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Product inhibition of mammalian thiamine pyrophosphokinase is an important mechanism for maintaining thiamine diphosphate homeostasis.

Biochimica et biophysica acta. General subjects

Sambon M, Pavlova O, Alhama-Riba J, Wins P, Brans A, Bettendorff L.
PMID: 34942318
Biochim Biophys Acta Gen Subj. 2021 Dec 20;1866(3):130071. doi: 10.1016/j.bbagen.2021.130071. Epub 2021 Dec 20.

BACKGROUND: Thiamine diphosphate (ThDP), an indispensable cofactor for oxidative energy metabolism, is synthesized through the reaction thiamine + ATP ⇆ ThDP + AMP, catalyzed by thiamine pyrophosphokinase 1 (TPK1), a cytosolic dimeric enzyme. It was claimed that the equilibrium...

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Sambon M, Pavlova O, Alhama-Riba J, et al. Product inhibition of mammalian thiamine pyrophosphokinase is an important mechanism for maintaining thiamine diphosphate homeostasis. Biochim Biophys Acta Gen Subj. 2021;1866(3):130071doi: 10.1016/j.bbagen.2021.130071.
Sambon, M., Pavlova, O., Alhama-Riba, J., Wins, P., Brans, A., & Bettendorff, L. (2021). Product inhibition of mammalian thiamine pyrophosphokinase is an important mechanism for maintaining thiamine diphosphate homeostasis. Biochimica et biophysica acta. General subjects, 1866(3), 130071. https://doi.org/10.1016/j.bbagen.2021.130071
Sambon, Margaux, et al. "Product inhibition of mammalian thiamine pyrophosphokinase is an important mechanism for maintaining thiamine diphosphate homeostasis." Biochimica et biophysica acta. General subjects vol. 1866,3 (2021): 130071. doi: https://doi.org/10.1016/j.bbagen.2021.130071
Sambon M, Pavlova O, Alhama-Riba J, Wins P, Brans A, Bettendorff L. Product inhibition of mammalian thiamine pyrophosphokinase is an important mechanism for maintaining thiamine diphosphate homeostasis. Biochim Biophys Acta Gen Subj. 2021 Dec 20;1866(3):130071. doi: 10.1016/j.bbagen.2021.130071. Epub 2021 Dec 20. PMID: 34942318.
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Proteomic consequences of the deletion of cytochrome P450 (CYP450) reductase in mice.

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences

Gethings LA, Gray N, Plumb RS, Wilson ID.
PMID: 34218094
J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Aug 01;1179:122803. doi: 10.1016/j.jchromb.2021.122803. Epub 2021 Jun 17.

Microsomal cytochrome P450 (CYP450) reductase enzymes play a major role in drug and xenobiotic metabolism. Mice which are deficient in hepatic CYP450 reductase serve as excellent models in understanding CYP450 drug metabolism and alterations in the underlying biology and...

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Gethings LA, Gray N, Plumb RS, et al. Proteomic consequences of the deletion of cytochrome P450 (CYP450) reductase in mice. J Chromatogr B Analyt Technol Biomed Life Sci. 2021;1179:122803doi: 10.1016/j.jchromb.2021.122803.
Gethings, L. A., Gray, N., Plumb, R. S., & Wilson, I. D. (2021). Proteomic consequences of the deletion of cytochrome P450 (CYP450) reductase in mice. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1179122803. https://doi.org/10.1016/j.jchromb.2021.122803
Gethings, Lee A, et al. "Proteomic consequences of the deletion of cytochrome P450 (CYP450) reductase in mice." Journal of chromatography. B, Analytical technologies in the biomedical and life sciences vol. 1179 (2021): 122803. doi: https://doi.org/10.1016/j.jchromb.2021.122803
Gethings LA, Gray N, Plumb RS, Wilson ID. Proteomic consequences of the deletion of cytochrome P450 (CYP450) reductase in mice. J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Aug 01;1179:122803. doi: 10.1016/j.jchromb.2021.122803. Epub 2021 Jun 17. PMID: 34218094.
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Temporal synthesis and radiolabelling of the sorghum 3-deoxyanthocyanidin phytoalexins and the anthocyanin, cyanidin 3-dimalonyl glucoside.

The New phytologist

Wharton PS, Nicholson RL.
PMID: 33862912
New Phytol. 2000 Mar;145(3):457-469. doi: 10.1046/j.1469-8137.2000.00600.x.

Sorghum (Sorghum bicolor) synthesizes a complex mixture of 3-deoxyanthocyanidin phytoalexins in response to inoculation with the non-pathogenic fungus Bipolaris maydis. The anthocyanin cyanidin 3-dimalonyl glucoside, is also synthesized naturally in response to light. To determine the order and time...

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Wharton PS, Nicholson RL. Temporal synthesis and radiolabelling of the sorghum 3-deoxyanthocyanidin phytoalexins and the anthocyanin, cyanidin 3-dimalonyl glucoside. New Phytol. 2000;145(3):457-469doi: 10.1046/j.1469-8137.2000.00600.x.
Wharton, P. S., & Nicholson, R. L. (2000). Temporal synthesis and radiolabelling of the sorghum 3-deoxyanthocyanidin phytoalexins and the anthocyanin, cyanidin 3-dimalonyl glucoside. The New phytologist, 145(3), 457-469. https://doi.org/10.1046/j.1469-8137.2000.00600.x
Wharton, Phillip S, and Nicholson, Ralph L. "Temporal synthesis and radiolabelling of the sorghum 3-deoxyanthocyanidin phytoalexins and the anthocyanin, cyanidin 3-dimalonyl glucoside." The New phytologist vol. 145,3 (2000): 457-469. doi: https://doi.org/10.1046/j.1469-8137.2000.00600.x
Wharton PS, Nicholson RL. Temporal synthesis and radiolabelling of the sorghum 3-deoxyanthocyanidin phytoalexins and the anthocyanin, cyanidin 3-dimalonyl glucoside. New Phytol. 2000 Mar;145(3):457-469. doi: 10.1046/j.1469-8137.2000.00600.x. PMID: 33862912.
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Showing 253 to 255 of 255 entries