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The structure of SGCE10, the acp-polyene thioesterase involved in C- 1027 biosynthesis
Analyse The structure of SGCE10, the acp-polyene thioesterase involved in C- 1027… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4I4J
- Type
- protein
- Length
- 1,119 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Acp-polyene thioesterase
- UniProt
- Q8GME8
- Pockets
- 11 · best druggability 0.86
Structure
x-ray diffraction · 6 distinct chains · 26% helix, 41% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Acp-polyene thioesterase | protein | 140 | 24% helix, 42% strand | Q8GME8 |
| D | Acp-polyene thioesterase | protein | 136 | 24% helix, 41% strand | Q8GME8 |
| E | Acp-polyene thioesterase | protein | 138 | 26% helix, 40% strand | Q8GME8 |
| F | Acp-polyene thioesterase | protein | 142 | 27% helix, 42% strand | Q8GME8 |
| G | Acp-polyene thioesterase | protein | 142 | 26% helix, 42% strand | Q8GME8 |
| H | Acp-polyene thioesterase | protein | 141 | 26% helix, 42% strand | Q8GME8 |
Ligands and binding sites
- TAR · D(-)-tartaric acid · additive · 3 copies · chains A, B, D, C
- GOL · Glycerol · additive · 2 copies · chains E, F, G, H
- EDO · 1,2-ethanediol · additive · chains C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
11 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1121 | 0.86 | 0.87 | 102 | GOL |
| 2 | 1175 | 0.83 | 0.84 | 99 | TAR |
| 3 | 137 | 0.78 | 0.95 | 26 | empty |
| 4 | 154 | 0.78 | 0.94 | 26 | empty |
| 5 | 194 | 0.77 | 0.92 | 30 | EDO |
Interfaces
14 interfaces between chains.
- C–D · 1183 Ų buried · 11 hydrogen bonds · protein-protein
- G–H · 1175 Ų buried · 12 hydrogen bonds · protein-protein
- A–B · 1159 Ų buried · 11 hydrogen bonds · protein-protein
- E–F · 1116 Ų buried · 10 hydrogen bonds · protein-protein
- E–H · 617 Ų buried · 3 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 16 modified (engineered).
Compared structures
- 4I4J · The structure of SgcE10, the ACP-polyene thioesterase involved in C-1027 biosynthesis · 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 Q8GME8
- Elsewhere: RCSB PDB 4I4J · PDBe 4I4J · UniProt Q8GME8
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