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X-ray crystal structure of gamma-glutamyl phosphate reductase from burkholderia thailandensis

Analyse X-ray crystal structure of gamma-glutamyl phosphate reductase from burkholderia… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4GHK
Type
protein
Length
1,612 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Gamma-glutamyl phosphate reductase
EC
1.2.1.41
UniProt
Q2SZ88
Pockets
20 · best druggability 0.80

Structure

x-ray diffraction · 4 distinct chains · 47% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGamma-glutamyl phosphate reductase (EC 1.2.1.41)protein40446% helix, 21% strandQ2SZ88
BGamma-glutamyl phosphate reductase (EC 1.2.1.41)protein41048% helix, 22% strandQ2SZ88
CGamma-glutamyl phosphate reductase (EC 1.2.1.41)protein39846% helix, 21% strandQ2SZ88
DGamma-glutamyl phosphate reductase (EC 1.2.1.41)protein40046% helix, 22% strandQ2SZ88

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111550.800.82122empty
29660.770.8080empty
34490.770.8551empty
44570.750.8457empty
53830.600.7645empty

Interfaces

6 interfaces between chains.

  • C–D · 2883 Ų buried · 53 hydrogen bonds · protein-protein
  • A–B · 2873 Ų buried · 47 hydrogen bonds · protein-protein
  • B–C · 956 Ų buried · 15 hydrogen bonds · protein-protein
  • A–D · 944 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 273 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 4GHK · X-ray Crystal Structure of Gamma-glutamyl phosphate reductase from Burkholderia… · the same entry in another collection · chain D against D, TM-score 1.00
  • Q2SZ88 · AlphaFold monomer V2.0 prediction for gamma-glutamyl phosphate reductase (Q2SZ88) · a predicted model of the same protein · chain B against A, TM-score 0.99

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