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Dihydroxylphenyl amides as inhibitors of the HSP90 molecular chaperone

Analyse Dihydroxylphenyl amides as inhibitors of the HSP90 molecular chaperone in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3EKO
Type
protein
Length
434 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Heat shock protein HSP 90-alpha
UniProt
P07900
Ligands
PYU, PO4
Pockets
3 · best druggability 0.62

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHeat shock protein HSP 90-alphaprotein21742% helix, 23% strandP07900
BHeat shock protein HSP 90-alphaprotein21740% helix, 23% strandP07900

Ligands and binding sites

  • PYU · 2-(1H-pyrrol-1-ylcarbonyl)benzene-1,3,5-triol · ligand · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12710.620.8028PYU
22910.610.7933PYU
32490.520.7640PO4

Interfaces

1 interface between chains.

  • A–B · 313 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 3EKO · Dihydroxylphenyl amides as inhibitors of the Hsp90 molecular chaperone · the same entry in another collection · chain A against A, TM-score 1.00

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