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Structure of rat brain nnos heme domain complexed with S- ethyl-N-[4-(TRIFLUOROMETHYL)PHENYL] isothiourea

Analyse Structure of rat brain nnos heme domain complexed with S… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1K2U
Type
protein
Length
817 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
P29476
Ligands
HEM, H4B, TFM, ZN
Pockets
10 · best druggability 0.86

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
ANitric-oxide synthase (EC 1.14.13.39)protein40740% helix, 15% strandP29476
BNitric-oxide synthase (EC 1.14.13.39)protein41040% helix, 15% strandP29476

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
  • TFM · S-ethyl-N-[4-(trifluoromethyl)phenyl]isothiourea · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · chains A, B
  • ACT · Acetate ion · additive · 2 copies · chains A, B

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
16090.860.9199HEM, H4B, TFM
23410.790.8949HEM, H4B, TFM
32250.540.7737empty
4540.420.8314empty
51140.420.7719empty

Interfaces

1 interface between chains.

  • A–B · 2761 Ų buried · 46 hydrogen bonds · protein-protein

Compared structures

  • 1K2U · Structure of rat brain nNOS heme domain complexed with… · the same entry in another collection · chain A against A, TM-score 1.00

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