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Pyrr, the regulator of the pyrimidine biosynthetic operon in bacillus caldolyticus, nucleotide-bound form

Analyse Pyrr, the regulator of the pyrimidine biosynthetic operon in bacillus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1XZ8
Type
protein
Length
323 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pyrr bifunctional protein
EC
2.4.2.9
UniProt
P41007
Ligands
5GP, 3GP, U5P, MG
Pockets
3 · best druggability 0.43

Structure

x-ray diffraction · 2 distinct chains · 33% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APyrr bifunctional protein (EC 2.4.2.9)protein16233% helix, 31% strandP41007
BPyrr bifunctional protein (EC 2.4.2.9)protein16134% helix, 32% strandP41007

Ligands and binding sites

  • 5GP · Guanosine-5'-monophosphate · ligand · chains A
  • 3GP · Guanosine-3'-monophosphate · ligand · chains A
  • U5P · Uridine-5'-monophosphate · ligand · chains B
  • MG · Magnesium ion · metal · 2 copies · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11470.430.7522MG, 5GP
21220.400.7524MG, U5P
31160.380.7519empty

Interfaces

1 interface between chains.

  • A–B · 829 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 1XZ8 · Pyrr, The Regulator Of The Pyrimidine Biosynthetic Operon In Bacillus caldolyticus… · the same entry in another collection · chain A against A, TM-score 1.00
  • P41007 · AlphaFold monomer V2.0 prediction for bifunctional protein pyrr (P41007) · a predicted model of the same protein · chain B against A, TM-score 0.97

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