1w8m | pdb_00001w8m

From Proteopedia
Revision as of 11:53, 30 October 2007 by OCA (talk | contribs)
Jump to navigationJump to search

ENZYMATIC AND STRUCTURAL CHARACTERISATION OF NON PEPTIDE LIGAND CYCLOPHILIN COMPLEXES

File:1w8m.gif


1w8m, resolution 1.65Å

Drag the structure with the mouse to rotate

Overview

Piperidine ligands are described that provide the first examples of, non-peptidic ligand structures for the cyclophilin family of proteins., Crystal structures of two ligand complexes are compared with the, unliganded protein and show ligand-induced changes in side-chain, conformation and water binding. A peptidylprolyl cis-trans-isomerase assay, showed the dissociation constants of the two ligands to be 320 and 25 mM., This study also provides the first published data for both enzymatic, activity and three-dimensional structure for any protein-ligand complex, that binds with a high-millimolar dissociation constant. The structures, may be of relevance in the field of drug design, as they suggest starting, points for the design of larger tighter-binding analogues.

About this Structure

1W8M is a [Single protein] structure of sequence from [Homo sapiens] with E1P as [ligand]. Active as [Peptidylprolyl isomerase], with EC number [5.2.1.8]. Structure known Active Site: AC1. Full crystallographic information is available from [OCA].

Reference

Enzymatic and structural characterization of non-peptide ligand-cyclophilin complexes., Kontopidis G, Taylor P, Walkinshaw MD, Acta Crystallogr D Biol Crystallogr. 2004 Mar;60(Pt 3):479-85. Epub 2004, Feb 25. PMID:14993672

Page seeded by OCA on Tue Oct 30 13:58:29 2007

Proteopedia Page Contributors and Editors (what is this?)

OCA