GL1X · GenesisL1 explorer

Research workbench

The crystal structure of the 2009 H1N1 pa endonuclease wild type in complex with SJ000988632

Analyse The crystal structure of the 2009 H1N1 pa endonuclease wild type in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6V9E
Type
protein
Length
177 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Polymerase acidic protein
UniProt
C6H0Y9
Ligands
QQP, Y24, MN, SO4
Pockets
1 · best druggability 0.65

Structure

x-ray diffraction · 1 distinct chain · 51% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APolymerase acidic proteinprotein17751% helix, 13% strandC6H0Y9

Ligands and binding sites

  • QQP · N-[2-(6-amino-9H-purin-9-yl)ethyl]-5-hydroxy-6-oxo-2-[2-(trifluoromethyl)phenyl]-1,6-dihydropyrimidine-4-carboxamide · ligand · chains A
  • Y24 · 1,1',1'',1''',1''''-[(3R,5S,7S,9R)-decane-1,3,5,7,9-pentayl]penta(pyrrolidin-2-one) · ligand · chains A
  • MN · Manganese (II) ion · metal · 2 copies · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14530.650.7851MN, QQP

Compared structures

  • 6V9E · The crystal structure of the 2009 H1N1 PA endonuclease wild type in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.