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Crystal structure of SARS-cov-2 main protease (mpro) E166N mutant

Analyse Crystal structure of SARS-cov-2 main protease (mpro) E166N mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
8DDI
Type
protein
Length
305 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
P0DTD1
Pockets
2 · best druggability 0.43

Structure

x-ray diffraction · 1 distinct chain · 26% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A3C-like proteinase NSP5 (EC 3.4.22.69)protein30526% helix, 28% strandP0DTD1

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11390.430.7530empty
21170.410.7618empty

Compared structures

  • 8DDI · Crystal Structure of SARS-CoV-2 Main Protease (Mpro) E166N Mutant · the same entry in another collection · chain A against A, TM-score 1.00

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