Research workbench
Solution structure of CA2+-S100A1-RYRP12
Analyse Solution structure of CA2+-S100A1-RYRP12 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2K2F
- Type
- protein
- Length
- 210 residues
- Chains
- 4
- Method
- solution nmr
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Ryanodine receptor 1 peptide; Protein S100-A1
- UniProt
- P35467
- Ligands
- CA
- Pockets
- 3 · best druggability 0.80
Structure
solution nmr · 2 distinct chains · 66% helix, 6% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| C, D | Ryanodine receptor 1 peptide | protein | 12 | 83% helix, 0% strand | — |
| A, B | Protein S100-A1 | protein | 93 | 63% helix, 6% strand | P35467 |
Ligands and binding sites
- CA · Calcium ion · metal · 4 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 826 | 0.80 | 0.82 | 76 | empty |
| 2 | 142 | 0.63 | 0.85 | 26 | empty |
| 3 | 133 | 0.62 | 0.86 | 28 | empty |
Interfaces
4 interfaces between chains.
- A–B · 1184 Ų buried · 12 hydrogen bonds · protein-protein
- C–A · 379 Ų buried · 1 hydrogen bond · protein-protein
- D–B · 366 Ų buried · 1 hydrogen bond · protein-protein
- C–D · 13 Ų buried · 0 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 P35467
- Elsewhere: RCSB PDB 2K2F · PDBe 2K2F · UniProt P35467
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