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Mechanistic and Structural Analysis of Substrate Recognition and Cofactor Binding by an Unusual Bacterial Prolyl Hydroxylase - Co-BaP4H-MLI

Analyse Mechanistic and Structural Analysis of Substrate Recognition and Cofactor… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5IAV
Type
protein
Length
390 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.7
Source
Bacillus anthracis
Molecule
Procollagen-Proline Dioxygenase
UniProt
A0A0F7R8C5
Ligands
CO
Pockets
5 · best druggability 0.63

Structure

x-ray diffraction · resolution 1.7 · 2 distinct chains · 20% helix, 35% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProcollagen-Proline Dioxygenaseprotein19620% helix, 35% strandA0A0F7R8C5
BProcollagen-Proline Dioxygenaseprotein19420% helix, 35% strandA0A0F7R8C5

Ligands and binding sites

  • CO · Cobalt (II) ion · metal · 2 copies · chains A, B
  • MLI · Malonate ion · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11030.630.8823MLI
2910.550.8520MLI
31320.420.7626empty
4610.260.7219empty
5560.260.7316empty

Interfaces

1 interface between chains.

  • A–B · 1134 Ų buried · 20 hydrogen bonds · protein-protein

Compared structures

  • 5IAV · Mechanistic and structural analysis of substrate recognition and cofactor binding by an… · the same entry in another collection · chain A against A, TM-score 1.00

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