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Genome Res. Jul 2003; 13(7): 1563–1571.
PMCID: PMC403752

An Evolutionarily Structured Universe of Protein Architecture


Protein structural diversity encompasses a finite set of architectural designs. Embedded in these topologies are evolutionary histories that we here uncover using cladistic principles and measurements of protein-fold usage and sharing. The reconstructed phylogenies are inherently rooted and depict histories of protein and proteome diversification. Proteome phylogenies showed two monophyletic sister-groups delimiting Bacteria and Archaea, and a topology rooted in Eucarya. This suggests three dramatic evolutionary events and a common ancestor with a eukaryotic-like, gene-rich, and relatively modern organization. Conversely, a general phylogeny of protein architectures showed that structural classes of globular proteins appeared early in evolution and in defined order, the α/β class being the first. Although most ancestral folds shared a common architecture of barrels or interleaved β-sheets and α-helices, many were clearly derived, such as polyhedral folds in the all-α class and β-sandwiches, β-propellers, and β-prisms in all-β proteins. We also describe transformation pathways of architectures that are prevalently used in nature. For example, β-barrels with increased curl and stagger were favored evolutionary outcomes in the all-β class. Interestingly, we found cases where structural change followed the α-to-β tendency uncovered in the tree of architectures. Lastly, we traced the total number of enzymatic functions associated with folds in the trees and show that there is a general link between structure and enzymatic function.

Proteins are numerous, extraordinarily diverse in sequence, and varied in function. They display unique three-dimensional structures and contain protein domains (Doolittle 1995; Ponting and Russell 2002), minimal building blocks (modules) that share common ancestry (Riley and Labedan 1997; Murzin 1998; Apic et al. 2001; Aravind et al. 2002a) and can be unified into a comparatively small set of folding architectures (Murzin et al. 1995; Swindells et al. 1998). The universe of protein topology is therefore finite and structurally redundant, with protein folds being among the most conserved elements in biology (Gerstein and Hegyi 1998). The number of fold categories is at present curbed by progress in structural genomics and acquisition of entire protein complements (proteomes) from organisms spanning all branches of the universal tree of life (Teichmann et al. 1999). Because protein diversity apparently originated from a limited set of architectural designs (Koonin et al. 2000), the challenge is to find these designs imprinted as ancestral signatures in extant molecules. In evolutionary studies, genomes have been organized hierarchically in trees (Wolf et al. 2002) that were derived using measurements of order, sharing or usage of protein sequences (e.g., gene content; Snel et al. 1999) and structures (e.g., fold occurrence; Gerstein 1998). These genome trees describe overall similarities between the proteomes of different organisms, and are therefore phenetic in nature. In the present study, we used cladistic principles to uncover phylogenetic histories of organismal and protein-fold diversification. A general scheme recently applied to the study of evolved RNA structure (Caetano-Anollés 2002a,b) was used to infer phylogenetic relationships on the basis of shared and derived characteristics in protein fold-usage. Using this approach, we reconstructed inherently rooted phylogenetic trees of proteomes and protein folds, identified ancestral fold configurations, and revealed interesting patterns of evolution in protein architecture.


Cladistic Method and Character Argumentation

We used cladistic tools to trace the evolution and compare systematically the architecture of protein molecules that fall within the different fold categories in the Structural Classification of Proteins (SCOP) database. We characterized each fold using attributes (characters) that describe numerically its genomic abundance (G), distribution, and sharing (G and f). These metrics were here used to reconstruct phylogenetic relationships in three steps. First, values were normalized to compensate for differences in genome size, converted into linearly ordered multistate characters using gap-recoding techniques, and compared in alignment matrices. Second, maximum states were specified as being ancestral (plesiomorphic) to all other, establishing an evolutionary direction of character transformation. And third, the alignment matrices were analyzed with maximum parsimony, reconstructing branching histories of inheritance in the form of phylogenetic trees. The model of character evolution proposed here is supported by the survey and comparison of protein architectures, statistical analyses of genome sequences, and arguments of evolutionary divergence that postulate that new protein structures arise by descent with modification from an ever smaller set of ancestral designs. Character argumentation, the logical process of determining ancestral states in a transformation series, rests on the following considerations.

1. Distribution of Protein Folds Across Domains

Distribution patterns of fold architectures are good indicators of how proteins have diversified, especially if patterns are studied across a wide organismal transect. Uniform distribution patterns are suggestive of common ancestry and long-term architectural stability, and are spread by vertical descent (Hegyi et al 2002). Uneven distribution patterns are suggestive of horizontal gene transfer (HGT), gene loss, convergence, and rapid divergence (Eisen 2000). We studied the frequency of fold distribution and extent of architectural sharing across domains. Seven major distribution patterns were evident and are depicted in the Venn diagram of Figure 1A. Almost half of the protein folds were common to Eucarya, Archaea, and Bacteria (EAB). Almost all folds in Archaea and the majority of folds containing the large superfamilies were part of this distribution pattern. Eucarya and Bacteria shared about 20% of folds (EB). These probably resulted from the transfer of bacterial genes from primitive organelles to the nucleus, following ancestral processes of endocytosis and other HGT events (Eisen 2000). In contrast, only 2% were shared between the two prokaryotic domains (AB), perhaps reflecting remnants of common ancestry. Finally, about 18%, 9%, and 1% were unique to Eucarya (E), Bacteria (B) and Archaea (A), respectively, and were probably the result of coupled gene transfer and gene loss (nonorthologous displacement), rapid evolution, and HGT events postulated to be pervasive in prokaryotes (Koonin et al. 2000). Interestingly, the frequency of all these patterns of fold distribution did not change significantly despite the continuous increase of known folds in the databases (cf. Wolf et al. 1999).

Figure 1
Fold distribution, power-law behavior, and history of fold diversification in the three domains of life. (A) The Venn diagram shows the distribution of phylogenetically informative SCOP 1.59 folds in Eucarya, Archaea, and Bacteria (genomes analyzed ...

2. Statistical Analysis of Genome Sequences

Genome surveys have shown that fold occurrence follows a power-law distribution (Quian et al. 2001), with only a few popular fold designs occurring amid many that are infrequent. This pattern has been described with a graph that connects evolutionarily related architectures (vertices) in a scale-free network (Apic et al. 2001) that grows when connections establish preferentially with the more highly connected vertices (Jeong et al. 2000). These networks have been used to describe many phenomena, including metabolic pathways, social networks, and the World Wide Web. Linear regression analysis in double-logarithmic plots demonstrates that the frequency of folds (F) displaying a given occurrence decays according to the equation F = aG-b, for both genomes considered individually and those pooled by organismal domain. Figure 1B shows plots for sets of genomes of eucaryal, archaeal, and bacterial origin. Prokaryotic genomes produce steeper decay gradients (i.e., larger b exponents) than eukaryotic genomes, rejecting a null hypothesis of slope homogeneity (ANCOVA, P < 0.0001) and showing that there is a larger level of architectural redundancy in proteomes from complex organisms. This power-law behavior implies a preference for duplication of genes encoding folds that are already common, as recently summarized in an evolutionary model that takes into account both duplication of existing genes and acquisition (and loss) of novel genes by lateral transfer (especially in prokaryotes; Quian et al. 2001). Gene duplication has long been considered a major evolutionary mechanism responsible for genetic diversity and innovation (Ohno 1970). Strong support for this view comes from recent statistical analyses of genome sequences that suggest that the proteome renews every ~100 million years by gene duplication alone (Lynch and Conery 2000; Bailey et al. 2002; Moundsey et al. 2002). Gene duplication entails innovation in structure and function. Advances in protein structure determination reveal instances where structural innovation appears driven by changes in folding pathways, divergence, and convergence to stable architectures, shuffling of structural components and topologies, and generation of single-chain multidomain arrangements (Apic et al. 2001; Grishin 2001). Sequence and structure comparisons also suggest that innovations result from architectural divergence in paralogous molecules (Aravind et al. 2002b) and exchange of more primitive components by lateral transfer (Riley and Labedan 1997; Lupas et al. 2001).

3. Fold Sharing Across Domains

The extent of fold sharing was measured within each organismal domain or combination of domains with the G and f metrics. These two statistics rendered similar results; those using G are shown in Figure 1C. Most EAB and EB fold architectures were widely shared within each domain and followed Poisson-like distributions characteristic of a random graph. In fact the connectivity of folds in these exponential networks was statistically homogeneous (data not shown). All other fold distribution patterns contained relatively few architectures that were widely shared. In most of these cases, fold-sharing patterns resembled a power law characteristic of a scale-free network, which is highly heterogeneous (Fig. 1C). The null hypothesis of slope homogeneity was rejected (ANCOVA, P = 0.0001) in double logarithmic plots, and decay gradients and correlation coefficients were significantly larger for fold distributions other than EAB. The contrasting behavior of patterns of fold distribution (Fig. 1C) suggests that the spread of protein folds across organismal domains is complex and can be described by both homogeneous (random network) and heterogeneous (scale-free network) processes. Both lateral transfer (stochastic) and vertical descent (ordered) mechanisms probably delimit these architectural redundancy patterns.

4. The Evolution of Patterns of Fold Distribution

We used parsimony reasoning to establish phylogenetic relationships between the patterns of fold distribution themselves. In doing so, we tested our model of character evolution. Fold occurrence was averaged across populated domains for each distribution pattern and for each of the six major structural classes of proteins, and the resulting matrix was used to generate a most-parsimonious tree reconstruction (Fig. 1D). Characters were polarized by simply considering ancestral those fold distributions that were more frequent. This reasoning is based on two basic assumptions: (1) lineages can be traced to a common ancestor, and (2) redundancy is a favored evolutionary outcome. The tree was rooted in the group of folds that is shared among the three domains of life, with groups following the sequence EAB>EB>E>B>AB>EA=A, from ancestral to derived. This tree constitutes a hierarchical statement of ontogenetic reasoning, in which molecular features widely shared appear ancestral. If correct, this tree fails to reject the null hypothesis that fold occurrence increases in the course of evolution, and is therefore consistent with the model that supports character argumentation. A corollary of this statement is that Bacteria originated earlier than Archaea when evolving from the primitive cenancestor.

5. Phylogenetic Reconstruction Using Characters of Usage and Sharing of Protein Architectures

Finally, we tried to falsify our hypothesis of character polarity by comparing phylogenies reconstructed using independent characters sets (Kitching 1992; Maddison and Maddison 1999). Universal genome trees generated using G and f produced identical three-domain statements, all of them rooted in Eucarya (Fig. 2). This indicates that characters defined by the usage and sharing of protein architectures were cladistically compatible.

Figure 2
Phylogenetic reconstruction of a universal tree. Phylogenetic relationships were inferred from genomic abundance values of SCOP 1.59 fold categories. Bootstrap support (BS) values >80% are shown above nodes. (A) Reduced phylogenetic tree reconstructed ...

Given all five considerations discussed above, we can assume safely that extant proteins that have originated from a common ancestor retain memory of its ancestral structure and function, and consequently, that protein architectures prevalently used and shared by a wide range of organisms originate from innovations which occurred earlier in evolutionary time.

Proteome Phylogenies

We reconstructed phylogenetic trees from fold occurrence data, and tested the effect of character coding and progress in database entry (see Supplemental Material available at www.genome.org). Polarized multistate characters were used to reconstruct rooted phylogenies from a set of 32 genomes that have been completely sequenced and belong to organisms spanning the three domains of life (Fig. 2A). Distribution of cladogram lengths and PTP tests showed strong cladistic structure in the data (P < 0.01). The global topology of the universal tree was reasonably supported by double decay (data not shown) and bootstrap (BS) analysis. However, many branches were not well resolved, and some groups in Bacteria were polyphyletic (such as the γ-proteobacteria and the Spirochaetales). Two clear monophyletic groups were evident and comprised genomes from Archaea (95% BS) and Bacteria (82% BS). These prokaryotic groups exhibited a strong sister-clade relationship (99% BS) and were derived. In contrast, genomes in Eucarya were basal, suggesting a eukaryotic rooting of the tree of life. The topology and rooting of the genome tree were also recovered when examining patterns of fold distribution and sharing among the three organismal domains (Fig. 2B,C). Identical three-domain statements rooted in Eucarya were reconstructed from fold occurrence data averaged across genomes and from the fraction of genomes in Archaea, Bacteria, and Eucarya that share individual folds. Venn diagrams reveal that almost half of fold architectures were common, and that only about one in four folds were characteristic of individual domains (Fig. 1). Phylogenetic analysis of folds shared by the three domains revealed again the same tree topology rooted in the eukaryotic branch (Fig. 2D).

Phylogenetic Trees of Protein Architectures

In order to study evolutionary patterns embedded in protein architecture, we generated phylogenetic histories of protein diversification from fold occurrence data. Studies involved small and large subsets of protein folds, and complete data sets matching two releases of SCOP. Figure 3 shows the phylogenetic relationship of 536 folds in SCOP 1.59. Although there was strongcladistic structure in the data (P < 0.01), only 32 characters (with 20 states) were used to describe fold occurrence in different genomes, and consequently, most branches of the tree were poorly supported by bootstrap analysis. Despite this limitation, general evolutionary patterns in protein structure were clearly recovered. Cumulative frequency plots revealed order and rate of appearance of folds falling within each of the six major structural classes of globular proteins (Fig. 3A). Considering that folds are finite, the total number of nodes (ranging from 418–424 cladogenic events) and node distances (range 84–90) in the trees defined a relative but total time frame of protein diversification. All classes appeared very early in the tree of architectures, within the first 42 cladogenic events (9.7%) and within a distance of 24 nodes from the root (0.28 in a relative 0–1 scale). Folds in the α/β protein class arose first and were followed by those in the α+β, all-α, all-β, small, and multidomain classes, in that order. These folds accumulated at different levels. The α/β folds occurred at relatively constant rates and were prevalent in the bottom half of the tree. In contrast, the α+β folds started to accumulate significantly later but with increasing rates until these folds became the most prevalent class. Folds in all other classes followed this same pattern of accumulation but with lower rates. Maximum rates diminished in the order of fold appearance in the tree; that is, all-α, all-β, small, and multidomain proteins. These general evolutionary patterns were robust and were similarly inferred from trees reconstructed using G (see below) and folds defined by SCOP 1.49 and 20 genomes (data not shown).

Figure 3
Phylogenetic reconstruction of a universal tree of protein architecture. (A) Cumulative frequency plots illustrate the accumulation of folds in the six major classes of protein architecture along optimal (continuous lines) and suboptimal phylogenetic ...

Evolutionary Patterns and Pathways of Protein Architecture

The general tree of protein architectures identified three α/β folds as the most ancestral (Fig. 3B). These were the P-loop hydrolase (c.37), the TIM β/α-barrel (c.1), and the Rossmann (c.2) fold, in order from ancestral to derived. Phylogenies reconstructed separately from folds belonging to each protein class were more informative and contained better-supported branches than the general tree. These trees revealed ancestral fold configurations in each class and clear evolutionary patterns (Fig. 4). Ancestral folds were generally folds with top genomic representation and included barrel folds (e.g., c.1, b.40 [OB-fold], b.43 [reductase/elongation factor], and b.84 [barrel-sandwich hybrid]) and classic folds with helices packed on either side (e.g., c.37, c.2, c.23 [flavodoxin-like], and d.104 [SH2-like fold]) or onto a single face (e.g., d.58 [ferredoxin-like], c.3 [FAD/NAD(P)-binding], and d.142 [ATP-grasp fold]) of a central β-sheet arrangement. Ancestral folds in the α/β class were generally superfolds widely distributed amonggenomes (Gerstein 1998; Wolf et al. 1999). Remarkably and with the exception of the TIM β/α-barrel, they all shared a common architecture of interleaved β-sheets and α-helices. The ferredoxin-like fold (d.58) was the most ancestral architecture in the α+β class. This fold contains simple and irregular protein architectures and packs an α+β sandwich with an antiparallel β-sheet. Ancestral folds in the all-α class were mostly composed of bundles of longhelices, sometimes constituting a layer packing arrangement. This suggests that all-α folds that fit a polyhedron model (roughly half of SCOP entries in this protein class; Chothia et al. 1997) are evolutionarily derived architectures. Hence, evolution of the all-α protein class appears driven by a search for order in protein packing. Ancestral folds in the all-β class were β-barrels (of n = 5,6 and S = 8–10 with Greek-key) (b.40 and b.43), a barrel sandwich hybrid (b.84), and a left-handed β-helix with turns composed of three short β-strands (b.81). These ancestral folds have β-sheets staggered into closed, partly open, or open β-barrel architectures, or are packed in prism-like fashion into a 3-sheet β-helix arrangement (see UDP N-acetylglucosamine acyltransferase [1lxa]). This suggests that β-sandwiches, β-propellers, and β-prisms are all derived fold architectures, and that β-helices (which are mostly right-handed) derive from left-handed and closely packed superhelical structures. Interestingly, an evolutionary tendency towards right-handedness in β-helices is supported thermodynamically by folding pathways of β-β-β units in β-sheets that favor right-handed connections (Chothia et al. 1997).

Figure 4
Reduced cladograms representing the phylogenetic relationships of folds belonging to individual protein classes. Branches with BS values <50% were collapsed into multifurcations (triangles with areas proportional to the number of folds unified ...

Protein transformation pathways that describe likely scenarios of structural evolution (Murzin 1998; Grishin 2001) could be traced in our tree of architectures (see Supplemental Material). Similarly, evolutionary patterns of architectural design were also evident in individual protein classes. For example, we selected all-β folds that had barrel-like structures and were phylogenetically informative, pooled them in groups according to β-sheet topology (Greek-key, meander, and complex; Chothia et al. 1997), reconstructed phylogenetic trees, and searched for patterns in structure (Fig. 5). In the three groups, there was a clear increase in barrel strand (n) and shear (S) number. Moreover, open and partly open barrel structures were derived characteristics. Furthermore, analysis of ancestral folds from each group showed an evolutionary progression in β-sheet topology from the highly ordered Greek-key and the simple up-and-down meander pattern to more complex topological arrangements.

Figure 5
Phylogenetic trees of all-β protein folds with β-barrel-like architecture. Maximum parsimony was used to reconstruct a general tree of β-barrel-like folds with different β-sheet topologies and barrel mimic folds (A) ...

Evolution of Enzymatic Function

Lastly, we explored the relationship between protein architecture and function by tracing the total number of enzymatic functions associated with folds in the trees (Fig. 6). As expected, the most ancestral folds had generally the most enzymatic functions associated with them. This evolutionary tendency was seen in ancestral folds sampled throughout the tree of architectures and in a tree of protein classes. Squared-change parsimony allowed inference of the number of functions associated with the hypothetical ancestors of each protein class, which also decreased in time.

Figure 6
Tracing the evolutionary association of enzymatic function and protein architecture. Cladograms show the phylogenetic relationship of primitive folds (A) and protein classes (B) and were derived from a single tree of 907 steps (CI = 0.690, RI = 0.809; ...


Character attributes represent transformation pathways and hypotheses of relationship (amenable to Popperian falsification) that link character states to each other by specific evolutionary processes (Kitching 1992; Maddison and Maddison 1999). Our phylogenetic study rests on the central assumption that protein folds are more prevalent and more widely shared the more ancestral is their origin, with characters transforming from one state to another in pathways which are linear (restrictive statement that prohibits branched or reticulate arrangements), directed (statement of asymmetry in transformation costs), and polarized (statement that invokes ancestral states). This simple (and perhaps simplistic) model of character evolution is based on the parsimony principle of preferring simple explanations to complex ones (Ockham's razor: “Pluralitas non est ponenda sine neccesitate”) and is supported by patterns in the distribution and sharing of protein folds across domains, statistical analyses and scale-free network behavior of protein fold occurrence, and a phylogenetic study of the evolution of patterns of fold distribution (Fig. 1). The model and supporting results are compatible with the findings and evolutionary model of Quian et al. (2001). More complex models may be warranted however in the future to account for possible factors such as variation in evolutionary rates across characters and branches of the trees, and changes in the size of the protein universe expected to have occurred during evolution.

The reconstruction of histories of proteome diversification showed two monophyletic sister-groups delimiting Bacteria and Archaea, and a topology rooted in Eucarya (Fig. 2). The rooting of the universal tree constitutes a highly debated and controversial issue. Genomic analysis has shown that lateral gene transfer and lineage-specific gene loss are common phenomena (at least in prokaryotes; Koonin et al. 2000), casting doubt on the existence of a universal common ancestor (the `cenancestor'; Fitch and Upper 1987), and complicating parsimony-based reasoning(Woese 1998; Doolittle 1999). On the other hand, the analysis of complete genomes has rescued the notion of the universal tree, as sufficient phylogenetic signal in the sequence, content, and order of gene complements enabled tree reconstruction (Wolf et al. 2002). These unrooted trees continue to support the three-domain classification of life (Woese et al. 1990) but failed to define deep phylogenetic relationships. Other approaches had to be sought (Doolittle 2000). For example, a rooted universal tree was recently recovered from rRNA structure using cladistic principles and considerations in statistical mechanics (Caetano-Anollés 2002a,b). These phylogenies were suggestive of three dramatic evolutionary events and an equally parsimonious eukaryotic or prokaryotic origin of diversified life. Our results complement these findings, by reflecting global evolutionary relationships at a genomic scale. However, they conflict with the accepted view of a prokaryotic ancestor (Woese et al. 1990), supporting instead recent proposals that describe the genome of the cenancestor as an eukaryotic-like, gene-rich, and relatively modern architecture (Forterre and Philippe 1999; Penny and Poole 1999). We favor the view that molecular evolution is driven by a search for innovation that increases molecular complexity and modularity in all lineages of the universal tree (see below).

A general phylogeny of protein architectures showed that protein classes appeared early in evolution and in defined order (Figs. (Figs.33,,5). 5). Our results suggest that the most primitive protein forms contained interspersed α-helical and β-sheet elements (as in the α/β class) that in the course of evolution were first segregated within their structure (α+β class) and then confined to separate molecules (all-α and all-β classes). It is likely that during this time, structural simplification and re-arrangement occurred pervasively and at low levels (Lupas et al. 2001), resulting in the slow accumulation of small proteins and multidomain folds. This hypothetical scenario is consistent with patterns of modularity and simplification in molecular design (Ancel and Fontana 2000; Hartwell et al. 1999), recently revealed in rRNA structure (Caetano-Anollés 2002b), and in the suggestion that diversity in protein architecture originated by stochastic processes expressed in both protein sequence and structure (the random origin hypothesis; White 1994).

Proteins belonging to a fold category maintain a core of three-dimensional packing delimited by topological connections of α-helices and β-sheets, but they harbor peripheral elements of secondary structure and turn and coil regions that can be substantially variable, in both size and conformation. In SCOP, fold categories are also delimited by evolutionary considerations (Murzin et al. 1995; Lo Conte et al. 2002). In the absence of significant sequence similarity, functional features such as catalytic or binding sites, and structural characteristics such as unusual motifs or loops are used as evidence of common ancestry. It is therefore of interest to understand how topological connections defining fold categories have changed during protein diversification from a structural perspective. Phylogenies reconstructed from small and large subsets of protein folds allowed reliable identification of the most ancestral fold categories, and uncovered general patterns of evolution in fold architecture. We found that most ancestral folds shared a common architecture of barrels or interleaved β-sheets and α-helices (Fig. 4). We also uncovered interesting evolutionary patterns when studying the evolution of certain fold architectures that are prevalently used in nature. For example, β-barrels are simple highly geometrical structures that represent about a third of folds in the all-β protein class and appear quite early in evolution (Figs. (Figs.44,,5). 5). The study of these β-barrel folds showed an evolutionary tendency to increase: (1) the tilt of the β-strands in relation to the barrel axis in the context of the “n, S model” (by increasing n and S; McLachlan 1979), (2) the frequency of partly-open or open barrel structures, and (3) the complexity of strand topology in the curled β-sheets (Fig. 5). These tendencies suggest that barrel architectures with increased curl and stagger of β-sheets (sensu Taylor 2002) should be regarded as favored evolutionary outcomes.

It was also possible to trace changes in fold structure that have an impact on fold architecture. Grishin (2001) recently provided examples of architectural transformations in evolutionarily related proteins. Several of these examples involved insertions/deletions (indels), circular permutations, and strand re-arrangements that induce changes in structure capable of modifying general architecture. One example is the conversion of an α-helix into a three-stranded β-meander that replaces the α-β-α layered fold architecture characteristic of NAD(P)-binding Rossmann-fold domain (c.2) in lactate dehydrogenase (1ldn) by the β-β-α architecture characteristic of the FAD/NAD(P)-binding domain (c.3) in NADH peroxidase (1npx; Aravind et al. 2002b). This conversion is of significance as it is rather common in Rossmann fold proteins. Phylogenetic analysis (Figs. (Figs.33,,4) 4) showed that the classical Rossmann c.2 fold is ancestral to the c.3 architecture, suggesting that structural change follows the general α-to-β tendency revealed in the universal tree of protein architectures (Fig. 3). This same tendency can be observed in other pathways involving insertions, deletions, substitutions, circular permutations, and re-arrangements in β-sheet topologies (see Supplemental Material).

Lastly, we traced the total number of enzymatic functions associated with folds and found that their number increased towards the base of the trees (Fig. 6). These results suggest that architectural multifunctionality in proteins was replaced by specialized function. It is tempting to speculate that this evolutionary tendency is also associated with the rise of modular design in proteins.

Taken together, statistical and phylogenetic studies suggest a likely evolutionary scenario. At an early evolutionary stage, divergence in structure and function resulted in massive proliferation of proteins that were functionally versatile, had numerous lineage-specific variants, and clustered in large structural ensembles. The resulting architectures were common and widely distributed across taxa and domains, forming random exponential networks of relationships, and ultimately large structural superfamilies. With time, certain architectures behaved as modules, combined by “domain shuffling”, and gave rise to structural innovations associated with specific functions. Driven by strong selection pressures, each innovation was rare but spread across lineages, perhaps during horizontal transfer events that occurred progressively and at different levels in informational and operational gene sets (Jain et al. 1999). This ultimately produced scale-free networks of relationships that were more robust (error tolerant) than the originating networks.

However, results argue against mass lateral transfer of genes among the domains of life, as this would have obscured phylogenetic signal in the data. Results also show that diversity in architecture appears prevalent in Eucarya. This could stem from the early appearance of eukaryotic-like ancestors or from natural selection forces acting on gene duplication. Eucaryotic organisms are believed to be the subject of K-selection, taking advantage of the carrying capacity of the environment rather than rapid growth in times of nutrient availability (Carlile 1982). They also harbor multiple centers of replication that could enhance possibilities of gene duplication, genomic redundancy, and architectural diversification. Given that genetic redundancy is common and can be stable (Nowak et al. 1997), mutation and selection on `structural' and `functional' replicates would ultimately result in increased architectural innovation.

The evolutionary patterns revealed here are important but rely on how thorough and extensive are the protein databases analyzed. Results may be affected by biases such as over- and underrepresentation of certain sequences and structures, incorrect structural assignment of proteins to fold categories, and genome sampling (Gerstein and Hegyi 1998). PDB databanks are biased by research preferences for targets and organisms and physical constraints imposed by crystallography and NMR spectroscopy. At present, repositories classify only a small subset (averaging ~35%) of sequences into fold categories, and fold classification remains an empirical endeavor. Fortunately, the number of `orphan' sequences without a structure will diminish with progress in structural genomics. Our approach is general and will benefit by the constant increase in number and breadth of genomes that are being sequenced. We do not expect significant changes in the SCOP classification, especially because SCOP organizes protein architectures robustly according to both structural similarity and evolutionary origin (Swindells et al. 1998). Notwithstanding, discovery of new folds and accretion of fold categories will continue. The analysis of proteomes defined by two releases of SCOP recovered similar phylogenies of genomes and folds (data not shown). Consequently, the use of larger character sets in future analyses will only enhance the confidence of our phylogenetic statements.


The Structural Classification of Proteins (SCOP) database describes the evolutionary and structural relationship of proteins with known atomic structure (Murzin et al. 1995). Release 1.59 (May 2002) clusters 15,979 PDB structural entries and 39,893 domains into 686 fold categories, encompassing 1073 superfamilies and 1827 families (Lo Conte el al. 2002). Protein entries matching fold categories in SCOP were retrieved from the PEDANT 1.0.2 database (Frishman et al 2001) in a set of six eukaryotic, nine archaeal, and 17 bacterial genomes sampled over 100 finished genomic sequences. Out of 138,377 entries, an average of 38.4±1.5 (SE) % (range 9.7%–48.6%) matched SCOP domains, and 19.5±0.8 % (range 9.5%–28.3%) had enzymatic activities associated with them. For comparison purposes, we also used a data set that matched 420 fold categories in SCOP 1.39 and was generated by PSI-BLAST comparisons between PDB and genome sequence entries in the first 20 genomes ever to be sequenced (Hegyi et al. 2002). We considered soluble proteins that grouped into major structural classes: all-α proteins with structures composed mostly of α-helices (α), all-β proteins with mostly β-sheets (β), α/β proteins with interspersed α-helices and β-sheets (α/β), α+β proteins containing segregated α-helices and β-sheet regions (α+β), multidomain proteins containing domains belonging to different classes and without known homologs (M), and small proteins (S). The usage and sharing of protein folds was characterized with three metrics: fold occurrence (Gij), average genome occurrence (Gi), and fraction of genomes harboring a fold (fi). Gij defines how often a protein fold (i) occurs in a given proteome (j). Gi represents averages of Gij values. Gi and fi measure the extent of fold sharing within each domain or combination of domains. Values were converted into linearly ordered multistate characters using the gap-recoding technique of Thiele (1993), normalized using an arbitrary scale (generally 0–20) to compensate for differences in genome size, and compared in alignment matrices. These matrices constitute frequency ensembles of protein architectures. Character states were represented by a discrete alphanumerical format with numbers 0–9 and letters A–Q, and matrices encoded in the NEXUS format. Phylogenetic relationships were inferred using PAUP* v.4.0 (Swofford 1999). Characters were polarized with the ANCSTATES command. Trees were reconstructed using maximum parsimony as the optimality criterion, and were automatically rooted at the point where the hypothetical ancestor connected to the tree. Phylogenetic reliability was evaluated by the nonparametric bootstrap method (Felsenstein 1985; implemented using 2 × 103 pseudoreplicates) and by double decay analysis (Wilkinson et al. 2000) using RadCon (Thorley and Page 2000). The structure of phylogenetic signal in the data was tested by the skewness (g1) of the length distribution of 104 random trees, and permutation tail probability (PTP) tests of cladistic covariation using 103 replicates. Ensemble consistency (CI) and retention (RI) indices were used to measure homoplasy and synapomorphy. The homogeneity of partitions was analyzed using a modified Michevich-Farris index of incongruence among data sets and 103 heuristic search replicates (Farris et al. 1995). Topological congruence was measured with several tree comparison metrics and randomization tools using Component (Page 1993). Cumulative frequency plots were used to illustrate the accumulation of folds belonging to a protein class alonga phylogenetic tree. Cumulative fold number was given as a function of distance in nodes from the root. These plots can be considered time plots of lineages (Nee et al. 1994) with a time axis defined in relative units (e.g., cladogenic events). Enzymatic functions were retrieved from the Kyoto Encyclopedia of Genes and Genomes (KEGG) v. 24 (Wixon and Kell 2000). They were defined up to the third level of the Enzyme Commission (EC) classification (IUPAC-IUBMB), and their number was traced on the trees using MacClade v. 3.08 (Maddison and Maddison 1999). Square-change parsimony was used to reconstruct the ancestral states of continuous-valued characters (Maddison 1991). Data matrices can be retrieved from the TreeBase repository (http://herbaria.harvard.edu/treebase/).


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Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.1161903.


[Supplemental material is available online at www.genome.org.]


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