Research workbench
Crystal structure of the acyltransferase domain from second module 14 of salinomycin polyketide synthase
Analyse Crystal structure of the acyltransferase domain from second module 14 of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6IYT
- Type
- protein
- Length
- 856 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Type I modular polyketide synthase
- UniProt
- H1ZZU1
- Pockets
- 3 · best druggability 0.69
Structure
x-ray diffraction · 2 distinct chains · 45% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Type I modular polyketide synthase | protein | 432 | 44% helix, 16% strand | H1ZZU1 |
| B | Type I modular polyketide synthase | protein | 424 | 45% helix, 16% strand | H1ZZU1 |
Pockets
3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 663 | 0.69 | 0.77 | 79 | empty |
| 2 | 684 | 0.67 | 0.76 | 59 | empty |
| 3 | 291 | 0.66 | 0.82 | 44 | empty |
Interfaces
1 interface between chains.
- A–B · 146 Ų buried · 0 hydrogen bonds · protein-protein
Compared structures
- 6IYT · Crystal Structure of the acyltransferase domain from second module 14 of salinomycin… · 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 H1ZZU1
- Elsewhere: RCSB PDB 6IYT · PDBe 6IYT · UniProt H1ZZU1
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.