Tertiary structural constraints on protein evolutionary diversity: templates, key residues and structure prediction
- PMID: 1978340
- DOI: 10.1098/rspb.1990.0077
Tertiary structural constraints on protein evolutionary diversity: templates, key residues and structure prediction
Abstract
The pattern of residue substitution in divergently evolving families of globular proteins is highly variable. At each position in a fold there are constraints on the identities of amino acids from both the three-dimensional structure and the function of the protein. To characterize and quantify the structural constraints, we have made a comparative analysis of families of homologous globular proteins. Residues are classified according to amino acid type, secondary structure, accessibility of the sidechain, and existence of hydrogen bonds from sidechain to other sidechains or peptide carbonyl or amide functions. There are distinct patterns of substitution especially where residues are both solvent inaccessible and hydrogen bonded through their sidechains. The patterns of residue substitution can be used to construct templates or to identify 'key' residues if one or more structures are known. Conversely, analysis of conversation and substitution across a large family of aligned sequences in terms of substitution profiles can allow prediction of tertiary environment or indicate a functional role. Similar analyses can be used to test the validity of putative structures if several homologous sequences are available.
Similar articles
-
Environment-specific amino acid substitution tables: tertiary templates and prediction of protein folds.Protein Sci. 1992 Feb;1(2):216-26. doi: 10.1002/pro.5560010203. Protein Sci. 1992. PMID: 1304904 Free PMC article.
-
Alignment and searching for common protein folds using a data bank of structural templates.J Mol Biol. 1993 Jun 5;231(3):735-52. doi: 10.1006/jmbi.1993.1323. J Mol Biol. 1993. PMID: 8515448
-
Functional restraints on the patterns of amino acid substitutions: application to sequence-structure homology recognition.Proteins. 2005 Dec 1;61(4):722-31. doi: 10.1002/prot.20617. Proteins. 2005. PMID: 16193489
-
Structural and functional restraints in the evolution of protein families and superfamilies.Biochem Soc Trans. 2009 Aug;37(Pt 4):727-33. doi: 10.1042/BST0370727. Biochem Soc Trans. 2009. PMID: 19614584 Review.
-
Predicting the conformation of proteins from sequences. Progress and future progress.J Mol Recognit. 1995 Jan-Apr;8(1-2):9-28. doi: 10.1002/jmr.300080104. J Mol Recognit. 1995. PMID: 7598957 Review.
Cited by
-
Pattern of amino acid substitutions in transmembrane domains of β-barrel membrane proteins for detecting remote homologs in bacteria and mitochondria.PLoS One. 2011;6(11):e26400. doi: 10.1371/journal.pone.0026400. Epub 2011 Nov 1. PLoS One. 2011. PMID: 22069449 Free PMC article.
-
HOMSTRAD: a database of protein structure alignments for homologous families.Protein Sci. 1998 Nov;7(11):2469-71. doi: 10.1002/pro.5560071126. Protein Sci. 1998. PMID: 9828015 Free PMC article.
-
Assessing the impact of secondary structure and solvent accessibility on protein evolution.Genetics. 1998 May;149(1):445-58. doi: 10.1093/genetics/149.1.445. Genetics. 1998. PMID: 9584116 Free PMC article.
-
Structure-function relationships in the cysteine proteinases actinidin, papain and papaya proteinase omega. Three-dimensional structure of papaya proteinase omega deduced by knowledge-based modelling and active-centre characteristics determined by two-hydronic-state reactivity probe kinetics and kinetics of catalysis.Biochem J. 1991 Nov 15;280 ( Pt 1)(Pt 1):79-92. doi: 10.1042/bj2800079. Biochem J. 1991. PMID: 1741760 Free PMC article.
-
Structure-based identification and clustering of protein families and superfamilies.J Comput Aided Mol Des. 1994 Feb;8(1):5-27. doi: 10.1007/BF00124346. J Comput Aided Mol Des. 1994. PMID: 8035212
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources