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PDBsum entry 3sfc

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protein ligands Protein-protein interface(s) links
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
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
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
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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