Unexpected tolerance of glycosylation by udp-galnac:polypeptide α- N -acetylgalactosaminyltransferase revealed by electron capture dissociation mass spectrometry: Carbohydrate as potential protective groups

Biochemistry

Volumn 49, Issue 28, 2010, Pages 5929-5941

  Yoshimura, Yayoi ^a   Matsushita, Takahiko ^a   Fujitani, Naoki ^a   Takegawa, Yasuhiro ^a   Fujihira, Haruhiko ^a   Naruchi, Kentarou ^a   Gao, Xiao Dong ^a   Manri, Naomi ^b   Sakamoto, Takeshi ^b   Kato, Kentaro ^a   Hinou, Hiroshi ^a   Nishimura, Shin Ichiro ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b HITACHI LTD   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANOMERIC CARBON; CATALYTIC DOMAINS; DESIRED POSITION; ELECTRON CAPTURE DISSOCIATION; ELECTROSPRAY SOURCE; ENZYMATIC SYNTHESIS; GLYCOPEPTIDES; GLYCOSYLATED; HYDROXYL GROUPS; ION TRAPS; ISOFORMS; KEY ENZYMES; NOVEL CONCEPT; O-GLYCANS; O-GLYCOSYLATION; PEPTIDE LINKAGES; POST-TRANSLATIONAL MODIFICATIONS; PRECURSOR IONS; PROTECTIVE GROUP; STRUCTURAL CHARACTERIZATION; SUGAR RESIDUES; SYNTHETIC PEPTIDE; TOF MASS SPECTROMETER;

CARBOHYDRATES; DISSOCIATION; ENZYMES; ESTERIFICATION; FUNCTIONAL GROUPS; GLYCOPROTEINS; GLYCOSYLATION; INTERNET PROTOCOLS; IONS; MASS SPECTROMETRY; REDUCTION; STEREOCHEMISTRY; SUGAR (SUCROSE); SYNTHESIS (CHEMICAL);

PEPTIDES;

CARBOHYDRATE; CARBON; FUCOSYLGALACTOSE ALPHA N ACETYLGALACTOSAMINYLTRANSFERASE; GLYCOPEPTIDE; HYDROXYL GROUP; ISOPROTEIN; MUCIN; URIDINE DIPHOSPHATE N ACETYLGALACTOSAMINE;

ARTICLE; CARBOHYDRATE ANALYSIS; DECOMPOSITION; ELECTRON CAPTURE DISSOCIATION MASS SPECTROMETRY; ENZYME ACTIVE SITE; ENZYME SYNTHESIS; GLYCOSYLATION; HUMAN; ION TRAP MASS SPECTROMETRY; MALE; MASS SPECTROMETRY; PRIORITY JOURNAL; PROTEIN PROCESSING; PROTEIN SYNTHESIS; STEREOCHEMISTRY;

CARBOHYDRATES; CATALYTIC DOMAIN; ELECTRONS; GLYCOPEPTIDES; GLYCOSYLATION; HUMANS; LECTINS; MASS SPECTROMETRY; MUCINS; N-ACETYLGALACTOSAMINYLTRANSFERASES; PEPTIDES; POLYSACCHARIDES; THREONINE; URIDINE DIPHOSPHATE;

EID: 77954599524     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi100623g     Document Type: Article

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