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Crystal structure of propionate catabolism operon regulatory protein prpr

Analyse Crystal structure of propionate catabolism operon regulatory protein prpr in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2PJU
Type
protein
Length
766 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Propionate catabolism operon regulatory protein
UniProt
P77743
Pockets
8 · best druggability 0.80

Structure

x-ray diffraction · 4 distinct chains · 50% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APropionate catabolism operon regulatory proteinprotein18648% helix, 21% strandP77743
BPropionate catabolism operon regulatory proteinprotein18451% helix, 21% strandP77743
CPropionate catabolism operon regulatory proteinprotein18852% helix, 22% strandP77743
DPropionate catabolism operon regulatory proteinprotein20850% helix, 20% strandP77743

Pockets

8 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17670.800.8375empty
25430.730.8148empty
32240.700.8639empty
42390.620.8133empty
51920.610.8234empty

Interfaces

3 interfaces between chains.

  • C–D · 1281 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 902 Ų buried · 7 hydrogen bonds · protein-protein
  • B–D · 225 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 2PJU · Crystal structure of propionate catabolism operon regulatory protein prpR · the same entry in another collection · chain D against D, TM-score 1.00
  • P77743 · AlphaFold monomer V2.0 prediction for propionate catabolism operon regulatory protein… · a predicted model of the same protein · chain B against A, TM-score 0.93

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