Research workbench
Structure of liver pyruvate kinase in complex with anthraquinone derivative 29
Analyse Structure of liver pyruvate kinase in complex with anthraquinone derivative 29 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5SC9
- Type
- protein
- Length
- 3,366 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Pyruvate kinase
- EC
- 2.7.1.40
- UniProt
- Q16716
- Ligands
- FBP, OXL, I7K, MG
- Pockets
- 20 · best druggability 0.87
Structure
x-ray diffraction · 6 distinct chains · 48% helix, 17% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, E | Pyruvate kinase (EC 2.7.1.40) | protein | 414 | 48% helix, 17% strand | Q16716 |
| B, F | Pyruvate kinase (EC 2.7.1.40) | protein | 431 | 49% helix, 16% strand | Q16716 |
| C | Pyruvate kinase (EC 2.7.1.40) | protein | 417 | 47% helix, 17% strand | Q16716 |
| D | Pyruvate kinase (EC 2.7.1.40) | protein | 419 | 49% helix, 17% strand | Q16716 |
| G | Pyruvate kinase (EC 2.7.1.40) | protein | 419 | 47% helix, 17% strand | Q16716 |
| H | Pyruvate kinase (EC 2.7.1.40) | protein | 421 | 48% helix, 17% strand | Q16716 |
Ligands and binding sites
- FBP · 1,6-di-O-phosphono-beta-D-fructofuranose · ligand · 8 copies · chains A, B, C, G, D, E, F, H
- OXL · Oxalate ion · ligand · 8 copies · chains A, B, C, D, E, F, G, H
- I7K · 1-(3,4-dihydroxy-9,10-dioxo-9,10-dihydroanthracene-2-sulfonyl)piperidine-4-carboxylic acid · ligand · 7 copies · chains A, C, B, D, E, F, G, H
- MG · Magnesium ion · metal · 10 copies · chains A, B, C, D, E, F, G, H
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 877 | 0.87 | 0.89 | 57 | empty |
| 2 | 335 | 0.86 | 0.95 | 42 | empty |
| 3 | 334 | 0.86 | 0.95 | 47 | empty |
| 4 | 333 | 0.86 | 0.95 | 44 | empty |
| 5 | 337 | 0.85 | 0.94 | 46 | empty |
Interfaces
13 interfaces between chains.
- B–D · 2688 Ų buried · 38 hydrogen bonds · protein-protein
- E–G · 2657 Ų buried · 38 hydrogen bonds · protein-protein
- A–C · 2642 Ų buried · 35 hydrogen bonds · protein-protein
- F–H · 2637 Ų buried · 39 hydrogen bonds · protein-protein
- E–F · 1691 Ų buried · 26 hydrogen bonds · protein-protein
Compared structures
- 5SC9 · Structure of liver pyruvate kinase in complex with anthraqui derivative 29 · 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 Q16716
- Elsewhere: RCSB PDB 5SC9 · PDBe 5SC9 · UniProt Q16716
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