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Structure of mhpco Y270F mutant, 5-hydroxynicotinic acid complex

Analyse Structure of mhpco Y270F mutant, 5-hydroxynicotinic acid complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4H2R
Type
protein
Length
738 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase
EC
1.14.12.4
UniProt
Q988D3
Ligands
FAD, 5HN
Pockets
6 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase (EC 1.14.12.4)protein36934% helix, 29% strandQ988D3

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 2 copies · chains A, B
  • 5HN · 5-hydroxypyridine-3-carboxylic acid · ligand · chains A
  • GOL · Glycerol · additive · 5 copies · chains A, B
  • BME · Beta-mercaptoethanol · additive · chains A

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

Pockets

6 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11320.790.9624GOL
25750.790.8570FAD
38450.790.8278FAD, BME, 5HN
4690.690.9621empty
54050.570.7451empty

Interfaces

1 interface between chains.

  • A–B · 955 Ų buried · 17 hydrogen bonds · protein-protein

Compared structures

  • 4H2R · Structure of MHPCO Y270F mutant, 5-hydroxynicotinic acid complex · the same entry in another collection · chain A against A, TM-score 1.00

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