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Structure of pbp-a, L158E mutant. acyl-enzyme complex with penicillin- G.

Analyse Structure of pbp-a, L158E mutant. acyl-enzyme complex with penicillin- G. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2JBF
Type
protein
Length
1,067 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
TLL2115 protein
EC
3.4.16.4
UniProt
Q8DH45
Ligands
PNM
Pockets
5 · best druggability 0.71

Structure

x-ray diffraction · 3 distinct chains · 42% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CTLL2115 protein (EC 3.4.16.4)protein26442% helix, 20% strandQ8DH45
BTLL2115 protein (EC 3.4.16.4)protein26542% helix, 20% strandQ8DH45
DTLL2115 protein (EC 3.4.16.4)protein27441% helix, 19% strandQ8DH45

Ligands and binding sites

  • PNM · Open form - penicillin G · ligand · 4 copies · chains A, B, C, D
  • GOL · Glycerol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17500.710.7852PNM
26940.700.7868PNM
31600.520.7931PNM
41900.500.7721empty
51070.350.7319empty

Interfaces

3 interfaces between chains.

  • C–D · 365 Ų buried · 3 hydrogen bonds · protein-protein
  • A–C · 289 Ų buried · 2 hydrogen bonds · protein-protein
  • A–B · 173 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 4 covalent (covalent ligand).

Compared structures

  • 2JBF · Structure of PBP-A, L158E mutant. Acyl-enzyme complex with penicillin- G. · the same entry in another collection · chain A against A, TM-score 1.00

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