Protein-protein docking: is the glass half-full or half-empty?

Abstract:

:Are current docking methods capable of building complexes from putative component protein structures? Results of recent computational studies, including those of the CAPRI (Critical Assessment of Protein Interactions) competition, were used to determine the key properties for successful docking and introduce a classification of protein complexes based on docking difficulty. Enzyme-inhibitor complexes could be determined with reasonable accuracy - possibly to within a few alternative structures. Results for antigen-antibody pairs are less predictable, and data for small signaling complexes are generally poor. However, moderate amounts of experimental data can remove uncertainty and the methodology is rapidly improving. Transient complexes with large interface areas undergo substantial conformational change and are beyond the reach of current docking methods. The docking of such complexes might therefore require fundamentally new approaches.

journal_name

Trends Biotechnol

journal_title

Trends in biotechnology

authors

Vajda S,Camacho CJ

doi

10.1016/j.tibtech.2004.01.006

subject

Has Abstract

pub_date

2004-03-01 00:00:00

pages

110-6

issue

3

eissn

0167-7799

issn

1879-3096

pii

S0167-7799(04)00022-8

journal_volume

22

pub_type

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