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Structure of dengue virus protease with an allosteric inhibitor that blocks replication

Analyse Structure of dengue virus protease with an allosteric inhibitor that blocks… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6MO0
Type
protein
Length
328 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
FLAVIVIRUS_NS2B/PEPTIDASE S7
UniProt
A0A0B4L2Y4, Q91H74
Ligands
JVJ
Pockets
4 · best druggability 0.51

Structure

x-ray diffraction · 1 distinct chain · 4% helix, 44% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BFLAVIVIRUS_NS2B/PEPTIDASE S7protein1644% helix, 44% strandA0A0B4L2Y4, Q91H74

Ligands and binding sites

  • JVJ · 1-(4-{3-[4-(furan-3-yl)phenyl]-5-[(piperidin-4-yl) methoxy]pyrazin-2-yl}phenyl)methanamine · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11560.510.7821empty
21010.460.8019empty
31800.440.7529empty
41060.430.7815empty

Interfaces

1 interface between chains.

  • A–B · 287 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 6MO0 · Structure of dengue virus protease with an allosteric Inhibitor that blocks replication · the same entry in another collection · chain A against A, TM-score 1.00

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