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PDBsum entry 3rql

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protein ligands metals Protein-protein interface(s) links
Oxidoreductase/inhibitor PDB id
3rql

 

 

 

 

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Contents
Protein chains
409 a.a.
Ligands
HEM ×2
H4B ×2
ACT ×2
X2D ×2
Metals
_ZN
Waters ×312
PDB id:
3rql
Name: Oxidoreductase/inhibitor
Title: Structure of the neuronal nitric oxide synthase heme domain in complex with 6-(((3r,4r)-4-(2-((1s,2r/1r,2s)-2-(3-clorophenyl) cyclopropylamino)ethoxy)pyrrolidin-3-yl)methyl)-4-methylpyridin-2- amine
Structure: Nitric oxide synthase, brain. Chain: a, b. Fragment: unp residues 297-718. Synonym: bnos, constitutive nos, nc-nos, nos type i, neuronal nos, n- nos, nnos, peptidyl-cysteine s-nitrosylase nos1. Engineered: yes
Source: Rattus norvegicus. Brown rat,rat,rats. Organism_taxid: 10116. Gene: nos1, bnos. Expressed in: escherichia coli. Expression_system_taxid: 469008.
Resolution:
1.93Å     R-factor:   0.193     R-free:   0.235
Authors: H.Li,S.L.Delker,T.L.Poulos
Key ref: H.Li et al. (2013). Cyclopropyl- and methyl-containing inhibitors of neuronal nitric oxide synthase. Bioorg Med Chem Lett, 21, 1333-1343. PubMed id: 23352768
Date:
28-Apr-11     Release date:   02-May-12    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
P29476  (NOS1_RAT) -  Nitric oxide synthase 1 from Rattus norvegicus
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1429 a.a.
409 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.1.14.13.39  - nitric-oxide synthase (NADPH).
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: 2 L-arginine + 3 NADPH + 4 O2 + H+ = 2 L-citrulline + 2 nitric oxide + 3 NADP+ + 4 H2O
2 × L-arginine
+ 3 × NADPH
+ 4 × O2
+ H(+)
= 2 × L-citrulline
+ 2 × nitric oxide
+ 3 × NADP(+)
+ 4 × H2O
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    reference    
 
 
Bioorg Med Chem Lett 21:1333-1343 (2013)
PubMed id: 23352768  
 
 
Cyclopropyl- and methyl-containing inhibitors of neuronal nitric oxide synthase.
H.Li, F.Xue, J.M.Kraus, H.Ji, K.J.Labby, J.Mataka, S.L.Delker, P.Martásek, L.J.Roman, T.L.Poulos, R.B.Silverman.
 
  ABSTRACT  
 
No abstract given.

 

 

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