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Sepiapterin reductase in complex with compound 1

Analyse Sepiapterin reductase in complex with compound 1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6I6F
Type
protein
Length
521 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sepiapterin reductase
EC
1.1.1.153
UniProt
P35270
Ligands
NAP, H4E
Pockets
7 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 48% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASepiapterin reductase (EC 1.1.1.153)protein26548% helix, 16% strandP35270
BSepiapterin reductase (EC 1.1.1.153)protein25648% helix, 18% strandP35270

Ligands and binding sites

  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
  • H4E · ethyl 4-azanyl-3-bromanyl-benzoate · ligand · chains A
  • EDO · 1,2-ethanediol · additive · 13 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14550.760.8449NAP, H4E, EDO
24880.750.8352NAP
3800.380.7718empty
4600.370.7917EDO
5520.350.7914empty

Interfaces

1 interface between chains.

  • A–B · 1944 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 6I6F · Sepiapterin reductase in complex with compound 1 · the same entry in another collection · chain A against A, TM-score 1.00
  • P35270 · AlphaFold monomer V2.0 prediction for sepiapterin reductase (P35270) · a predicted model of the same protein · chain B against A, TM-score 1.00

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