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Summary Structural Experimental Function Sequence Neighbor Download Link


<Asymmetric unit>
= <Biological unit>

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( jV3 / Jmol ) *1
PDB ID1npv  sequence information (FASTA format)   
DescriptorPOL polyprotein [Contains: Protease, {1-BENZYL-3-[2-BENZYL-3-OXO-4-(1-OXO-1,2,3,4-TETRAHYDRO- ISOQUINOLIN-4-YL)-2,3-DIHYDRO-1H-PYRROL-2-YL]-2- HYDROXY-PROPYL}-CARBAMIC ACID TETRAHYDRO-FURAN-3-YL ESTER
TitleCrystal structure of HIV-1 protease complexed with LDC271
Functional KeywordsProtease, Hydrolase
HYDROLASE
Biological sourceHuman immunodeficiency virus 1
Total number of polymer chains2
Total molecular weight22203.3 (the details in Structural Details Page)
AuthorsSmith, A.B. (deposition date : 2003-01-20, release date : 2003-02-04)
Primary citationSmith, A.B. , Cantin, L.D. , Pasternak, A. , Guise-Zawacki, L. , Yao, W. , Charnley, A.K. , Barbosa, J. , Sprengeler, P.A. , Hirschmann, R. , Munshi, S. , Olsen, D.B. , Schleif, W.A. , Kuo, L.C.
Design, synthesis, and biological evaluation of monopyrrolinone-based HIV-1 protease inhibitors.
J.Med.Chem., 46:1831 - 1844, 2003.(PubMed : 12723947)  (DOI: 10.1021/jm0204587)
Experimental methodX-RAY DIFFRACTION ( 2.[Å] )
Other Database Information
Yorodumi , CATH , CE , FSSP , SCOP , VAST , UniProt ( P03366 ) , eF-site , KEGG ( EC 3.4.23.16 ) , PISA