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Crystal structure of NSP15 endoribonuclease from SARS cov-2 in the complex with potential repurposing drug tipiracil

Analyse Crystal structure of NSP15 endoribonuclease from SARS cov-2 in the complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6WXC
Type
protein
Length
695 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Uridylate-specific endoribonuclease
EC
3.1.-.-
UniProt
P0DTD1
Ligands
CMU, PO4
Pockets
7 · best druggability 0.58

Structure

x-ray diffraction · 2 distinct chains · 22% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUridylate-specific endoribonuclease (EC 3.1.-.-)protein34822% helix, 31% strandP0DTD1
BUridylate-specific endoribonuclease (EC 3.1.-.-)protein34722% helix, 31% strandP0DTD1

Ligands and binding sites

  • CMU · 5-chloro-6-(1-(2-iminopyrrolidinyl) methyl) uracil · ligand · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 9 copies · chains A, B
  • FMT · Formic acid · additive · 4 copies · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12100.580.8025empty
22370.580.7934empty
31310.400.7418empty
41330.390.7322EDO
5930.340.7420empty

Interfaces

1 interface between chains.

  • A–B · 32 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6WXC · Crystal Structure of NSP15 Endoribonuclease from SARS CoV-2 in the Complex with potential… · the same entry in another collection · chain A against A, TM-score 1.00

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