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Crystal structure of penicillin-binding protein 2 from neisseria gonorrhoeae containing an A501T mutation associated with cephalosporin resistance

Analyse Crystal structure of penicillin-binding protein 2 from neisseria gonorrhoeae… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5KSH
Type
protein
Length
886 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Penicillin-binding protein 2
EC
3.4.16.4
UniProt
P08149
Ligands
SO4
Pockets
8 · best druggability 0.63

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APenicillin-binding protein 2 (EC 3.4.16.4)protein45032% helix, 25% strandP08149
BPenicillin-binding protein 2 (EC 3.4.16.4)protein43632% helix, 25% strandP08149

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 12 copies · chains A, B
  • GOL · Glycerol · additive · 3 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16110.630.7467GOL, SO4
21260.590.8527empty
31140.580.8526empty
41410.490.7824empty
51200.390.7525empty

Interfaces

1 interface between chains.

  • A–B · 234 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (phosphorylation).

Compared structures

  • 5KSH · Crystal structure of penicillin-binding protein 2 from Neisseria gonorrhoeae containing… · the same entry in another collection · chain A against A, TM-score 1.00
  • P08149 · AlphaFold monomer V2.0 prediction for probable peptidoglycan D,D-transpeptidase pena… · a predicted model of the same protein · chain B against A, TM-score 0.98

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