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Structural and mechanistic studies on a cephalosporin esterase from the clavulanic acid biosynthesis pathway

Analyse Structural and mechanistic studies on a cephalosporin esterase from the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2XFS
Type
protein
Length
844 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ORF12
UniProt
Q83Z62
Ligands
J01
Pockets
13 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 45% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AORF12protein42044% helix, 22% strandQ83Z62
BORF12protein42445% helix, 22% strandQ83Z62

Ligands and binding sites

  • J01 · (2R,3Z,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid · ligand · 4 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15290.730.8153J01
25020.720.8156J01
32960.680.8349empty
43080.610.7834J01
53120.610.7830J01

Interfaces

1 interface between chains.

  • A–B · 677 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 2XFS · Structural and mechanistic studies on a cephalosporin esterase from the clavulanic acid… · the same entry in another collection · chain A against A, TM-score 1.00

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