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Crystal structure of the putative proline racemase from brucella melitensis, northeast structural genomics target LR31

Analyse Crystal structure of the putative proline racemase from brucella melitensis… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1TM0
Type
protein
Length
622 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proline racemase
EC
5.1.1.4
UniProt
Q8YFD6
Pockets
10 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 20% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BProline racemase (EC 5.1.1.4)protein31120% helix, 37% strandQ8YFD6

Pockets

10 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11770.800.9528empty
23580.560.7556empty
3900.520.8420empty
42300.510.7634empty
51030.490.8117empty

Interfaces

1 interface between chains.

  • A–B · 685 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 20 modified (engineered).

Compared structures

  • 1TM0 · Crystal Structure of the putative proline racemase from Brucella melitensis, Northeast… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q8YFD6 · AlphaFold monomer V2.0 prediction for protein BMEI1586 (Q8YFD6) · a predicted model of the same protein · chain A against A, TM-score 0.97

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