Evolutionary cores of domain co-occurrence networks
BMC Evolutionary Biology volume 5, Article number: 24 (2005)
The modeling of complex systems, as disparate as the World Wide Web and the cellular metabolism, as networks has recently uncovered a set of generic organizing principles: Most of these systems are scale-free while at the same time modular, resulting in a hierarchical architecture. The structure of the protein domain network, where individual domains correspond to nodes and their co-occurrences in a protein are interpreted as links, also falls into this category, suggesting that domains involved in the maintenance of increasingly developed, multicellular organisms accumulate links. Here, we take the next step by studying link based properties of the protein domain co-occurrence networks of the eukaryotes S. cerevisiae, C. elegans, D. melanogaster, M. musculus and H. sapiens.
We construct the protein domain co-occurrence networks from the PFAM database and analyze them by applying a k-core decomposition method that isolates the globally central (highly connected domains in the central cores) from the locally central (highly connected domains in the peripheral cores) protein domains through an iterative peeling process. Furthermore, we compare the subnetworks thus obtained to the physical domain interaction network of S. cerevisiae. We find that the innermost cores of the domain co-occurrence networks gradually grow with increasing degree of evolutionary development in going from single cellular to multicellular eukaryotes. The comparison of the cores across all the organisms under consideration uncovers patterns of domain combinations that are predominately involved in protein functions such as cell-cell contacts and signal transduction. Analyzing a weighted interaction network of PFAM domains of Yeast, we find that domains having only a few partners frequently interact with these, while the converse is true for domains with a multitude of partners. Combining domain co-occurrence and interaction information, we observe that the co-occurrence of domains in the innermost cores (globally central domains) strongly coincides with physical interaction. The comparison of the multicellular eukaryotic domain co-occurrence networks with the single celled of S. cerevisiae (the overlap network) uncovers small, connected network patterns.
We hypothesize that these patterns, consisting of the domains and links preserved through evolution, may constitute nucleation kernels for the evolutionary increase in proteome complexity. Combining co-occurrence and physical interaction data we argue that the driving force behind domain fusions is a collective effect caused by the number of interactions and not the individual interaction frequency.
Many complex systems can best be analyzed as networks where the basic building blocks of the system are represented as nodes and their interactions as links: Recent studies of systems as disparate as the network of scientific co-authorships, sexual contacts and the World-Wide-Web have revealed unexpected similarities, suggesting that their structure and growth is ruled by a set of generic organizing principles [1, 2]. A variety of biological systems, like food webs and the various biochemical interactions between genes, proteins and metabolites, have been found to exhibit similar large-scale traits [3–6]. The most prominent is the scale-free property of the connectivity distribution. When combined with a modular structure, the resulting network consists of a hierarchy of interwoven clusters [7–10].
Protein crystallography reveals that the fundamental unit of protein structure is the domain. Independent of neighboring sequences, this region of a polypeptide chain folds into a distinct structure and mediates biological functionality . Comparing domain architectures of proteins in multicellular organisms evidence emerged that preexisting domain architectures have predominantly been supplemented with single domains at their terminal sites [12, 13].
Functional links between proteins have also been detected by analyzing the fusion patterns of protein domains. Two separate proteins A and B in one organism may be expressed as a fusion protein in other species. A protein sequence containing both A and B is termed a Rosetta Stone sequence. However, this framework only applies in a minority of cases .
The structure of the protein domain network, where individual domains are nodes and their co-occurrences in a protein are interpreted as links, also displays a scale-free structure [15–17]. Domains that are involved in cell-cell interactions, signal transduction and cell differentiation have been found to accumulate links, reflecting increasing complexity of the organisms specific evolutionary development in going from bacteria to eukaryotes.
In a recent study , we classified yeast proteins as being either globally or locally central according to the number and density of links in their network neighborhoods. In particular, we applied an iterative decomposition method (see Methods) that systematically uncovered core networks with nodes having degrees of at least k. In nesting through the different cores, we gradually defined highly connected proteins in the innermost cores as globally central while we call proteins that have been placed in cores on the periphery locally central. This categorization allowed us to demonstrate that globally central proteins participate in a substantial number of complexes while simultaneously displaying a high level of evolutionary conservation. Here, we apply this core decomposition method to study the properties of the protein domain co-occurrence networks of the eukaryotes S. cerevisiae, C. elegans, D. melanogaster, M. musculus and H. sapiens, allowing us to classify the various domains as either globally or locally central. In going from the single celled Yeast to the considered highly evolved multi cellular organisms we find that the number of globally central domains increases with the organisms level of evolutionary development. Also the overlap network which consists only of the nodes and links shared by all the organisms specific cores reveals those domain fusions that have been preserved through evolution. Comparing the co-occurrence networks to the physical protein domain interaction network of S. cerevisiae [17, 19] we find that links that appear in the innermost cores of the co-occurrence network of higher eukaryotes strongly coincide with physical interactions. The co-occurrences of domains that make them end up in the innermost cores of the co-occurrence networks might represent evolutionary patterns that serve as a putative proteome backbone. Since we find the driving force behind fusion events not to be a high frequency of interactions between a given protein domain pair but a large number of individual interaction partners, we conclude that links appearing in the innermost cores of the co-occurring networks are the result of underlying important domain interactions.
Statistics of domain networks
Table 1 summarizes basic statistics of the domain co-occurrence networks of H. sapiens, M. musculus, C. elegans, D. melanogaster and S. cerevisiae. All the domain co-occurrence networks have a major component containing the vast majority of the nodes, co-existing with many small, connected components. Both the average degree ⟨k⟩ and the clustering coefficients ⟨C⟩ of the networks gradually increase with elevated level of the organisms development. Determining the number of domains N proteins in the proteomes of H. sapiens, M. musculus, C. elegans, D. melanogaster and S. cerevisiae contain, we observe the presence of power-laws in frequency distributions thus obtained, P(N) ~ N-δ(Fig. 1b). This result confirms that the vast majority of proteins contains only a single domain , while a minority accumulates more domains. In Fig. 1c, we find that N shows a positive power-law correlation from the mean number of co-occurring domains – the degree – ⟨k⟩ ~ Nε, suggesting that on average frequently occurring domains are combined with an increasing number of changing partners. All co-occurrence networks display a scale-free degree distribution  (Fig. 1d), as exemplified by the presence of power-laws, P(k) ~ k-θ. Similarly, we find a power-law dependence of the clustering coefficient from the degree exemplified by a generalized Zipf-law ⟨C(k)⟩ = α(β + k)-γ, indicating the network's inherent modularity (Fig. 1e). As summarized in Table 1, the dependence of the power-law exponents in Figs. 1b–e well mirrors the level of an organisms evolutionary development. In particular, the higher the level of the organisms development, the smaller the values we find for δ (Fig. 1b), θ (Fig. 1d) and γ (Fig. 1e). In turn, we find the opposite for ε (Fig. 1c). Obviously, the increase in complexity of the organisms development coincides with an elevated networks heterogeneity. Since we find similar numbers of domains in the higher eukaryotes (Table 1), we assume that an elevated degree of development presumably is increasingly obtained by frequent domain combinations.
Cores of domain networks
Due to the size of the domain co-occurrence networks considered we find different numbers of k-cores. While the networks of H. sapiens and M. musculus are decomposed into 8 nested k-cores, where k = 1, ..., 8 we find 6 k-cores in D. melanogaster and C. elegans (k = 1, ..., 6). There are only 4 in S. cerevisiae (k = 1, ..., 4). The placement of a node in a certain core allows an assessment of its meaning for the topology. A hub – a highly connected node – that is only a member of the peripheral k-cores is defined as locally central, while nodes (not necessarily the biggest hubs of the whole network) being members of the innermost cores are globally central (Fig. 2f). In Table 2, we compiled lists of the highest connected domains in each core layer, being the set of nodes two consecutive cores do not have in common. Notably, the innermost k-core is not populated by the largest hubs, indicating that a high degree alone does not necessarily imply a central placement in the network. In fact, we observe that with even a considerably low degree domains can be placed in the innermost cores.
In Fig. 2a–e we show the two innermost cores of the protein domain networks of S. cerevisiae, C. elegans, D. melanogaster, M. musculus and H. sapiens, respectively. We observe that the increase in the organisms complexity is not only reflected by higher numbers of cores, but the innermost cores differs in size. We find, that H. sapiens has 43 domains in the innermost core, while we find 30 in M. musculus and D. melanogaster, 14 in C. elegans and 5 in S. cerevisiae. Reflecting the increasing evolutionary development of the underlying organism, the cores are enriched with domains predominantly associated with functions such as cell-cell contact and signal transduction. This observation agrees well with the known evolutionary development from the single cellular S. cerevisiae to the multicellular higher eukaryotes. In particular, the innermost core of S. cerevisiae (panel a) consists of the following clique of interconnected domains: (i) pkinase and (ii) pkinaseC which are signal transduction domains, (iii) DAG-PE-bind, a domain which binds Diacyl-glycerol, activating the family of the previously mentioned kinases, (iv) HR1 which is involved in binding the small G-protein rho, and (v) C2, a Ca2+-dependent membrane-targeting module found in many cellular proteins that are involved in both signal transduction and membrane trafficking.
Nesting through the innermost cores of the more evolved organisms, we find that the initial small innermost core of Yeast is enriched with clusters of densely connected domains (Fig. 2b–e). Obviously, this expansion of the innermost core is mostly caused by domains which are involved in signal transduction and cell-cell contacts as well as cell development, suggesting that the demand to maintain a multicellular organism is the driving force for fusing protein domains. In particular, we observe that domains providing these functions, such as PDZ, efhand, SH2 and SH3 to name a few (Fig. 2b–e, Table 2), increasingly populate the innermost cores. However, the affiliation of one domain to a certain core is not inevitably constant. In fact, we observe that pkinaseC which appears in the innermost core of the Yeast domain network occurs in the 2-core of the network of the multicellular organisms. The affiliation of HR1 to the innermost core of Yeast appears to be the effect of a single protein architecture which contains numerous domains, since this particular domain does not appear in the inner cores of the other organisms. Since the majority of Yeast proteins only has one to two domains, being teamed up with a reasonably large number of domains in a given protein is beneficial for a domain to make it to the innermost cores. In multicellular organisms, the number of proteins with a large number of domains increases, inevitably resulting in an inflation of the inner cores. Consequently, the evolutionary significance of a domain is well reflected in its ability to remain present in the inner cores of different organisms.
Domain interaction network
Information about protein domain interactions as of the InterDom database  constitute an undirected network of Yeast protein domain interactions. In contrast to domain co-occurrence networks, each link has a weight which reflects the frequency of the corresponding interactions relative to a random background distribution . The degree distribution of the domain interaction network (Fig. 3a) is well fitted by a generalized Zipf-law P(k) ~ α(β + k)-γ, suggesting that a few ubiquitous domains (hubs) dominate the web of domain interactions. The network's inherent modularity is expressed by the power-law form of the degree dependent clustering coefficient ⟨C(k)⟩ ~ k-δ(Fig. 3a, inset). In order to combine the impact of topology and weights, Barrat et al.  introduced a series of measures that allowed a more significant assessment of the impact weights have on the networks statistical properties. In a weighted representation of a domain interaction network the strength of a domain is the sum of the weights w ij carried on each link, (Note, that the strength s i of a node i is the degree k i if we consider a network where all weights are 1). In the inset of Fig. 3b, we observe that the strength of the average interaction weakly decreases with increasing degree k. Assessing the distribution of weights, we define the average strength per link by . This measure allows us to observe a decreasing trend of s(k) with k (Fig. 3b) as a power-law, suggesting that domains with many interaction partners only occasionally interact with each partner.
How is then the domain interaction network related to the domain co-occurrence network? In each core of the domain co-occurrence networks, we calculated the fraction of links present in the Yeast domain interaction network. Fig. 4a shows these frequencies of links for the eukaryotes S. cerevisiae, C. elegans, D. melangaster, M. musculus and H. sapiens, all displaying a decreasing trend that a fusion is accompanied by the physical interactions of domains when going from the innermost to the outermost core. Calculating the mean strength of domains based on the links that are present in the different cores by superimposing the respective weights w ij from the domain interaction network, we observe an ascending trend when nesting outwards toward the periphery of the domain co-occurrence networks (Fig. 4b). We interpret the observations that (i) domains which appear in the inner cores likely physically interact with (ii) a low average strength as follows: Domains with numerous interaction partners have an elevated chance of being fused in a higher eukaryote, while domains which interact frequently are less likely to be fused. Indeed, the innermost cores display the lowest average strengths, confirming that the driving force behind the fusion of a domain pair is not their frequent interaction, but rather the engagement of the two domains in a multitude of interactions with other domains.
Overlap of domain network cores
Many of the domains appear ubiquitous to the innermost eukaryotic cores of the co-occurrence network (see e.g. Fig. 2). As already mentioned, the evolutionary and functional significance of a domain is indicated by its presence in the innermost cores of many organisms. Similarly, the conservation of links represents an evolutionary and functional signal. So far, it is unclear if links between these globally central domains have been preserved in all the eukaryotes. Fig. 5b–d shows the domain links simultaneously present in the four central cores of S. cerevisiae, C. elegans, D. melanogaster, M. musculus and H. sapiens. Note that all the links in Fig. 5 have been preserved during evolution, suggesting the existence of a deeper reason why these domains seemingly always appear together in proteins. To be more specific: The central core of this domain-overlap network consists of a triangle set up by C2, pkinase and DAG-PE-bind (Fig. 5b, red nodes). Nesting outward through the cores, we find a further accumulation of triangles, all established by such prominent domains as PH, SH3 and RasGEF (Fig. 5b, yellow and red). In the subsequent overlap of cores (Fig 5c and 5d) we observe the presence of the important signaling domains zf-CCCH, zf-C2H2 and zf-C3HC4 from the zinc-finger family. Note that all of the (co-occurrence) links in the overlap networks correspond to physical interactions between the domains, i.e. the fraction of links in the overlap cores that are present in the interaction network is 1.0.
Discussion & conclusions
Although the PFAM database provides comprehensive domain information, it covers only a part of the considered proteomes. Similarly, the determination of putative domain interactions depends on the quality and completeness of the underlying sets of protein interactions. Yet, the heterogeneity of scale-free networks indicates that the general characteristics of domain co-occurrence and interaction networks are independent of the webs actual size . In particular, such networks are governed by the presence of highly connected hubs and cohesive areas, factors that not only influence their integrity but also the determination of k-cores. Since biological networks have been found to be stable upon random perturbations, we expect that the addition of new data will not dramatically impact our findings. The idea of analyzing the protein domain co-occurrence network as a sequence of nested cores and comparing the overlap between the central cores of eukaryotic organisms with increasing level of evolutionary development, gives new and fundamental insights into the qualitative arrangement and evolutionary utilization of the proteome. The evolutionary trend toward multicellularity requires proteomes capable of new and additional complex cellular processes such as signal transduction or cell-cell contacts. On a node based level, this trend toward higher complexity is reflected by an considerable heightened connectivity of domains that support such functions in multicellular organisms . Turning our attention to a link-based level, panels in Fig. 2 suggest an analogous result. The steadily increasing size of the innermost k-cores allows us to observe that the demand of maintaining complex cellular process does not only impact the level of single domains, but also operates on a combinatorial level of domain arrangements. Nevertheless, many protein families involved in inter- and intracellular signaling pathways, apoptosis , development, and immune and neural functions [12, 13], are indeed augmented in H. sapiens relative to D. melanogaster and C. elegans. Although human phenotypic complexity by far exceeds that of D. melanogaster and C. elegans, proteome dimensions remain surprisingly similar, allowing us to conclude that increased functional complexity is not simply a matter of proteome size but strongly underlines the role of innovations on the level of domain (re-) arrangements.
In fact, a significant portion of the protein architecture is found to be homolog in H. sapiens and D. melanogaster while substantial innovation in the creation of new protein architectures also has been detected . The expansion of selected domain families and the accompanying evolution of complex domain architectures by joining presumably pre-existing domains coincides with the increase in the organisms level of evolutionary development. In particular, changes in the domain architectures are the consequence of a cellular mechanism commonly known as 'domain shuffling', appearing in different disguises . In simple cases of creating a new domain architecture, domains are simply inserted in already preexisting domain arrangements, a mechanism known as domain insertion while domain duplication refers to the internal duplication of at least one domain in a gene. Comparing domain architectures of proteins in multicellular organisms evidence emerged that preexisting domain architectures have been supplemented with single domains at their terminal sites, another mechanism that is known as domain accretion . Our results do not favor one mechanism over the other. Yet, the panels in Fig. 2 support the assumption that domain (re-)arrangements massively helped to evolve complex proteomes that are capable to maintain complex cellular processes, that have not been possible with the extension of single protein domain families alone. In the same way, network patterns we obtained from the comparison of cores which appear in all organisms under consideration will not tell us which mechanism predominantly gave rise to their emergence. Yet, we see that such small sized network patterns (see Fig. 5) presumably represent a repository of domain combinations around which the individual proteomes unfolded. These patterns predominately contain domains that play dominant roles in proteins which are essential for the inner workings of a multicellular organism, presumably serving as a possible backbone for the evolution of proteins mainly involved in signal transduction and cell-cell contacts.
The decomposition of the domain co-occurrence networks into k-cores allows us to uncover those sets of domains that are embedded in densely connected areas of the networks. The high connectivity as well as the nature of the partners those domains appear with indicate a central topological and functional role in the proteome of the considered organisms. Nesting toward the innermost cores the significance of these links is supported by the observation that pairs of co-occurring domains increasingly are present as physical interactions in Yeast. Utilizing the combined information of the co-occurrence network and the physical interaction network, we also find that domains tend to interact infrequently if they have many different interaction partners. In contrast, we observe that domains interact increasingly frequently once they have a small number of partners. Although we considered domain fusions on an indirect and qualitative basis this series of observations suggests that the driving force behind domain fusion events is not frequent interactions. In fact, it seems that the number of interactors, the connectivity, of the domains mainly influences a domains propensity to fuse with other interactors. The trend to spatially organize otherwise randomly diffusing domains might help to organize the flow of information in cells. Concluding, we find that domain fusion is a tool to superannuate the random diffusive interaction of a domain pair by embedding them in an architecture which ensures their interactions that would be difficult by random diffusion in a cell alone.
An undirected unweighted network of n nodes is conveniently represented as an symmetric n × n adjacency matrix A = (a ij ), where a ij = 1 if there exists an edge between nodes i and j and a ij = 0 otherwise. In a weighted network, the adjacency matrix reads as A = (a ij w ij ), where w ij represents the weight of edge ij. Consistently, the degree being the number of neighbors a node i has is . As a generalization of a nodes degree the strength s i of a node i is defined as .
Proteome databases and domain co-occurrence network
The Integr8 database [24, 25] provides comprehensive statistical and comparative analyzes of the proteomes of fully sequenced organisms. Every predicted protein is annotated with the domains it contains, utilizing the combined efforts of different domain sequence sources. For our analysis, we focused on the domain data retrieved from the PFAM database, a reliable collection of multiple sequence alignments of protein families and profile hidden Markov models . We construct the protein domain networks by considering all PFAM domains (or nodes) that are co-occurring in a protein to be a fully connected clique of undirected links (see Fig. la). In Integr8 we find 19,061 proteins that have a PFAM annotation in H.sapiens, as well as 18, 953 of M. musculus, 9, 785 of D. melanogaster, 12, 587 of C. elegans and 3, 791 of S. cerevisae. Although domain combinations ij potentially occur repeatedly in a proteome, we assign weight w ij = 1 to every link between domains i and j. Following this procedure, we generated domain networks for the proteomes of H. sapiens, M. musculus, C. elegans, D. melanogaster and S. cerevisiae.
Domain interaction data
The Interdom database [21, 27, 28] provides computationally derived putative domain interactions of Yeast. Based on PFAM domain information  for each set of protein interactions including pairwise protein interactions, protein complexes and Rosetta Stone sequences the presence of potential domain interactions is determined. The occurrence of a domain interaction in each protein interaction set is evaluated by comparing the observed frequencies to a random background model. A score thus obtained reflects the abundance of a particular pair-wise domain interaction, allowing the assessment of the reliability and the significance of the considered domain interaction. Considering these scores as weights w ij of interactions between protein domains ij, we generate an undirected network of 3, 353 domains that are embedded in 28, 339 weighted interactions.
Network degree distribution
The simplest way to characterize a network is by the degree k (or connectivity) of the nodes, reflecting the number of neighbors each node has. Accordingly, we define the average degree of a network as ⟨k⟩ = (1/N) k i , where N is the total number of nodes. Recent studies of biological networks have produced compelling evidence that the network degree distribution – the probability that a node has k neighbors – is scale-free with the functional form P(k) ~ k-γ[1, 9]. An important feature of the power-law distribution is the presence of a minority of nodes, carrying a vast number of connections, called 'hubs'.
Another important feature of biological networks is their tendency to exhibit cohesive areas: The clustering coefficient  of a node i measures the actual number of triangles that node i is a member of, relative to the possible number of triangles. Formally, it is defined as
where n i denotes the number of triangles. Accordingly, we define the average clustering coefficient as ⟨C⟩ = (1/N) C i . The clustering coefficient of a network also carries information about its modular nature, since ⟨C⟩ ~ 1 necessitates the presence of tightly interconnected clusters of nodes. Note that the network has a hierarchical architecture when ⟨C(k)⟩ ~ k-α, allowing the existence of discernible, yet topologically overlapping, functional modules. Apparently, networks with this structure are observed in most types of biological systems where a small subset of hubs play the important role of linking, and hence bridging, the various network modules [9, 32].
The k-core of a graph is defined as the largest subgraph for which every node has at least k links (Fig. 2): For each choice of k, we determine the k-cores by recursively pruning all nodes with degree lower than k and their incident links. In particular, we applied the following recursive algorithm: (1) sort nodes according to their present degree, and (2) remove the nodes with degree lower than k [18, 33, 34]. The layer l k of two consecutive cores k, k + 1 is defined as the set of nodes that both cores do not have in common, i.e. nodes which only occur in the larger core. Since the innermost core does not have a successive core, we define the innermost core to be equivalent to a layer.
Albert R, Barabási AL: Statistical mechanics of complex networks. Rev Mod Phys. 2002, 74: 47-10.1103/RevModPhys.74.47.
Barabási A, Albert R: Emergence of Scaling in Random Networks. Science. 1999, 286: 509-512. 10.1126/science.286.5439.509.
Jeong H, Tombor B, Albert R, Oltvai Z, Barabási AL: The large-scale organization of metabolic networks. Nature. 2000, 407: 651-654. 10.1038/35036627.
Fell D, Wagner A: The small world of metabolism. Nature Biotech. 2000, 189: 1121-1122. 10.1038/81025.
Wagner A, Fell DA: The small world inside large metabolic networks. Proc Roy Soc London Series B. 2001, 268: 1803-1810. 10.1098/rspb.2001.1711.
Wuchty S: Small-Worlds in RNA. Nucl Acids Res. 2003, 31: 1108-1117. 10.1093/nar/gkg162.
Ravasz E, Somera A, Mongru D, Oltvai Z, Barabaśi A: Hierarchical organization of modularity in metabolic networks. Science. 2002, 297: 1551-1555. 10.1126/science.1073374.
Holme P, Huss M, Jeong H: Subnetwork hierarchies in biochemical pathways. Bioinformatics. 2003, 19 (4): 532-538. 10.1093/bioinformatics/btg033.
Barabaśi A, Oltvai Z: Network Biology: Understanding the Cell's Functional Organization. Nature Rev Gen. 2004, 101-113. 10.1038/nrg1272. 5
Rives A, Galitski T: Modular organisation of cellular networks. Proc Nail Acad Sci USA. 2003, 100: 1128-1133. 10.1073/pnas.0237338100.
Janin J, Chothia C: Domains in proteins: definitions, location, and structural principles. Methods Enzym. 1985, 115: 420-430.
International Human Genome Sequencing Consortium: Initial sequencing and analysis of the human genome. Nature. 2001, 409: 860-921. 10.1038/35057062.
Venter J, Adams M, Myers E, (271 co-authors): The sequence of the Human Genome. Science. 2001, 291: 1304-1351. 10.1126/science.1058040.
Marcotte E, Pellegrini M, Ng HL, Rice D, Yeates T, Eisenberg D: Detecting Protein Function and Protein-Protein Interactions from Genom Sequences. Science. 1999, 285: 751-753. 10.1126/science.285.5428.751.
Wuchty S: Scale-Free Behavior in Protein Domain Networks. Mol Biol Evol. 2001, 18: 1694-1702.
Apic G, Gough J, Teichmann S: Domain Combinations in Archaeal, Eubacterial and Eukaryotic Proteomes. J Mol Biol. 2001, 310 (2): 311-325. 10.1006/jmbi.2001.4776.
Wuchty S: Interaction and Domain Networks of Yeast. Proteomics. 2002, 2: 1715-1723. 10.1002/1615-9861(200212)2:12<1715::AID-PROT1715>3.0.CO;2-O.
Wuchty S, Almaas E: Peeling the Yeast Interaction Network. Proteomics. 2004,
Park J, Lappe M, Teichmann A: Mapping Protein Family Interations: Intramolecular and Intermolecular Protein Family Interaction Repertoires in the PDB and Yeast. J Mol Biol. 2001, 307: 929-938. 10.1006/jmbi.2001.4526.
Doolittle R: The Multiplicity of Domains in Proteins. Ann Rev Biochem. 1995, 64: 287-314. 10.1146/annurev.bi.64.070195.001443.
Ng S, Zhang Z, Tan S, Lin K: InterDom: a database of putative interacting protein domains for validating predicted protein interactions and complexes. Nucl Acids Res. 2003, 31: 251-254. 10.1093/nar/gkg079.
Barrat A, Barthélemy M, Pastor-Satorras R, Vespignani A: The architecture of complex weighted networks. Proc Natl Acad Sci USA. 2004, 101 (11): 3747-3752. 10.1073/pnas.0400087101.
Aravind L, Dixit V, Koonin E: Apoptotic Molecular Machinery: Vastly Increased Complexity in Vertebrates Revealed by Genome Comparisons. Science. 2001, 291: 1279-1284. 10.1126/science.291.5507.1279.
Pruess M, Fleischmann W, Kanapin A, Karavidopoulou Y, Kersey P, Kriventseva E, Mittard V, Mulder N, Phan I, Servant F, Apweiler R: The Proteome Analysis database: a tool for the in silico analysis of whole proteomes. Nucl Acids Res. 2003, 31: 414-417. 10.1093/nar/gkg105.
Integr8 proteome database. [http://www.ebi.ac.uk/integr8]
Bateman A, Coin L, Durbin R, Finn R, Hollich V, Griffiths-Jones S, Khanna A, Marshall M, Moxon S, Sonnhammer E, Studholme D, Yeats C, Eddy S: The Pfam protein families database. Nucl Acids Res. 2004, 32: D138-D141. 10.1093/nar/gkh121.
Ng S, Zhang Z, Tan S: Integrative approach for Computationally Inferring Protein Domain Interactions. Bioinformatics. 2003, 19 (8): 923-929. 10.1093/bioinformatics/btg118.
Interdom database of interacting domains. [http://interdom.lit.org.sg]
Jeong H, Mason S, Barabási AL, Oltvai Z: Lethality and centrality in protein networks. Nature. 2001, 411: 41-42. 10.1038/35075138.
Wuchty S: Topology and Evolution in Yeast Interaction Networks. Genome Res. 2004, 14: 1310-1314. 10.1101/gr.2300204.
Watts DJ, Strogatz SH: Collective dynamics of small-world networks. Nature. 1998, 393: 440-442. 10.1038/30918.
Han J, Bertin N, Hao T, Goldberg DS, Berriz G, Zhang L, Dupuy D, Walhout A, Cusick M, Roth F, Vidal M: Evidence for dynamically organized modularity in the yeast protein-protein interaction network. Nature. 2004, 430: 88-93. 10.1038/nature02555.
Seidman S: Network Structure And Minimum Degree. Social Networks. 1983, 5: 269-287. 10.1016/0378-8733(83)90028-X.
Batagelj V, Zaveršnik M: An O(m) Algorithm for Cores Decomposition of Networks. University of Ljubljana, preprint series. 2002, 40: 799-[http://vlado.fmf.uni-lj.si/pub/preprint/imfm0798.pdf]
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Wuchty, S., Almaas, E. Evolutionary cores of domain co-occurrence networks. BMC Evol Biol 5, 24 (2005). https://doi.org/10.1186/1471-2148-5-24