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Crystal structure of heme binding protein hutx from vibrio cholerae

Analyse Crystal structure of heme binding protein hutx from vibrio cholerae in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5EXV
Type
protein
Length
994 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemin-degrading HEMS.CHUX domain protein
UniProt
A0A085SE34
Pockets
11 · best druggability 0.66

Structure

x-ray diffraction · 4 distinct chains · 32% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemin-degrading HEMS.CHUX domain proteinprotein16328% helix, 33% strandA0A085SE34
B, E, FHemin-degrading HEMS.CHUX domain proteinprotein16736% helix, 35% strandA0A085SE34
CHemin-degrading HEMS.CHUX domain proteinprotein16530% helix, 33% strandA0A085SE34
DHemin-degrading HEMS.CHUX domain proteinprotein16535% helix, 33% strandA0A085SE34

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17250.660.7558empty
26110.640.7570empty
34480.620.7657empty
44290.600.7543empty
53490.580.7641empty

Interfaces

7 interfaces between chains.

  • A–B · 1108 Ų buried · 19 hydrogen bonds · protein-protein
  • E–F · 1108 Ų buried · 22 hydrogen bonds · protein-protein
  • C–D · 1088 Ų buried · 12 hydrogen bonds · protein-protein
  • C–F · 927 Ų buried · 13 hydrogen bonds · protein-protein
  • B–D · 484 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 5EXV · Crystal structure of heme binding protein HutX from Vibrio cholerae · the same entry in another collection · chain A against A, TM-score 1.00

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