PYRUVATE METABOLIC PATHWAY (PW:0000043)

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Description

The pyruvate metabolic pathway, the sum of biochemical reactions involving pyruvate, is at the intersection of pathways important for glucose and energy homeostasis. Reaction 10 at the end of glycolysis, carried out by pyruvate kinases, converts phosphoenolpyruvate (PEP) to ATP and pyruvate which can be converted to acetyl-CoA or anaerobically to lactate (considered the end of anaerobic glycolysis). Pyruvate, and to a much lesser extent acetyl-CoA, can also be derived from the breakdown of sever

Pathway Diagram:

Ariadne Genomics Inc. Pdp members Pdk members Dld Dlat Pdha1 pyruvate ---> acetyl-CoA Pdhx Pdhb thiamine-diphosphate Pkm2 Pklr Pc oxaloacetate ---> acetyl-CoA oxaloacetate ---> gluconeogenesis pathway pyruvate ---> oxaloacetate pyruvate fatty acid beta degradation pathway ---> acetyl-CoA acetyl-CoA ---> fatty acid biosynthetic pathway glycolysis pathway ---> pyruvate oxaloacetate acetyl-CoA ---> citrate cycle pathway acetyl-CoA acetyl-CoA <--> ketone bodies metabolic pathway Pdk members ---| Pdha1 Pdp members --+> Pdha1 glycolysis pathway gluconeogenesis pathway citrate cycle pathway ketone bodies metabolic pathway fatty acid beta degradation pathway fatty acid biosynthetic pathway
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Genes in Pathway:

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pyruvate metabolic pathway term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Acaca acetyl-CoA carboxylase alpha JBrowse link 10 71,519,392 71,719,910 RGD:6907045
RGD:10402751
G Acacb acetyl-CoA carboxylase beta JBrowse link 12 48,127,149 48,238,969 RGD:6907045
G Acat1 acetyl-CoA acetyltransferase 1 JBrowse link 8 58,166,990 58,195,884 RGD:6907045
RGD:10402751
G Acat2 acetyl-CoA acetyltransferase 2 JBrowse link 1 47,972,399 47,992,654 RGD:6907045
G Acot12 acyl-CoA thioesterase 12 JBrowse link 2 20,857,056 20,901,656 RGD:6907045
RGD:10402751
G Acss1 acyl-CoA synthetase short-chain family member 1 JBrowse link 3 146,420,346 146,470,293 RGD:6907045
G Acss2 acyl-CoA synthetase short-chain family member 2 JBrowse link 3 151,032,925 151,075,856 RGD:6907045
RGD:10402751
G Acyp1 acylphosphatase 1 JBrowse link 6 109,097,065 109,110,266 RGD:6907045
RGD:10402751
G Acyp2 acylphosphatase 2 JBrowse link 14 114,891,245 115,052,497 RGD:6907045
G Akr1b1 aldo-keto reductase family 1 member B JBrowse link 4 61,706,866 61,720,959 RGD:6907045
RGD:10402751
G Aldh1a1 aldehyde dehydrogenase 1 family, member A1 JBrowse link 1 238,222,689 238,264,381 RGD:6907045
G Aldh1a7 aldehyde dehydrogenase family 1, subfamily A7 JBrowse link 1 240,584,233 240,601,843 RGD:6907045
G Aldh1b1 aldehyde dehydrogenase 1 family, member B1 JBrowse link 5 61,382,351 61,387,359 RGD:6907045
G Aldh2 aldehyde dehydrogenase 2 family (mitochondrial) JBrowse link 12 40,466,418 40,498,813 RGD:6907045
RGD:10402751
G Aldh3a2 aldehyde dehydrogenase 3 family, member A2 JBrowse link 10 47,525,486 47,546,535 RGD:6907045
G Aldh7a1 aldehyde dehydrogenase 7 family, member A1 JBrowse link 18 51,619,007 51,651,267 RGD:6907045
G Aldh9a1 aldehyde dehydrogenase 9 family, member A1 JBrowse link 13 85,580,828 85,597,497 RGD:6907045
G Dlat dihydrolipoamide S-acetyltransferase JBrowse link 8 55,062,549 55,087,832 RGD:2307427
RGD:6907045
RGD:10402751
G Dld dihydrolipoamide dehydrogenase JBrowse link 6 50,597,677 50,618,694 RGD:2307427
RGD:6907045
RGD:10402751
G Glo1 glyoxalase 1 JBrowse link 20 9,273,589 9,291,608 RGD:6907045
RGD:10402751
G Grhpr glyoxylate and hydroxypyruvate reductase JBrowse link 5 60,528,981 60,538,410 RGD:10402751
G Hagh hydroxyacyl glutathione hydrolase JBrowse link 10 14,215,913 14,230,506 RGD:6907045
RGD:10402751
G Ldha lactate dehydrogenase A JBrowse link 1 102,900,288 102,909,713 RGD:6907045
G Ldhal6b lactate dehydrogenase A-like 6B JBrowse link 1 46,307,853 46,309,276 RGD:6907045
G Ldhb lactate dehydrogenase B JBrowse link 4 176,701,980 176,719,999 RGD:6907045
G Ldhc lactate dehydrogenase C JBrowse link 1 102,914,875 102,931,843 RGD:6907045
G Ldhd lactate dehydrogenase D JBrowse link 19 43,826,989 43,848,937 RGD:6907045
RGD:10402751
G Mdh1 malate dehydrogenase 1 JBrowse link 14 106,378,349 106,393,642 RGD:6907045
RGD:10402751
G Mdh2 malate dehydrogenase 2 JBrowse link 12 23,941,451 23,954,406 RGD:6907045
G Me1 malic enzyme 1 JBrowse link 8 94,256,830 94,368,834 RGD:6907045
RGD:10402751
G Me2 malic enzyme 2 JBrowse link 18 69,737,515 69,784,099 RGD:6907045
RGD:10402751
G Me3 malic enzyme 3 JBrowse link 1 153,861,535 154,058,608 RGD:6907045
G Pc pyruvate carboxylase JBrowse link 1 219,759,157 219,859,854 RGD:1601554
RGD:6907045
RGD:10402751
G Pck1 phosphoenolpyruvate carboxykinase 1 JBrowse link 3 171,213,936 171,219,885 RGD:6907045
RGD:10402751
G Pck2 phosphoenolpyruvate carboxykinase 2 (mitochondrial) JBrowse link 15 34,216,735 34,224,357 RGD:6907045
G Pdha1 pyruvate dehydrogenase E1 alpha 1 subunit JBrowse link X 37,329,779 37,343,410 RGD:2307427
RGD:6907045
RGD:10402751
G Pdha2 pyruvate dehydrogenase E1 alpha 2 subunit JBrowse link 2 246,736,449 246,737,997 RGD:2307427
RGD:6907045
G Pdhb pyruvate dehydrogenase E1 beta subunit JBrowse link 15 18,540,826 18,546,855 RGD:2307427
RGD:6907045
RGD:10402751
G Pdhx pyruvate dehydrogenase complex, component X JBrowse link 3 92,910,300 92,933,725 RGD:2307427
G Pdk1 pyruvate dehydrogenase kinase 1 JBrowse link 3 58,530,870 58,561,494 RGD:2307427
RGD:2307428
G Pdk2 pyruvate dehydrogenase kinase 2 JBrowse link 10 82,838,270 82,852,758 RGD:2307427
RGD:2307428
G Pdk3 pyruvate dehydrogenase kinase 3 JBrowse link X 62,836,131 62,904,114 RGD:2307427
RGD:2307428
G Pdk4 pyruvate dehydrogenase kinase 4 JBrowse link 4 30,546,772 30,556,774 RGD:2307427
RGD:2307428
G Pdp1 pyruvate dehyrogenase phosphatase catalytic subunit 1 JBrowse link 5 25,577,593 25,584,325 RGD:2307428
G Pdp2 pyruvate dehyrogenase phosphatase catalytic subunit 2 JBrowse link 19 597,427 601,556 RGD:2307428
G Pklr pyruvate kinase, liver and RBC JBrowse link 2 188,449,158 188,458,034 RGD:2302790
RGD:6907045
RGD:10402751
G Pkm pyruvate kinase, muscle JBrowse link 8 64,480,963 64,502,957 RGD:2302790
G RGD1562690 similar to L-lactate dehydrogenase A chain (LDH-A) (LDH muscle subunit) (LDH-M) JBrowse link 8 33,075,109 33,076,725 RGD:6907045

Additional Elements in Pathway:

(includes Gene Groups, Small Molecules, Other Pathways..etc.)
Object TypePathway ObjectPathway Object Description
Functional ClassPdk memberspyruvate dehydrogenase kinase members
Functional ClassPdp memberspyruvate dehydrogenase phosphatase members

Pathway Gene Annotations

Disease Annotations Associated with Genes in the pyruvate metabolic pathway
Disease TermsGene Symbols
Abnormalities, MultipleDlat , Pdha1
Acetyl-Coa Carboxylase DeficiencyAcaca
Acidosis, LacticPdha1
Acute Coronary SyndromeLdhb
Adenosine Triphosphate, Elevated, of ErythrocytesPklr
AlbuminuriaAkr1b1
Alcohol Sensitivity, AcuteAldh2
Alcohol-Induced DisordersAldh2
AlcoholismAldh2
Alzheimer DiseaseAldh2 , Pck1
Anemia, Hemolytic, Congenital NonspherocyticPklr
AnoxiaPck2
Anxiety DisordersGlo1
ArteriosclerosisAcat1 , Acat2 , Akr1b1
AsthmaAldh2
Autism Spectrum DisorderAcaca
Autistic DisorderGlo1
Bardet-Biedl SyndromeMdh1
Beta Ketothiolase DeficiencyAcat1
Bone DiseasesAldh7a1
Brain DiseasesMdh2
Brain InfarctionAldh2
Brain IschemiaMdh2
Breast NeoplasmsLdhal6b , Ldhb
Burkitt LymphomaPc
BurnsPklr
Carbohydrate Metabolism, Inborn ErrorsAcat1
CarcinomaMdh2 , Pkm
Carcinoma, HepatocellularAcaca , Akr1b1 , Me1 , Pck1 , Pkm
Carcinoma, Intraductal, NoninfiltratingLdhb
Carcinoma, Renal CellAldh1a1 , Ldhb , Pdhb
CardiomyopathiesLdha , Pdk2
CataractAkr1b1
Charcot-Marie-Tooth Disease, X-Linked Dominant, 6Pdk3
CholestasisAldh1b1
Chromosome 17q12 Deletion SyndromeAcaca
ColobomaAldh7a1
Colonic NeoplasmsAldh1b1
Colorectal NeoplasmsAldh2
Congenital Thrombotic Disease, due to Protein C DeficiencyPc
Coronary Artery DiseaseAcat2
Creutzfeldt-Jakob SyndromeAldh1a1
Cytosolic Acetoacetyl-CoA Thiolase DeficiencyAcat2
Depressive DisorderGlo1
Dermatitis, OccupationalAldh2
Diabetes ComplicationsAkr1b1 , Aldh2 , Glo1
Diabetes Insipidus, NephrogenicAkr1b1
Diabetes Mellitus, ExperimentalAkr1b1 , Pc , Pck1 , Pdk4 , Pklr
Diabetes Mellitus, Type 1Aldh2
Diabetes Mellitus, Type 2Akr1b1 , Aldh2 , Glo1 , Pc , Pck1
Diabetic NephropathiesAkr1b1 , Glo1
Diabetic NeuropathiesAkr1b1 , Aldh2
Diabetic RetinopathyAkr1b1 , Glo1
Disease ProgressionAldh7a1 , Pdha1
Drug-Induced Liver InjuryAldh2 , Mdh1 , Pdk4
Endometrial NeoplasmsAkr1b1
EndometriosisAkr1b1
EndotoxemiaPck1 , Pck2
Endotoxin-Induced UveitisAkr1b1
Enterocolitis, NecrotizingAldh2
Epilepsy, Idiopathic GeneralizedMe2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51Mdh2
Esophageal NeoplasmsAldh2
Esophageal Squamous Cell CarcinomaAldh2 , Glo1
Fanconi SyndromeLdha
Fatty LiverAcaca , Acacb
Fatty Liver, AlcoholicAldh2
Fetal Growth RetardationPck1
FlushingAldh2
GalactosemiasAkr1b1
Gaucher DiseasePklr
Genetic Diseases, InbornAcat1 , Dlat , Pdha1
Genetic Predisposition to DiseaseAldh2
Hearing Loss, Cisplatin-Induced, Susceptibility ToAcyp2
Heart DiseasesAldh2
Heart FailureAcaca , Mdh2 , Pck1
Heart InjuriesAldh2
Heart Septal Defects, VentricularAcyp1
HepatomegalyAldh1b1
HyperalgesiaAkr1b1
HyperglycemiaAkr1b1 , Ldha , Pck1 , Pklr
HyperinsulinismPklr
Hyperoxaluria, PrimaryGrhpr
HypersensitivityAkr1b1
HypertensionAldh2 , Mdh1
HypokalemiaAkr1b1
Immunodeficiency 23Me1
Infertility, MaleAldh2 , Ldhc
InflammationAkr1b1
Insulin ResistanceAcaca , Acacb , Pklr
Intellectual DisabilityPdhx
Kidney Failure, ChronicAcat1 , Glo1
Kidney Reperfusion InjuryAldh2 , Glo1
Lactate Dehydrogenase B DeficiencyLdhb
Lactate Dehydrogenase Deficiency Type ALdha
Lactic Acidosis, Congenital Infantile, Due To LAD DeficiencyDld
Leigh DiseaseDld
Leigh Syndrome, X-LinkedPdha1
Liver Cirrhosis, ExperimentalAcat1 , Akr1b1 , Aldh1a1 , Aldh1b1 , Aldh2 , Hagh , Ldhb , Mdh1 , Pc , Pck1 , Pck2 , Pklr
Liver DiseasesAldh2
Lung DiseasesLdhc
MalariaPklr
Mammary Neoplasms, AnimalMdh2 , Pkm
Mammary Neoplasms, ExperimentalMdh2 , Pkm
Maple Syrup Urine DiseaseDld
MelanomaGlo1 , Pck1
Metabolic Syndrome XAcat2
Metabolism, Inborn ErrorsLdhb
Myocardial InfarctionAldh2 , Ldha , Mdh2
Myocardial IschemiaAkr1b1 , Aldh2 , Dlat , Pdha1 , Pdk4
Myocardial Reperfusion InjuryAldh2
MyoglobinuriaLdha
Neoplasm InvasivenessLdhb , Pkm
Neoplasms, ExperimentalLdha
Nephrotic SyndromeAcat1
ObesityAcacb , Me1 , Pck1 , Pdp1 , Pklr
Opioid-Related DisordersMe2
OsteoarthritisPdha1
Osteogenesis ImperfectaPdk2
OsteoporosisPkm
Pancreatic NeoplasmsAldh1a1 , Aldh2
Parkinsonian DisordersAldh1a1
Phosphoenolpyruvate Carboxykinase 2 DeficiencyPck2
Phosphoenolpyruvate Carboxykinase DeficiencyPck1
Pleomorphic Xanthoastrocytoma Akr1b1 , Dld , Mdh2 , Pdk4
Precancerous ConditionsAldh2
Primary hyperoxaluria type 2Grhpr
Prostatic NeoplasmsAldh9a1 , Dlat , Grhpr , Ldhb , Pdha1 , Pdk4 , Pdp2
Pyridoxine-Dependent EpilepsyAldh7a1
Pyruvate Carboxylase Deficiency DiseasePc
Pyruvate Dehydrogenase Complex Deficiency DiseaseDlat , Dld , Pdha1 , Pdhb , Pdhx
Pyruvate Dehydrogenase E1 Alpha DeficiencyPdha1
Pyruvate Dehydrogenase E1-Beta DeficiencyPdhb
Pyruvate Dehydrogenase E2 DeficiencyDlat
Pyruvate Dehydrogenase E3-Binding Protein DeficiencyPdhx
Pyruvate dehydrogenase phosphatase deficiencyPdp1
Pyruvate Kinase Deficiency of Red CellsPklr
Pyruvate Metabolism, Inborn ErrorsPdha1
Reperfusion InjuryPklr
Respiratory Distress Syndrome, AdultAkr1b1 , Mdh1
Retinitis PigmentosaAcacb
SeizuresAcat1 , Aldh7a1 , Pdha1
Sjogren-Larsson SyndromeAldh3a2
Sleep DeprivationDlat
Smith-Magenis SyndromeAcaca , Aldh3a2 , Pdk2
Stomach NeoplasmsAkr1b1 , Aldh7a1 , Pdha1
Thrombophilia, Hereditary, due to Protein C Deficiency, Autosomal RecessivePc
Vascular DiseasesAldh2 , Glo1
Ventricular DysfunctionAldh2
Weight GainMe1
Pathway Annotations Associated with Genes in the pyruvate metabolic pathway
Pathway TermsGene Symbols
2-aminoadipic 2-oxoadipic aciduria disease pathwayAcat1 , Aldh7a1 , Dld
3-hydroxy-3-methylglutaryl-CoA lyase deficiency pathwayAcat1 , Aldh2 , Dld
3-hydroxyacyl-CoA dehydrogenase deficiency pathwayAcat1
3-hydroxyisobutyric aciduria pathwayAcat1 , Aldh2 , Dld
3-methylcrotonyl CoA carboxylase 1 deficiency pathwayAcat1 , Aldh2 , Dld
alanine metabolic pathwayPc
alendronate pharmacodynamics pathwayAcat2
altered galactose metabolic pathwayAkr1b1
arginine and proline metabolic pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
ascorbate and aldarate metabolic pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
beta-alanine metabolic pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
butanoate metabolic pathwayAcat1 , Acat2 , Pdha1 , Pdha2 , Pdhb
carnitine biosynthetic pathwayAldh9a1
carnitine palmitoyl transferase deficiency type I pathwayAcat1
carnosinemia disease pathwayAldh2
cholesterol biosynthetic pathwayAcat2
cholesterol ester storage disease pathwayAcat2
choline metabolic pathwayAldh7a1
citric acid cycle pathwayDlat , Dld , Mdh1 , Mdh2 , Pc , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb
congenital hemidysplasia with ichthyosiform erythroderma and limb defects disease pathwayAcat2
cyclophosphamide pharmacodynamics pathwayAldh1a1
cyclophosphamide pharmacokinetics pathwayAldh1a1
cysteine and methionine metabolic pathwayLdha , Ldhal6b , Ldhb , Ldhc , RGD1562690
D-glycericacidemia disease pathwayAkr1b1
desmosterolosis disease pathwayAcat2
diabetic nephropathy pathwayAkr1b1
dihydropyrimidine dehydrogenase deficiency pathwayAldh2 , Dld
dimethylglycine dehydrogenase deficiency pathwayAldh2 , Dld
disulfiram pharmacodynamics pathwayAcss1 , Acss2 , Aldh1b1 , Aldh2
dopa responsive dystonia disease pathwayAkr1b1
eicosanoid signaling pathway via peroxisome proliferator-activated receptor gammaMe1 , Pck1 , Pck2
epidermal growth factor/neuregulin signaling pathwayPdk1
ethylmalonic encephalopathy disease pathwayAcat1
fanconi syndrome pathwayPklr
fatty acid beta degradation pathwayAcat1 , Acss1 , Acss2
fatty acid biosynthetic pathwayAcaca , Acacb
fatty acid metabolic pathwayAcat1 , Acat2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
Fc epsilon receptor mediated signaling pathwayPdk1
folate cycle metabolic pathwayDld
forkhead class A signaling pathwayPck1 , Pklr
fructose and mannose metabolic pathwayAkr1b1
fructose intolerance pathwayAkr1b1
fructose-1,6-diphosphatase deficiency pathwayMdh2 , Pc , Pck1
fructosuria disease pathwayAkr1b1
fumaric aciduria disease pathwayDlat , Dld , Mdh2 , Pc , Pdha1 , Pdhb
galactose metabolic pathwayAkr1b1
GALT deficiency pathwayAkr1b1
gamma aminobutyric acid transaminase deficiency pathwayAldh2
gluconeogenesis pathwayAcss1 , Acss2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dlat , Dld , Ldha , Ldhal6b , Ldhb , Ldhc , Mdh2 , Pc , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb , Pklr , RGD1562690
glutaric aciduria type I disease pathwayAcat1 , Aldh7a1 , Dld
glycerolipid metabolic pathwayAkr1b1 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
glycine, serine and threonine metabolic pathwayAldh7a1 , Dld
glycogen storage disease pathway, type IAMdh2 , Pc , Pck1
glycogen storage disease pathway, type IBMdh2 , Pc , Pck1
glycogen storage disease pathway, type VIIPklr
glycolysis pathwayAcss1 , Acss2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dlat , Dld , Ldha , Ldhal6b , Ldhb , Ldhc , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb , Pklr , Pkm , RGD1562690
glycolysis/gluconeogenesis pathwayAcss1 , Acss2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dlat , Dld , Ldha , Ldhal6b , Ldhb , Ldhc , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb , Pklr , RGD1562690
glyoxalase metabolic pathwayGlo1 , Hagh , Ldhd
glyoxylate and dicarboxylate metabolic pathwayAcat1 , Acat2 , Mdh1 , Mdh2
hepatitis C virus infection pathwayPdk1
histidine metabolic pathwayAldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
histidinemia disease pathwayAldh2
hypercholesterolemia disease pathwayAcat2
hyperglycerolemia disease pathwayAkr1b1
hyperlipoproteinemia type I disease pathwayAkr1b1
hyperlysinemias disease pathwayAcat1 , Aldh7a1 , Dld
hypoxia inducible factor pathwayLdha , Pkm
ibandronate pharmacodynamics pathwayAcat2
ifosfamide pharmacodynamics pathwayAldh1a1
ifosfamide pharmacokinetics pathwayAldh1a1
insulin signaling pathwayAcaca , Acacb , Pck1 , Pck2 , Pklr
isobutyryl-CoA dehydrogenase deficiency pathwayAcat1 , Aldh2 , Dld
isovaleric acidemia disease pathwayAcat1 , Aldh2 , Dld
ketone bodies metabolic pathwayAcat1 , Acat2
lactic acidosis pathwayPc
Leigh syndrome pathwayAcaca , Acat1 , Acot12 , Acss2 , Acyp1 , Akr1b1 , Aldh2 , Dlat , Dld , Glo1 , Grhpr , Hagh , Ldhd , Mdh1 , Me1 , Me2 , Pc , Pck1 , Pdha1 , Pdhb , Pklr
lysine biosynthetic pathwayAldh7a1
lysine degradation pathwayAcat1 , Acat2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dld
malonic aciduria disease pathwayAcaca , Acat1 , Acss1
malonic aciduria pathwayAcaca , Acat1 , Acss1
maple syrup urine disease pathwayAcat1 , Aldh2 , Dld
maturity onset diabetes of the young pathwayPklr
medium-chain acyl-CoA dehydrogenase deficiency pathwayAcat1
methylmalonate semialdehyde dehydrogenase deficiency pathwayAcat1 , Aldh2 , Dld
methylmalonic acidemia disease pathwayAcat1 , Aldh2 , Dld
methylmalonic aciduria, cobalamin-related, disease pathwayAcaca , Acat1 , Acss1
mevalonate kinase deficiency pathwayAcat2
mitochondrial complex II deficiency pathwayDlat , Dld , Mdh2 , Pc , Pdha1 , Pdhb
neurotrophic factor signaling pathwayPdk1
neviparine pharmacokinetics pathwayAldh1a1
nicotinamide adenine dinucleotide metabolic pathwayMdh1 , Mdh2
nitrogenous bisphosphonate pharmacodynamics pathwayAcat2
nonketotic hyperglycinemia disease pathwayAldh2 , Dld
Nonketotic hyperglycinemia disease pathwayAldh2 , Dld
pamidronate pharmacodynamics pathwayAcat2
pentose and glucuronate interconversion pathwayAkr1b1 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2
phosphoenolpyruvate carboxykinase deficiency pathwayMdh2 , Pc , Pck1
phytanic acid degradation pathwayAldh3a2
polyol pathwayAkr1b1
primary hyperoxaluria type 1 disease pathwayPc
primary hyperoxaluria type 2 disease pathwayAcaca , Acat1 , Acot12 , Acss2 , Acyp1 , Akr1b1 , Aldh2 , Dlat , Dld , Glo1 , Grhpr , Hagh , Ldhd , Mdh1 , Me1 , Me2 , Pc , Pck1 , Pdha1 , Pdhb , Pklr
propanoate metabolic pathwayAcaca , Acacb , Acat1 , Acat2 , Acss1 , Acss2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Ldha , Ldhal6b , Ldhb , Ldhc , RGD1562690
propionic acidemia disease pathwayAcat1 , Aldh2 , Dld
prostaglandin biosynthetic pathwayAkr1b1
purine metabolic pathwayPklr
pyruvate carboxylase deficiency disease pathwayPc
pyruvate dehydrogenase complex deficiency pathwayAcaca , Acat1 , Acot12 , Acss2 , Acyp1 , Akr1b1 , Aldh2 , Dlat , Dld , Glo1 , Grhpr , Hagh , Ldhd , Mdh1 , Me1 , Me2 , Pc , Pck1 , Pdha1 , Pdhb , Pklr
pyruvate dehydrogenase E1 deficiency pathwayAcaca , Acat1 , Acot12 , Acss2 , Acyp1 , Akr1b1 , Aldh2 , Dlat , Dld , Glo1 , Grhpr , Hagh , Ldhd , Mdh1 , Me1 , Me2 , Pc , Pck1 , Pdha1 , Pdhb , Pklr
pyruvate dehydrogenase E2 deficiency pathwayDlat , Dld , Mdh2 , Pc , Pdha1 , Pdhb
pyruvate dehydrogenase E3 deficiency pathwayDlat , Dld , Mdh2 , Pc , Pdha1 , Pdhb
pyruvate kinase deficiency pathwayAcaca , Acat1 , Acot12 , Acss2 , Acyp1 , Akr1b1 , Aldh2 , Dlat , Dld , Glo1 , Grhpr , Hagh , Ldhd , Mdh1 , Me1 , Me2 , Pc , Pck1 , Pdha1 , Pdhb , Pklr
pyruvate metabolic pathwayAcaca , Acacb , Acat1 , Acat2 , Acot12 , Acss1 , Acss2 , Acyp1 , Acyp2 , Akr1b1 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dlat , Dld , Glo1 , Grhpr , Hagh , Ldha , Ldhal6b , Ldhb , Ldhc , Ldhd , Mdh1 , Mdh2 , Me1 , Me2 , Me3 , Pc , Pck1 , Pck2 , Pdha1 , Pdha2 , Pdhb , Pdhx , Pdk1 , Pdk2 , Pdk3 , Pdk4 , Pdp1 , Pdp2 , Pklr , Pkm , RGD1562690
Refsum disease pathwayAldh3a2
remethylation pathway of homocysteine metabolism - cobalamin independent, betaine dependentAldh7a1
retinoic acid metabolic pathwayAldh1a1
retinol metabolic pathwayAldh1a1
risedronate pharmacodynamics pathwayAcat2
saccharopinuria disease pathwayAcat1 , Aldh7a1 , Dld
sarcosinemia disease pathwayAldh2 , Dld
Segawa syndrome pathwayAkr1b1
short-chain acyl-CoA dehydrogenase deficiency pathwayAcat1
Smith-Lemli-Opitz Syndrome pathwayAcat2
statin pharmacodynamics pathwayAcat2
succinyl-CoA:3-oxoacid transferase deficiency pathwayAcat1
T cell receptor signaling pathwayPdk1
terpenoid biosynthetic pathwayAcat1 , Acat2
Toxoplasma gondii infection pathwayPdk1
trifunctional protein deficiency pathwayAcat1
triosephosphate isomerase deficiency pathwayMdh2 , Pc , Pck1
tryptophan metabolic pathwayAcat1 , Acat2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1
type 2 diabetes mellitus pathwayPklr
type I 3-Methylglutaconic aciduria disease pathwayAcat1 , Aldh2 , Dld
type III 3-Methylglutaconic aciduria disease pathwayAcat1 , Aldh2 , Dld
valine, leucine and isoleucine biosynthetic pathwayPdha1 , Pdha2 , Pdhb
valine, leucine and isoleucine degradation pathwayAcat1 , Acat2 , Aldh1a1 , Aldh1a7 , Aldh1b1 , Aldh2 , Aldh3a2 , Aldh7a1 , Aldh9a1 , Dld
very long-chain acyl-CoA dehydrogenase deficiency pathwayAcat1
vitamin A deficiency pathwayAldh1a1
Wolman disease pathwayAcat2
X-linked dominant chondrodysplasia punctata 2 disease pathwayAcat2
zoledronate pharmacodynamics pathwayAcat2
Phenotype Annotations Associated with Genes in the pyruvate metabolic pathway
Phenotype TermsGene Symbols
alcohol preferenceAldh1a1 , Aldh2

References Associated with the pyruvate metabolic pathway:

Ontology Path Diagram:

paths to the root

Import into Pathway Studio: