Research workbench
Crystal structure of NITRATE/NITRITE exchanger nark
Analyse Crystal structure of NITRATE/NITRITE exchanger nark in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4JR9
- Type
- protein
- Length
- 833 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Nitrite extrusion protein 1; Immunoglobulin gamma-2A, heavy chain; Immunoglobulin kappa…
- UniProt
- P10903
- Ligands
- GYP
- Pockets
- 9 · best druggability 0.60
Structure
x-ray diffraction · 3 distinct chains · 41% helix, 27% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Nitrite extrusion protein 1 | protein | 409 | 78% helix, 1% strand | P10903 |
| H | Immunoglobulin gamma-2A, heavy chain | protein | 213 | 7% helix, 52% strand | — |
| L | Immunoglobulin kappa, light chain | protein | 211 | 6% helix, 53% strand | — |
Ligands and binding sites
- GYP · methyl alpha-D-glucopyranoside · ligand · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
9 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 317 | 0.60 | 0.78 | 38 | empty |
| 2 | 226 | 0.45 | 0.73 | 29 | empty |
| 3 | 106 | 0.44 | 0.79 | 20 | empty |
| 4 | 69 | 0.44 | 0.81 | 12 | GYP |
| 5 | 139 | 0.43 | 0.75 | 36 | empty |
Interfaces
3 interfaces between chains.
- H–L · 1793 Ų buried · 7 hydrogen bonds · protein-protein
- A–H · 577 Ų buried · 20 hydrogen bonds · protein-protein
- A–L · 224 Ų buried · 4 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 P10903
- Elsewhere: RCSB PDB 4JR9 · PDBe 4JR9 · UniProt P10903
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