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Pathways

PathWhiz ID Pathway Meta Data

PW013090

Pw013090 View Pathway
metabolic

TG Test

Arabidopsis thaliana
In higher plants, the primary seed storage reserve is triacylglycerol rather than carbohydrates. Thus, triacylglycerol degradation is an important pathway from which plants obtain energy for growth. First, triacylglycerol lipase, an enzyme localized to the oil body (storage vacuole) membrane, catalyzes the conversion of a triglyceride into a 1,2-diglyceride. Second, the predicted enzyme diglyceride lipase (coloured orange in the image) is theorized to catalyze the conversion of a 1,2-diglyceride iinto a 2-acylglycerol. Third, a 2-acylglycerol is spontaneously converted into a 1-monoglyceride. Fourth, acylhydrolase catalyzes the conversion of a 1-monoglyceride into glycerol. Fifth, glycerol kinase catalyzes the conversion of glycerol into glycerol 3-phosphate. Sixth, glycerol-3-phosphate dehydrogenase (coloured dark green in the image), localized to the mitochondrial inner membrane, catalyzes the conversion of glycerol 3-phosphate into glycerone phosphate.

PW123678

Pw123678 View Pathway
metabolic

TG Test

Saccharomyces cerevisiae
A triglyceride (TG, triacylglycerol, TAG, or triacylglyceride) is an ester derived from glycerol and three fatty acids. The biosynthesis of triacylglycerol is localized to the endoplasmic reticulum membrane and starts with glycerol 3-phosphate reacting with acyl-CoA through a glycerol-3-phosphate O-acyltransferase resulting in the release of lysophosphatidic acid (LPA). This, in turn, reacts with an acyl-CoA through a lipase complex resulting in the release of CoA and phosphatidic acid. Phosphatidic acid reacts with water through a phosphatidic acid phosphohydrolase 1 resulting in the release of a phosphate and a diacylglycerol. This reaction can be reversed through a CTP-dependent diacylglycerol kinase. The diacylglycerol reacts in the endoplasmic reticulum with an acyl-CoA through a diacylglycerol O-acyltransferase resulting in the release of coenzyme A and a triacylglycerol. Triacylglycerol metabolism begins with a reaction with water through lipase resulting in the release of a fatty acid, hydrogen ion, and a diacylglycerol. Diacylglycerol then reacts with a lipase 3 resulting in the release of a fatty acid and a monoacylglycerol. Monoacylglycerol reacts with monoglyceride lipase resulting in the release of a fatty acid in glycerol.

PW552591

Pw552591 View Pathway
signaling

TGF beta Signaling

Homo sapiens
The TGF beta signaling pathway plays a role in regulating various cellular processes, including growth, differentiation, and immune responses. It is initiated when TGF beta activates the TGF beta receptor, triggering a cascade of signaling events. This receptor activation leads to the activation of PI3K, which in turn activates the Akt complex. The Akt complex further activates Serine/threonine-protein kinase mTOR, a key regulator of cell growth and metabolism. mTOR then activates Ribosomal protein S6 kinase beta-1, involved in protein synthesis. Additionally, TGF-beta receptor type-1 activates the GRB2-SOS-IRS-SHC complex, which stimulates Ras-related protein Ral-A, leading to the activation of the RAF proto-oncogene serine/threonine-protein kinase without zinc. The signaling also involves the activation of TRAF4/6, which in turn activates the TRAF6-TAK1 complex. This complex activates MAP kinase-interacting serine/threonine-protein kinase 1 (MKNK1), which subsequently activates JNK (c-Jun N-terminal kinase). JNK then activates ATF-2 and Jun, important transcription factors. Moreover, MKNK1 also activates Proto-oncogene c-Fos, a key transcription factor involved in cellular responses. Another branch of the pathway involves the activation of Rho-related GTP-binding protein RhoC, which activates Rho-associated protein kinase 1. This kinase activates the Cofilin-actin-CAP1 complex, involved in cytoskeletal dynamics. Regarding cellular transport, Proto-oncogene c-Fos is translocated from the cytosol to the nucleus, where it regulates gene expression. These interactions collectively contribute to the modulation of cell behavior, including cell cycle progression, migration, and differentiation.

PW565784

Pw565784 View Pathway
signaling

TGF beta SMAD Signaling

Homo sapiens
The TGF-β pathway is initiated when TGF-β activates TGF-β receptors (type-1/2) on the cell surface. This receptor activation leads to the phosphorylation of the receptors, which in turn activates downstream signaling components. One important result is the phosphorylation of Mothers against decapentaplegic homolog 2 (SMAD2), forming a complex called SMAD2 with phosphate. This phosphorylated SMAD2 then activates a critical downstream signaling cascade involving SMAD2-3-4, which translocates from the cytosol to the nucleus, where it regulates gene expression and various cellular responses. However, the pathway is also tightly regulated. SMAD 6/7 interacts with SMURF 1/2, which acts as a negative regulator by inhibiting the phosphorylation of the TGF-β receptor. This feedback mechanism helps to balance the activation of the TGF-β pathway to ensure proper cellular responses.

PW092100

Pw092100 View Pathway
signaling

TGF-Beta and Cav1

Mus musculus

PW002525

Pw002525 View Pathway
disease

TGFB

Homo sapiens

PW002362

Pw002362 View Pathway
signaling

TGFbcoreandaltered

Homo sapiens

PW145135

Pw145135 View Pathway
drug action

Thalidomide Drug Metabolism Action Pathway

Homo sapiens

PW176528

Pw176528 View Pathway
metabolic

Thalidomide Predicted Metabolism Pathway

Homo sapiens
Metabolites of Thalidomide are predicted with biotransformer.

PW146083

Pw146083 View Pathway
drug action

Thallous chloride Drug Metabolism Action Pathway

Homo sapiens