Mevalonate kinase deficiency (MKD) is an autosomal recessive metabolic disorder that disrupts the biosynthesis of cholesterol and isoprenoids. It is a...
17 KB (1,960 words) - 22:12, 13 November 2024
Mevalonate kinase is an enzyme (specifically a kinase) that in humans is encoded by the MVK gene. Mevalonate kinases are found in a wide variety of organisms...
14 KB (1,367 words) - 12:41, 7 January 2024
diseases such as osteoporosis) A number of diseases affect the mevalonate pathway: Mevalonate Kinase Deficiency Mevalonic Aciduria Hyperimmunoglobulinemia D...
9 KB (756 words) - 19:22, 14 January 2025
classified mevalonate diphosphate decarboxylase as an enzyme in the GHMP kinase family (galactokinase, homoserine kinase, mevalonate kinase, and phosphomevalonate...
16 KB (1,611 words) - 13:53, 26 August 2023
code North Macedonia, ISO 3166-1 alpha-3 code and IOC country code Mevalonate kinase deficiency, a metabolic disorder mkd (software), a documentation extractor...
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The non-mevalonate pathway—also appearing as the mevalonate-independent pathway and the 2-C-methyl-D-erythritol 4-phosphate/1-deoxy-D-xylulose 5-phosphate...
17 KB (1,657 words) - 15:33, 9 January 2025
infection. Episodic and multisystem AIDs (NLRP12-associated disease, mevalonate kinase deficiency, PFAPA (periodic fever syndrome, aphthous stomatitis, pharyngitis...
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periodic syndrome (TRAPS), hyperimmunoglobulin D syndrome (HIDS)/mevalonate kinase deficiency (MKD), and familial mediterranean fever (FMF). In June...
15 KB (1,294 words) - 22:06, 7 March 2025
and in two additional autoinflammatory recurrent fever syndromes: mevalonate kinase deficiency (hyper-immunoglobulin D syndrome, or HIDS) and tumor necrosis...
25 KB (2,684 words) - 06:10, 8 April 2025
phytol kinase EC 2.7.1.183: glycoprotein-mannosyl O6-kinase EC 2.7.1.184: sulfofructose kinase EC 2.7.1.185: mevalonate 3-kinase EC 2.7.1.186: mevalonate-3-phosphate...
215 KB (21,664 words) - 05:19, 27 April 2025
(HIDS). This is now (along with mevalonic aciduria) defined as a mevalonate kinase deficiency 260920 MVK TNF receptor associated periodic syndrome (TRAPS)...
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kinase family is a family of kinase enzymes. Members of this family include homoserine kinases EC 2.7.1.39, galactokinases EC 2.7.1.6, and mevalonate...
3 KB (309 words) - 10:09, 6 July 2021
(or CDP-ME) is an intermediate in the MEP pathway (non-mevalonate pathway) of isoprenoid precursor biosynthesis. It is produced by the enzyme...
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for Familial Mediterranean fever, Hyper-IgD syndrome also known as Mevalonate kinase deficiency, and TNF receptor associated periodic syndrome (TRAPS)...
25 KB (2,148 words) - 22:52, 25 April 2025
Statin (redirect from Mevalonate inhibition)
competitively inhibiting HMG-CoA reductase, the rate-limiting enzyme of the mevalonate pathway. Because statins are similar in structure to HMG-CoA on a molecular...
136 KB (13,282 words) - 12:40, 15 May 2025
Phosphomevalonate kinase is an enzyme (EC 2.7.4.2) in the mevalonate pathway that in humans is encoded by the PMVK gene. GRCh38: Ensembl release 89: ENSG00000163344...
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its original members: galactokinase, homoserine kinase, mevalonate kinase, and phosphomevalonate kinase. Members of the GHMP superfamily have great three-dimensional...
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"Isopentenyl diphosphate biosynthesis via a mevalonate-independent pathway: isopentenyl monophosphate kinase catalyzes the terminal enzymatic step". Proceedings...
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within the peroxisomes of the apocrine glands by enzymes such as mevalonate kinases. Pheromones are a factor seen in the mating selection and reproduction...
46 KB (5,238 words) - 01:11, 13 May 2025
encompasses both hereditary types (familial Mediterranean fever, mevalonate kinase deficiency, TNF receptor associated periodic syndrome, cryopyrin-associated...
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mut-0 Methylmalonyl-Coenzyme A mutase deficiency Methemoglobinemia Mevalonate kinase deficiency Mevalonicaciduria Meyenburg–Altherr–Uehlinger syndrome...
28 KB (2,470 words) - 15:50, 17 May 2025
This enzyme is also called CDP-ME kinase, and IspE. This enzyme participates in the MEP pathway (non-mevalonate pathway) of isoprenoid precursor biosynthesis...
3 KB (311 words) - 12:39, 26 August 2023
receptor associated periodic syndrome (TRAPS) Hyper-IgD syndrome (Mevalonate kinase deficiency) CIAS1-related diseases: Muckle–Wells syndrome Familial...
19 KB (1,849 words) - 07:31, 11 May 2025
is activated on perception, which then converts HMG-CoA into mevalonate. This mevalonate acts as a second messenger and activates a nuclear K+ cation...
53 KB (4,793 words) - 15:45, 30 December 2024
Hyperimmunoglobulin D syndrome in 50% of cases is associated with mevalonate kinase deficiency which can be measured in the leukocytes.[citation needed]...
10 KB (1,193 words) - 03:25, 23 September 2024
enzyme (NADH-dependent, EC 1.1.1.88; NADPH-dependent, EC 1.1.1.34) of the mevalonate pathway, the metabolic pathway that produces cholesterol and other isoprenoids...
34 KB (4,113 words) - 16:29, 29 July 2024
of the HMG-CoA reductase pathway. The product of HMG CoA reductase is mevalonate. By combining precursors with 5 carbons, the pathway subsequently produces...
15 KB (1,810 words) - 16:46, 26 June 2024
(plague) Controls ASC-mediated apoptosis Familial Mediterranean fever (FMF), mevalonate kinase deficiency (MKD), hyperimmunoglobulinemia D syndrome (HIDS)...
14 KB (1,166 words) - 21:32, 14 April 2025
The resulting mevalonate is then sequentially phosphorylated by two separate kinases, mevalonate kinase and phosphomevalonate kinase, to form 5-pyrophosphomevalonate...
10 KB (945 words) - 23:27, 8 December 2024
(or mevalonate-5-pyrophosphate, or 5-pyrophosphomevalonate) is an intermediate in the mevalonate pathway. Mevalonic acid Phosphomevalonate kinase Pyrophosphomevalonate...
2 KB (41 words) - 19:59, 29 June 2024