MolNFT v1 · #182037 · protein
A biphenyl inhibitor of EIF4E targeting an internal binding site enables the design of cell-permeable protac-degraders
7MEU: “A biphenyl inhibitor of EIF4E targeting an internal binding site enables the design of cell-permeable…”. X-ray diffraction, 2 ligands (MGP, Z5D). MolNFT v1 #182037 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 7MEU
- Type
- protein
- Length
- 368 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- P06730
- Ligands
- MGP, Z5D
Structure
x-ray diffraction · 1 distinct chain.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | — | protein | 184 | — | P06730 |
Ligands and binding sites
- MGP · 7-methyl-guanosine-5'-triphosphate · ligand · 2 copies · chains A, B
- Z5D · (2E)-2-{2-[4-([1,1'-biphenyl]-4-yl)-1,3-thiazol-2-yl]hydrazinylidene}-3-(2-nitrophenyl)propanoic acid · ligand · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Compared structures
- 7MEU · A biphenyl inhibitor of eIF4E targeting an internal binding site enables the design of… · 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 P06730
- Elsewhere: RCSB PDB 7MEU · PDBe 7MEU · UniProt P06730
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.