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Carbamate kinase from enterococcus faecalis

Analyse Carbamate kinase from enterococcus faecalis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1B7B
Type
protein
Length
1,228 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Carbamate kinase
EC
2.7.2.2
UniProt
P0A2X8
Ligands
SO4
Pockets
20 · best druggability 0.65

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DCarbamate kinase (EC 2.7.2.2)protein30740% helix, 23% strandP0A2X8

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15250.650.7668SO4
24790.640.7764SO4
35100.630.7666SO4
44590.630.7665SO4
53580.530.7335empty

Interfaces

5 interfaces between chains.

  • B–D · 2124 Ų buried · 27 hydrogen bonds · protein-protein
  • A–C · 2115 Ų buried · 28 hydrogen bonds · protein-protein
  • A–D · 119 Ų buried · 3 hydrogen bonds · protein-protein
  • A–B · 37 Ų buried · 0 hydrogen bonds · protein-protein
  • C–D · 19 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 1B7B · Carbamate kinase from Enterococcus faecalis · the same entry in another collection · chain A against A, TM-score 1.00
  • P0A2X8 · AlphaFold monomer V2.0 prediction for carbamate kinase 1 (P0A2X8) · a predicted model of the same protein · chain A against A, TM-score 0.98

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