| Literature DB >> 11527443 |
A Babajide1, R Farber, I L Hofacker, J Inman, A S Lapedes, P F Stadler.
Abstract
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 PROSA pair potential and a neural network based potential, are used to verify these claims. Copyright 2001 Academic Press.Mesh:
Year: 2001 PMID: 11527443 DOI: 10.1006/jtbi.2001.2343
Source DB: PubMed Journal: J Theor Biol ISSN: 0022-5193 Impact factor: 2.691