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NADPH complex of imine reductase from amycolatopsis orientalis

Analyse NADPH complex of imine reductase from amycolatopsis orientalis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5A9S
Type
protein
Length
562 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Imine reductase
EC
1.5.1.48
UniProt
R4SNK4
Ligands
NAP, CA
Pockets
3 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 57% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AImine reductase (EC 1.5.1.48)protein28056% helix, 13% strandR4SNK4
BImine reductase (EC 1.5.1.48)protein28257% helix, 12% strandR4SNK4

Ligands and binding sites

  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15500.730.8149empty
24230.730.8342NAP
31060.700.9219empty

Interfaces

1 interface between chains.

  • A–B · 4124 Ų buried · 28 hydrogen bonds · protein-protein

Compared structures

  • 5A9S · NADPH complex of Imine Reductase from Amycolatopsis orientalis · the same entry in another collection · chain A against A, TM-score 1.00

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