PDB ID: 2G8E
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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0M6 | N-[(2s)-1,4-dihydroxybutan-2-yl]-N~2~-(phenylcarbamothioyl)-L-leucinamide | PoSSuM | |||
CA | Calcium ion | PoSSuM | |||
MES | 2-(N-morpholino)-ethanesulfonic acid | PoSSuM |
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Download interaction data: 2G8E
Structure summary
Code : | 2G8E PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||
Title : | Calpain 1 proteolytic core in complex with SNJ-1715, a cyclic hemiacetal-type inhibitor | ||||||||||||
Release Data : | 2006-06-06 | ||||||||||||
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Authors : | Cuerrier, D., Moldoveanu, T., Davies, P.L., Campbell, R.L. | ||||||||||||
Keywords : | protease, peptidase, inhibitor, cyclic hemiacetal, aldehyde, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.25 Å ) | ||||||||||||
Citation : |
Calpain Inhibition by alpha-Ketoamide and Cyclic Hemiacetal Inhibitors Revealed by X-ray Crystallography
Cuerrier, D.,Moldoveanu, T.,Inoue, J.
et al.
PubMed: 16768440 |
Reaction
Chain : | A | ||||||||
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UniProt : | P97571 (CAN1_RAT) | ||||||||
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