MolNFT v1 · #167928 · protein
The 1.9 a crystal structure of NSP15 endoribonuclease from SARS cov-2 in the complex with a citrate
6W01 · Uridylate-specific endoribonuclease: “The 1.9 a crystal structure of NSP15 endoribonuclease from SARS cov-2 in the complex with a citrate”. X-ray diffraction, 6 pockets (best druggability 0.59). MolNFT v1 #167928 on GenesisL1: 3D…
- PDB
- 6W01
- Type
- protein
- Length
- 694 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Uridylate-specific endoribonuclease
- EC
- 3.1.-.-
- UniProt
- P0DTD1
- Pockets
- 6 · best druggability 0.59
Structure
x-ray diffraction · 1 distinct chain · 21% helix, 31% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Uridylate-specific endoribonuclease (EC 3.1.-.-) | protein | 347 | 21% helix, 31% strand | P0DTD1 |
Ligands and binding sites
- EDO · 1,2-ethanediol · additive · 22 copies · chains A, B
- PEG · Di(hydroxyethyl)ether · additive · 3 copies · chains A, B
- CIT · Citric acid · additive · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 265 | 0.59 | 0.79 | 31 | empty |
| 2 | 223 | 0.59 | 0.80 | 28 | EDO |
| 3 | 204 | 0.45 | 0.73 | 26 | empty |
| 4 | 86 | 0.33 | 0.74 | 21 | EDO |
| 5 | 70 | 0.31 | 0.75 | 17 | empty |
Interfaces
1 interface between chains.
- A–B · 60 Ų buried · 0 hydrogen bonds · protein-protein
Compared structures
- 6W01 · The 1.9 A Crystal Structure of NSP15 Endoribonuclease from SARS CoV-2 in the Complex with… · the same entry in another collection · chain B against B, 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 P0DTD1
- Elsewhere: RCSB PDB 6W01 · PDBe 6W01 · UniProt P0DTD1
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