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Structure of penicillin V acylase from agrobacterium tumefaciens

Analyse Structure of penicillin V acylase from agrobacterium tumefaciens in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5J9R
Type
protein
Length
1,268 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Choloylglycine hydrolase
EC
3.5.1.24
UniProt
A0A083ZJN8
Pockets
14 · best druggability 0.56

Structure

x-ray diffraction · 1 distinct chain · 23% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, D, CCholoylglycine hydrolase (EC 3.5.1.24)protein31723% helix, 31% strandA0A083ZJN8

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1550.560.9016empty
2610.380.7916empty
3760.370.7719empty
4680.350.7719empty
5630.350.7713empty

Interfaces

6 interfaces between chains.

  • A–B · 1747 Ų buried · 16 hydrogen bonds · protein-protein
  • D–C · 1717 Ų buried · 19 hydrogen bonds · protein-protein
  • B–C · 505 Ų buried · 7 hydrogen bonds · protein-protein
  • A–D · 502 Ų buried · 6 hydrogen bonds · protein-protein
  • B–D · 216 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 5J9R · Structure of Penicillin V acylase from Agrobacterium tumefaciens · the same entry in another collection · chain A against A, TM-score 1.00

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