Research workbench
Ntca from synechococcus elongatus: active and inactive
Analyse Ntca from synechococcus elongatus: active and inactive in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2XKP
- Type
- protein
- Length
- 1,228 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Global nitrogen regulator
- UniProt
- P29283
- Ligands
- AKG
- Pockets
- 20 · best druggability 0.79
Structure
x-ray diffraction · 3 distinct chains · 41% helix, 28% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D | Global nitrogen regulator | protein | 207 | 41% helix, 29% strand | P29283 |
| B, E | Global nitrogen regulator | protein | 211 | 43% helix, 27% strand | P29283 |
| C, F | Global nitrogen regulator | protein | 196 | 39% helix, 29% strand | P29283 |
Ligands and binding sites
- AKG · 2-oxoglutaric acid · ligand · 6 copies · chains A, B, C, D, E, F
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1095 | 0.79 | 0.81 | 90 | empty |
| 2 | 72 | 0.72 | 0.96 | 21 | empty |
| 3 | 66 | 0.70 | 0.96 | 18 | empty |
| 4 | 236 | 0.61 | 0.80 | 34 | empty |
| 5 | 228 | 0.60 | 0.80 | 34 | empty |
Interfaces
7 interfaces between chains.
- D–E · 2174 Ų buried · 17 hydrogen bonds · protein-protein
- A–B · 2174 Ų buried · 17 hydrogen bonds · protein-protein
- C–F · 1311 Ų buried · 8 hydrogen bonds · protein-protein
- A–C · 501 Ų buried · 6 hydrogen bonds · protein-protein
- C–E · 389 Ų buried · 4 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 P29283
- Elsewhere: RCSB PDB 2XKP · PDBe 2XKP · UniProt P29283
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