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Summary Structural Experimental Function Sequence Neighbor Download Link


<Asymmetric unit>
= <Biological unit>

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( jV3 / Jmol ) *1
PDB ID1t7j  sequence information (FASTA format)   
RELATED PDB ID1f7a, 1t3r
DescriptorPol Polyprotein (E.C.3.4.23.16)
Titlecrystal structure of inhibitor amprenavir in complex with a multi-drug resistant variant of HIV-1 protease (L63P/V82T/I84V)
Functional KeywordsHIV-1 PROTEASE, DRUG RESITANCE, THERMODYNAMICS, SUBSTRATE ENVELOPE, HYDROLASE
Biological sourceHuman immunodeficiency virus 1
Cellular location [UNP - P35963] Matrix protein p17: Virion (Potential). Capsid protein p24: Virion (Potential). Nucleocapsid protein p7: Virion (Potential). Reverse transcriptase/ribonuclease H: Virion (Potential). Integrase: Virion (Potential)
Total number of polymer chains2
Total molecular weight22405.2 (the details in Structural Details Page)
AuthorsKing, N.M. , Prabu-Jeyabalan, M. , Nalivaika, E.A. , Wigerinck, P.B.T.P. , De Bethune, M.-P. , Schiffer, C.A. (deposition date : 2004-05-10, release date : 2005-05-10)
Primary citationSurleraux, D.L.N.G. , Tahri, A. , Verschueren, W.G. , Pille, G.M.E. , de Kock, H.A. , Jonckers, T.H.M. , Peeters, A. , De Meyer, S. , Azijn, H. , Pauwels, R. , de Bethune, M.-P. , King, N.M. , Prabu-Jeyabalan, M. , Schiffer, C.A. , Wigerinck, P.B.T.P.
Discovery and selection of TMC114, a next generation HIV-1 protease inhibitor
J.Med.Chem., 48:1813 - 1822, 2005.(PubMed : 15771427)  (DOI: 10.1021/jm049560p)
Experimental methodX-RAY DIFFRACTION ( 2.20[Å] )
Other Database Information
Yorodumi , CATH , CE , FSSP , SCOP , VAST , UniProt ( P35963 ) , eF-site , KEGG ( EC 3.4.23.16 ) , PISA