- Research article
- Open Access
An automatic method for assessing structural importance of amino acid positions
© Sadowski and Jones; licensee BioMed Central Ltd. 2009
- Received: 05 August 2008
- Accepted: 04 March 2009
- Published: 04 March 2009
A great deal is known about the qualitative aspects of the sequence-structure relationship, for example that buried residues are usually more conserved between structurally similar homologues, but no attempts have been made to quantitate the relationship between evolutionary conservation at a sequence position and change to global tertiary structure. In this paper we demonstrate that the Spearman correlation between sequence and structural change is suitable for this purpose.
Buried residues, bends, cysteines, prolines and leucines were significantly more likely to occupy positions highly correlated with structural change than expected by chance. Some buried residues were found to be less informative than expected, particularly residues involved in active sites and the binding of small molecules.
The correlation-based method generates predictions of structural importance for superfamily positions which agree well with previous results of manual analyses, and may be of use in automated residue annotation piplines. A PERL script which implements the method is provided.
- Solvent Accessibility
- Interface Residue
- Functional Residue
- Relative Solvent Accessibility
- Structural Importance
Over the course of evolutionary time proteins which retain a particular molecular function accumulate neutral mutations to their sequences; these mutations in turn generate functionally neutral changes to the structure of the protein .
The location of an amino acid residue in the sequence and structure constrains its mutability according to how easily the mutation can be accommodated without disruption [2, 3]. Thus buried positions generally accept mutations less readily than those exposed to solvent and where function is conserved it is extremely rare to find mutations to active site residues [4, 5].
These broad details of the relationship between protein sequence and structure are well established but more detailed patterns are difficult to assess on a global scale and it becomes necessary to examine superfamilies individually to determine which positions may be most important for maintaining structure and function.
A large number of manual analyses have been published [e.g. [6–10]] which identify structurally important residues in particular protein families, however these are time-consuming, rely on extensive knowledge of the details of the family in question and may be subjective. A quantitative assessment of the importance of particular amino acid sites in a family of proteins by an automatic method would be an important step towards standardising such assessments.
Such a method would also be useful as an input for incorporation into analysis pipelines such as those used to annotate functional residues or predict the mutational consequences of SNPs [e.g. [11, 12]].
In this paper we present a quantitative examination of the structural importance of amino acid positions in six superfamilies taken from the CATH database  using a modified version of a method originally developed for predicting functionally important residues . This method simply compares global structural change with the degree of mutational difference at a given position in a multiple alignment and corrects for the overall level of mutation as a measure of the degree of mutational constraint experienced by that position as a consequence of its importance for the structure.
The results are found to agree with known principles of protein sequence-structure relationships in general and in a specific case-study of the globin superfamily. We further show that similarity scores using subsets of structurally important residues are highly correlated with structural similarities of distantly related proteins. We demonstrate that the results are generally robust to changes in the definitions of the categories and the measures of residue similarity and structural divergence, indicating that they are not critically dependent on the details of these definitions.
We conclude that this method produces a meaningful ranking of the importance of amino acid residues for protein structure and is a potentially useful addition to protein residue annotation pipelines. A PERL script which implements the method is provided [see additional file 1].
The method aims to determine which sequence positions in a superfamily are most strongly indicative of global structural change by finding the correlation between mutational changes at a given position with a global RMSD score.
The Distribution of Site-Specific Sequence/Structure Correlations Varies By Superfamily
Although the raw correlations at the majority of positions are highly significant the partial correlations for most of the superfamilies show strong peaks around zero, suggesting that the majority of positions in these alignments provide information about structural similarity only as far as they contribute to the overall sequence similarity.
However, all six families also contain positions with partial correlations of -0.3 or better, which are highly significant given the large number of pairs in each dataset. The proportion of strongly correlated positions varies from 2% for the globins to 13% for the snake venom toxins. The most strongly correlated sequence position is found in the viral capsids and has a partial correlation value of just over -0.7. This residue is highly conserved within each of the three major groups of viral coat protein domains in this dataset, but the residue found in each group differs in each case.
Structurally Informative Positions Reproduce Previous Structural Observations
We examined the composition of the multiple alignment columns with respect to their degree of correlation with structural change. In order to determine whether the structural correlations were meaningful we examined the relationship between amino-acid composition, secondary structure and structural position with the correlation measure using chi-squared tests (see methods for category definitions).
The column containing each residue was assigned to one of three categories: significantly correlated, significantly anticorrelated and uncorrelated according to the consensus of four partial correlation coefficients (derived using two RMSD measures and two different score matrices, see methods). To aid clarity we refer to these classes as Structurally Informative, Structurally Uninformative and Structurally Neutral respectively.
Associations between structural correlations and residue types
Associations between structural correlations and secondary structure types
Associations between structural correlations and residue types
Buried core residues were found to be in structurally informative columns more often than expected by chance, exposed residues were more likely to be neutral and functional residues were more likely to be uninformative. These results were unaffected by removal of any single dataset or the change of criteria of classification (see below).
Intermediately exposed residues were significantly more likely to be informative than expected from a random distribution of residues, however this effect disappeared with the removal of either the globin or snake venom toxin datasets.
Interface residues were significantly more likely to be informative than expected, however this effect was exclusively due to the viral capsid proteins, which contained a substantially greater number of interface residues than the other superfamilies. Once these were removed the interface residues for the remainder were significantly more likely to be uninformative.
For the secondary structure classes, four results were consistently unchanged by removing each dataset: bend residues were always significantly overrepresented in informative columns; 3–10 helix residues were always significantly overrepresented in uninformative columns and coil and strand residues were always significantly overrepresented in neutral columns. Alpha-helical residues were more likely to be uninformative than expected, however this was solely due to the globin dataset, removal of which put these residues in the neutral class. Turn regions were found to be neutral except when the PLA2 sequences were removed, which moved them to the informative class. Isolated beta-bridge residues showed no consistent preference.
The sequence composition results similarly make sense in light of previous structural analyses. Cysteine, leucine and proline were consistently overrepresented in informative columns; tryptophan, tyrosine and glycine were similarly overrepresented in most cases. Arginine and aspartic acid were consistently overrepresented in structurally neutral columns; valine in the majority of cases. Phenylalanine was consistently overrepresented in uninformative columns, with asparagine and glutamic acid in 5/6 cases.
Overall the patterns agree with expectations based on earlier studies [1–5] although the observations relating to functional residues and secondary structures have not to our knowledge been previously described.
Of course it is always difficult to categorize data deriving from continuous scales in a consistently meaningful way and this may introduce some bias. To address this issue we varied the thresholds for the solvent accessibility based patterns and functional residues and found that although exposed and intermediate residues varied in their tendency to be neutral or uninformative the main results did not change significantly. Incorporating more residues surrounding non-protein atoms in the PDB files in the functional class also did not change the findings presented until a significant fraction of the sequence was included.
To further validate the method with a detailed case-study we used the globin superfamily, which has been the subject of considerable study, as a test case.
Structurally Informative Positions in the Globins
Gly 25 is known to be very highly-conserved in the globin family owing to its location where two helices cross . In 22 of the 70 sequences this residue has mutated. Many of these changes are conservative (e.g. G->A, S) however there are other classes of globin such as the truncated globins (e.g. 1kr7) in which more extreme changes are found (e.g. G->V); in such cases the closest approach of the two helices is greater by 0.5 Å or more. In all structures with a glycine at this position this is annotated by our method as a functional residue, however in every case where the residue has mutated its class has changed.
His 87 is involved in chelating the haem group. This position varies in only three cases: 1dly, 1mwb and 1ew6 which are from green algae, a cyanobacterium and a polychaete marine worm respectively and differ functionally from vertebrate globins, which are the majority of this set. Inspection of the alignment shows that the functionally equivalent histidines are at slightly different sequence positions in these examples. In these cases this residue is classed as exposed by the automatic annotation described above.
Ala 17 packs into the core from helix A (blue in the figure). This position is generally hydrophobic with its identity conserved only for close homologues. This suggests that it is useful in distinguishing relatively closely-related sequences from more distant ones.
Ile 10 extends from the centre of helix A into the core at the point where helices A, D and H meet. In vertebrate globins this is mostly valine but in others where the N-terminus is truncated it is generally a more polar site (e.g. serine), hence it may act as an indicator of the length of the N-terminus.
Tyr 140 is the penultimate residue in 1hbr and forms a side-chain/main-chain hydrogen bond with the oxygen of V93 in the loop preceding helix F. A similar interaction is conserved within groups (e.g. 1cqx, 1vhb, 1gvh) which conserve a particular residue (i.e. Tyr in most globins, Glu in 1cqx etc.) but with different details of interaction: where a tyrosine appears at this position we find the interaction to be a side-chain/main-chain hydrogen bond; in 1cqx etc. this is a side-chain/side-chain bond to more than one partner. This residue is absent in the truncated globins. The side-chain also forms part of the interface in 29 of the family members considered here. A tyrosine at this position is found to be a necessary, but not sufficient, condition for an involvement in an inter-chain interface.
Tyr 36 is a surface residue. It is not immediately obvious how this position is constrained by structure however its role in 1hbr may be suggestive: it is involved in a sidechain-sidechain hydrogen bond with glutamine Q103 in the penultimate helix. This non-local contact may be involved in formation of the final tertiary structure. The nature of this interaction differs slightly in other structures examined. For example, in the 101 m sperm whale myoglobin structure there is now an aromatic interaction between H36 and F106 with an additional hydrogen-bond to E109. In the truncated globin 1kr7 H18 packs against N81 although it is not apparently hydrogen-bonded. A local aromatic interaction with Y21 now occurs and this tyrosine hydrogen-bonds to N81. In 1tu9, another truncated globin structure, this position is now a serine, S32, which locally hydrogen bonds with Q34. In the marine worm globin 1ew6 this has become a hydrophobic interaction with the tyrosine at this position (Y28) now sandwiched between two lysines: K27 and K99. Within another closely-related group (1g0b, 1g08 et al.) this has become a Phe and now interacts with Leu100.
Lys 127 is highly conserved across a great evolutionary distance. Again a surface residue, this is also involved in a sidechain-sidechain hydrogen bond, this time with an aspartic acid at position 6, uniting the C- and N-termini. Where this residue has mutated this interaction is not conserved. In 1hbr this residue is an interface residue. Although this role is not completely conserved it is found in only one case where this residue is not lysine (1ith).
Pro 37 is very strongly conserved across the majority of the superfamily (D or Q in 6 of 70 sequences) and is adjacent to the lysine involved in a non-local sidechain hydrogen bond as found at position 36. As observed above the non-local interaction at this site is very highly conserved and where the proline has mutated this interaction seems to have altered concomitantly.
Trp 14 is a strongly-conserved aromatic residue, predominantly tryptophan. This is involved in packing between helices A/D and forms a "ridge" which fits into the "groove" made by L63, G67 and V70. Mutations to other residue types at this position are associated with different N-terminal conformations.
Asn 75 is highly solvent-accessible and conserved mostly over short evolutionary distances. In some cases the sidechain of the residue at this position is involved in a local hydrogen-bonding interaction. This residue is found to be exposed in nearly all family members.
Several core positions were anticorrelated, that is they were found to contribute more noise than signal to the level of sequence-structure correlation derived using them. In 1hbr these are positions 32, 105 and 109. Each of these has a mean of < 5% accessibility across the entire set of sequences. This may seem surprising as it is expected that core residues will be more greatly conserved, however two complementary explanations can be suggested.
In the first place these residues are consistently located in the hydrophobic core and therefore must conserve their hydrophobicity. Since there are several possible residues which are equally acceptable (e.g. I, V, L) these positions are candidates for multiple substitutions. In the second place their positioning in contact with other sidechain residues provides the maximum possible repacking in response to changes in shape or volume. Thus the structural effect on the backbone position is likely to be minimal.
Conservation of Structurally Informative Residues Can Improve Predictions of Structural Similarity for Distant Homologues
As a final test of this method we examined whether the conservation of the more highly correlated residues was more indicative of structural similarity than that of the least highly correlated residues. Although we expect this to be the case it is possible that the combination of several residues might not increase the amount of information since they may be correlated or anticorrelated with one another.
For distantly related pairs the correlation based ranking is clearly effective, with a minimum correlation of -0.778 compared to -0.676 for the full sequence similarity score. Using the Fisher transformation this difference has a Z-score of 23 and accounts for ~14% more of the variance in the relationship. This is achieved using only the top five positions. Scoring with the ranks reversed shows that the positions at the bottom of the list are indeed more noisy than would be expected and cumulatively push the overall correlation above zero. The steep correction before returning to the full sequence correlation score again shows that the highly correlated residues contribute significant information.
By contrast the closely-related sequence pairs do not at any point exceed the level of correlation attained by the full sequence similarity scores but instead gradually approach the correlation of the full ID score from above. For both the forward and the reversed rankings there is an initial steep drop as sufficient information to make a reasonable classification is reached (about 20 residues), however after this the correlation of the forward ranked set continues to drop whereas the reverse rankings plateau very early.
In this paper we present an automatic method for assigning relative structural importance to sequence positions and shown that the results accord well with prior expectations. The main results are summarised and discussed below.
Most Buried Positions are Better Correlated with Structural Change Than Sequence Change
Buried core positions are significantly correlated with structure, over the level expected based on overall sequence-structure correlation. Similarly, exposed positions are overall equally correlated with structure as would be expected from the relationship with overall sequence change. Given that buried positions experience mutational constraints as a result of their structural location this makes sense and agrees with previous results. Exposed positions are similarly explicable. We also find that some buried positions are apparently able to mutate without affecting the structure, which is somewhat more surprising. One possible explanation is for a position to be in contact with sidechains with sufficient degrees of freedom to adopt a different packing without altering the backbone conformation.
The overall neutrality of interface residues outside the viral capsid proteins was surprising to us as many of the more detailed analyses suggested that these positions were frequently strongly correlated. However given that these are essentially exposed positions which have acquired a functional constraint they could be regarded as a more slowly-evolving class of exposed residue, therefore providing information about structural change in concert with overall sequence changes. Residues which expose an intermediate level of surface area to the solvent are similarly correlated with sequence and structural change to the same extent, which accords with the existence of an intermediate level of mutational constraint due to structure.
Residues in contact with non-protein atoms in the structures, which can be regarded as functional residues, are found to be poorly correlated with structural change. Once the relationship with sequence change is accounted for these positions actually provide less information on structural changes than would be expected. Varying the threshold for the contact distance to be more permissive only strengthened the relationship until the point at which a large proportion of the sequence was being included. This shows that the relatively smaller number of these residues compared to the other types was not the cause of this result.
The reason for this is simply that on the whole these residues are much more correlated than the majority of columns. Consequently there is a much greater range of structural similarities given conservation of a functional residue than for many more variable positions.
In any case, since the main selection pressure in these groups is to maintain function any structural changes we observe (assuming function has not changed) must be neutral as far as functional change is concerned; therefore conservation of such sites could be expected to be uninformative. The interesting conclusion is that while functional residues are crucial for distinguishing correct from incorrect (super)family assignments they are detrimental in determining which of a set of sequences is likely to be the most similar structurally.
Bends correlated, 3/10-Helices anticorrelated, Coils, Strands uncorrelated
We find that elements in bends contain more information about structural change than would be expected from their correlation with sequence similarity. Conversely, mutations to residues in 3–10 helices are significantly likely to correlate poorly with structural change given their correlation with sequence change. Turns, coils, helices and strands are more likely to be uncorrelated than expected.
Overall this suggests that most secondary structure types do not bias the importance of residues for the structure compared to the significant effect of solvent accessibility. Since a residue in a secondary structure can be buried or exposed this is hardly surprising. Bends are perhaps explicable in terms of torsional restraints on compatible residues: if a bend is conserved from one protein to another it is likely to be necessary to maintain particular residues compatible with the local curvature; where a bend and a non-bend are aligned a mutation may well indicate the loss of this local pattern. 3–10 helices are unusual but make up ~5% of the residues in our dataset.
Bulky Hydrophobic residues, Cysteines, Prolines & Glycines are Informative
Analysis of correlation patterns with reference to sequence composition finds cysteine to be the most significantly likely to exist in a column with more information on structural change than expected. Since many of the proteins in this study contain disulphide bonds in varying patters this is another expected result. Proline and glycine are similarly overrepresented (although glycine inconsistently so), which given their torsional properties is also as expected.
In addition to these cases two other residues are significantly informative: leucine, and tryptophan. Given their hydrophobicity this is likely to be associated with their tendency to be buried; additionally the size of tryptophan is likely to be a factor since mutation to or from these in a buried position is likely to entail repacking to accommodate the volumetric change.
Residues which tend to be exposed are likely to be less informative, which accords with the observations above, however we also found F and V to be less well correlated than expected.
Sequence Identity Scores Using Subsets of Structurally Informative Positions can Improve Prediction of Structural Similarity
Generating restricted sequence identity scores for subsets of aligned positions using this method would in principle allow the range over which structural similarity can be reliably predicted to be increased: at present for most superfamilies once < 20% ID is reached the most similar structures cannot be distinguished from the least similar since for very distantly related proteins the majority of positions have become mutationally saturated and therefore contribute only chance similarities.
Figure 3 shows that conservation of the positions most highly ranked by this method remains informative within this range, although naturally the limited information available adds noise to the comparison between more similar sequences.
It is interesting that although the more highly correlated residues are clearly useful for closely homologous proteins the best correlated score in the globin superfamily was only reached with the full sequence identity. This suggests that for closely related pairs we are simply removing information by ignoring certain positions. Alternatively it may be the result of the sensitivity of the correlation coefficient to outliers in the data: if one structure in a set is very different from the remainder this method will assign high correlations to positions which discriminate the highly divergent structure from the remainder.
To address this it would be better to separate the dataset into closely related pairs and distantly related pairs by some method and generate a decomposition of the superfamily into positions which are important for structural change in close homologues compared to positions important for distantly related proteins.
This is potentially useful for improving the selection of templates for modelling proteins using distant templates however it requires a very accurate alignment between the templates and the target which may be difficult to achieve.
We have presented the results of applying a simple correlation based method previously used in the identification of functional residues to the question of determining a relative scale of structural importance for residue positions in a set of aligned protein sequences. The results agree well with common knowledge of protein sequence-structure relationships but also provide some novel insights. This method should be useful in future analyses of protein sequence/structure/function relationships.
Data Derivation and Preparation
Six superfamilies of homologous proteins (Table 1) were chosen from the CATH database version 3.0 . The families were chosen to provide a reasonably diverse set with structural pairs distributed as evenly as possible over a wide range of similarity values and cover each of the three structural classes (mostly alpha, mostly beta, alpha and beta).
All structures within a family were first structurally aligned as pairs using the TM-align program . The percentage identity was calculated for each pair from these alignments. To reduce bias in the analysis, we derived the largest non-redundant set of structures (with less than 90% mutual pairwise sequence identity derived from the structural alignments) using a greedy, graph-based method which generates a data set by removing the sequence with the most neighbours of 90% or greater identity at each step until only singletons remain. The sets were manually examined to ensure that structures of low quality were identified and removed if necessary; however this was avoided where possible since this is difficult to automate.
The process for manual vetting of results was as follows: the sequence identity and RMSD values produced by TM-align were plotted for each family. Points lying substantially outside the trend for that superfamily were examined and if it was found that the plot for an individual structure against all other superfamily members had an unusual trend it was removed from the set. Where a small number of examples of a single family were found these were also removed as they would bias the analysis. The multiple alignments of the six superfamilies are provided as an additional file [see additional file 2].
For each non redundant set, we then generated a structure-based multiple sequence alignment using 3D-COFFEE , which generates a progressive multiple sequence alignment guided by pairwise structural alignments generated with SAP .
Structural Similarity Scores
Pairwise structural similarity scores were calculated in two ways: the RMSD score returned by TM-align was used directly from the results of the structural alignment. However since this process also optimizes the set of equivalent residues it is sometimes inconsistent where families have large loops. As a second measure we also derived RMSD scores using superpositions based on equivalences taken from the multiple alignments. All columns without gaps were used to calculate these. Initially we also generated RMSD values with SAP  however these did not substantially differ from those generated by TM-align  and therefore were not used in the analysis.
Positional Sequence/Structure Correlations
Information about the relationship between positional change and structural change was derived with a modification of the mutational behaviour method of Mesa et al.  which was previously applied to the determination of functionally important residues.
Where ρxy is the columnwise Spearman correlation with the RMSD score, ρxz is the columnwise Spearman correlation with sequence similarity scores and ρyz is the global correlation between RMSD scores and sequence similarity scores.
Significance of Structural Correlations
We used a T-threshold of 1.96 to define a column as non-neutral in the appropriate direction.
Residues were grouped according to three classifications: residue type, secondary structural state and solvent accessibility. Residue types were used directly, as were secondary structural states, which were taken from DSSP . Functional residues were assigned using direct analysis of the structures as previously described in reference . We defined five classes of residue: Functional, Interface, Buried Core, Exposed and Intermediate. Residues were assigned to the Functional class if any sidechain atom was within 4 Å of a non-protein group in the structure, excluding water and sulphates. Relative solvent accessibilities were calculated for non-functional residues using reference values for extended G-G-X-G-G pentapeptides as in reference  and assigned to one of four classes: residues which were < 5% accessible in the single domain structure were assigned to the Buried Core class; residues less accessible in the quaternary structure (as defined by PQS, ) than the single domain structure were assigned to the Interface class; residues exposing > 25% of their area to solvent in both structures were assigned to the Exposed class. All other residues were assigned to the Intermediate class (following the scheme in ref. ).
We assessed the strength of the association between structurally informative residues and predefined classes using chi-square tests. In each case the null hypothesis was of random associations between the class and the three structural types. In each case we applied the Bonferroni correction for multiple hypotheses.
Subset Similarity Scoring
Similarity scores for subsets of residues were the mean Cvaldar conservation scores  over aligned residues in the selected subset, calculated using the BLOSUM62 matrix. This score essentially normalizes substitution matrix scores to the interval [0–1].
This work was supported by the Biosapiens Network of Excellence, funded by the European Commission within its FP6 Programme, under the thematic area Life sciences, Genomics and Biotechnology for Health, contract number LSHG-CT-2003-503265. The authors thank Kevin Bryson for reading early drafts of the paper. This work was also part-funded by Wellcome Trust grant reference GR068233.
- Sasidharan R, Chothia C: The selection of acceptable protein mutations. Proc Natl Acad Sci USA 2007, 104: 10080–10085. 10.1073/pnas.0703737104PubMed CentralView ArticlePubMedGoogle Scholar
- Chothia C: Principles that determine the structures of proteins. Ann Rev Biochem 1984, 53: 537–572. 10.1146/annurev.bi.53.070184.002541View ArticlePubMedGoogle Scholar
- Robinson DM, Jones DT, Kishino H, Goldman N, Thorne JL: Protein evolution with dependence among codons due to tertiary structure. Mol Biol Evol 2003, 20: 1692–1704. 10.1093/molbev/msg184View ArticlePubMedGoogle Scholar
- Krissinel E: On the relationship between sequence and structure similarities in proteomics. Bioinformatics 2007, 23: 717–723. 10.1093/bioinformatics/btm006View ArticlePubMedGoogle Scholar
- Cheng G, Qian B, Samudrala R, Baker D: Improvement in protein functional site prediction by distinguishing structural and functional constraints on protein family evolution using computational design. Nucl Acid Res 2005, 33: 5861–5867. 10.1093/nar/gki894View ArticleGoogle Scholar
- Lesk AM, Chothia C: How different amino-acid-sequences determine similar protein structures – structure and evolutionary dynamics of the globins. J Mol Biol 1980, 136: 225–270. 10.1016/0022-2836(80)90373-3View ArticlePubMedGoogle Scholar
- Chothia C, Lesk AM: Helix movements and the reconstruction of the heme pocket during the evolution of the cytochrome-C family. J Mol Biol 1985, 182: 151–158. 10.1016/0022-2836(85)90033-6View ArticlePubMedGoogle Scholar
- Bashford D, Chothia C, Lesk AM: Determinants of a protein fold – unique features of the globin amino-acid-sequences. J Mol Biol 1987, 196: 199–216. 10.1016/0022-2836(87)90521-3View ArticlePubMedGoogle Scholar
- Betzel C, Genov N, Rajashankar KR, Singh TP: Modulation of Phospholipase A 2 activity generated by molecular evolution. Cell Mol Life Sci 1999, 56: 384–397. 10.1007/s000180050440View ArticlePubMedGoogle Scholar
- Chelvanayagam G, Heringa J, Argos P: Anatomy and evolution of proteins displaying the viral capsid jellyroll topology. J Mol Biol 1992, 228: 220–242. 10.1016/0022-2836(92)90502-BView ArticlePubMedGoogle Scholar
- Tang YR, Sheng ZY, Chen YZ, Zhang ZD: An improved prediction of catalytic residues in enzyme structures. PEDS 2008, 21: 295–302.PubMedGoogle Scholar
- Worth CL, Bickerton GRJ, Schreyer A, Forman JR, Cheng TMK, Lee S, Gong S, Burke DF, Blundell TL: A structural bioinformatics approach to the analysis of nonsynonymous single nucleotide polymorphisms (nsSNPs) and their relation to disease. J Bioinform Comput Biol 2007, 6: 1297–1318. 10.1142/S0219720007003120View ArticleGoogle Scholar
- Pearl F, Todd A, Sillitoe I, Dibley M, Redfern O, Lewis T, Bennett C, Marsden R, Grant A, Lee D, Akpor A, Maibaum M, Harrison A, Dallman T, Reeves G, Diboun I, Addou S, Lise S, Johnston C, Sillero A, Thornton J, Orengo C: The CATH Domain Structure Database and related resources Gene3D and DHS provide comprehensive domain family information for genome analysis. Nucl Acid Res 33: D247-D251. 10.1093/nar/gki024Google Scholar
- Mesa AD, Pazos F, Valencia A: Automatic methods for predicting functionally important residues. J Mol Biol 2003, 326(4):1289–1302. 10.1016/S0022-2836(02)01451-1View ArticleGoogle Scholar
- Knapp JE: The structural and functional analysis of the hemoglobin D component from chicken. J Biol Chem 1999, 274: 6411–6420. 10.1074/jbc.274.10.6411View ArticlePubMedGoogle Scholar
- Zhang Y, Skolnick J: TM-align: a protein structure alignment algorithm based on the TM-Score. Nucl Acid Res 2005, 33: 2302–2309. 10.1093/nar/gki524View ArticleGoogle Scholar
- O'Sullivan O, Suhre K, Abergel C, Higgins DG, Notredame C: 3DCoffee: Combining Protein Sequences and Structures within Multiple Sequence Alignments. J Mol Biol 2004, 85: 385–395. 10.1016/j.jmb.2004.04.058View ArticleGoogle Scholar
- Taylor WR: Protein structure comparison using iterated double dynamic programming. Protein Sci 1999, 8(3):654–665.PubMed CentralView ArticlePubMedGoogle Scholar
- Henikoff S, Henikoff JG: Amino-acid substitution matrices from protein blocks. Proc Natl Acad Sci USA 1992, 89: 10915–10919. 10.1073/pnas.89.22.10915PubMed CentralView ArticlePubMedGoogle Scholar
- Jones DT, Taylor WR, Thornton JM: The rapid generation of mutation data matrices from protein sequences. CABIOS 1992, 8: 275–282.PubMedGoogle Scholar
- Kabsch W, Sander C: Dictionary of protein secondary structure: Pattern recognition of hydrogen-bonded and geometrical features. Biopolymers 1983, 22: 2577–2637. 10.1002/bip.360221211View ArticlePubMedGoogle Scholar
- Sadowski MI, Jones DT: Benchmarking template selection and model quality assessment for high-resolution comparative modeling. Proteins: Struct Func Bioinf 2007, 69: 476–485. 10.1002/prot.21531View ArticleGoogle Scholar
- Brooksbank C, Camon E, Harris MA, Magrane M, Martin MJ, Mulder N, O'Donovan C, Parkinson H, Tuli MA, Apweiler R, Birney E, Brazma A, Henrick K, Lopez R, Stoesser G, Stoehr P, Cameron G: The European Bioinformatics Institute's data resources. Nucl Acid Res 2003, 31: 43–50. 10.1093/nar/gkg066View ArticleGoogle Scholar
- Russell RB, Barton GJ: Structural features can be unconserved in proteins with similar folds: An analysis of side chain to side-chain contacts, secondary structure and accessibility. J Mol Biol 1994, 244: 332–350. 10.1006/jmbi.1994.1733View ArticlePubMedGoogle Scholar
- Valdar WSJ: Scoring amino acid conservation. Proteins: Struct Func Genet 2002, 43: 227–241. 10.1002/prot.10146View ArticleGoogle Scholar
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