| Literature DB >> 8995274 |
J D McCarter1, D L Burgoyne, S Miao, S Zhang, J W Callahan, S G Withers.
Abstract
Human lysosomal beta-galactosidase catalyzes the hydrolysis of beta-galactosides via a double displacement mechanism involving a covalent glycosyl enzyme intermediate. By use of the slow substrate 2,4-dinitrophenyl-2-deoxy-2-fluoro-beta-D-galactopyranoside, a glycosyl enzyme intermediate has been trapped on the enzyme. This has allowed the catalytic nucleophile to be identified as Glu-268 by peptic and tryptic digestion of the inactivated enzyme followed by high performance liquid chromatography-electrospray ionization tandem mass spectrometry of the peptide mixture. This glutamic acid is fully conserved in a sequence-related family of enzymes (Family 35), consistent with its essential role.Entities:
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Year: 1997 PMID: 8995274 DOI: 10.1074/jbc.272.1.396
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157