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MolNFT v1 · #24923 · protein

Inducible nitric oxide synthase oxygenase domain complexed with the inhibitor ar-R17477

1VAF · Nitric oxide synthase, inducible: “Inducible nitric oxide synthase oxygenase domain complexed with the inhibitor ar-R17477”. X-ray diffraction, 4 ligands (HEM, H4B, ARR), 8 pockets (best druggability 0.80). MolNFT v1 #24923 on…

PDB
1VAF
Type
protein
Length
838 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Nitric oxide synthase, inducible
EC
1.14.13.39
UniProt
P29477
Ligands
HEM, H4B, ARR, ZN
Pockets
8 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 38% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BNitric oxide synthase, inducible (EC 1.14.13.39)protein41938% helix, 15% strandP29477

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • H4B · 5,6,7,8-tetrahydrobiopterin · ligand · 2 copies · chains A, B
  • ARR · N-(4-{2-[(3-chlorobenzyl)amino]ethyl}phenyl)thiophene-2-carboximidamide · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110380.800.8169HEM, H4B, ARR
210530.800.8171HEM, H4B, ARR
33200.580.7630empty
4970.500.8217empty
51370.450.7725empty

Interfaces

1 interface between chains.

  • A–B · 115 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 1VAF · Inducible nitric oxide synthase oxygenase domain complexed with the inhibitor AR-R17477 · the same entry in another collection · chain A against A, TM-score 1.00

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