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Crystal structure of bacb, an enzyme involved in bacilysin synthesis, in monoclinic form

Analyse Crystal structure of bacb, an enzyme involved in bacilysin synthesis, in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3H7J
Type
protein
Length
448 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bacilysin biosynthesis protein bacb
UniProt
P39639
Ligands
PPY, CO, FE
Pockets
5 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 4% helix, 54% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BBacilysin biosynthesis protein bacbprotein2244% helix, 54% strandP39639

Ligands and binding sites

  • PPY · 3-phenylpyruvic acid · ligand · 2 copies · chains A, B
  • CO · Cobalt (II) ion · metal · 4 copies · chains A, B
  • FE · Fe (III) ion · metal · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110830.790.80100empty
2570.710.9820PPY
3550.700.9720PPY
4800.370.7621empty
5580.350.7819empty

Interfaces

1 interface between chains.

  • A–B · 478 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 3H7J · Crystal structure of BacB, an enzyme involved in Bacilysin synthesis, in monoclinic form · the same entry in another collection · chain A against A, TM-score 1.00
  • P39639 · AlphaFold monomer V2.0 prediction for H2HPP isomerase (P39639) · a predicted model of the same protein · chain B against A, TM-score 0.99

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