Research workbench
The RIM1ALPHA C2B domain
Analyse The RIM1ALPHA C2B domain in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2Q3X
- Type
- protein
- Length
- 286 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Regulating synaptic membrane exocytosis protein 1
- UniProt
- Q9JIR4
- Ligands
- NA, SO4, CL
- Pockets
- 2 · best druggability 0.70
Structure
x-ray diffraction · 2 distinct chains · 5% helix, 53% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Regulating synaptic membrane exocytosis protein 1 | protein | 142 | 5% helix, 53% strand | Q9JIR4 |
| B | Regulating synaptic membrane exocytosis protein 1 | protein | 144 | 5% helix, 53% strand | Q9JIR4 |
Ligands and binding sites
- NA · Sodium ion · metal · chains B
- SO4 · Sulfate ion · ion · 7 copies · chains A, B
- CL · Chloride ion · ion · 3 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 61 | 0.70 | 0.96 | 23 | empty |
| 2 | 57 | 0.35 | 0.78 | 17 | SO4 |
Interfaces
1 interface between chains.
- A–B · 1019 Ų buried · 11 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 9 modified (engineered).
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 Q9JIR4
- Elsewhere: RCSB PDB 2Q3X · PDBe 2Q3X · UniProt Q9JIR4
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