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PDBsum entry 3sfc
Go to PDB code:
Hydrolase/hydrolase inhibitor
PDB id
3sfc
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Contents
Protein chain
340 a.a.
Ligands
NAG
×2
GOL
×4
S53
×3
Waters
×483
PDB id:
3sfc
Links
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ProSAT
Name:
Hydrolase/hydrolase inhibitor
Title:
Structure-based optimization of potent 4- and 6-azaindole-3- carboxamides as renin inhibitors
Structure:
Renin. Chain: a, b. Fragment: unp residues 67-406. Synonym: angiotensinogenase. Engineered: yes
Source:
Homo sapiens. Human. Organism_taxid: 9606. Gene: ren. Expressed in: homo sapiens. Expression_system_taxid: 9606. Expression_system_cell_line: hek
Resolution:
2.10Å
R-factor:
0.212
R-free:
0.243
Authors:
B.Scheiper,H.Matter,H.Steinhagen,Z.Bocskei,V.Fleury,G.Mccort
Key ref:
B.Scheiper et al. (2011). Structure-based optimization of potent 4- and 6-azaindole-3-carboxamides as renin inhibitors.
Bioorg Med Chem Lett
,
21
, 5480-5486.
PubMed id:
21840218
Date:
13-Jun-11
Release date:
31-Aug-11
PROCHECK
Headers
References
Protein chains
?
P00797
(RENI_HUMAN) - Renin from Homo sapiens
Seq:
Struc:
406 a.a.
340 a.a.
Key:
PfamA domain
Secondary structure
CATH domain
Enzyme reactions
Enzyme class:
E.C.3.4.23.15
- renin.
[IntEnz]
[ExPASy]
[KEGG]
[BRENDA]
Reaction:
Cleaves Leu-|- bond in angiotensinogen to generate angiotensin I.
Bioorg Med Chem Lett
21
:5480-5486 (2011)
PubMed id:
21840218
Structure-based optimization of potent 4- and 6-azaindole-3-carboxamides as renin inhibitors.
B.Scheiper,
H.Matter,
H.Steinhagen,
Z.Böcskei,
V.Fleury,
G.McCort.
ABSTRACT
No abstract given.
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