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Ligands
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0QB (2s)-2-[(2-amino-1,3-thiazol-4-yl)methyl]-N~1~-{(1s,2s)-1-(cyclohexylmethyl)-2-hydroxy-2-[(3r)-1,5,5-trimethyl-2-oxopyrrolidin-3-yl]ethyl}-N~4~-[2-(dimethylamino)-2-oxoethyl]-N~4~-[(1s)-1-phenylethyl]butanediamide
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Code : 1BIM   PDBj   RCSB PDB   PDBe
Header : HYDROLASE/HYDROLASE INHIBITOR
Title : CRYSTALLOGRAPHIC STUDIES ON THE BINDING MODES OF P2-P3 BUTANEDIAMIDE RENIN INHIBITORS
Release Data : 1996-01-29
Compound :
mol_id molecule chains synonym
1 Renin A,B Angiotensinogenase
ec: 3.4.23.15
other_details: GLYCOSYLATED
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Canis lupus familiaris  (taxid:9615)
gene: CMV IE-HUMAN PREPRORENIN CDNA, REN
expression_system_common: Dog
expression_system_strain: familiaris
expression_system_plasmid: PMNC RETROVIRAL VECTOR
expression_system_gene: CMV IE-HUMAN PREPRORENIN CDNA
other_details: STABLY TRANSFERRED
Authors : Tong, L.
Keywords : ASPARTIC PROTEINASE, Aspartyl protease, Cleavage on pair of basic residues, Disease mutation, Disulfide bond, Glycoprotein, Hydrolase, Membrane, Protease, Secreted, Zymogen, HYDROLASE-HYDROLASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 2.8 Å )
Citation :

Crystallographic studies on the binding modes of P2-P3 butanediamide renin inhibitors.

Tong, L.,Pav, S.,Lamarre, D.  et al.
(1995)  J.Biol.Chem.  270 : 29520 - 29524

PubMed: 7493993
DOI: 10.1074/jbc.270.49.29520

Chain : A, B
UniProt : P00797 (RENI_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
Cleavage of Leu-|-Xaa bond in angiotensinogen to generate angiotensin I. 3.4.23.15 PubMed:12045255, PubMed:20927107
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