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TitleL-Enantiomers of transition state analogue inhibitors bound to human purine nucleoside phosphorylase.
Journal, issue, pagesJ. Am. Chem. Soc., Vol. 130, Page 842-844, Year 2008
Publish dateJun 7, 2007 (structure data deposition date)
AuthorsRinaldo-Matthis, A. / Murkin, A.S. / Ramagopal, U.A. / Clinch, K. / Mee, S.P. / Evans, G.B. / Tyler, P.C. / Furneaux, R.H. / Almo, S.C. / Schramm, V.L.
External linksJ. Am. Chem. Soc. / PubMed:18154341
MethodsX-ray diffraction
Resolution2.099 - 2.9 Å
Structure data

PDB-2q7o:
Structure of human purine nucleoside phosphorylase in complex with L-Immucillin-H
Method: X-RAY DIFFRACTION / Resolution: 2.9 Å

PDB-3bgs:
Structure of human purine nucleoside phosphorylase with L-DADMe-ImmH and phosphate
Method: X-RAY DIFFRACTION / Resolution: 2.099 Å

Chemicals

ChemComp-PO4:
PHOSPHATE ION

ChemComp-IMH:
1,4-DIDEOXY-4-AZA-1-(S)-(9-DEAZAHYPOXANTHIN-9-YL)-D-RIBITOL / inhibitor*YM

ChemComp-HOH:
WATER

ChemComp-DIH:
7-[[(3R,4R)-3-(hydroxymethyl)-4-oxidanyl-pyrrolidin-1-ium-1-yl]methyl]-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / purine nucleoside phosphorylase / PNP / transition state analogue / L-enantiomer

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