Skip to main content

Modular architecture of protein structures and allosteric communications: potential implications for signaling proteins and regulatory linkages

Abstract

Background

Allosteric communications are vital for cellular signaling. Here we explore a relationship between protein architectural organization and shortcuts in signaling pathways.

Results

We show that protein domains consist of modules interconnected by residues that mediate signaling through the shortest pathways. These mediating residues tend to be located at the inter-modular boundaries, which are more rigid and display a larger number of long-range interactions than intra-modular regions. The inter-modular boundaries contain most of the residues centrally conserved in the protein fold, which may be crucial for information transfer between amino acids. Our approach to modular decomposition relies on a representation of protein structures as residue-interacting networks, and removal of the most central residue contacts, which are assumed to be crucial for allosteric communications. The modular decomposition of 100 multi-domain protein structures indicates that modules constitute the building blocks of domains. The analysis of 13 allosteric proteins revealed that modules characterize experimentally identified functional regions. Based on the study of an additional functionally annotated dataset of 115 proteins, we propose that high-modularity modules include functional sites and are the basic functional units. We provide examples (the Gα s subunit and P450 cytochromes) to illustrate that the modular architecture of active sites is linked to their functional specialization.

Conclusion

Our method decomposes protein structures into modules, allowing the study of signal transmission between functional sites. A modular configuration might be advantageous: it allows signaling proteins to expand their regulatory linkages and may elicit a broader range of control mechanisms either via modular combinations or through modulation of inter-modular linkages.

Background

Allosteric communications play crucial roles in many cellular signaling processes. Perturbations caused by factors such as ligand binding at one functional site affect a distant site, thereby regulating binding affinity and catalytic activity [1, 2]. Since the allosteric model proposed by Monod and coworkers [1], decades of research have extended the common view of allostery associated with multi-domain proteins to single domain proteins. The allosteric behavior displayed by single domain proteins, such as myoglobin [3], called into question the existing allosteric dogma. In the 'new view' of protein allostery, all proteins are potentially allosteric when thought of in terms of population redistribution upon ligand binding causing conformational change in a second binding site [1].

Dynamic models have been proposed to explain the conformational changes involved in signal transmission between functional sites [4, 5]. In particular, the role of the pre-existing equilibrium of conformational sub-states in allostery proposed already over 20 years ago [6] is increasingly receiving attention, emphasizing the key role of protein dynamics in this process [1, 7–9]. Although experimental methods such as double mutant cycle analysis [10] have provided insights into allosteric communications, understanding the general principles of the transmission of information between distant functional surfaces remains a challenge in structural biology. Several theoretical methods based on sequence and structural considerations have been proposed for the identification of key amino acids for long-range communications [11–13]. Among these, an interesting sequence-based approach has been proposed by Ranganathan and coworkers [14, 15] for estimating the thermodynamic coupling between amino acids in several examples of protein families. Recently, we introduced a model based on a network representation of protein structures. The model allows us to determine fold centrally conserved residues (FCCRs). These residues are responsible for maintaining the shortest pathways between all amino acids and, thus, play key roles in signal transmission [13]. Analysis of several protein families showed an agreement between our results and experimental data, illustrating the importance of protein topology in network communications. Perceiving protein structures as information processing networks, it is reasonable to assume that mutations of amino acids crucial for network communications could impair signal transmission.

The rationale for modular organization of proteins in allosteric behavior has been discussed previously [16–18]. Modular domains can act cooperatively, leading to new input (and output) relationships. The Src family proteins constitute a clear example of this modular architecture: these proteins contain amino-terminal SH3 and SH2 domains, which flank a kinase domain by intra-molecular SH3-binding and SH2-binding sites [16]. It is further known that modular functional units display certain degrees of functional specificity in a number of proteins. In several cases of protein-protein interactions, which are involved in cell signaling, some parts of the interacting interface participate in the information transfer, whereas other interacting regions appear to contribute solely to binding affinity [19]. Examples of proteins exhibiting this binding site modular configuration include Myosin, C5a receptor, and the protein kinase R activator PACT among others [19]. Here, we aim to obtain the modular decomposition of allosteric proteins and to explore a relationship between the modules and the allosteric activity. We expect that such a relationship, if it exists, would lead to deeper insight into functional mechanisms. We develop a new approach for decomposing protein structures into modules using their residue network representations. Our methodology is based on the edge-betweenness clustering algorithm proposed by Newman and Girvan [20, 21], which has been previously applied to a wide variety of problems [22–25]. This method uses edge centrality to detect module boundaries and finds the assignation of nodes into modules [20].

The small-world topology of protein structures suggests that the key amino acids for signal transmission should lie in the shortcuts linking different regions of the structure. The removal of the most central contacts forming these shortcuts divides the structure into modules. We characterize these modules from a structural point of view. Our results, derived from a non-redundant dataset of multi-domain proteins, reveal that, in the vast majority of the cases, modules tend to be located within rather than across domains. Therefore, modules can be considered as sub-domains. Further analysis shows that the percentage of long-range interactions at the modular boundaries is much higher than that in non-boundary regions. Residues forming inter-modular contacts fluctuate less than those participating only in the intra-modular interactions. One possible explanation of this finding is that most central residues, which have been shown to be important for the allosteric communications, are located at the inter-modular interfaces and, therefore, tend to be more rigid to maintain their contacts. Inspection of 13 allosteric proteins shows that functionally annotated regions exhibit a modular architecture, with modules interconnected by FCCRs, which are responsible for mediating the shortest pathways between all amino acids and, thus, play crucial roles in allosteric communications [13]. Functional sites are often contained in one module; however, there are also examples of functional sites shared by two or more modules. Some of these cases correspond to binding sites divided into two modules belonging to different domains. The Gα s subunit and P450 cytochromes are examples of functional sites shared between modules. Interestingly, the modular decomposition of the Gα s subunit reflects binding site partitioning into regions involved in different sub-functional specialization, general binding and information transfer regions [26]. The P450eryF active site is divided into a module containing the ligand-binding site, and a module comprising the effector-binding site, whereas the P450cam substrate binds to one module, and the product binds mainly to another module. A detailed analysis of a large dataset of proteins with functional annotations revealed that modules exhibiting high modularity tend to include functional sites.

Our results lead us to propose that the modular architecture of protein structures yields a more efficient performance of the functional activity. Modules may possess certain functional independence; and, they are interconnected through amino acids previously shown to mediate signaling in proteins. Modules consist of groups of highly cooperative residues. Evolution has organized proteins as systems consisting of modules linked by amino acids that maintain the shortest pathways between all amino acids and are, thus, crucial for signal transmission, leading to robust and efficient communication networks. This organization is advantageous and, as such, has been conserved by evolution.

Results and discussion

Here we propose a novel way to decompose protein structures into modules based on their representation as residue interacting networks (see Materials and methods). Our approach relies on the edge-betweenness clustering algorithm presented by Newman and Girvan [20, 21]. Modular decomposition allows us to identify functionally important regions in proteins.

Structural properties of modules

We carried out the modular decomposition of protein structures of a non-redundant dataset of 100 multi-domain proteins (described in Materials and methods). Results show that the majority of the modules have most of their residues in one domain (Figure 1). That is, modules tend to be located within rather than across domains, and hence may be considered as sub-domains. Comparison of contacts between amino acids belonging to different modules (inter-modular contacts) and those between amino acids belonging to the same module (intra-modular contacts) revealed that the percentage of long-range interactions is larger in the inter-modular contacts (Figure 2). This finding is in agreement with the rationale that long-range interactions often mediate the shortest pathways between most residues in the protein.

Figure 1
figure 1

Mapping of modules into domains for the dataset of multi-domain proteins. The abscissa axis shows the percentage of a module contained in one domain. The bars indicate the percentage of all modules corresponding to each interval of the abscissa axis.

Figure 2
figure 2

Percentage of long-range interactions for each protein of the multi-domain protein dataset. The interactions were calculated separately for the set of the inter-modular residues and for the set of intra-modular residues. The ordinate axis shows the percentage of long-range interactions for the inter-modular interfaces (in red) and for the intra-modular regions (in blue).

A detailed analysis of 115 proteins (described in Materials and methods) with available structures in different conformational states and temperature B-factors showed that residues with inter-modular contacts fluctuate less than those forming exclusively intra-modular contacts. Figure 3 clearly illustrates this situation: the normalized root mean square deviation (RMSD) values and the B-factors of the residues involved in inter-modular interactions tend to be lowerthan those of the residues involved in intra-modular interactions. This result could suggest that intra-modular regions, which include most of the protein or ligand binding sites, absorb conformational changes due to perturbations. In contrast, the boundaries between modules are more rigid, allowing them to maintain key residue contacts for the integration and transmission of the information between modules.

Figure 3
figure 3

Modular flexibility for each protein of the dataset of proteins with conformers. (a) Averages of normalized residue temperature B-factors for inter-modular residues (red) and intra-modular residues (blue) for each protein. (b) Averages of normalized residue RMSDs for inter-modular residues (red) and intra-modular residues (blue) for each protein.

Modularity of protein function

The modular decomposition of protein structures provides information about functional sites and signal transmission. We selected a dataset of 13 allosteric proteins based on previously analyzed examples [13] and new examples with experimental information. A detailed study of these proteins revealed that many modules contain functional regions, which are interconnected by residues mediating the shortest pathways between most amino acids in the structure (FCCRs). A majority (72%) of the FCCRs connect modules (Additional data file 1). Table 1 summarizes the analyzed examples, including the assignment of functional sites to modules (detailed information is provided in Table 3 of Additional data file 1).

Table 1 Modular division and FCCRs connecting functional modules for the studied allosteric proteins

Modular division of functional sites

Functional sites can be decomposed into modules. In some cases, the modules are located in different domains. An illustrative example of this situation is the pyruvate kinase (PDB ID 1liu, chain A). The catalytic site is divided into two modules belonging to different domains and exhibiting different degrees of flexibility [27] (Table 1). In other examples, the functional site is contained in one domain and is divided into two or more modules. Such is the case of tyrosine phosphatase 1B (PDB ID 1pty), with the catalytic residues located in two modules. One of these modules comprises a loop, whose flexibility is important for the transition from the open to the closed conformation [28] (Table 1). The Gα s subunit and Cytochrome P450eryF and P450cam examples are discussed in detail below.

Guanine nucleotide-binding protein G(s) subunit alpha (Bos Taurus)

A well-studied example of signal transmission is the regulation of adenylyl cyclase by the Gα s subunit [19, 29]. It is known that the Gα s subunit undergoes significant conformational changes upon exchange of GDP by GTP, affecting its affinity for adenylyl cyclase [29]. It has been experimentally verified that the Gα s subunit involves three main regions for its interaction with this enzyme effector - the switch I and switch II regions and the α 3-β5 loop [26]. Although the Gα s subunit activation of adenylyl cyclase is a complex process, experimental results indicate that the switch I and switch II regions, which display conformational flexibility, mainly mediate information transfer, whereas the α 3-β5 loop is solely involved in the ligand binding affinity [26]. Interestingly, the modular decomposition of the Gα s subunit (1azs, chain C) shows that the adenylyl cyclase-binding site is divided into two modules: one of the modules contains the switch I and switch II regions and the other module comprises the α 3-β5 loop (Figure 4). Thus, in this example we find a correspondence between the modular decomposition of the binding site and its partition into signal-transfer and general binding regions.

Figure 4
figure 4

Binding site of the G-protein α s subunit (PDB ID 1azs) divided into two modules. This division coincides with the specialized regions of this binding site for ligand binding only (pink module) and ligand binding and information transfer (blue module). The binding site residues are depicted in spacefill. Modular regions not involved in the binding site are depicted in green.

Cytochromes P450

P450eryF (Saccharopolyspora erythraea)

P450eryF, a cytochrome P450 involved in erythromycin biosynthesis, exhibits no cooperativity with its natural substrate 6-deoxyerythronolide, while showing sigmoidal substrate saturation curves with other smaller substrates [30]. The presence of multiple binding sites within the same binding pocket is believed to be a primary cause of allostery in cytochromes P450 [31]. Since P450eryF has a large active site, it is assumed that P450eryF is capable of binding the large substrates of the mammalian P450s [32]. X-ray crystallographic studies and other experimental results indicate that two androstenediones are simultaneously present in the active site, interacting with each other, and, therefore, exhibiting a certain degree of homotropic cooperativity [32]. Binding of one androstenedion (Andro2) induces conformational changes in the active site and increases its hydrophobicity, resulting in increased binding affinity to the other androstenedion (Andro1) [32]. The modular decomposition of this protein indicates that the two modules share the active site. Each of these modules contains one of the two androstenedion-binding sites (Figure 5a).

Figure 5
figure 5

Modular division of the Cytochromes binding sites. (a) Modular division of the Cytochrome P450eryF (PDB ID 1eup) binding site. Two androstenedione molecules (Andro1 and Andro2 colored in blue and purple, respectively) are bound to the protein. The binding site (in spacefill) for the androstenedione is divided into two modules (highlighted in red and yellow) corresponding to the binding area for each of these two molecules. Modular regions not involved in the binding site are depicted in green. (b) Modular division of the Cytochrome P450cam (PDB ID 1noo) binding site. Two camphor molecules (camphor and 5-exo-OH camphor) can bind to the protein. The binding site (in spacefill) for the camphor is highlighted in yellow and orange. The binding site (in spacefill) for the 5-exo-OH camphor is highlighted in red and orange. Residues in orange are the ones that can bind both camphor and hydroxycamphor. Catalytic residues (in spacefill) are highlighted in light blue and purple. The ones in purple can also bind hydroxycamphor. The residues forming each of the four modular regions (and not involved in any of the functions previously described) are depicted in magenta, blue, green and brown.

P450cam (Pseudomonas putida)

The camphor monoxygenase P450cam catalyzes the 5-exo hydroxylation of camphor [33]. Its active site may be considered to have two functionally different subsites: the substrate binding region (site I) and the L6 position of the iron to which oxygen binds upon reduction (site II) [33]. Allosteric interactions between these subsites are reflected in the fact that site I binding can inhibit site II ligation and vice versa. Furthermore, the presence of the product 5-exo-OH camphor inhibits binding of the substrate camphor (and vice versa) [33]. The modular decomposition of the P450cam structure (PDB ID 1noo) shows that the substrate (camphor) and product (5-exo-OH camphor) binding sites are mainly located in different modules, sharing common central residues, which are likely to be important for the allosteric communication between these sites. Figure 5b shows that residues comprising the 5-exo-OH camphor binding site tend to be located closest to the heme central ion, whereas amino acids forming the camphor binding site tend to be positioned distal from the heme group.

These examples suggest that the modular design of functional sites might be related to their sub-functional specialization. Each module contains a portion of the active site and is mainly involved in a specific sub-function, such as the binding of the substrate, the product or an allosteric ligand.

Modularity and functional significance of modules

Analysis of the previously studied dataset of 115 proteins with functional site annotations (described in Materials and methods) indicates that modules exhibiting high modularity values tend to comprise functional sites. The analysis of all modules illustrates that a large percentage of modules comprising functional regions exhibit above average modularity values (Figure 6a). Figure 6b clearly illustrates that there is a correlation between the percentages of functional modules and the modularity values.

Figure 6
figure 6

Relationship between functionally annotated modules and modularity. (a) Z-score distribution of the modularity values for functional modules. The abscissa axis represents the Z-score modularity values calculated for all modules. The vertical line at Z-score = 0 represents the averaged modularity of all modules. The bars stand for the number of functional modules for each Z-score interval shown in the abscissa. (b) Distribution of modularity values for functional modules. The abscissa axis shows the different intervals of modularity. The bars represent the percentage of functional modules for each interval of modularity. The number of functional modules for each range of modularity is indicated at the top of the graph.

Conclusion

In signaling proteins, modular domains can act as switches mediating activation, repression and integration of diverse input functions. Experimental studies confirm that inter-domain linker regions are crucial for the domain coupling required for the information transfer [16]. Our approach decomposes protein structures into modules, allowing us to study functional sites linked by signal transmission. To detect module peripheries, we rely on the identification and removal of the most central residue contacts, assuming that the interactions of these amino acids are crucial for information transfer. Our results show that modules, which often characterize functional sites, can be considered as building blocks of protein domains. Hence, the question arises, how is the transmission between distinct modules achieved? Although a very complex process, which is not fully understood, our findings suggest that inter-modular boundaries are essential for integrating and transmitting the information between functional regions. The majority of the fold centrally conserved residues, recently shown to play a key role in signal transmission by maintaining the short path lengths between all residues in the structure [12], are those responsible for the inter-modular interactions. Furthermore, boundary residues are rigid, sustaining key amino acid interactions for the communication between modules. On the other hand, intra-modular regions, which include most of the protein or ligand binding sites, form a flexible cushion. Most of the inter-modular residue interactions form long-range contacts, which are predominantly involved in mediating signaling. A detailed study of 13 allosteric proteins showed that functional sites are often contained within one module. However, there are cases of active sites divided into two or more modules. The analysis of the Gα s subunit and of Cytochromes P450eryF and P450cam illustrate that the modular architecture of the active site may relate to its sub-functions. Modules containing functional sites display high modularity, suggesting that modularity can be used to identify functional modules.

To conclude, our approach decomposes protein domains into modules. Mapping annotated functional regions onto the decomposed structures illustrates that the modules characterize functional sites. We observe that most inter-modular boundary residues provide the shortcuts in the communication wires. These residues maintain the shortest pathways between all amino acids, leading to robust and efficient signal transmission communication networks. Functional specificity and regulation relies on the communication between modules. This advantageous organization has been conserved by evolution. Furthermore, due to the possible functional independence of modules, changes in boundary residues may lead to new functions or to functional alterations as might be needed in a changing environment. Therefore, a modular configuration might allow signaling proteins to increase their regulatory links, and to expand the range of control mechanisms either via new modular combinations or through modulation of inter-modular linkages. Since our results indicate that boundary residues are crucial in efficient short communication pathways, both mechanisms appear possible.

Materials and methods

Protein datasets

A non-redundant dataset of 100 multi-domain proteins was selected from NCBI [34]. The domain information was extracted from the CATH database [35, 36]. This dataset was used to analyze the distribution of protein modules into domains and to calculate the distribution of the long-range interactions at the inter-modular interfaces and in the intra-modular regions. Using the definition of Green and Higman [37], we considered the interactions as long range if they occur between amino acid residues that are ten or more residues apart in the sequence. While residues close in sequence are close in space, we adopt this standard notation, which has been used in numerous studies. The analyses of flexibility and modularity of modules were based on a different dataset of 115 proteins with conformers. This dataset was compiled using the database of macromolecular movements: [38–40] undergoing distinct molecular motions. Only conformers with more than 60% sequence identity were chosen. The annotations of functional sites were taken from PDBsum [41, 42]. We annotated a module as functional if more than 30% of its residues belong to a functional site. We selected 13 examples of proteins displaying allosteric activities with existing PDB structures. All protein structure images were created using DS ViewerPro 6.0 [43].

Network analysis of protein structures

Each protein structure was modeled as an undirected graph, where amino acid residues corresponded to vertices, and their contacts were represented as edges. Residues i and j were considered to be in contact if at least one atom corresponding to residue i was at a distance of less than or equal to 5.0 Ã… from an atom from residue j. This value approximates the upper limit for attractive London-van-der-Waals forces [12, 37].

FCCRs were calculated as in del Sol et al. [13]. Protein networks were decomposed into modules using the edge-betweenness clustering algorithm of Girvan and Newman [21] based on the iterative removal of the highest betweenness edges. We used the parallel implementation PEBC (parallel edge betweenness clustering) [44] of the Girvan and Newman algorithm. We modified the program to obtain the modular decomposition after removing 80% of the network edges. This cutoff was obtained empirically for optimizing the correspondence in the mapping of functional sites into modules. Based on the expression of network modularity introduced by Guimerà and Nunes Amaral [45], we defined the modularity of protein modules Q m as follows:

Q m = l m L − ( d m 2 L ) 2 MathType@MTEF@5@5@+=feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2Caerbhv2BYDwAHbqedmvETj2BSbqee0evGueE0jxyaibaiKI8=vI8tuQ8FMI8Gi=hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqai=hGuQ8kuc9pgc9s8qqaq=dirpe0xb9q8qiLsFr0=vr0=vr0dc8meaabaqaciGacaGaaeqabaqadeqadaaakeaacaWGrbWaaSbaaSqaaiaad2gaaeqaaOGaeyypa0ZaaSaaaeaacaWGSbWaaSbaaSqaaiaad2gaaeqaaaGcbaGaamitaaaacqGHsisldaqadaqaamaalaaabaGaamizamaaBaaaleaacaWGTbaabeaaaOqaaiaaikdacaWGmbaaaaGaayjkaiaawMcaamaaCaaaleqabaGaaGOmaaaaaaa@4038@

where L is the number of edges in the network, l m is the number of edges between nodes in module m, and d m is the sum of the degrees of the nodes in module m. The rationale for this modularity measure is as follows: modules with high modularity values must contain many within module links and as few as possible between-module links. The equation above imposes Q m = 0 in cases when the module comprises the whole network or if nodes are placed randomly into modules.

Protein flexibility analysis

The analysis was carried out over the dataset of 115 proteins with conformers in two ways. We first calculated the averaged main chain residue RMSD considering all pairs of structurally aligned conformers. The structural alignments were obtained using MultiProt [46, 47]. We also calculated the main chain temperature B-factor of each residue. The normalizations of the RMSDs and B-factors were calculated using the standard definition of the Z-score values.

Additional data files

The following additional data are available with the online version of this paper. Additional data file 1 contains figures with additional examples of protein modularity and tables with the data sets used for the analyses.

References

  1. Gunasekaran K, Ma B, Nussinov R: Is allostery an intrinsic property of all dynamic proteins?. Proteins. 2004, 57: 433-443. 10.1002/prot.20232.

    Article  PubMed  CAS  Google Scholar 

  2. Changeux JP, Edelstein SJ: Allosteric mechanisms of signal transduction. Science. 2005, 308: 1424-1428. 10.1126/science.1108595.

    Article  PubMed  CAS  Google Scholar 

  3. Frauenfelder H, McMahon BH, Fenimore PW: Myoglobin: the hydrogen atom of biology and a paradigm of complexity. Proc Natl Acad Sci USA. 2003, 100: 8615-8617. 10.1073/pnas.1633688100.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  4. Xu C, Tobi D, Bahar I: Allosteric changes in protein structure computed by a simple mechanical model: hemoglobin T↔R2 transition. J Mol Biol. 2003, 333: 153-168. 10.1016/j.jmb.2003.08.027.

    Article  PubMed  CAS  Google Scholar 

  5. Hawkins RH, McLeish TCB: Coupling of global and local vibrational modes in dynamic allostery of proteins. Biophys J. 2006, 91: 2055-2062. 10.1529/biophysj.106.082180.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  6. Monod J, Wyman J, Changeux JP: On the nature of allosteric transitions: a plausible model. J Mol Biol. 1965, 12: 88-118.

    Article  PubMed  CAS  Google Scholar 

  7. Swain JF, Gierasch LM: The changing landscape of protein allostery. Curr Opin Struct Biol. 2006, 16: 102-108. 10.1016/j.sbi.2006.01.003.

    Article  PubMed  CAS  Google Scholar 

  8. Kern D, Zuiderweg ERP: The role of dynamics in allosteric regulation. Curr Opin Struct Biol. 2003, 13: 748-757. 10.1016/j.sbi.2003.10.008.

    Article  PubMed  CAS  Google Scholar 

  9. Popovych N, Sun Sh, Ebright RH, Kalodimos ChG: Dynamically driven protein allostery. Nat Struct Mol Biol. 2006, 13: 831-838. 10.1038/nsmb1132.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  10. Aharoni A, Horovitz A: Detection of changes in pairwise interactions during allosteric transitions: coupling between local and global conformational changes in GroEL. Proc Natl Acad Sci USA. 1997, 94: 1698-1702. 10.1073/pnas.94.5.1698.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  11. Kass I, Horovitz A: Mapping pathways of allosteric communication in GroEl by analysis of correlated mutations. Proteins. 2002, 48: 611-617. 10.1002/prot.10180.

    Article  PubMed  CAS  Google Scholar 

  12. Fodor AA, Aldrich RW: On evolutionary conservation of thermodynamic coupling in proteins. J Biol Chem. 2004, 279: 19046-19050. 10.1074/jbc.M402560200.

    Article  PubMed  CAS  Google Scholar 

  13. del Sol A, Fujihashi H, Amoros D, Nussinov R: Residues crucial formaintaining short paths in network communication mediate signaling in proteins. Mol Syst Biol. 2006, 2: 2006.0019-10.1038/msb4100063. doi:10.1038/msb4100063

    Article  PubMed  PubMed Central  Google Scholar 

  14. Lockless SW, Ranganathan R: Evolutionarily conserved pathways of energetic connectivity in protein families. Science. 1999, 286: 295-299. 10.1126/science.286.5438.295.

    Article  PubMed  CAS  Google Scholar 

  15. Süel GM, Lockless SW, Wall MA, Ranganathan R: Evolutionary conserved networks of residues mediate allosteric communication in proteins. Nat Struct Biol. 2002, 10: 59-69. 10.1038/nsb881.

    Article  Google Scholar 

  16. Lim WA: The modular logic of signaling proteins: building allosteric switches from simple binding domains. Curr Opin Struct Biol. 2002, 12: 61-68. 10.1016/S0959-440X(02)00290-7.

    Article  PubMed  CAS  Google Scholar 

  17. Dueber JE, Yeh BJ, Chak K, Lim WA: Reprogramming control of an allosteric signaling switch trough modular recombination. Science. 2003, 301: 1904-1908. 10.1126/science.1085945.

    Article  PubMed  CAS  Google Scholar 

  18. Dueber JE, Yeh BJ, Bhattacharyya RP, Lim WA: Rewiring cell signaling: the logic and plasticity of eukaryotic protein circuitry. Curr Opin Struct Biol. 2004, 14: 690-699. 10.1016/j.sbi.2004.10.004.

    Article  PubMed  CAS  Google Scholar 

  19. Buck E, Iyengar R: Organization and functions of interacting domains for signaling by protein-protein interactions. Sci STKE. 2003, 2003: re14-

    PubMed  Google Scholar 

  20. Newman MEJ, Girvan M: Finding and evaluating community structure in networks. Phys Rev E. 2004, 69: 026113-10.1103/PhysRevE.69.026113.

    Article  CAS  Google Scholar 

  21. Girvan M, Newman MEJ: Community structure in social and biological networks. Proc Natl Acad Sci USA. 2002, 99: 7821-7826. 10.1073/pnas.122653799.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  22. Dunn R, Dudbridge F, Sanderson CM: The use of edge-betweenness clustering to investigate biological function in protein interaction networks. BMC Bioinformatics. 2005, 6: 39-10.1186/1471-2105-6-39.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Holme P, Huss M, Jeong H: Subnetwork hierarchies of biochemical pathways. Bioinformatics. 2003, 19: 532-538. 10.1093/bioinformatics/btg033.

    Article  PubMed  CAS  Google Scholar 

  24. Newman MEJ: Detecting community structure in networks. Eur Phys J B. 2004, 38: 321-330. 10.1140/epjb/e2004-00124-y.

    Article  CAS  Google Scholar 

  25. Kashtan N, Alon U: Spontaneous evolution of modularity and network motifs. Proc Natl Acad Sci USA. 2005, 102: 13773-13778. 10.1073/pnas.0503610102.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  26. Chen Y, Yoo B, Lee JB, Weng G, Iyengar R: The signal transfer regions of Gαs. J Biol Chem. 2001, 276: 45751-45754. 10.1074/jbc.M107191200.

    Article  PubMed  CAS  Google Scholar 

  27. Fenton AW, Blair JB: Kinetic and allosteric consequences of mutations in the subunit and domain interfaces and the allosteric site of yeast pyruvate kinase. Arch Biochem Biophys. 2002, 397: 28-39. 10.1006/abbi.2001.2634.

    Article  PubMed  CAS  Google Scholar 

  28. Wiesmann C, Barr KJ, Kung J, Zhu J, Erlanson DA, Shen W, Fahr BJ, Zhong M, Taylor L, Randal M, et al: Allosteric inhibition of protein tyrosine phosphatase 1B. Nat Struct Mol Biol. 2004, 11: 730-737. 10.1038/nsmb803.

    Article  PubMed  CAS  Google Scholar 

  29. Grishina G, Berlot CH: Identification of common and distinct residues involved in the interaction of αi2 and αs with adenylyl cyclase. J Biol Chem. 1997, 272: 20619-20626. 10.1074/jbc.272.33.20619.

    Article  PubMed  CAS  Google Scholar 

  30. Davydov DR, Botchkareva AE, Kumar S, He YQ, Halpert JR: An electrostatic driven conformational transition is involved in the mechanism of substrate binding in cytochrome P450eryF. Biochemistry. 2004, 43: 6475-6485. 10.1021/bi036260l.

    Article  PubMed  CAS  Google Scholar 

  31. Khan KK, He YA, He YQ, Halpert JR: Site-directed mutagenesis of cytochrome P450eryF: implications for substrate oxidation, cooperativity, and topology of the active site. Chem Res Toxicol. 2002, 15: 843-853. 10.1021/tx025539k.

    Article  PubMed  CAS  Google Scholar 

  32. Cupp-Vickery J, Anderson R, Hatziris Z: Crystal structures of ligand complexes of P450eryF exhibiting homotropic cooperativity. Proc Natl Acad Sci USA. 2000, 97: 3050-3055. 10.1073/pnas.050406897.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  33. Narasimhulu S: Differential behavior of the sub-sites of cytochrome 450 active site in binding of substrates, and products (implications for coupling/uncoupling). Biochim Biophys Acta. 2007, 1770: 360-375.

    Article  PubMed  CAS  Google Scholar 

  34. National Center for Biotechnology Information. [http://www.ncbi.nlm.nih.gov]

  35. Orengo CA, Michie AD, Jones S, Jones DT, Swindells MB, Thornton JM: CATH- A hierarchic classification of protein domain structures. Structure. 1997, 5: 1093-1108. 10.1016/S0969-2126(97)00260-8.

    Article  PubMed  CAS  Google Scholar 

  36. CATH Protein Structure Classification Database. [http://www.cathdb.info/latest/index.html]

  37. Green L, Higman V: Uncovering network systems within protein structures. J Mol Biol. 2003, 334: 781-791. 10.1016/j.jmb.2003.08.061.

    Article  Google Scholar 

  38. Gerstein M, Krebs W: A database of macromolecular motions. Nucleic Acids Res. 1998, 26: 4280-4290. 10.1093/nar/26.18.4280.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  39. Database of Macromolecular Movements. [http://molmovdb.org]

  40. Krebs WG, Alexandrov V, Wilson CA, Echols N, Yu H, Gerstein M: Normal mode analysis of macromolecular motions in a database framework: developing mode concentration as a useful classifying statistic. Proteins. 2002, 48: 682-695. 10.1002/prot.10168.

    Article  PubMed  CAS  Google Scholar 

  41. Laskowski RA, Chistyakov VV, Thornton JM: PDBsum more: New summaries and analyses of the known 3D structures of proteins and nucleic acids. Nucleic Acids Res. 2005, 33: D266-D268. 10.1093/nar/gki001.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  42. PDBsum Database. [http://www.ebi.ac.uk/thornton-srv/databases/pdbsum/]

  43. Accelrys DS Viewer Pro. [http://www.accelrys.com/dstudio/ds_viewer/index.html]

  44. Yang Q, Lonardi S: A parallel edge-betweenness clustering tool for protein interaction networks. Int J Data Mining Bioinformatics. 2007, 1: 241-247. 10.1504/IJDMB.2007.011611.

    Article  Google Scholar 

  45. Guimerà R, Nunes Amaral LA: Functional cartography of complex metabolic networks. Nature. 2005, 433: 895-900. 10.1038/nature03288.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Shatsky M, Nussinov R, Wolfson HJ: A method for simultaneous alignment of multiple protein structures. Proteins. 2004, 56: 143-56. 10.1002/prot.10628.

    Article  PubMed  CAS  Google Scholar 

  47. MultiProt. [http://bioinfo3d.cs.tau.ac.il/MultiProt]

  48. Paoli M, Liddington R, Tame J, Wilkinson A, Dodson G: Crystal structure of T state haemoglobin with oxygen bound at all four haems. J Mol Biol. 1996, 256: 775-792. 10.1006/jmbi.1996.0124.

    Article  PubMed  CAS  Google Scholar 

  49. Perutz MF, Wilkinson AJ, Paoli M, Dodson GG: The stereochemical mechanism of the cooperative effects in hemoglobin revisited. Annu Rev Biophys Biomol Struct. 1998, 27: 1-34. 10.1146/annurev.biophys.27.1.1.

    Article  PubMed  CAS  Google Scholar 

  50. Johnson LN: Glycogen phosphorylase: control by phosphorylation and allosteric effectors. FASEB J. 1992, 6: 2274-82.

    PubMed  CAS  Google Scholar 

  51. Oikonomakos NG, Schnier JB, Spyros EZ, Skamnaki VT, Tsitsanou KE, Johnson LN: Flavopiridol inhibits glycogen phosphorylase by binding at the inhibitor site. J Biol Chem. 2000, 275: 34566-34573. 10.1074/jbc.M004485200.

    Article  PubMed  CAS  Google Scholar 

  52. Oikonomakos NG, Skamnaki VT, Tsitsanou KE, Gavalas NG, Johnson LN: A new allosteric site in glycogen phosphorylase B as a target for drug interactions. Structure. 2000, 8: 575-584. 10.1016/S0969-2126(00)00144-1.

    Article  PubMed  CAS  Google Scholar 

  53. Mitchell EP, Withers G, Ermert P, Vasella AT, Garman EF, Oikonomakos NG, Johnson LN: Ternary complex crystal structures of glycogen phosphorylase with the transition state analogue nojirimycin tetrazole and phosphate in the T and R states. Biochemistry. 1996, 35: 7341-7355. 10.1021/bi960072w.

    Article  PubMed  CAS  Google Scholar 

  54. Schulman AI, Larson C, Mangelsdorf DJ, Ranganathan R: Structural determinants of allosteric ligand activation in RXR heterodimers. Cell. 2004, 116: 417-429. 10.1016/S0092-8674(04)00119-9.

    Article  Google Scholar 

  55. Gampe RT, Montana VG, Lambert MH, Wisely B, Milburn MV, Xu HE: Structural basis for autorepression of retinoid X receptor by tetramer formation and the AF-2 helix. Genes Dev. 2000, 14: 2229-2241. 10.1101/gad.802300.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  56. Gampe RT, Montana VG, Lambert MH, Miller AB, Bledsoe RK, Milburn MV, Kliewer SA, Willson TM, Xu HE: Assymetry in the PPARγ/RXRα crystal structure reveals the molecular basis of heterodimerization among nuclear receptors. Mol Cell. 2000, 5: 545-555. 10.1016/S1097-2765(00)80448-7.

    Article  PubMed  CAS  Google Scholar 

  57. Busby S, Ebright RH: Transcription activation by catabolite activator protein (CAP). J Mol Biol. 1999, 293: 199-213. 10.1006/jmbi.1999.3161.

    Article  PubMed  CAS  Google Scholar 

  58. Passner JM, Schultz SC, Steitz TA: Modeling the cAMP-induced allosteric transition using the crystal structure of CAP-cAMP at 2.1 A resolution. J Mol Biol. 2000, 304: 847-859. 10.1006/jmbi.2000.4231.

    Article  PubMed  CAS  Google Scholar 

  59. Harman JG: Allosteric regulation of the cAMP receptor protein. Biochim Biophys Acta. 2001, 1547: 1-17.

    Article  PubMed  CAS  Google Scholar 

  60. Fic E, Polit A, Wasylewsky Z: Kinetic and structural studies of the allosteric conformational changes induced by binding of cAMP receptor protein from Escherichia coli. Biochemistry. 2006, 45: 373-380. 10.1021/bi051586a.

    Article  PubMed  CAS  Google Scholar 

  61. Passner JM, Steitz TA: The structure of a CAP-DNA complex having two cAMP molecules bound to each monomer. Proc Natl Acad Sci USA. 1997, 94: 2843-2847. 10.1073/pnas.94.7.2843.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  62. Smith TJ, Peterson PE, Schmidt T, Fang J, Stanley CA: Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulation. J Mol Biol. 2001, 307: 707-720. 10.1006/jmbi.2001.4499.

    Article  PubMed  CAS  Google Scholar 

  63. Smith TJ, Schmidt T, Fang J, Wu J, Siuzdak G, Stanley CA: The structure of Apo human glutamate dehydrogenase details subunit communication and allostery. J Mol Biol. 2002, 318: 765-777. 10.1016/S0022-2836(02)00161-4.

    Article  PubMed  CAS  Google Scholar 

  64. Peterson EP, Smith TJ: The structure of bovine glutamate dehydrogenase provides insights into the mechanism of allostery. Structure. 1999, 7: 769-782. 10.1016/S0969-2126(99)80101-4.

    Article  PubMed  CAS  Google Scholar 

  65. Madabushi S, Gross AK, Philippi A, Meng EC, Wensel TG, Lichtarge O: Evolutionary trace of G protein-coupled receptors reveals clusters of residues that determine global and class-specific functions. J Biol Chem. 2004, 279: 8126-8132. 10.1074/jbc.M312671200.

    Article  PubMed  CAS  Google Scholar 

  66. Palczewski K, Kumasaka T, Hori T, Behnke CA, Motoshima H, Fox BA, Trong IL, Teller DC, Okada T, Stenkamp RE, et al: Crystal structure of rhodopsin: A G protein-coupled receptor. Science. 2000, 289: 739-745. 10.1126/science.289.5480.739.

    Article  PubMed  CAS  Google Scholar 

  67. Acharya S, Saad Y, Karnik SS: Transducin-α C-terminal peptide binding site consists of C-D and E-F loops of rhodopsin. J Biol Chem. 1997, 272: 6519-6524. 10.1074/jbc.272.10.6519.

    Article  PubMed  CAS  Google Scholar 

  68. Ballesteros JA, Shi L, Javitch JA: Structural mimicry in G protein-coupled receptors: implications of the high-resolution structure of rhodopsin for structure-function analysis of rhodopsin-like receptors. Mol Pharmacol. 2001, 60: 1-19.

    PubMed  CAS  Google Scholar 

  69. Brabazon DM, Abdulaev NG, Marino JP, Ridge KD: Evidence for structural changes in carboxyl-terminal peptides of transducin α-subunit upon binding a soluble mimic of light-activated rhodopsin. Biochemistry. 2003, 42: 302-311. 10.1021/bi0268899.

    Article  PubMed  CAS  Google Scholar 

  70. Valentini G, Chiarelli LR, Fortin R, Dolzan M, Galizzi A, Abraham DJ, Wang Ch, Bianchi P, Zanella A, Mattevi A: Structure and function of human erythrocyte pyruvate kinase. J Biol Chem. 2002, 277: 23807-23814. 10.1074/jbc.M202107200.

    Article  PubMed  CAS  Google Scholar 

  71. Muñoz ME, Ponce E: Pyruvate kinase: current status of regulatory and functional properties. Comp Biochem Physiol B Biochem Mol Biol. 2003, 135: 197-218. 10.1016/S1096-4959(03)00081-2.

    Article  PubMed  Google Scholar 

  72. Fenton AW, Paricharttanakul NM, Reinhart GD: Identification of substrate contact residues important for the allosteric regulation of phosphofructokinase from Escherichia coli. Biochemistry. 2003, 42: 6453-6459. 10.1021/bi034273t.

    Article  PubMed  CAS  Google Scholar 

  73. Fenton AW, Paricharttanakul NM, Reinhart GD: Disentangling the web of allosteric communication in a homotetramer: heterotropic activation in phosphofructokinase from Escherichia coli. Biochemistry. 2004, 43: 14104-14110. 10.1021/bi048569q.

    Article  PubMed  CAS  Google Scholar 

  74. Lau FT, Fersht AR: Dissection of the effector-binding site and complementation studies of Escherichia coli phosphofructokinase using site-directed mutagenesis. Biochemistry. 1989, 28: 6841-6847. 10.1021/bi00443a010.

    Article  PubMed  CAS  Google Scholar 

  75. Hedstrom L, Perona JJ, Rutter WJ: Converting trypsin to chymotrypsin: residue 172 is a substrate specificity determinant. Biochemistry. 1994, 33: 8757-8763. 10.1021/bi00195a017.

    Article  PubMed  CAS  Google Scholar 

  76. Hung SH, Hedstrom L: Converting trypsin to elastase: substitution of the S1 site and adjacent loops reconstitutes esterase specificity but not amidase activity. Protein Eng. 1998, 11: 669-673. 10.1093/protein/11.8.669.

    Article  PubMed  CAS  Google Scholar 

  77. Szabo E, Venekei I, Bocskei Z, Naray-Szabo G, Graf L: Three dimensional structures of S189D chymotrypsin and D189S trypsin mutants: the effect of polarity at site 189 on a protease-specific stabilization of the substrate-binding site. J Mol Biol. 2003, 331: 1121-1130. 10.1016/S0022-2836(03)00849-0.

    Article  PubMed  CAS  Google Scholar 

  78. Szabo E, Bocskei Z, Naray-Szabo G, Graf L: The three-dimensional structure of Asp189Ser trypsin provides evidence for an inherent structural plasticity of the protease. Eur J Biochem. 1999, 263: 20-26. 10.1046/j.1432-1327.1999.00452.x.

    Article  PubMed  CAS  Google Scholar 

  79. Buck E, Iyengar R: Modular design of Gβ as the basis for reversible specificity in effector stimulation. J Biol Chem. 2001, 276: 36014-36019. 10.1074/jbc.M103228200.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

This project has been funded in whole or in part with Federal funds from the National Cancer Institute, National Institutes of Health, under contract number NO1-CO-12400. The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the US Government. This research was supported (in part) by the Intramural Research Program of the NIH, National Cancer Institute, Center for Cancer Research.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Antonio del Sol.

Electronic supplementary material

Authors’ original submitted files for images

Rights and permissions

Reprints and permissions

About this article

Cite this article

del Sol, A., Araúzo-Bravo, M.J., Amoros, D. et al. Modular architecture of protein structures and allosteric communications: potential implications for signaling proteins and regulatory linkages. Genome Biol 8, R92 (2007). https://doi.org/10.1186/gb-2007-8-5-r92

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/gb-2007-8-5-r92

Keywords