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HDM2 (17-111, wild type) complexed with compound 12 at 1.8A; structural states of HDM2 and hdmx: X-ray elucidation of adaptations and binding interactions for different chemical compound classes

Analyse HDM2 (17-111, wild type) complexed with compound 12 at 1.8A; structural states… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6Q96
Type
protein
Length
173 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
E3 ubiquitin-protein ligase MDM2
EC
2.3.2.27
UniProt
Q00987
Ligands
HRE, SO4
Pockets
2 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 44% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AE3 ubiquitin-protein ligase MDM2 (EC 2.3.2.27)protein8743% helix, 15% strandQ00987
BE3 ubiquitin-protein ligase MDM2 (EC 2.3.2.27)protein8645% helix, 15% strandQ00987

Ligands and binding sites

  • HRE · 4-[(4~{S})-5-(5-chloranyl-2-oxidanylidene-1~{H}-pyridin-3-yl)-2-[2-(dimethylamino)-4-methoxy-pyrimidin-5-yl]-6-oxidanylidene-3-propan-2-yl-4~{H}-pyrrolo[3,4-c]pyrazol-4-yl]benzenecarbonitrile · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14170.760.8434HRE
21030.430.7719HRE

Interfaces

1 interface between chains.

  • A–B · 588 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6Q96 · HDM2 (17-111, WILD TYPE) COMPLEXED WITH COMPOUND 12 AT 1.8A; Structural states of Hdm2… · the same entry in another collection · chain A against A, TM-score 1.00

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