PathWhiz ID | Pathway | Meta Data |
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PW125974View Pathway |
Tutorial May 12Arabidopsis thaliana
Coniferin is
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Creator: Eponine Oler Created On: May 12, 2021 at 14:08 Last Updated: May 12, 2021 at 14:08 |
PW124463View Pathway |
Tutorial PathwayCannabis sativa
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Creator: Eponine Oler Created On: January 19, 2021 at 15:19 Last Updated: January 19, 2021 at 15:19 |
PW145714View Pathway |
drug action
Tyloxapol Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 16:27 Last Updated: October 07, 2023 at 16:27 |
PW123839View Pathway |
signaling
Type I Interferon pathwayHomo sapiens
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Creator: mu Created On: March 19, 2020 at 02:02 Last Updated: March 19, 2020 at 02:02 |
PW064716View Pathway |
Type II Methanotroph PathwayMethylosinus trichosporium OB3b
Type II methanotroph pathway
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Creator: Guest: Anonymous Created On: April 16, 2018 at 13:07 Last Updated: April 16, 2018 at 13:07 |
PW130839View Pathway |
Typhoid vaccine Drug MetabolismHomo sapiens
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Creator: Selena Created On: September 14, 2023 at 22:59 Last Updated: September 14, 2023 at 22:59 |
PW146100View Pathway |
drug action
Tyropanoic acid Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 17:24 Last Updated: October 07, 2023 at 17:24 |
PW000806View Pathway |
Tyrosine BiosynthesisEscherichia coli
Tyrosine is one of the amino acid used in protein synthesis. The tyrosine biosynthesis pathways is connected with the chorismate biosynthesis pathway. Chorismate biosynthesis produce the chorismate, which can further be converted to prephenate by T-protein. Combined with cofactor, NAD, prephenate has been further converted to 4-Hydroxyphenylpyruvic acid by T-protein with generated NADH and carbon dioxide. Tyrosine aminotransferase catalyzes 4-Hydroxyphenylpyruvic acid to tyrosine, and also converts glutamic acid to oxoglutaric acid. Tyrosine will be further catalyzed into various molecules such as 2-iminoacetate, p-Cresol, 5'Deoxyadenosine and L-Methionine; or it will be exported from cell via the lysine exporter.
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Creator: miguel ramirez Created On: March 15, 2015 at 16:37 Last Updated: March 15, 2015 at 16:37 |
PW144277View Pathway |
drug action
Tyrosine Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 13:05 Last Updated: October 07, 2023 at 13:05 |
PW000473View Pathway |
disease
Tyrosine Hydroxylase DeficiencyHomo sapiens
Tyrosine Hydroxylase (TH) Deficiency is a rare inborn error of metabolism (IEM) and autosomal recessive disorder of catecholamines pathways. The disorder is caused by defects in the Tyrosine hydroxylase (TH) gene which encodes for the enzyme tyrosine hydroxylase. This enzyme is part of the production of catecholamines such as dopamine, norepinephrine and epinephrine are all essential for normal nervous system function. Dopamine transmits signals to help the brain control physical movement and emotional behavior. Norepinephrine and epinephrine are involved in the autonomic nervous system. Mutations in the TH gene result in reduced activity of the tyrosine hydroxylase enzyme. As a result, the body produces less dopamine, norepinephrine and epinephrine. Symptoms of the disorder include abnormal movements, autonomic dysfunction, and other neurological problems. Treatments can include the administration of levodopa; however patient responses can vary greatly. The frequency of Tyrosine Hydroxylase Deficiency is unknown.
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Creator: WishartLab Created On: August 29, 2013 at 10:38 Last Updated: August 29, 2013 at 10:38 |