Research workbench
P-glycoprotein cocrystallised with qz-phe
Analyse P-glycoprotein cocrystallised with qz-phe in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4Q9L
- Type
- protein
- Length
- 1,193 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Multidrug resistance protein 1A; (30F)F(30F)F(30F)F peptide
- EC
- 3.6.3.44
- UniProt
- P21447
- Ligands
- 30F
- Pockets
- 13 · best druggability 0.80
Structure
x-ray diffraction · 2 distinct chains · 64% helix, 9% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Multidrug resistance protein 1A (EC 3.6.3.44) | protein | 1187 | 64% helix, 9% strand | P21447 |
| B, C | (30F)F(30F)F(30F)F peptide | protein | 3 | 0% helix, 0% strand | — |
Ligands and binding sites
- 30F · (2Z)-2-amino-3-selanylprop-2-enoic acid · ligand · 6 copies · chains A, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
13 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 938 | 0.80 | 0.82 | 83 | 30F |
| 2 | 869 | 0.74 | 0.78 | 75 | 30F |
| 3 | 270 | 0.62 | 0.80 | 30 | empty |
| 4 | 149 | 0.56 | 0.81 | 34 | empty |
| 5 | 188 | 0.53 | 0.79 | 23 | empty |
Interfaces
3 interfaces between chains.
- A–B · 441 Ų buried · 0 hydrogen bonds · protein-protein
- A–C · 332 Ų buried · 0 hydrogen bonds · protein-protein
- B–C · 93 Ų buried · 0 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 12 covalent (covalent ligand).
Compared structures
- 4Q9L · P-glycoprotein cocrystallised with QZ-Phe · 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 P21447
- Elsewhere: RCSB PDB 4Q9L · PDBe 4Q9L · UniProt P21447
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