Ionization state of pyridoxal 5′-phosphate in D-serine dehydratase, dialkylglycine decarboxylase and tyrosine phenol-lyase and the influence of monovalent cations as inferred by 31P NMR spectroscopy

Biochimica et Biophysica Acta - Proteins and Proteomics

Volumn 1764, Issue 2, 2006, Pages 230-238

  Schnackerz, Klaus D ^a   Keller, John ^b   Phillips, Robert S ^c   Toney, Michael D ^d  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b UNIVERSITY OF ALASKA FAIRBANKS   (United States)

^c UNIVERSITY OF GEORGIA   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

31P chemical shift; D serine dehydratase; Dialkylglycine decarboxylase; Monovalent cations; Ppyridoxal 5 phosphate; Tyrosine phenol lyase

Indexed keywords

ALKALI METAL; DEXTRO SERINE DEHYDRATASE; DIALKYLGLYCINE DECARBOXYLASE; ENZYME; METAL ION; MONOVALENT CATION; PHOSPHATE; PYRIDOXAL 5 PHOSPHATE; TYROSINE PHENOL LYASE; UNCLASSIFIED DRUG;

ARTICLE; BINDING SITE; ENZYME STRUCTURE; IONIZATION; NONHUMAN; PH; PHOSPHORUS NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 33644543360     PISSN: 15709639     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbapap.2005.10.009     Document Type: Article

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