Research workbench
Structure of the SARS-cov-2 main protease in complex with halicin
Analyse Structure of the SARS-cov-2 main protease in complex with halicin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7TUU
- Type
- protein
- Length
- 306 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 3C-like proteinase NSP5
- EC
- 3.4.22.69
- UniProt
- P0DTC1
- Ligands
- U88
- Pockets
- 2 · best druggability 0.50
Structure
x-ray diffraction · 1 distinct chain · 25% helix, 28% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | 3C-like proteinase NSP5 (EC 3.4.22.69) | protein | 306 | 25% helix, 28% strand | P0DTC1 |
Ligands and binding sites
- U88 · 5-nitro-1,3-thiazole · ligand · 3 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 210 | 0.50 | 0.76 | 25 | U88 |
| 2 | 210 | 0.49 | 0.75 | 29 | empty |
Modifications
Observed in the structure: 3 covalent (covalent ligand).
Compared structures
- 7TUU · Structure of the SARS-CoV-2 main protease in complex with halicin · 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 P0DTC1
- Elsewhere: RCSB PDB 7TUU · PDBe 7TUU · UniProt P0DTC1
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