Brand  (β version)

PDB ID: 6CID

Hetero Atom Contents

  The number of atoms exceeds 100,000.
  So, it can not be displayed here.

Select unit:

Select hetatm:   

close
information
centroid:
interaction residue:

Select chain:   Sequence  

Data format:   

Color scheme of protein:

Ligands
Code Name Style Show Link
F2J N-[1-(piperidin-4-yl)-1h-indol-5-yl]thiophene-2-carboximidamide PoSSuM
GOL Glycerol PoSSuM
H4B 5,6,7,8-tetrahydrobiopterin PoSSuM
HEM Protoporphyrin ix containing Fe PoSSuM
ZN Zinc ion PoSSuM
Non-standard Residues
Code Name Show
Glycosylation
Code Name Emphasize
Modification
Code Name Show

Structure summary

Code : 6CID   PDBj   RCSB PDB   PDBe
Header : OXIDOREDUCTASE
Title : Structure of human neuronal nitric oxide synthase R354A/G357D mutant heme domain in complex with N-(1-(Piperidin-4-yl)indolin-5-yl)thiophene-2-carboximidamide
Release Data : 2018-10-31
Compound :
mol_id molecule chains synonym
1 Nitric oxide synthase, brain A,B Constitutive NOS,NC-NOS,NOS type I,Neuronal NOS,nNOS,Peptidyl-cysteine S-nitrosylase NOS1,bNOS
ec: 1.14.13.39
mutation: R354A, G357D
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:469008)
organ: brain
gene: NOS1
expression_system_strain: BL21(DE3)
expression_system_vector_type: plasmid
expression_system_plasmid: pCWori
Authors : Li, H., Poulos, T.L.
Keywords : nitric oxide synthase inhibitor complex heme enzyme, OXIDOREDUCTASE
Exp. method : X-RAY DIFFRACTION ( 1.75 Å )
Citation :

Structural Basis for Isoform Selective Nitric Oxide Synthase Inhibition by Thiophene-2-carboximidamides.

Li, H.,Evenson, R.J.,Chreifi, G.  et al.
(2018)  Biochemistry  57 : 6319 - 6325

PubMed: 30335983
DOI: 10.1021/acs.biochem.8b00895

Reaction

Chain : A, B
UniProt : P29475 (NOS1_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
H(+) + 2 L-arginine + 3 NADPH + 4 O2 = 4 H2O + 2 L-citrulline + 3 NADP(+) + 2 nitric oxide 1.14.13.39 PubMed:35772285
left-to-right