GL1X · GenesisL1 explorer

MolNFT v1 · #154950 · protein

Peroxiredoxin from aeropyrum pernix K1 (apprx) 0CYS F80A mutant

6KRQ: “Peroxiredoxin from aeropyrum pernix K1 (apprx) 0CYS F80A mutant”. X-ray diffraction, 20 pockets (best druggability 0.62). MolNFT v1 #154950 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
6KRQ
Type
protein
Length
2,440 residues
Chains
10
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peroxiredoxin
EC
1.11.1.15
UniProt
Q9Y9L0
Pockets
20 · best druggability 0.62

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, JPeroxiredoxin (EC 1.11.1.15)protein24434% helix, 23% strandQ9Y9L0

Ligands and binding sites

  • CIT · Citric acid · additive · 10 copies · chains A, B, C, D, E, F, G, H, I, J

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

Pockets

20 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14270.620.7746CIT
23880.620.7744CIT
33980.620.7748CIT
43840.610.7750CIT
53660.610.7745CIT

Interfaces

20 interfaces between chains.

  • C–D · 3643 Ų buried · 57 hydrogen bonds · protein-protein
  • G–H · 3636 Ų buried · 56 hydrogen bonds · protein-protein
  • E–F · 3619 Ų buried · 55 hydrogen bonds · protein-protein
  • I–J · 3571 Ų buried · 54 hydrogen bonds · protein-protein
  • A–B · 3563 Ų buried · 54 hydrogen bonds · protein-protein

Compared structures

  • 6KRQ · Peroxiredoxin from Aeropyrum pernix K1 (ApPrx) 0Cys F80A mutant · the same entry in another collection · chain A against A, TM-score 1.00

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