Journal
CURRENT OPINION IN STRUCTURAL BIOLOGY
Volume 12, Issue 1, Pages 36-40Publisher
CURRENT BIOLOGY LTD
DOI: 10.1016/S0959-440X(02)00286-5
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Funding
- NIGMS NIH HHS [GM61867-01] Funding Source: Medline
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Rigid body protein docking methods frequently yield false positive structures that have good surface complementarity, but are far from the native complex. The main reason for this is the uncertainty of the protein structures to be docked, including the positions of solvent-exposed sidechains. Substantial efforts have been devoted to finding near-native structures by rescoring the docked conformations and employing various filters. An alternative approach emulates the process of protein-protein association, that is, first finding the region in which binding is likely to occur and then refining the complex while allowing for flexibility.
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