PathWhiz

PathWhiz ID	Pathway	Meta Data
PW088190 View Pathway	metabolic Alpha Linolenic Acid and Linoleic Acid Metabolism Bos taurus Linoleic acid (LNA) is a polyunsaturated fatty acid (PUFA) precursor to the longer n−6 fatty acids commonly known as omega-6 fatty acids. Omega-6 fatty acids are characterized by a carbon-carbon double bond at the sixth carbon from the methyl group. Similarly, the PUFA alpha-linoleic acid (ALA) is the precursor to n-3 fatty acids known as omega-3 fatty acids which is characterized by a carbon-carbon double bond at the third carbon from the methyl group. Both LNA and ALA are essential dietary requirements for all mammals since they cannot be synthesized natively in the body. Both undergo a series of similar conversions to reach their final fatty acid form. LNA enters the cell and is catalyzed to gamma-linolenic acid (GLA) by acyl-CoA 6-desaturase (delta-6-desaturase/fatty acid desaturase 2). GLA is then converted to dihomo-gammalinolenic acid (DGLA) by elongation of very long chain fatty acids protein 5 (ELOVL5). DGLA is then converted to arachidonic acid (AA) by acyl-CoA (8-3)-desaturase (delta-5-desaturase/fatty acid desaturase 1). Arachidonic acid is then converted to a series of short lived metabolites called eicosanoids before finally reaching it's final fatty acid form. BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: Ana Marcu Created On: August 10, 2018 at 10:48 Last Updated: August 10, 2018 at 10:48
PW000006 View Pathway	metabolic Alpha Linolenic Acid and Linoleic Acid Metabolism Homo sapiens Linoleic acid (LNA) is a polyunsaturated fatty acid (PUFA) precursor to the longer n−6 fatty acids commonly known as omega-6 fatty acids. Omega-6 fatty acids are characterized by a carbon-carbon double bond at the sixth carbon from the methyl group. Similarly, the PUFA alpha-linoleic acid (ALA) is the precursor to n-3 fatty acids known as omega-3 fatty acids which is characterized by a carbon-carbon double bond at the third carbon from the methyl group. Both LNA and ALA are essential dietary requirements for all mammals since they cannot be synthesized natively in the body. Both undergo a series of similar conversions to reach their final fatty acid form. LNA enters the cell and is catalyzed to gamma-linolenic acid (GLA) by acyl-CoA 6-desaturase (delta-6-desaturase/fatty acid desaturase 2). GLA is then converted to dihomo-gammalinolenic acid (DGLA) by elongation of very long chain fatty acids protein 5 (ELOVL5). DGLA is then converted to arachidonic acid (AA) by acyl-CoA (8-3)-desaturase (delta-5-desaturase/fatty acid desaturase 1). Arachidonic acid is then converted to a series of short lived metabolites called eicosanoids before finally reaching it's final fatty acid form. BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: WishartLab Created On: August 01, 2013 at 13:54 Last Updated: August 01, 2013 at 13:54
PW088298 View Pathway	metabolic Alpha Linolenic Acid and Linoleic Acid Metabolism Rattus norvegicus Linoleic acid (LNA) is a polyunsaturated fatty acid (PUFA) precursor to the longer n−6 fatty acids commonly known as omega-6 fatty acids. Omega-6 fatty acids are characterized by a carbon-carbon double bond at the sixth carbon from the methyl group. Similarly, the PUFA alpha-linoleic acid (ALA) is the precursor to n-3 fatty acids known as omega-3 fatty acids which is characterized by a carbon-carbon double bond at the third carbon from the methyl group. Both LNA and ALA are essential dietary requirements for all mammals since they cannot be synthesized natively in the body. Both undergo a series of similar conversions to reach their final fatty acid form. LNA enters the cell and is catalyzed to gamma-linolenic acid (GLA) by acyl-CoA 6-desaturase (delta-6-desaturase/fatty acid desaturase 2). GLA is then converted to dihomo-gammalinolenic acid (DGLA) by elongation of very long chain fatty acids protein 5 (ELOVL5). DGLA is then converted to arachidonic acid (AA) by acyl-CoA (8-3)-desaturase (delta-5-desaturase/fatty acid desaturase 1). Arachidonic acid is then converted to a series of short lived metabolites called eicosanoids before finally reaching it's final fatty acid form. BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: Ana Marcu Created On: August 10, 2018 at 13:21 Last Updated: August 10, 2018 at 13:21
PW146772 View Pathway	drug action alpha-Amyl cinnamaldehyde Drug Metabolism Action Pathway Homo sapiens BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: Ray Kruger Created On: October 07, 2023 at 19:00 Last Updated: October 07, 2023 at 19:00
PW132280 View Pathway	metabolic alpha-Arbutin Drug Metabolism Homo sapiens alpha-Arbutin is a drug that is not metabolized by the human body as determined by current research and biotransformer analysis. alpha-Arbutin passes through the liver and is then excreted from the body mainly through the kidney. BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: Ray Kruger Created On: September 21, 2023 at 20:36 Last Updated: September 21, 2023 at 20:36
PW146757 View Pathway	drug action alpha-Arbutin Drug Metabolism Action Pathway Homo sapiens BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: Ray Kruger Created On: October 07, 2023 at 18:57 Last Updated: October 07, 2023 at 18:57
PW144275 View Pathway	drug action alpha-Linolenic acid Drug Metabolism Action Pathway Homo sapiens BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: Ray Kruger Created On: October 07, 2023 at 13:05 Last Updated: October 07, 2023 at 13:05
PW122524 View Pathway	metabolic alpha-Linolenic Acid Metabolism Arabidopsis thaliana alpha-Linolenic acid is a poly-unsaturated fatty acid with an 18-carbon chain and three cis double bonds. Its primary role in Arabidopsis thaliana is in being a precursor of the phytohormone jasmonic acid. Being a precursor for jasmonic acid, it plays a role in gene responses to feeding from insects. It is also a precursor to other molecules involved in defense signalling such as cis-3-hexenyl acetate. alpha-Linolenic acid itself modulates gene transcription in response to hyperosmotic salinity, heat acclimation, and oxidative stress. alpha-Linolenic acid is released from the hydrolysis of a phosphatidylcholine membrane lipid. It then has a hydroperoxy group added by a dioxygenase in either the 2, 9, or 13 position to form 2(R)-HPOT, 9(S)-HPOT, or 13(S)-HPOT respectively. The oxidation of alpha-linolenic acid to 13(S)-HPOT is the first step in the jasmonic acid synthesis and leads to that separate pathway. 2(R)-HPOT is formed in an oil body and undergoes a spontaneous decarboxylation to form a heptadecatrienal. 9(S)-HPOT, or 13(S)-HPOT are both formed in a chloroplast and cleaved by probable inactive linolenate hydroperoxide lyase to form an aldehyde and an oxo-carboxylic acid. The hexenal from 13(S)-HPOT is reduced by alcohol dehydrogenase class-P to form a hexenol, which undergoes an esterification with acetyl-CoA to form 3-hexenyl acetate. BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: William Created On: June 10, 2019 at 11:55 Last Updated: June 10, 2019 at 11:55
PW146733 View Pathway	drug action alpha-Tocopherol acetate Drug Metabolism Action Pathway Homo sapiens BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: Ray Kruger Created On: October 07, 2023 at 18:54 Last Updated: October 07, 2023 at 18:54
PW146731 View Pathway	drug action alpha-Tocopherol succinate Drug Metabolism Action Pathway Homo sapiens BioPAX SVG SBGN SBML PWML All files (.zip)	Creator: Ray Kruger Created On: October 07, 2023 at 18:54 Last Updated: October 07, 2023 at 18:54