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3NFA

Structural basis for a new mechanism of inhibition of HIV integrase identified by fragment screening and structure based design

Summary for 3NFA
Entry DOI10.2210/pdb3nfa/pdb
Related1bhl 1bi4 1biu 1ex4 1k6y 3NF6 3NF7 3NF8 3NF9
DescriptorIntegrase, SULFATE ION, 6-[(5-bromo-2,3-dioxo-2,3-dihydro-1H-indol-1-yl)methyl]-2,3-dihydro-1,4-benzodioxine-5-carboxylic acid, ... (5 entities in total)
Functional Keywordsintegrase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHuman immunodeficiency virus 1
Total number of polymer chains2
Total formula weight42830.89
Authors
Peat, T.S.,Newman, J.,Deadman, J.J.,Rhodes, D. (deposition date: 2010-06-10, release date: 2011-04-27, Last modification date: 2024-03-20)
Primary citationRhodes, D.I.,Peat, T.S.,Vandegraaff, N.,Jeevarajah, D.,Le, G.,Jones, E.D.,Smith, J.A.,Coates, J.A.,Winfield, L.J.,Thienthong, N.,Newman, J.,Lucent, D.,Ryan, J.H.,Savage, G.P.,Francis, C.L.,Deadman, J.J.
Structural basis for a new mechanism of inhibition of HIV-1 integrase identified by fragment screening and structure-based design
ANTIVIR.CHEM.CHEMOTHER., 21:155-168, 2011
Cited by
PubMed: 21602613
DOI: 10.3851/IMP1716
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.95 Å)
Structure validation

217705

건을2024-03-27부터공개중

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