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Bovine endothelial nitric oxide synthase heme domain complexed with 1400W(H4B-free)

Analyse Bovine endothelial nitric oxide synthase heme domain complexed with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1FOI
Type
protein
Length
830 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Nitric-oxide synthase
EC
1.14.13.39
UniProt
P29473
Ligands
HEM, 14W, ZN
Pockets
14 · best druggability 0.85

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANitric-oxide synthase (EC 1.14.13.39)protein41640% helix, 15% strandP29473
BNitric-oxide synthase (EC 1.14.13.39)protein41439% helix, 15% strandP29473

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • 14W · N-(3-(aminomethyl)benzyl)acetamidine · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · chains A, B
  • ACT · Acetate ion · additive · 2 copies · chains A, B
  • CAC · Cacodylate ion · additive · 2 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains A, B

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

Pockets

14 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110920.850.8696ACT, HEM, 14W, GOL
211560.840.8594ACT, HEM, 14W, GOL
3940.720.9521empty
4980.560.8519empty
5960.540.8419empty

Interfaces

1 interface between chains.

  • A–B · 2847 Ų buried · 47 hydrogen bonds · protein-protein

Compared structures

  • 1FOI · Bovine endothelial nitric oxide synthase heme domain complexed with 1400W(H4B-free) · the same entry in another collection · chain A against A, TM-score 1.00

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