Research workbench
Galactoside acetyltransferase in complex with coenzyme a
Analyse Galactoside acetyltransferase in complex with coenzyme a in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1KQA
- Type
- protein
- Length
- 600 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Galactoside O-acetyltransferase
- EC
- 2.3.1.18
- UniProt
- P07464
- Ligands
- COA
- Pockets
- 3 · best druggability 0.84
Structure
x-ray diffraction · 1 distinct chain · 19% helix, 27% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Galactoside O-acetyltransferase (EC 2.3.1.18) | protein | 200 | 19% helix, 27% strand | P07464 |
Ligands and binding sites
- COA · Coenzyme A · ligand · 3 copies · chains A, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
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 | 975 | 0.84 | 0.85 | 104 | COA |
| 2 | 790 | 0.76 | 0.81 | 74 | COA |
| 3 | 757 | 0.76 | 0.80 | 72 | COA |
Interfaces
3 interfaces between chains.
- A–C · 1606 Ų buried · 8 hydrogen bonds · protein-protein
- B–C · 1601 Ų buried · 7 hydrogen bonds · protein-protein
- A–B · 1561 Ų buried · 10 hydrogen bonds · protein-protein
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 P07464
- Elsewhere: RCSB PDB 1KQA · PDBe 1KQA · UniProt P07464
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