Research workbench
Structure of TrkH-TrkA in complex with ATP
Analyse Structure of TrkH-TrkA in complex with ATP in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6V4J
- Type
- protein
- Length
- 2,697 residues
- Chains
- 8
- Method
- electron microscopy
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 2.97
- Source
- Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633)
- Molecule
- Trk system potassium uptake protein TrkH; Potassium uptake protein TrkA
- UniProt
- Q87TN7, Q87KD2
- Pockets
- 20 · best druggability 0.89
Structure
electron microscopy · resolution 2.97 · 5 distinct chains · 59% helix, 2% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Trk system potassium uptake protein TrkH | protein | 447 | 60% helix, 0% strand | Q87TN7 |
| B | Trk system potassium uptake protein TrkH | protein | 434 | 62% helix, 0% strand | Q87TN7 |
| C | Trk system potassium uptake protein TrkH | protein | 442 | 61% helix, 0% strand | Q87TN7 |
| D | Trk system potassium uptake protein TrkH | protein | 438 | 63% helix, 0% strand | Q87TN7 |
| E, F, G, H | Potassium uptake protein TrkA | protein | 234 | 39% helix, 18% strand | Q87KD2 |
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 | 1047 | 0.89 | 0.91 | 168 | empty |
| 2 | 523 | 0.85 | 0.91 | 79 | empty |
| 3 | 513 | 0.85 | 0.91 | 86 | empty |
| 4 | 509 | 0.85 | 0.91 | 89 | empty |
| 5 | 430 | 0.83 | 0.90 | 90 | empty |
Interfaces
12 interfaces between chains.
- C–D · 1417 Ų buried · 4 hydrogen bonds · protein-protein
- A–B · 1388 Ų buried · 6 hydrogen bonds · protein-protein
- F–H · 624 Ų buried · 24 hydrogen bonds · protein-protein
- E–G · 610 Ų buried · 18 hydrogen bonds · protein-protein
- B–E · 437 Ų buried · 7 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 disulfide (disulfide).
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 Q87TN7
- Every structure of UniProt Q87KD2
- Elsewhere: RCSB PDB 6V4J · PDBe 6V4J · UniProt Q87TN7 · UniProt Q87KD2
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