Exploring protein sequence space using knowledge-based potentials

被引:37
作者
Babajide, A
Farber, R
Hofacker, IL
Inman, J
Lapedes, AS
Stadler, PF
机构
[1] Univ Vienna, Inst Theoret Chem & Mol Strukturbiol, A-1090 Vienna, Austria
[2] Los Alamos Natl Lab, Div Theoret, Los Alamos, NM 87545 USA
[3] Santa Fe Inst, Santa Fe, NM 87501 USA
[4] Natl Ctr Genome Resources, Santa Fe, NM 87505 USA
关键词
D O I
10.1006/jtbi.2001.2343
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Knowledge-based potentials can be used to decide whether an amino. acid sequence is likely to fold into a prescribed native protein structure. We use this idea to survey the sequence-structure relations in protein space. In particular, we test the following two propositions which were found to be important for efficient evolution: the sequences folding into a particular native fold form extensive neutral networks that percolate through sequence space. The neutral networks of any two native folds approach each other to within a few point mutations. Computer simulations using two very different potential functions, M. Sippl's PP,OSA pair potential and a neural network based potential, are used to verify these claims. (C) 2001 Academic Press.
引用
收藏
页码:35 / 46
页数:12
相关论文
共 53 条
[1]   REFINEMENT OF RECOMBINANT ONCOMODULIN AT 1.30-ANGSTROM RESOLUTION [J].
AHMED, FR ;
ROSE, DR ;
EVANS, SV ;
PIPPY, ME ;
TO, R .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 230 (04) :1216-1224
[2]  
[Anonymous], ORIGIN ORDER
[4]   Neutral networks in protein space: a computational study based on knowledge-based potentials of mean force [J].
Babajide, A ;
Hofacker, IL ;
Sippl, MJ ;
Stadler, PF .
FOLDING & DESIGN, 1997, 2 (05) :261-269
[5]   Neutral evolution of model proteins: Diffusion in sequence space and overdispersion [J].
Bastolla, U ;
Roman, HE ;
Vendruscolo, M .
JOURNAL OF THEORETICAL BIOLOGY, 1999, 200 (01) :49-64
[6]   AN IMPROVED PAIR POTENTIAL TO RECOGNIZE NATIVE PROTEIN FOLDS [J].
BAUER, A ;
BEYER, A .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1994, 18 (03) :254-261
[7]   THE 2.0 A X-RAY CRYSTAL-STRUCTURE OF CHICKEN EGG-WHITE CYSTATIN AND ITS POSSIBLE MODE OF INTERACTION WITH CYSTEINE PROTEINASES [J].
BODE, W ;
ENGH, R ;
MUSIL, D ;
THIELE, U ;
HUBER, R ;
KARSHIKOV, A ;
BRZIN, J ;
KOS, J ;
TURK, V .
EMBO JOURNAL, 1988, 7 (08) :2593-2599
[8]   How are model protein structures distributed in sequence space? [J].
BornbergBauer, E .
BIOPHYSICAL JOURNAL, 1997, 73 (05) :2393-2403
[9]   A METHOD TO IDENTIFY PROTEIN SEQUENCES THAT FOLD INTO A KNOWN 3-DIMENSIONAL STRUCTURE [J].
BOWIE, JU ;
LUTHY, R ;
EISENBERG, D .
SCIENCE, 1991, 253 (5016) :164-170
[10]   IDENTIFICATION OF PROTEIN FOLDS - MATCHING HYDROPHOBICITY PATTERNS OF SEQUENCE SETS WITH SOLVENT ACCESSIBILITY PATTERNS OF KNOWN STRUCTURES [J].
BOWIE, JU ;
CLARKE, ND ;
PABO, CO ;
SAUER, RT .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1990, 7 (03) :257-264