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Human peroxiredoxin 2 oxidized (ss)

Analyse Human peroxiredoxin 2 oxidized (ss) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5IJT
Type
protein
Length
1,683 residues
Chains
10
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peroxiredoxin-2
EC
1.11.1.15
UniProt
P32119
Ligands
ZN
Pockets
20 · best druggability 0.75

Structure

x-ray diffraction · 10 distinct chains · 28% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeroxiredoxin-2 (EC 1.11.1.15)protein16230% helix, 29% strandP32119
BPeroxiredoxin-2 (EC 1.11.1.15)protein17128% helix, 27% strandP32119
CPeroxiredoxin-2 (EC 1.11.1.15)protein15727% helix, 29% strandP32119
DPeroxiredoxin-2 (EC 1.11.1.15)protein15827% helix, 30% strandP32119
EPeroxiredoxin-2 (EC 1.11.1.15)protein17830% helix, 26% strandP32119
FPeroxiredoxin-2 (EC 1.11.1.15)protein17728% helix, 27% strandP32119
GPeroxiredoxin-2 (EC 1.11.1.15)protein16429% helix, 29% strandP32119
HPeroxiredoxin-2 (EC 1.11.1.15)protein16729% helix, 28% strandP32119
IPeroxiredoxin-2 (EC 1.11.1.15)protein17327% helix, 27% strandP32119
JPeroxiredoxin-2 (EC 1.11.1.15)protein17628% helix, 27% strandP32119

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains B, F, H

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

Pockets

20 pockets found on a 1 Å grid, 18 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11660.750.9228empty
22210.730.8847empty
3570.720.9921empty
44470.720.8260empty
52540.700.8545empty

Interfaces

14 interfaces between chains.

  • E–F · 1938 Ų buried · 27 hydrogen bonds · protein-protein
  • I–J · 1752 Ų buried · 26 hydrogen bonds · protein-protein
  • A–B · 1362 Ų buried · 20 hydrogen bonds · protein-protein
  • G–H · 980 Ų buried · 13 hydrogen bonds · protein-protein
  • F–H · 785 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 5IJT · Human Peroxiredoxin 2 Oxidized (SS) · the same entry in another collection · chain J against J, TM-score 1.00
  • P32119 · AlphaFold monomer V2.0 prediction for peroxiredoxin-2 (P32119) · a predicted model of the same protein · chain D against A, TM-score 0.97

Analyse

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