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Structure of human nnos R354A G357D mutant heme domain in complex with 4-methyl-6-(2-(5-(4-methylpiperazin-1-yl) pyridin-3-YL)ETHYL)PYRIDIN-2-amine

Analyse Structure of human nnos R354A G357D mutant heme domain in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5FVU
Type
protein
Length
821 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Nitric oxide synthase, brain
EC
1.14.13.39
UniProt
P29475
Ligands
HEM, H4B, W64, ZN
Pockets
9 · best druggability 0.84

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
ANitric oxide synthase, brain (EC 1.14.13.39)protein41339% helix, 15% strandP29475
BNitric oxide synthase, brain (EC 1.14.13.39)protein40840% helix, 15% strandP29475

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
  • W64 · 4-methyl-6-(2-(5-(4-methylpiperazin-1-yl)pyridin-3-yl)ethyl)pyridin-2-amine · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · chains A, B
  • EDO · 1,2-ethanediol · additive · chains A

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

Pockets

9 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111650.840.85105HEM, H4B, W64
211480.840.8588HEM, H4B, W64, EDO
31120.400.7621empty
4950.390.7717empty
5790.390.7820empty

Interfaces

1 interface between chains.

  • A–B · 2854 Ų buried · 42 hydrogen bonds · protein-protein

Compared structures

  • 5FVU · Structure of human nNOS R354A G357D mutant heme domain in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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