MolNFT v1 · #32561 · protein
Crystal structures of human pyruvate dehydrogenase kinase 2 containing physiological and synthetic ligands
2BU6 · Pyruvate dehydrogenase kinase isoenzyme 2: “Crystal structures of human pyruvate dehydrogenase kinase 2 containing physiological and synthetic ligands”. X-ray diffraction, 1 ligand (TF2), 4 pockets (best druggability 0.66). MolNFT…
- PDB
- 2BU6
- Type
- protein
- Length
- 353 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Pyruvate dehydrogenase kinase isoenzyme 2
- EC
- 2.7.1.99
- UniProt
- Q15119
- Ligands
- TF2
- Pockets
- 4 · best druggability 0.66
Structure
x-ray diffraction · 1 distinct chain · 53% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Pyruvate dehydrogenase kinase isoenzyme 2 (EC 2.7.1.99) | protein | 353 | 53% helix, 16% strand | Q15119 |
Ligands and binding sites
- TF2 · (N-{4-[(ethylanilino)sulfonyl]-2-methylphenyl}-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide · ligand · 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 | 132 | 0.66 | 0.88 | 25 | empty |
| 2 | 75 | 0.60 | 0.88 | 13 | TF2 |
| 3 | 173 | 0.52 | 0.79 | 29 | empty |
| 4 | 79 | 0.37 | 0.77 | 17 | empty |
Compared structures
- 2BU6 · crystal structures of human pyruvate dehydrogenase kinase 2 containing physiological and… · the same entry in another collection · chain A against A, TM-score 1.00
- Q15119 · AlphaFold monomer V2.0 prediction for [pyruvate dehydrogenase (acetyl-transferring)]… · a predicted model of the same protein · chain A against A, TM-score 0.98
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 Q15119
- Elsewhere: RCSB PDB 2BU6 · PDBe 2BU6 · UniProt Q15119
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