Ontology highlight
ABSTRACT:
SUBMITTER: Ivetac A
PROVIDER: S-EPMC3271729 | biostudies-literature | 2011
REPOSITORIES: biostudies-literature
Ivetac Anthony A McCammon J Andrew JA
Current pharmaceutical design 20110101 17
A protein's flexibility is well recognized to underlie its capacity to engage in critical functions, such as signal transduction, biomolecular transport and biochemical reactivity. Molecular recognition is also tightly linked to the dynamics of the binding partners, yet protein flexibility has largely been ignored by the growing field of structure-based drug design (SBDD). In combination with experimentally determined structures, a number of computational methods have been proposed to model prot ...[more]