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Crystal structure of SARS coronavirus main protease complexed with ac- nsfsq-H (soaking)

Analyse Crystal structure of SARS coronavirus main protease complexed with ac- nsfsq-H… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3SNA
Type
protein
Length
306 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
3C-like proteinase; Peptide aldehyde inhibitor ac-nsfsq-H
EC
3.4.22.-
UniProt
P0C6U8
Ligands
ACE
Pockets
2 · best druggability 0.41

Structure

x-ray diffraction · 2 distinct chains · 24% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A3C-like proteinase (EC 3.4.22.-)protein30124% helix, 28% strandP0C6U8
HPeptide aldehyde inhibitor ac-nsfsq-Hprotein50% helix, 20% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · chains H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11270.410.7526empty
2570.290.7515empty

Interfaces

1 interface between chains.

  • A–H · 491 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent, 1 modified (covalent ligand, nonstandard).

Compared structures

  • 3SNA · Crystal structure of SARS coronavirus main protease complexed with Ac-NSFSQ-H (soaking) · the same entry in another collection · chain A against A, TM-score 1.00

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