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Structure of a putative peptidoglycan glycosyltransferase from atopobium parvulum in complex with penicillin V

Analyse Structure of a putative peptidoglycan glycosyltransferase from atopobium… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4QJG
Type
protein
Length
834 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peptidoglycan glycosyltransferase
EC
2.4.1.129
UniProt
C8W8H7
Ligands
35P
Pockets
6 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 34% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeptidoglycan glycosyltransferase (EC 2.4.1.129)protein41734% helix, 24% strandC8W8H7
BPeptidoglycan glycosyltransferase (EC 2.4.1.129)protein41734% helix, 24% strandC8W8H7

Ligands and binding sites

  • 35P · (2R,4S)-5,5-dimethyl-2-{(1R)-2-oxo-1-[(phenoxyacetyl)amino]ethyl}-1,3-thiazolidine-4-carboxylic acid · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110920.760.7810835P
2590.490.8620empty
3600.460.8420empty
4550.360.7920empty
5660.360.7814empty

Interfaces

1 interface between chains.

  • A–B · 622 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 26 modified, 2 covalent (engineered, covalent ligand).

Compared structures

  • 4QJG · Structure of a putative peptidoglycan glycosyltransferase from Atopobium parvulum in… · the same entry in another collection · chain A against A, TM-score 1.00

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