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Crystal analysis of DELTA1-pyrroline-5-carboxylate dehydrogenase from thermus thermophilus with bound L-alanine

Analyse Crystal analysis of DELTA1-pyrroline-5-carboxylate dehydrogenase from thermus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2EJD
Type
protein
Length
1,032 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
1-pyrroline-5-carboxylate dehydrogenase
EC
1.5.1.12
UniProt
Q5SI02
Ligands
ALA, NA
Pockets
8 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 41% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B1-pyrroline-5-carboxylate dehydrogenase (EC 1.5.1.12)protein51641% helix, 21% strandQ5SI02

Ligands and binding sites

  • ALA · Alanine · ligand · 2 copies · chains A, B
  • NA · Sodium ion · metal · 2 copies · chains A, B
  • MPD · (4S)-2-methyl-2,4-pentanediol · additive · 13 copies · chains A, B
  • ACT · Acetate ion · additive · 2 copies · chains A, B

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

Pockets

8 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16400.810.8661MPD
23450.720.8466ALA, MPD
33630.690.8266ALA, MPD
45150.690.7946MPD
54710.680.7941MPD

Interfaces

1 interface between chains.

  • A–B · 3133 Ų buried · 56 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (oxidation).

Compared structures

  • 2EJD · Crystal analysis of delta1-pyrroline-5-carboxylate dehydrogenase from Thermus… · the same entry in another collection · chain A against A, TM-score 1.00

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