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Crystal structure of apo virginiamycin B lyase from staphylococcus aureus

Analyse Crystal structure of apo virginiamycin B lyase from staphylococcus aureus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2Z2O
Type
protein
Length
1,185 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Virginiamycin B lyase
EC
4.2.99.-, 5.5.1.-
UniProt
Q53744
Ligands
CL
Pockets
13 · best druggability 0.76

Structure

x-ray diffraction · 4 distinct chains · 1% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AVirginiamycin B lyase (EC 4.2.99.-, 5.5.1.-)protein2981% helix, 51% strandQ53744
BVirginiamycin B lyase (EC 4.2.99.-, 5.5.1.-)protein2931% helix, 52% strandQ53744
CVirginiamycin B lyase (EC 4.2.99.-, 5.5.1.-)protein2991% helix, 52% strandQ53744
DVirginiamycin B lyase (EC 4.2.99.-, 5.5.1.-)protein2951% helix, 52% strandQ53744

Ligands and binding sites

  • CL · Chloride ion · ion · 5 copies · chains A, B, C, D

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

Pockets

13 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18920.760.7991empty
22540.700.8552empty
33930.690.8136empty
44000.680.8137empty
53590.680.8137empty

Interfaces

4 interfaces between chains.

  • A–D · 924 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 509 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 464 Ų buried · 8 hydrogen bonds · protein-protein
  • C–D · 35 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 2Z2O · Crystal Structure of apo virginiamycin B lyase from Staphylococcus aureus · the same entry in another collection · chain A against A, TM-score 1.00

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