Nucleoside phosphorothioates as probes of the nucleotide binding site of brain pyridoxal kinase.
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چکیده
منابع مشابه
Nucleoside phosphorothioates as probes of the nucleotide binding site of brain pyridoxal kinase.
N-Dansyl-2-oxopyrrolidine, a competitive inhibitor with respect to ATP, was used as a probe of the nucleotide binding site of pyridoxal kinase. It binds to an hydrophobic region of the catalytic site with a KD = 6 microM. Time emission anisotropy measurements yielded a rotational correlation time of 38 ns for the bound inhibitor. N-Dansyl-2-oxopyrrolidine is immobilized by strong interactions w...
متن کاملBrain Pyridoxal Kinase
F’yridoxal kinase has been purified 2,000-fold from pig brain. The enzyme preparation migrates as a single protein and activity band on analytical gel electrophoresis. Pyridoxal kinase, 60,000 molecular weight, catalyzes the phosphorylation of pyridoxal (K,,, = 2.5 x 10m5 M) and pyridoxine (K, = 1.7 X lo-’ M). Pyridoxamine is not a substrate of the purified kinase. Irradiation of the kinase in ...
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Sphingosine kinase catalyzes the formation of sphingosine 1-phosphate, a lipid second messenger that has been implicated in a number of agonist-driven cellular responses including mitogenesis, anti-apoptosis, and expression of inflammatory molecules. Despite the importance of sphingosine kinase, very little is known regarding its structure or mechanism of catalysis. Moreover, sphingosine kinase...
متن کاملArrangement of the substrates at the active site of brain pyridoxal kinase.
The distances between enzyme-bound paramagnetic CrATP (a stable, beta, gamma-bidentate complex of Cr3+ and ATP) at the active site of sheep brain pyridoxal kinase and the protons of bound inhibitor 4-dPyr (4-deoxypyridoxine) were determined in the ternary enzyme-CrATP.4-dPyr complex by measuring the paramagnetic effects of Cr3+ on the longitudinal relaxation rates (1/T1p) of the protons of 4-dP...
متن کاملآنالیز پروفایل nbs (nucleotide binding-site) ژنهای مقاومت به بیماری در ارقام مختلف زیتون
به منظور مطالعه ژنهای مقاومت nbs-lrr و تنوع ژنتیکی آنها در بین ارقام بومی زیتون و همچنین مقایسه آن با ارقام خارجی، از تکنیک profiling nbs و آنالیزهای مولکولی استفاده شد. برای این منظور dna ژنومی تعداد 5 رقم خارجی و 5 رقم داخلی زیتون استخراج و با آنزیم های برشی alui و rsai هضم و با استفاده از 3 آغازگر دژنره( nbs2،nbs7،nbs5a) در دو مرحله تکثیر شدند و الگوی باندی حاصل از تکثیر انتخابی آنها در روی ...
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ژورنال
عنوان ژورنال: Journal of Biological Chemistry
سال: 1982
ISSN: 0021-9258
DOI: 10.1016/s0021-9258(18)33689-5