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5UOQ

CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS INTASOME WITH A 2- PYRIDINONE AMINAL INHIBITOR (COMPOUND 31)

Summary for 5UOQ
Entry DOI10.2210/pdb5uoq/pdb
Related5uop
DescriptorINTEGRASE, NUCLEOTIDE PREPROCESSED PFV DONOR DNA (NON-TRANSFERRED STRAND), NUCLEOTIDE PREPROCESSED PFV DONOR DNA (TRANSFERRED STRAND), ... (9 entities in total)
Functional Keywordstransferase-dna complex, dna integration, viral protein, recombination-inhibitor-dna complex, transferase-dna-inhibitor complex, transferase/dna/inhibitor
Biological sourceHuman spumaretrovirus (SFVcpz(hu))
More
Cellular locationIntegrase: Virion . Protease/Reverse transcriptase/ribonuclease H: Host nucleus : P14350
Total number of polymer chains4
Total formula weight101335.46
Authors
Klein, D.J. (deposition date: 2017-02-01, release date: 2017-03-29, Last modification date: 2024-03-06)
Primary citationSchreier, J.D.,Embrey, M.W.,Raheem, I.T.,Barbe, G.,Campeau, L.C.,Dubost, D.,McCabe Dunn, J.,Grobler, J.,Hartingh, T.J.,Hazuda, D.J.,Klein, D.,Miller, M.D.,Moore, K.P.,Nguyen, N.,Pajkovic, N.,Powell, D.A.,Rada, V.,Sanders, J.M.,Sisko, J.,Steele, T.G.,Wai, J.,Walji, A.,Xu, M.,Coleman, P.J.
Discovery and optimization of 2-pyridinone aminal integrase strand transfer inhibitors for the treatment of HIV.
Bioorg. Med. Chem. Lett., 27:2038-2046, 2017
Cited by
PubMed: 28285916
DOI: 10.1016/j.bmcl.2017.02.039
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.61 Å)
Structure validation

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