Literature DB >> 11746703

A unifold, mesofold, and superfold model of protein fold use.

Andrew F W Coulson1, John Moult.   

Abstract

As more and more protein structures are determined, there is increasing interest in the question of how many different folds have been used in biology. The history of the rate of discovery of new folds and the distribution of sequence families among known folds provide a means of estimating the underlying distribution of fold use. Previous models exploiting these data have led to rather different conclusions on the total number of folds. We present a new model, based on the notion that the folds used in biology fall naturally into three classes: unifolds, that is, folds found only in a single narrow sequence family; mesofolds, found in an intermediate number of families; and the previously noted superfolds, found in many protein families. We show that this model fits the available data well and has predicted the development of SCOP over the past 2 years. The principle implications of the model are as follows: (1) The vast majority of folds will be found in only a single sequence family; (2) the total number of folds is at least 10,000; and (3) 80% of sequence families have one of about 400 folds, most of which are already known. Copyright 2001 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2002        PMID: 11746703     DOI: 10.1002/prot.10011

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


  27 in total

1.  When proteome meets genome: the alpha helix and the beta strand of proteins are eschewed by mRNA splice junctions and may define the minimal indivisible modules of protein architecture.

Authors:  Sailen Barik
Journal:  J Biosci       Date:  2004-09       Impact factor: 1.826

Review 2.  Protein folds and protein folding.

Authors:  R Dustin Schaeffer; Valerie Daggett
Journal:  Protein Eng Des Sel       Date:  2010-11-03       Impact factor: 1.650

3.  Generation of a consensus protein domain dictionary.

Authors:  R Dustin Schaeffer; Amanda L Jonsson; Andrew M Simms; Valerie Daggett
Journal:  Bioinformatics       Date:  2010-11-09       Impact factor: 6.937

4.  Proteome evolution and the metabolic origins of translation and cellular life.

Authors:  Derek Caetano-Anollés; Kyung Mo Kim; Jay E Mittenthal; Gustavo Caetano-Anollés
Journal:  J Mol Evol       Date:  2010-11-17       Impact factor: 2.395

5.  A glimpse at the organization of the protein universe.

Authors:  Michele Vendruscolo; Christopher M Dobson
Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-12       Impact factor: 11.205

6.  Evolutionary plasticity of protein families: coupling between sequence and structure variation.

Authors:  Anna R Panchenko; Yuri I Wolf; Larisa A Panchenko; Thomas Madej
Journal:  Proteins       Date:  2005-11-15

7.  Universal sharing patterns in proteomes and evolution of protein fold architecture and life.

Authors:  Gustavo Caetano-Anollés; Derek Caetano-Anollés
Journal:  J Mol Evol       Date:  2005-04       Impact factor: 2.395

8.  A limited universe of membrane protein families and folds.

Authors:  Amit Oberai; Yungok Ihm; Sanguk Kim; James U Bowie
Journal:  Protein Sci       Date:  2006-07       Impact factor: 6.725

9.  The difficult road from sequence to function.

Authors:  Robert H White
Journal:  J Bacteriol       Date:  2006-05       Impact factor: 3.490

10.  Evolution of protein structural classes and protein sequence families.

Authors:  In-Geol Choi; Sung-Hou Kim
Journal:  Proc Natl Acad Sci U S A       Date:  2006-09-07       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.