PathWhiz ID | Pathway | Meta Data |
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PW353410View Pathway |
Trehalose Degradation I (Low Osmolarity)Trabulsiella guamensis ATCC 49490
In E.coli, trehalose can be only synthesized with high osmolarity, and if the osmolarity is low, then the source of trehalose can be only obtained from external via transportation with trehalose PTS permease. However, sugar can be degraded with both low or high osmolarity in E.coli. Glucokinase can phosphorylate free gluocose into glucose-6-phosphate and both glucose-6-phosphate moieties enter glycolysis.
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Creator: Julia Wakoli Created On: November 08, 2024 at 21:46 Last Updated: November 08, 2024 at 21:46 |
PW353388View Pathway |
Trehalose Degradation I (Low Osmolarity)Citrobacter youngae ATCC 29220
In E.coli, trehalose can be only synthesized with high osmolarity, and if the osmolarity is low, then the source of trehalose can be only obtained from external via transportation with trehalose PTS permease. However, sugar can be degraded with both low or high osmolarity in E.coli. Glucokinase can phosphorylate free gluocose into glucose-6-phosphate and both glucose-6-phosphate moieties enter glycolysis.
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Creator: Julia Wakoli Created On: November 08, 2024 at 21:24 Last Updated: November 08, 2024 at 21:24 |
PW353465View Pathway |
Trehalose Degradation I (Low Osmolarity)Providencia alcalifaciens DSM 30120
In E.coli, trehalose can be only synthesized with high osmolarity, and if the osmolarity is low, then the source of trehalose can be only obtained from external via transportation with trehalose PTS permease. However, sugar can be degraded with both low or high osmolarity in E.coli. Glucokinase can phosphorylate free gluocose into glucose-6-phosphate and both glucose-6-phosphate moieties enter glycolysis.
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Creator: Julia Wakoli Created On: November 08, 2024 at 22:06 Last Updated: November 08, 2024 at 22:06 |
PW353415View Pathway |
Trehalose Degradation I (Low Osmolarity)Edwardsiella tarda ATCC 23685
In E.coli, trehalose can be only synthesized with high osmolarity, and if the osmolarity is low, then the source of trehalose can be only obtained from external via transportation with trehalose PTS permease. However, sugar can be degraded with both low or high osmolarity in E.coli. Glucokinase can phosphorylate free gluocose into glucose-6-phosphate and both glucose-6-phosphate moieties enter glycolysis.
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Creator: Julia Wakoli Created On: November 08, 2024 at 21:53 Last Updated: November 08, 2024 at 21:53 |
PW012870View Pathway |
Trehalose metabolismHomo sapiens
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Creator: Guest: Anonymous Created On: January 24, 2017 at 12:52 Last Updated: January 24, 2017 at 12:52 |
PW132333View Pathway |
Treosulfan Drug MetabolismHomo sapiens
Treosulfan is a drug that is not metabolized by the human body as determined by current research and biotransformer analysis. Treosulfan passes through the liver and is then excreted from the body mainly through the kidney.
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Creator: Ray Kruger Created On: September 21, 2023 at 20:57 Last Updated: September 21, 2023 at 20:57 |
PW146425View Pathway |
drug action
Treosulfan Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 18:10 Last Updated: October 07, 2023 at 18:10 |
PW128116View Pathway |
drug action
Treprostinil Action PathwayHomo sapiens
Treprostinil is a stable tricyclic analogue of prostacyclin, it promotes vasodilation and inhibition of platelet aggregation. Treprostinil is administered either subcutaneously, orally or through inhalation used to treat pulmonary arterial hypertension as it acts as an anti-thrombotic agent and potent vasodilator. The drug binds and activates prostacyclin, prostaglandin D2 and P2Y purinoceptor 12 receptors that lead to activation and increased formation of cAMP levels. These elevated cAMP concentrations cause the efflux of calcium and calcium-activated potassium channels leading to cell hyperpolarization. Leading to the inhibition of platelet aggregation and vasodilation of the blood vessels. Treprostinil is metabolized by the liver by CYP2C8 and CYP2C into other metabolites that are excreted in urine.
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Creator: Selena Created On: July 19, 2023 at 11:15 Last Updated: July 19, 2023 at 11:15 |
PW144500View Pathway |
drug action
Treprostinil Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 13:46 Last Updated: October 07, 2023 at 13:46 |
PW175917View Pathway |
Triacylglyceride (TG) PathwayHomo sapiens
A triglyceride (TG, triacylglycerol, TAG, or triacylglyceride) is an ester derived from glycerol and three fatty acids. Triglycerides are the main constituents of body fat in humans and other animals, as well as vegetable fat. They are also present in the blood to enable the bidirectional transference of adipose fat and blood glucose from the liver, and are a major component of human skin oils (Wikipedia). Dihydroxyacetone phosphate (or glycerone phosphate) from glycolysis is used by the cytosolic enzyme glycerol-3-phosphate dehydrogenase [NAD(+)] to synthesize sn-glycerol 3-phosphate. Second, the mitochondrial outer membrane enzyme glycerol-3-phosphate acyltransferase esterifies an acyl-group to the sn-1 position of sn-glycerol 3-phosphate to form 1-acyl-sn-glycerol 3-phosphate (lysophosphatidic acid or LPA). The next three steps are localized to the endoplasmic reticulum membrane. The enzyme 1-acyl-sn-glycerol-3-phosphate acyltransferase converts LPA into phosphatidic acid (1,2-diacyl-sn-glycerol 3-phosphate) by esterifying an acyl-group to the sn-2 position of the glycerol backbone. Next, magnesium-dependent phosphatidate phosphatase catalyzes the conversion of phosphatidic acid into diacylglycerol. Last, the enzyme diacylglycerol O-acyltransferase synthesizes triacylglycerol from diacylglycerol and a fatty acyl-CoA.
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Creator: Omolola Created On: October 30, 2023 at 14:57 Last Updated: October 30, 2023 at 14:57 |