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TitlePrivileged Structures Meet Human T-Cell Leukemia Virus-1 (HTLV-1): C2-Symmetric 3,4-Disubstituted Pyrrolidines as Nonpeptidic HTLV-1 Protease Inhibitors.
Journal, issue, pagesJ. Med. Chem., Vol. 58, Page 4845-4850, Year 2015
Publish dateFeb 22, 2015 (structure data deposition date)
AuthorsKuhnert, M. / Blum, A. / Steuber, H. / Diederich, W.E.
External linksJ. Med. Chem. / PubMed:26000468
MethodsX-ray diffraction
Resolution2.804 - 3.25 Å
Structure data

PDB-4ydf:
Crystal structure of compound 9 in complex with HTLV-1 Protease
Method: X-RAY DIFFRACTION / Resolution: 2.804 Å

PDB-4ydg:
Crystal structure of compound 10 in complex with HTLV-1 Protease
Method: X-RAY DIFFRACTION / Resolution: 3.25 Å

Chemicals

ChemComp-4B1:
N-benzyl-N-[(3S,4S)-4-{benzyl[(4-nitrophenyl)sulfonyl]amino}pyrrolidin-3-yl]-3-nitrobenzenesulfonamide

ChemComp-SO4:
SULFATE ION

ChemComp-HOH:
WATER

ChemComp-G3G:
N,N'-(3S,4S)-PYRROLIDINE-3,4-DIYLBIS(4-AMINO-N-BENZYLBENZENESULFONAMIDE)

Source
  • human t-lymphotropic virus 1
  • human t-cell leukemia virus 1 (strain japan atk-1 subtype a)
KeywordsHYDROLASE / HTLV-1 protease

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