Research workbench
Crystal structure of danio rerio histone deacetylase 6 catalytic domain 2 (Y745F mutant) in complex with alpha tubulin K40 tripeptide substrate
Analyse Crystal structure of danio rerio histone deacetylase 6 catalytic domain 2… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5EFK
- Type
- protein
- Length
- 358 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HDAC6 protein; Alpha tubulin K40 tripeptide
- EC
- 3.5.1.98
- UniProt
- A7YT55
- Ligands
- MCM, K, ZN, NO3
Structure
x-ray diffraction · 2 distinct chains · 43% helix, 14% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B | HDAC6 protein (EC 3.5.1.98) | protein | 355 | 43% helix, 14% strand | A7YT55 |
| A | Alpha tubulin K40 tripeptide | protein | 3 | 0% helix, 0% strand | — |
Ligands and binding sites
- MCM · 7-amino-4-methyl-chromen-2-one · ligand · chains B, A
- K · Potassium ion · metal · 2 copies · chains B
- ZN · Zinc ion · metal · chains B, A
- NO3 · Nitrate ion · ion · chains B
- GOL · Glycerol · additive · chains B
- PEG · Di(hydroxyethyl)ether · additive · chains B
- EDO · 1,2-ethanediol · additive · chains B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Interfaces
1 interface between chains.
- B–A · 289 Ų buried · 6 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 1 covalent, 1 modified (covalent ligand, acetylation).
Compared structures
- 5EFK · Crystal structure of Danio rerio histone deacetylase 6 catalytic domain 2 (Y745F mutant)… · the same entry in another collection · chain B against B, 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 A7YT55
- Elsewhere: RCSB PDB 5EFK · PDBe 5EFK · UniProt A7YT55
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