Research workbench
Recombinant bovine skeletal calsequestrin, high-CA2+ form
Analyse Recombinant bovine skeletal calsequestrin, high-CA2+ form in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5KN1
- Type
- protein
- Length
- 1,042 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Calsequestrin
- UniProt
- Q05JF3
- Ligands
- CA, CL
- Pockets
- 18 · best druggability 0.82
Structure
x-ray diffraction · 2 distinct chains · 40% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Calsequestrin | protein | 346 | 41% helix, 20% strand | Q05JF3 |
| B, C | Calsequestrin | protein | 348 | 40% helix, 19% strand | Q05JF3 |
Ligands and binding sites
- CA · Calcium ion · metal · 40 copies · chains A, B, C
- CL · Chloride ion · ion · chains B
- MPD · (4S)-2-methyl-2,4-pentanediol · additive · 4 copies · chains A, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
18 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 534 | 0.82 | 0.88 | 56 | empty |
| 2 | 1055 | 0.78 | 0.79 | 72 | CA |
| 3 | 262 | 0.75 | 0.89 | 35 | empty |
| 4 | 342 | 0.71 | 0.84 | 28 | empty |
| 5 | 354 | 0.69 | 0.82 | 30 | empty |
Interfaces
2 interfaces between chains.
- B–C · 2420 Ų buried · 23 hydrogen bonds · protein-protein
- A–B · 481 Ų buried · 5 hydrogen bonds · protein-protein
Compared structures
- 5KN1 · Recombinant bovine skeletal calsequestrin, high-Ca2+ form · the same entry in another collection · chain A against A, TM-score 1.00
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 Q05JF3
- Elsewhere: RCSB PDB 5KN1 · PDBe 5KN1 · UniProt Q05JF3
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