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Structure of unphosphorylated IRE1 in complex with G-1749

Analyse Structure of unphosphorylated IRE1 in complex with G-1749 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6W39
Type
protein
Length
748 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
SERINE/THREONINE-protein KINASE/ENDORIBONUCLEASE IRE1
EC
2.7.11.1, 3.1.26.-
UniProt
O75460
Ligands
SJG
Pockets
9 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 48% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASERINE/THREONINE-protein KINASE/ENDORIBONUCLEASE IRE1 (EC 2.7.11.1, 3.1.26.-)protein37448% helix, 14% strandO75460
BSERINE/THREONINE-protein KINASE/ENDORIBONUCLEASE IRE1 (EC 2.7.11.1, 3.1.26.-)protein37448% helix, 14% strandO75460

Ligands and binding sites

  • SJG · ethyl ~{N}-[6-methyl-5-[3-[2-[[(3~{S})-piperidin-3-yl]amino]pyrimidin-4-yl]pyridin-2-yl]oxy-naphthalen-1-yl]carbamate · ligand · 2 copies · chains A, B

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

Pockets

9 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16910.770.8253empty
23450.700.8234SJG
33770.690.8139SJG
46620.680.7757empty
5550.460.8414empty

Interfaces

1 interface between chains.

  • A–B · 1429 Ų buried · 29 hydrogen bonds · protein-protein

Compared structures

  • 6W39 · Structure of unphosphorylated IRE1 in complex with G-1749 · the same entry in another collection · chain A against A, TM-score 1.00
  • O75460 · AlphaFold monomer V2.0 prediction for SERINE/THREONINE-protein KINASE/ENDORIBONUCLEASE… · a predicted model of the same protein · chain B against A, TM-score 0.98

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