Literature DB >> 10713986

An alternative view of protein fold space.

I N Shindyalov1, P E Bourne.   

Abstract

Comparing and subsequently classifying protein structures information has received significant attention concurrent with the increase in the number of experimentally derived 3-dimensional structures. Classification schemes have focused on biological function found within protein domains and on structure classification based on topology. Here an alternative view is presented that groups substructures. Substructures are long (50-150 residue) highly repetitive near-contiguous pieces of polypeptide chain that occur frequently in a set of proteins from the PDB defined as structurally non-redundant over the complete polypeptide chain. The substructure classification is based on a previously reported Combinatorial Extension (CE) algorithm that provides a significantly different set of structure alignments than those previously described, having, for example, only a 40% overlap with FSSP. Qualitatively the algorithm provides longer contiguous aligned segments at the price of a slightly higher root-mean-square deviation (rmsd). Clustering these alignments gives a discreet and highly repetitive set of substructures not detectable by sequence similarity alone. In some cases different substructures represent all or different parts of well known folds indicative of the Russian doll effect--the continuity of protein fold space. In other cases they fall into different structure and functional classifications. It is too early to determine whether these newly classified substructures represent new insights into the evolution of a structural framework important to many proteins. What is apparent from on-going work is that these substructures have the potential to be useful probes in finding remote sequence homology and in structure prediction studies. The characteristics of the complete all-by-all comparison of the polypeptide chains present in the PDB and details of the filtering procedure by pair-wise structure alignment that led to the emergent substructure gallery are discussed. Substructure classification, alignments, and tools to analyze them are available at http://cl.sdsc.edu/ce.html.

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Year:  2000        PMID: 10713986

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  44 in total

1.  CKAAPs DB: a conserved key amino acid positions database.

Authors:  W W Li; B V Reddy; I N Shindyalov; P E Bourne
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

2.  A database and tools for 3-D protein structure comparison and alignment using the Combinatorial Extension (CE) algorithm.

Authors:  I N Shindyalov; P E Bourne
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

3.  CKAAPs DB: a Conserved Key Amino Acid Positions DataBase.

Authors:  Wilfred W Li; Boojala V B Reddy; John G Tate; Ilya N Shindyalov; Philip E Bourne
Journal:  Nucleic Acids Res       Date:  2002-01-01       Impact factor: 16.971

4.  MAMMOTH (matching molecular models obtained from theory): an automated method for model comparison.

Authors:  Angel R Ortiz; Charlie E M Strauss; Osvaldo Olmea
Journal:  Protein Sci       Date:  2002-11       Impact factor: 6.725

5.  FoldMiner: structural motif discovery using an improved superposition algorithm.

Authors:  Jessica Shapiro; Douglas Brutlag
Journal:  Protein Sci       Date:  2004-01       Impact factor: 6.725

6.  An optimal structure-discriminative amino acid index for protein fold recognition.

Authors:  R H Leary; J B Rosen; P Jambeck
Journal:  Biophys J       Date:  2004-01       Impact factor: 4.033

Review 7.  Structural genomics: computational methods for structure analysis.

Authors:  Sharon Goldsmith-Fischman; Barry Honig
Journal:  Protein Sci       Date:  2003-09       Impact factor: 6.725

8.  A consensus view of fold space: combining SCOP, CATH, and the Dali Domain Dictionary.

Authors:  Ryan Day; David A C Beck; Roger S Armen; Valerie Daggett
Journal:  Protein Sci       Date:  2003-10       Impact factor: 6.725

9.  Database searching by flexible protein structure alignment.

Authors:  Yuzhen Ye; Adam Godzik
Journal:  Protein Sci       Date:  2004-07       Impact factor: 6.725

10.  CONTSOR--a new knowledge-based fold recognition potential, based on side chain orientation and contacts between residue terminal groups.

Authors:  Boris Vishnepolsky; Malak Pirtskhalava
Journal:  Protein Sci       Date:  2011-11-23       Impact factor: 6.725

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