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Structure of murine inos oxygenase domain with inhibitor ar-C95791

Analyse Structure of murine inos oxygenase domain with inhibitor ar-C95791 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3E7M
Type
protein
Length
837 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, AT2, ZN
Pockets
10 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANitric oxide synthase, inducible (EC 1.14.13.39)protein41641% helix, 15% strandP29477
BNitric oxide synthase, inducible (EC 1.14.13.39)protein42140% 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
  • AT2 · Ethyl 4-[(4-methylpyridin-2-yl)amino]piperidine-1-carboxylate · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 2 copies · chains A

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

Pockets

10 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19980.800.8170HEM, H4B, AT2
210310.800.8173HEM, H4B, AT2
32640.590.7830empty
41740.470.7630empty
5730.420.8115empty

Interfaces

1 interface between chains.

  • A–B · 203 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 3E7M · Structure of murine iNOS oxygenase domain with inhibitor AR-C95791 · the same entry in another collection · chain A against A, TM-score 1.00

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