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Crystal structure of human coronavirus NL63 3C-like protease

Analyse Crystal structure of human coronavirus NL63 3C-like protease in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7E6M
Type
protein
Length
598 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
3C-like proteinase
EC
3.4.22.-
UniProt
P0C6U6
Pockets
5 · best druggability 0.72

Structure

x-ray diffraction · 1 distinct chain · 24% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B3C-like proteinase (EC 3.4.22.-)protein29924% helix, 29% strandP0C6U6

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19560.720.7682empty
24880.650.7762empty
35070.630.7661empty
41460.430.7527empty
51060.380.7519empty

Interfaces

1 interface between chains.

  • A–B · 1045 Ų buried · 19 hydrogen bonds · protein-protein

Compared structures

  • 7E6M · Crystal structure of Human coronavirus NL63 3C-like protease · the same entry in another collection · chain A against A, TM-score 1.00

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