MolNFT v1 · #60614 · protein
Crystal structure of cagd from helicobacter pylori pathogenicity island
3CWX · Protein cagd: “Crystal structure of cagd from helicobacter pylori pathogenicity island”. X-ray diffraction, 3 pockets (best druggability 0.63). MolNFT v1 #60614 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 3CWX
- Type
- protein
- Length
- 375 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein cagd
- UniProt
- P94837
- Pockets
- 3 · best druggability 0.63
Structure
x-ray diffraction · 1 distinct chain · 30% helix, 28% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Protein cagd | protein | 125 | 30% helix, 28% strand | P94837 |
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 256 | 0.63 | 0.81 | 29 | empty |
| 2 | 154 | 0.49 | 0.78 | 19 | empty |
| 3 | 85 | 0.39 | 0.78 | 16 | empty |
Interfaces
3 interfaces between chains.
- A–B · 981 Ų buried · 12 hydrogen bonds · protein-protein
- A–C · 643 Ų buried · 8 hydrogen bonds · protein-protein
- B–C · 13 Ų buried · 0 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 9 modified, 4 disulfide (engineered, disulfide).
Compared structures
- 3CWX · Crystal structure of cagd from helicobacter pylori pathogenicity island · 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 P94837
- Elsewhere: RCSB PDB 3CWX · PDBe 3CWX · UniProt P94837
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.