MolNFT v1 · #186556 · protein
Cryo-EM structure of xenopus patched-1 in nanodisc
7RHR: “Cryo-EM structure of xenopus patched-1 in nanodisc”. Electron microscopy, 2 ligands (CLR, NAG), 9 pockets (best druggability 0.90). MolNFT v1 #186556 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 7RHR
- Type
- protein
- Length
- 974 residues
- Chains
- 1
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Patched-1
- UniProt
- Q98SW6
- Ligands
- CLR, NAG
- Pockets
- 9 · best druggability 0.90
Structure
electron microscopy · 1 distinct chain · 56% helix, 8% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Patched-1 | protein | 974 | 56% helix, 8% strand | Q98SW6 |
Ligands and binding sites
- CLR · Cholesterol · ligand · 3 copies · chains A
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · 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, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1128 | 0.90 | 0.91 | 127 | CLR |
| 2 | 284 | 0.76 | 0.88 | 34 | empty |
| 3 | 218 | 0.57 | 0.79 | 27 | empty |
| 4 | 178 | 0.52 | 0.78 | 19 | empty |
| 5 | 141 | 0.42 | 0.74 | 18 | CLR |
Modifications
Observed in the structure: 3 disulfide, 3 glycan (disulfide, N-glycosylation).
Compared structures
- 7RHR · Cryo-EM structure of Xenopus Patched-1 in nanodisc · 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 Q98SW6
- Elsewhere: RCSB PDB 7RHR · PDBe 7RHR · UniProt Q98SW6
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.