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Crystal structure and oxidative mechanism of human pyrroline-5- carboxylate reductase

Analyse Crystal structure and oxidative mechanism of human pyrroline-5- carboxylate… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2GER
Type
protein
Length
1,384 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pyrroline-5-carboxylate reductase 1
EC
1.5.1.2
UniProt
P32322
Pockets
20 · best druggability 0.67

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 9% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, D, EPyrroline-5-carboxylate reductase 1 (EC 1.5.1.2)protein27748% helix, 12% strandP32322
BPyrroline-5-carboxylate reductase 1 (EC 1.5.1.2)protein27645% helix, 7% strandP32322

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1680.670.9423empty
2510.650.9519empty
32250.560.7845empty
43440.540.7439empty
53910.540.7236empty

Interfaces

5 interfaces between chains.

  • C–D · 407 Ų buried · 3 hydrogen bonds · protein-protein
  • B–E · 402 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 389 Ų buried · 10 hydrogen bonds · protein-protein
  • A–E · 375 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 370 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide (disulfide).

Compared structures

  • 2GER · Crystal Structure and Oxidative Mechanism of Human Pyrroline-5-carboxylate Reductase · the same entry in another collection · chain B against B, TM-score 1.00
  • P32322 · AlphaFold monomer V2.0 prediction for pyrroline-5-carboxylate reductase 1, mitochondrial… · a predicted model of the same protein · chain A against A, TM-score 0.98

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