Research workbench
Cocaine esterase with mutation L169K, bound to dtt adduct
Analyse Cocaine esterase with mutation L169K, bound to dtt adduct in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3I2H
- Type
- protein
- Length
- 574 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Cocaine esterase
- EC
- 3.1.1.-
- UniProt
- Q9L9D7
- Ligands
- DBC, CL, SO4
- Pockets
- 4 · best druggability 0.62
Structure
x-ray diffraction · 1 distinct chain · 24% helix, 31% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Cocaine esterase (EC 3.1.1.-) | protein | 574 | 24% helix, 31% strand | Q9L9D7 |
Ligands and binding sites
- DBC · (4S,5S)-4,5-bis(mercaptomethyl)-1,3-dioxolan-2-ol · ligand · chains A
- CL · Chloride ion · ion · 8 copies · chains A
- SO4 · Sulfate ion · ion · chains A
- GOL · Glycerol · additive · 5 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
4 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 183 | 0.62 | 0.83 | 36 | DBC, GOL |
| 2 | 109 | 0.52 | 0.82 | 35 | empty |
| 3 | 76 | 0.50 | 0.84 | 17 | GOL |
| 4 | 68 | 0.29 | 0.73 | 17 | empty |
Modifications
Observed in the structure: 1 covalent (covalent ligand).
Compared structures
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 Q9L9D7
- Elsewhere: RCSB PDB 3I2H · PDBe 3I2H · UniProt Q9L9D7
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