MolNFT v1 · #82855 · protein
Crystal structure of human MDM2 with a dihydroimidazothiazole inhibitor
3VZV · E3 ubiquitin-protein ligase MDM2: “Crystal structure of human MDM2 with a dihydroimidazothiazole inhibitor”. X-ray diffraction, 1 ligand (VZV), 2 pockets (best druggability 0.69). MolNFT v1 #82855 on GenesisL1: 3D structure, binding…
- PDB
- 3VZV
- Type
- protein
- Length
- 170 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- E3 ubiquitin-protein ligase MDM2
- EC
- 6.3.2.-
- UniProt
- Q00987
- Ligands
- VZV
- Pockets
- 2 · best druggability 0.69
Structure
x-ray diffraction · 1 distinct chain · 44% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | E3 ubiquitin-protein ligase MDM2 (EC 6.3.2.-) | protein | 85 | 44% helix, 15% strand | Q00987 |
Ligands and binding sites
- VZV · 1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-6-methyl-3-(propan-2-yl)-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-N,N-dimethyl-L-prolinamide · ligand · 2 copies · chains A, B
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.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 500 | 0.69 | 0.79 | 37 | VZV |
| 2 | 97 | 0.43 | 0.77 | 18 | VZV |
Interfaces
1 interface between chains.
- A–B · 603 Ų buried · 1 hydrogen bond · protein-protein
Compared structures
- 3VZV · Crystal structure of human mdm2 with a dihydroimidazothiazole inhibitor · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt Q00987
- Elsewhere: RCSB PDB 3VZV · PDBe 3VZV · UniProt Q00987
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