Modules, multidomain proteins and organismic complexity. FEBS J. 272, 5064–5078 (2005).
Weiner, J., Moore, A. D. & Bornberg-Bauer, E. Just how versatile are domains?. BMC Evol. Biol. 8, 285 (2008).
Shahzad, K., Mittenthal, J. E. & Caetano-Anollés, G. The organization of domains in proteins obeys Menzerath-Altmann’s law of language. BMC Syst. Biol. 9, 44 (2015).
Vogel, C., Teichmann, S. A. & Pereira-Leal, J. The relationship between domain duplication and recombination. J. Mol. Biol. 346, 355–365 (2005).
Basu, M. K., Carmel, L., Rogozin, I. B. & Koonin, E. V. Evolution of protein domain promiscuity in eukaryotes. Genome Res. 18, 449–461 (2008).
Xie, X., Jin, J. & Mao, Y. Evolutionary versatility of eukaryotic protein domains revealed by their bigram networks. BMC Evol. Biol. 11, 244 (2011).
Taylor, W. R. Evolutionary transitions in protein fold space. Curr. Opin. Struct. Biol. 17, 354–361 (2007).
Alva, V., Remmert, M., Biegert, A., Lupas, A. N. & Söding, J. A galaxy of folds. Protein Sci. 19, 124–130 (2010).
Ferrada, E. & Wagner, A. Evolutionary innovations and the organization of protein functions in genotype space. PLoS ONE 5, e14172 (2010).
Taylor, W. R. A ‘periodic table’ for protein structures. Nature 416, 657–660 (2002).
Forslund, S. K., Kaduk, M. & Sonnhammer, E. L. L. Evolution of protein domain architectures. In Evolutionary Genomics, Methods in Molecular Biology Vol. 1910 (ed. Anisimova, M.) 469–504 (Humana, 2019).
Gerstein, M. Patterns of protein-fold usage in eight microbial genomes: a comprehensive structural census. Proteins Struct. Funct. Genet. 33, 518–534 (1998).
Abeln, S. & Deane, C. M. Fold usage on genomes and protein fold evolution. Proteins Struct. Funct. Genet. 60, 690–700 (2005).
Edwards, H., Abeln, S. & Deane, C. M. Exploring fold space preferences of new-born and ancient protein superfamilies. PLoS Comput. Biol. 9, e1003325 (2013).
Caetano-Anollés, G. & Caetano-Anollés, D. An evolutionarily structured universe of protein architecture. Genome Res. 13, 1563–1571 (2003).
Wang, M., Yafremava, L. S., Caetano-Anollés, D., Mittenthal, J. E. & Caetano-Anollés, G. Reductive evolution of architectural repertoires in proteomes and the birth of the tripartite world. Genome Res. 17, 1572–1585 (2007).
Wang, M. & Caetano-Anollés, G. Global phylogeny determined by the combination of protein domains in proteomes. Mol. Biol. Evol. 23, 2444–2454 (2006).
Nath, N., Mitchell, J. B. O. & Caetano-Anollés, G. The natural history of biocatalytic mechanisms. PLoS Comput. Biol. 10, e1003642 (2014).
Debès, C., Wang, M., Caetano-Anollés, G. & Gräter, F. Evolutionary optimization of protein folding. PLoS Comput. Biol. 9, e1002861 (2013).
Aziz, M. F., Caetano-Anollés, K. & Caetano-Anollés, G. The early history and emergence of molecular functions and modular scale-free network behavior. Sci. Rep. 6, 25058 (2016).
Wang, M. et al. A universal molecular clock of protein folds and its power in tracing the early history of aerobic metabolism and planet oxygenation. Mol. Biol. Evol. 28, 567–582 (2011).
Caetano-Anollés, D., Kim, K. M., Mittenthal, J. E. & Caetano-Anollés, G. Proteome evolution and the metabolic origins of translation and cellular life. J. Mol. Evol. 72, 14–33 (2011).
Mittenthal, J. E., Caetano-Anollés, D. & Caetano-Anollés, G. Biphasic patterns of diversification and the emergence of modules. Front. Genet. 3, 147 (2012).
Aziz, M. F. et al. Stress induces biphasic-rewiring and modularization patterns in the metabolomic networks of Escherichia coli. IEEE Intl. Conf. Bioinf. Biomed. https://doi.org/10.1109/BIBM.2012.6392626 (2012).
MacDougall, M. H. Simulating Computer Systems: Techniques and Tools (MIT Press, 1987).
Delaney, W. & Vaccari, E. Dynamic Models and Discrete Event Simulation (CRC Press, 1989).
Pidd, M. Computer simulation in management science. J. Oper. Res. Soc. 57, 327 (2006).
Caetano-Anollés, G., Kim, H. S. & Mittenthal, J. E. The origin of modern metabolic networks inferred from phylogenomic analysis of protein architecture. Proc. Natl. Acad. Sci. USA 104, 9358 (2007).
Caetano-Anollés, G., Kim, K. M. & Caetano-Anollés, D. The phylogenomic roots of modern biochemistry: origins of proteins, cofactors and protein biosynthesis. J. Mol. Evol. 74, 1–34 (2012).
Caetano-Anollés, K. & Caetano-Anollés, G. Structural phylogenomics reveals gradual evolutionary replacement of abiotic chemistries by protein enzymes in purine metabolism. PLoS ONE 8, e59300 (2013).
Caetano-Anollés, G. et al. The origin and evolution of modern metabolism. Int. J. Biochem. Cell Biol. 41, 285–297 (2009).
Barabási, A. L. & Albert, R. Emergence of scaling in random networks. Science 286, 509 (1999).
Pang, T. Y. & Maslov, S. Universal distribution of component frequencies in biological and technological systems. Proc. Natl. Acad. Sci. USA 110, 6235–6239 (2013).
Ravasz, E., Somera, A. L., Mongru, D. A., Oltvai, Z. N. & Barabási, A. L. Hierarchical organization of modularity in metabolic networks. Science 297, 1551–1555 (2002).
Erdős, P. & Rényi, A. Connectivity of random nets. Publ. Math. Inst. Hungarian Acad. Sci. 5, 17–61 (1960).
Bollobas, B. Random Graphs (Academic Press, 1985).
Strogatz, S. H. Exploring complex networks. Nature 410, 268–276 (2001).
Mughal, F. & Caetano-Anollés, G. MANET 3.0: hierarchy and modularity in evolving metabolic networks. PLoS ONE 14, e0224201 (2019).
Newman, M. E. J. & Girvan, M. Finding and evaluating community structure in networks. Phys. Rev. E 69, 26113 (2004).
Jeong, H., Tombor, B., Albert, R., Oltvai, Z. N. & Barabási, A. L. The large-scale organization of metabolic networks. Nature 407, 651–654 (2000).
Overbeek, R. et al. WIT: integrated system for high-throughput genome sequence analysis and metabolic reconstruction. Nucleic Acids Res. 28, 123–125 (2000).
Wagner, A. & Fell, D. A. The small world inside large metabolic networks. Proc. R. Soc. Lond. Ser. B Biol. Sci. 268, 1803–1810 (2001).
Wasserman, S. & Faust, K. Social Network Analysis: Methods and Applications (MIT Press, 1994).
Barrat, A., Barthelemy, M., Pastor-Satorras, R. & Vespignani, A. The architecture of complex weighted networks. Proc. Natl. Acad. Sci. USA 101, 3747–3752 (2004).
Watts, D. J. & Strogatz, S. H. Collective dynamics of ‘small-world’networks. Nature 393, 440–442 (1998).
Albert, R. & Barabási, A. L. Statistical mechanics of complex networks. Rev. Mod. Phys. 74, 47 (2002).
Newman, M. E. J., Strogatz, S. H. & Watts, D. J. Random graphs with arbitrary degree distributions and their applications. Phys. Rev. E 64, 26118 (2001).
Caetano-Anollés, G., Wang, M. & Caetano-Anollés, D. Structural phylogenomics retrodicts the origin of the genetic code and uncovers the evolutionary impact of protein flexibility. PLoS ONE 8, e72225 (2013).
Tal, G., Boca, S. M., Mittenthal, J. & Caetano-Anollés, G. A dynamic model for the evolution of protein structure. J. Mol. Evol. 82, 230–243 (2016).
Mrvar, A. & Batagelj, V. Analysis and visualization of large networks with program package Pajek. Complex Adapt. Syst. Model. 4, 1–8 (2016).
Csardi, G. & Nepusz, T. The igraph software package for complex network research. Int. J. Complex Syst. 1695, 1–9 (2006).
Van Eck, N. J. & Waltman, L. VOS: a new method for visualizing similarities between objects. In Advances in Data Analysis: Proceedings of the 30th Annual Conference of the German Classification Society 299–306 (Heidelberg: Springer Verlag, 2007).
Waltman, L., van Eck, N. J. & Noyons, E. C. M. A unified approach to mapping and clustering of bibliometric networks. J. Infometr. 4, 629–635 (2010).
Kamada, T. & Kawai, S. An algorithm for drawing general undirected graphs. Inf. Process. Lett. 31, 7–15 (1989).
Ihaka, R. & Gentleman, R. R: A language for data analysis and graphics. J. Comput. Graph. Stat. 5, 299–314 (1996).
R Core Team. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria (2014).
PHP-Group & others. PHP: Hypertext PreProcessor. Internet http://www.php.net (2012).
Newman, M. E. J. Power laws, Pareto distributions and Zipf’s law. Contemp. Phys. 46, 323–351 (2005).
Clauset, A., Shalizi, C. R. & Newman, M. E. J. Power-law distributions in empirical data. SIAM Rev. 51, 661–703 (2009).
Clauset, A., Newman, M. E. J. & Moore, C. Finding community structure in very large networks. Phys. Rev. E 70, 66111 (2004).
Borg, I. & Groenen, P. Modern multidimensional scaling: theory and applications. J. Educ. Meas. 40, 277–280 (2003).
Murtagh, F. & Legendre, P. Ward’s hierarchical agglomerative clustering method: Which algorithms implement ward’s criterion?. J. Classif. 31, 274–295 (2014).
Bartels, R. The rank version of von Neumann’s ratio test for randomness. J. Am. Stat. Assoc. 77, 40–46 (1982).
Erdős, P. & Rényi, A. On random graphs I. Publ. Math. 6, 290–297 (1959).
Research was supported by grants from the National Science Foundation (MCB-0749836 and OISE-1132791) and the United States Department of Agriculture (ILLU-802-909 and ILLU-483-625) to GCA. Materials and data necessary to interpret the findings of this paper have been included in the manuscript.
The authors declare no competing interests.
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Aziz, M.F., Caetano-Anollés, G. Evolution of networks of protein domain organization. Sci Rep 11, 12075 (2021). https://doi.org/10.1038/s41598-021-90498-8
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