Ontology highlight
ABSTRACT:
SUBMITTER: Lund O
PROVIDER: S-EPMC2143282 | biostudies-other | 1996 Nov
REPOSITORIES: biostudies-other
Lund O O Hansen J J Brunak S S Bohr J J
Protein science : a publication of the Protein Society 19961101 11
We evaluate to what extent the structure of proteins can be deduced from incomplete knowledge of disulfide bridges, surface assignments, secondary structure assignments, and additional distance constraints. A cost function taking such constraints into account was used to obtain protein structures using a simple minimization algorithm. For small proteins, the approximate structure could be obtained using one additional distance constraint for each amino acid in the protein. We also studied the ef ...[more]