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1 ackup" regulator of pathway flux relative to pantothenate kinase.
2 s the starting metabolite, phosphorylated by pantothenate kinase.
3 ions of the phosphoryl transfer mechanism of pantothenate kinase.
4 N-alkylpantothenamides are substrates for pantothenate kinase.
5 ural substrate PA for phosphorylation by the pantothenate kinase.
6 pathway and is mediated by four isoforms of pantothenate kinase.
11 disease have mutations in the gene encoding pantothenate kinase 2 (PANK2); these patients are said t
18 ry properties exhibited by the family of the pantothenate kinases allowed the rate of CoA biosynthesi
19 gulator, and antimetabolite binding sites on pantothenate kinase and provide a framework for studies
20 icated in neurodegenerative diseases such as pantothenate kinase-associated neurodegeneration (PKAN)
26 den-Spatz syndrome, the disorder was renamed pantothenate kinase-associated neurodegeneration after d
27 e shown great potential for the treatment of pantothenate kinase-associated neurodegeneration and pro
29 PanK2(G521R), the most frequent mutation in pantothenate kinase-associated neurodegeneration, was de
36 e structural information on Escherichia coli pantothenate kinase by determining the structure of the
43 CoA biosynthesis in bacteria and mammals is pantothenate kinase (CoaA), which governs the intracellu
44 , both active sites of the dimeric mammalian pantothenate kinases coordinately switch between the on
47 of two new classes of compounds that inhibit pantothenate kinase from M. tuberculosis are described,
48 coside phosphotransferase [APH(3')-IIIa] and pantothenate kinases from Escherichia coli (EcPanK) and
49 s, including the finding of mutations in the pantothenate kinase gene and ferritin light chain gene,
50 ow that HSS is caused by a defect in a novel pantothenate kinase gene and propose a mechanism for oxi
52 , especially given the existence of multiple pantothenate kinase genes in humans and multiple PanK2 t
53 spatial and chemical distribution of evolved pantothenate kinase immobilized onto two diverse, microp
56 trate the key role of feedback regulation of pantothenate kinase in the control of intracellular CoA
57 ns indicate that this type of "bifunctional" pantothenate kinase is conserved in other higher eukaryo
60 report here the characterization of a second pantothenate kinase of Arabidopsis, AtPANK2, as well as
63 In Bacillus anthracis, the novel type III pantothenate kinase (PanK(Ba); encoded by coaX) catalyze
64 al and animal coenzyme A (CoA) biosynthesis, pantothenate kinase (PANK) activity is critical in regul
78 The absence of feedback regulation at the pantothenate kinase step allows the accumulation of high
80 quence that is more similar to the mammalian pantothenate kinases than the prototypical bacterial Coa
81 in human brain, distinguishing it from other pantothenate kinases that do not possess mitochondrial-t
82 ate specificities associated with endogenous pantothenate kinase, the first enzyme in the CoA biosynt