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Structure of human MDM2 in complex with high affinity peptide

Analyse Structure of human MDM2 in complex with high affinity peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3G03
Type
protein
Length
192 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
E3 ubiquitin-protein ligase MDM2; High affinity synthetic peptide
EC
6.3.2.-
UniProt
Q00987
Pockets
1 · best druggability 0.72

Structure

x-ray diffraction · 3 distinct chains · 46% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AE3 ubiquitin-protein ligase MDM2 (EC 6.3.2.-)protein8745% helix, 18% strandQ00987
B, DHigh affinity synthetic peptideprotein1155% helix, 0% strand—
CE3 ubiquitin-protein ligase MDM2 (EC 6.3.2.-)protein8347% helix, 16% strandQ00987

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13120.720.8529empty

Interfaces

4 interfaces between chains.

  • C–D · 583 Ų buried · 3 hydrogen bonds · protein-protein
  • A–B · 530 Ų buried · 3 hydrogen bonds · protein-protein
  • A–C · 466 Ų buried · 6 hydrogen bonds · protein-protein
  • B–D · 58 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 3G03 · Structure of human MDM2 in complex with high affinity peptide · the same entry in another collection · chain A against A, TM-score 1.00

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