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Crystal structure of NS3/4A protease variant A156T in complex with mk- 5172

Analyse Crystal structure of NS3/4A protease variant A156T in complex with mk- 5172 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3SUG
Type
protein
Length
201 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NS3 protease, NS4A protein
UniProt
A8DG50
Ligands
SUE, ZN, SO4
Pockets
1 · best druggability 0.32

Structure

x-ray diffraction · 1 distinct chain · 14% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANS3 protease, NS4A proteinprotein20114% helix, 43% strandA8DG50

Ligands and binding sites

  • SUE · (1aR,5S,8S,10R,22aR)-5-tert-butyl-N-{(1R,2S)-1-[(cyclopropylsulfonyl)carbamoyl]-2-ethenylcyclopropyl}-14-methoxy-3,6-di oxo-1,1a,3,4,5,6,9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methanocyclopropa[18,19][1,10,3,6]dioxadiazacyclononadec ino[11,12-b]quinoxaline-8-carboxamide · ligand · chains A
  • ZN · Zinc ion · metal · chains A
  • SO4 · Sulfate ion · ion · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1680.320.7516empty

Compared structures

  • 3SUG · Crystal structure of NS3/4A protease variant A156T in complex with MK-5172 · the same entry in another collection · chain A against A, TM-score 1.00

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