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Alanine racemase with bound inhibitor derived from D- cycloserine

Analyse Alanine racemase with bound inhibitor derived from D- cycloserine in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1EPV
Type
protein
Length
762 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alanine racemase
EC
5.1.1.1
UniProt
P10724
Ligands
DCS
Pockets
9 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 33% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAlanine racemase (EC 5.1.1.1)protein38232% helix, 27% strandP10724
BAlanine racemase (EC 5.1.1.1)protein38033% helix, 27% strandP10724

Ligands and binding sites

  • DCS · D-[3-hydroxy-2-methyl-5-phosphonooxymethyl-pyridin-4-ylmethyl]-N,O-cycloserylamide · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12240.750.9051DCS
22220.740.8949DCS
33790.710.8375empty
4690.640.9224empty
51120.530.8220empty

Interfaces

1 interface between chains.

  • A–B · 3356 Ų buried · 51 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (carboxylation).

Compared structures

  • 1EPV · Alanine racemase with bound inhibitor derived from D-cycloserine · the same entry in another collection · chain A against A, TM-score 1.00
  • P10724 · AlphaFold monomer V2.0 prediction for alanine racemase (P10724) · a predicted model of the same protein · chain A against A, TM-score 1.00

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