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Crystal structure of the membrane proximal oxidoreductase domain of human STEAP3, the dominant ferric reductase of the erythroid transferrin cycle

Analyse Crystal structure of the membrane proximal oxidoreductase domain of human… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2VQ3
Type
protein
Length
361 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Metalloreductase STEAP3
EC
1.16.1.2, 1.16.1.-
UniProt
Q658P3
Ligands
NAP
Pockets
3 · best druggability 0.54

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMetalloreductase STEAP3 (EC 1.16.1.2, 1.16.1.-)protein18141% helix, 22% strandQ658P3
BMetalloreductase STEAP3 (EC 1.16.1.2, 1.16.1.-)protein18042% helix, 22% strandQ658P3

Ligands and binding sites

  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
  • CIT · Citric acid · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12310.540.7746NAP
22040.520.7738NAP
3690.310.7517empty

Interfaces

1 interface between chains.

  • A–B · 724 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 2VQ3 · Crystal Structure of the Membrane Proximal Oxidoreductase Domain of Human Steap3, the… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q658P3 · AlphaFold monomer V2.0 prediction for metalloreductase STEAP3 (Q658P3) · a predicted model of the same protein · chain A against A, TM-score 0.98

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