1utz
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CRYSTAL STRUCTURE OF MMP-12 COMPLEXED TO (2R)-3-({[4-[(PYRI DIN-4-YL)PHENYL]-THIEN-2-YL}CARBOXAMIDO)(PHENYL)PROPANOIC ACID
OverviewOverview
Human macrophage elastase (MMP-12) plays an important role in inflammatory, processes and has been implicated in diseases such as emphysema and, chronic obstructive pulmonary disease (COPD). It is therefore an, attractive target for therapeutic agents. As part of a structure-based, drug design programme to find new inhibitors of MMP-12, the crystal, structures of the MMP-12 catalytic domain (residues 106-268) complexed to, three different non-peptidic small molecule inhibitors have been, determined. The structures reveal that all three ligands bind in the S1', pocket but show varying degrees of interaction with the Zn atom. The, structures of the complexes with inhibitors CP-271485 and PF-00356231, reveal that their central morpholinone and thiophene rings, respectively, sit over the Zn ... [(full description)]
About this StructureAbout this Structure
1UTZ is a [Single protein] structure of sequence from [Homo sapiens] with ZN, CA, PF3 and HAE as [ligands]. Active as [Macrophage elastase], with EC number [3.4.24.65]. Structure known Active Site: ZN2. Full crystallographic information is available from [OCA].
ReferenceReference
Crystal structures of novel non-peptidic, non-zinc chelating inhibitors bound to MMP-12., Morales R, Perrier S, Florent JM, Beltra J, Dufour S, De Mendez I, Manceau P, Tertre A, Moreau F, Compere D, Dublanchet AC, O'Gara M, J Mol Biol. 2004 Aug 20;341(4):1063-76. PMID:15289103
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- Homo sapiens
- Macrophage elastase
- Single protein
- Beltra, J.
- Compere, D.
- Dublanchet, A.C.
- Dufour, S.
- Florent, J.M.
- Gara, M.O.
- Manceau, P.
- Mendez, I.De.
- Morales, R.
- Moreau, F.
- Perrier, S.
- Tertre, A.
- CA
- HAE
- PF3
- ZN
- Hydrolase
- Macrophage metalloelastase
- Metalloprotease
- Mmp inhibitor
- Mmp-12
- Non-zinc chelator