Research workbench
Cryoem structure of polycystin-2 in complex with calcium and lipids
Analyse Cryoem structure of polycystin-2 in complex with calcium and lipids in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5MKF
- Type
- protein
- Length
- 1,924 residues
- Chains
- 4
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Polycystin-2
- UniProt
- Q13563
- Ligands
- PLM, CHS, PX6, NAG, CA
- Pockets
- 20 · best druggability 0.83
Structure
electron microscopy · 1 distinct chain · 53% helix, 10% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Polycystin-2 | protein | 481 | 53% helix, 10% strand | Q13563 |
Ligands and binding sites
- PLM · Palmitic acid · ligand · 12 copies · chains A, B, C, D
- CHS · 4-amino-5-cyclohexyl-3-hydroxy-pentanoic acid · ligand · 8 copies · chains A, B, C, D
- PX6 · 1,2-dipalmitoyl-sn-glycero-3-phosphate · ligand · 4 copies · chains A, B, C, D
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 20 copies · chains A, B, C, D
- CA · Calcium ion · metal · 5 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 337 | 0.83 | 0.92 | 56 | empty |
| 2 | 336 | 0.83 | 0.92 | 55 | empty |
| 3 | 335 | 0.83 | 0.92 | 55 | empty |
| 4 | 335 | 0.83 | 0.92 | 57 | empty |
| 5 | 194 | 0.80 | 0.94 | 24 | CA |
Interfaces
6 interfaces between chains.
- A–B · 3236 Ų buried · 25 hydrogen bonds · protein-protein
- A–D · 3206 Ų buried · 22 hydrogen bonds · protein-protein
- C–D · 3205 Ų buried · 22 hydrogen bonds · protein-protein
- B–C · 3202 Ų buried · 23 hydrogen bonds · protein-protein
- A–C · 27 Ų buried · 0 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 16 glycan, 4 disulfide (N-glycosylation, 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 Q13563
- Elsewhere: RCSB PDB 5MKF · PDBe 5MKF · UniProt Q13563
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