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PathWhiz ID Pathway Meta Data

PW354108

Pw354108 View Pathway
metabolic

Trehalose Degradation I (Low Osmolarity)

Haemophilus haemolyticus M19501
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.

PW354146

Pw354146 View Pathway
metabolic

Trehalose Degradation I (Low Osmolarity)

Paenibacillus lactis 154
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.

PW354160

Pw354160 View Pathway
metabolic

Trehalose Degradation I (Low Osmolarity)

Roseburia inulinivorans DSM 16841
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.

PW354172

Pw354172 View Pathway
metabolic

Trehalose Degradation I (Low Osmolarity)

Megamonas funiformis YIT 11815
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.

PW353237

Pw353237 View Pathway
metabolic

Trehalose Degradation I (Low Osmolarity)

Fusobacterium periodonticum 1_1_41FAA
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.

PW012870

Pw012870 View Pathway
metabolic

Trehalose metabolism

Homo sapiens

PW132333

Pw132333 View Pathway
metabolic

Treosulfan Drug Metabolism

Homo 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.

PW146425

Pw146425 View Pathway
drug action

Treosulfan Drug Metabolism Action Pathway

Homo sapiens

PW128116

Pw128116 View Pathway
drug action

Treprostinil Action Pathway

Homo 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.

PW144500

Pw144500 View Pathway
drug action

Treprostinil Drug Metabolism Action Pathway

Homo sapiens