KEGG   PATHWAY: ko00984
Entry
ko00984                     Pathway                                
Name
Steroid degradation
Class
Metabolism; Xenobiotics biodegradation and metabolism
Pathway map
ko00984  Steroid degradation
ko00984

Other DBs
GO: 0006707
Orthology
K00632  fadA, fadI; acetyl-CoA acyltransferase [EC:2.3.1.16]
K01796  AMACR, mcr; alpha-methylacyl-CoA racemase [EC:5.1.99.4]
K01822  ksi; steroid Delta-isomerase [EC:5.3.3.1]
K03333  choD; cholesterol oxidase [EC:1.1.3.6]
K05296  E1.1.1.51; 3(or 17)beta-hydroxysteroid dehydrogenase [EC:1.1.1.51]
K05898  kstD; 3-oxosteroid 1-dehydrogenase [EC:1.3.99.4]
K15981  CYP125A; cholest-4-en-3-one 26-monooxygenase [EC:1.14.15.29]
K15982  kshA; 3-ketosteroid 9alpha-monooxygenase subunit A [EC:1.14.15.30]
K15983  kshB; 3-ketosteroid 9alpha-monooxygenase subunit B [EC:1.14.15.30]
K16045  hsd; 3beta-hydroxy-Delta5-steroid dehydrogenase / steroid Delta-isomerase [EC:1.1.1.145 5.3.3.1]
K16046  CYP142; cholest-4-en-3-one 26-monooxygenase [EC:1.14.15.28]
K16047  hsaA; 3-hydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione monooxygenase [EC:1.14.14.12]
K16048  hsaB; 3-hydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione monooxygenase reductase component [EC:1.5.1.-]
K16049  hsaC; 3,4-dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione 4,5-dioxygenase [EC:1.13.11.25]
K16050  hsaD; 4,5:9,10-diseco-3-hydroxy-5,9,17-trioxoandrosta-1(10),2-diene-4-oate hydrolase [EC:3.7.1.17]
K16051  tesI; 3-oxo-5alpha-steroid 4-dehydrogenase [EC:1.3.99.5]
K18364  bphH, xylJ, tesE; 2-oxopent-4-enoate/cis-2-oxohex-4-enoate hydratase [EC:4.2.1.80 4.2.1.132]
K18365  bphI, xylK, nahM, tesG; 4-hydroxy-2-oxovalerate/4-hydroxy-2-oxohexanoate aldolase [EC:4.1.3.39 4.1.3.43]
K18366  bphJ, xylQ, nahO, tesF; acetaldehyde/propanal dehydrogenase [EC:1.2.1.10 1.2.1.87]
K18687  fadD3; HIP---CoA ligase [EC:6.2.1.41]
K18688  fadD19; 3-oxocholest-4-en-26-oate---CoA ligase [EC:6.2.1.42]
K22818  fadE26; 3-oxocholest-4-en-26-oyl-CoA dehydrogenase alpha subunit [EC:1.3.99.-]
K22819  fadE27; 3-oxocholest-4-en-26-oyl-CoA dehydrogenase beta subunit [EC:1.3.99.-]
K22820  fadE34; 3-oxochol-4-en-24-oyl-CoA dehydrogenase [EC:1.3.99.-]
K22821  fadE28; 3-oxo-4-pregnene-20-carboxyl-CoA dehydrogenase alpha subunit [EC:1.3.99.-]
K22822  fadE29; 3-oxo-4-pregnene-20-carboxyl-CoA dehydrogenase beta subunit [EC:1.3.99.-]
K25621  chsH2; 3-oxo-4,17-pregnadiene-20-carboxyl-CoA hydratase alpha subunit
K25622  chsH1; 3-oxo-4,17-pregnadiene-20-carboxyl-CoA hydratase beta subunit
K25623  ltp2; 17-hydroxy-3-oxo-4-pregnene-20-carboxyl-CoA lyase
K28218  chsH3; 3-oxochol-4,22-dien-24-oyl-CoA hydratase (S-form)
K28219  chsB1, hsd4A; (22S)-hydroxy-3-oxochol-4-en-24-oyl-CoA dehydrogenase
K28220  scdG, IpdF; hydroxylacyl dehydrogenase
K28221  scdC1, fadE33, ipdE2; 5OH-HIP-CoA dehydrogenase
K28222  scdC2, fadE30, ipdE1; 5OH-HIP-CoA dehydrogenase
K28224  scdD; enoyl-CoA hydratase
K28225  scdE; 3-hydroxyl acyl-CoA dehydrogenase
K28226  scdK, ipdC; acyl-CoA dehydrogenase
K28227  scdY, echA20; HIEC-CoA hydrolase
K28228  scdL1, ipdA; COCHEA-CoA hydrolase alpha subunit
K28229  scdL2, ipdB; COCHEA-CoA hydrolase beta subunit
K28230  scdM1, fadE31; acyl-CoA dehydrogenase
K28231  scdM2, fadE32; acyl-CoA dehydrogenase
K28232  scdN; enoyl-CoA hydratase
Compound
C00022  Pyruvate
C00024  Acetyl-CoA
C00091  Succinyl-CoA
C00100  Propanoyl-CoA
C00187  Cholesterol
C00280  Androstenedione
C00479  Propanal
C00535  Testosterone
C00599  Cholest-4-en-3-one
C00674  5alpha-Androstane-3,17-dione
C01227  Dehydroepiandrosterone
C04793  3,4-Dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione
C04844  3-Hydroxy-5,9,17-trioxo-4,5:9,10-disecoandrosta-1(10),2-dien-4-oate
C06762  4-Hydroxy-2-oxohexanoic acid
C07635  Epiandrosterone
C11354  2-Hydroxy-cis-hex-2,4-dienoate
C14909  9alpha-Hydroxyandrosta-1,4-diene-3,17-dione
C19944  3-Hydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione
C20144  Androsta-1,4-diene-3,17-dione
C20199  3-[(3aS,4S,7aS)-7a-Methyl-1,5-dioxo-octahydro-1H-inden-4-yl]propanoate
C20252  5-Androstene-3,17-dione
C20838  3-[(3aS,4S,7aS)-7a-Methyl-1,5-dioxo-octahydro-1H-inden-4-yl]propanoyl-CoA
C20839  (25R)-3-Oxocholest-4-en-26-oate
C20840  (25S)-3-Oxocholest-4-en-26-oyl-CoA
C21076  Delta4-Dafachronic acid
C21906  3-Oxochol-4-en-24-oyl-CoA
C23003  3-[(3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-inden-4-yl]propanoyl-CoA
C23004  (2E)-3-[(3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-inden-4-yl]prop-2-enoyl-CoA
C23005  3-[(3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-inden-4-yl]-3-hydroxypropanoyl-CoA
C23006  3-[(3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-inden-4-yl]-3-oxopropanoyl-CoA
C23007  (3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-indene-4-carboxyl-CoA
C23009  (7aS)-7a-Methyl-1,5-dioxo-2,3,5,6,7,7a-hexahydro-1H-indene-4-carboxyl-CoA
C23010  3-Oxocholest-4,24-dien-26-oyl-CoA
C23011  (25R)-3-Oxocholest-4-en-26-oyl-CoA
C23012  24-Hydroxy-3-oxocholest-4-en-26-oyl-CoA
C23013  3,24-Dioxocholest-4-en-26-oyl-CoA
C23014  3-Oxochol-4,22-dien-24-oyl-CoA
C23015  (22S)-Hydroxy-3-oxochol-4-en-24-oyl-CoA
C23016  3,22-Dioxochol-4-en-24-oyl-CoA
C23017  3-Oxopregnene-20-carboxyl-CoA
C23018  3-Oxo-4,17-pregnadiene-20-carboxyl-CoA
C23019  17-Hydroxy-3-oxo-4-pregnene-20-carboxyl-CoA
C23020  (3R)-2-(2-carboxyethyl)-3-methyl-6-oxocyclohex-1-ene-1-carboxyl-CoA
C23021  9-Carboxy-6-methyl-3,7-dioxononanoyl-CoA
C23022  7-Carboxy-4-methyl-5-oxoheptanoyl-CoA
C23023  (2E)-7-Carboxy-4-methyl-5-oxohept-2-enoyl-CoA
C23024  7-Carboxy-3-hydroxy-4-methyl-5-oxoheptanoyl-CoA
C23025  7-Carboxy-4-methyl-3,5-dioxoheptanoyl-CoA
C23026  5-Carboxy-2-methyl-3-oxopentanoyl-CoA
Reference
  Authors
Olivera ER, Luengo JM.
  Title
Steroids as Environmental Compounds Recalcitrant to Degradation: Genetic  Mechanisms of Bacterial Biodegradation Pathways.
  Journal
Genes (Basel) 10 (2019)
DOI:10.3390/genes10070512
Reference
  Authors
Horinouchi M, Hayashi T, Kudo T
  Title
Steroid degradation in Comamonas testosteroni.
  Journal
J Steroid Biochem Mol Biol 129:4-14 (2012)
DOI:10.1016/j.jsbmb.2010.10.008
Reference
  Authors
Horinouchi M, Kurita T, Hayashi T, Kudo T
  Title
Steroid degradation genes in Comamonas testosteroni TA441: Isolation of genes encoding a Delta4(5)-isomerase and 3alpha- and 3beta-dehydrogenases and evidence for a 100 kb steroid degradation gene hot spot.
  Journal
J Steroid Biochem Mol Biol 122:253-63 (2010)
DOI:10.1016/j.jsbmb.2010.06.002
Reference
  Authors
Horinouchi M, Hayashi T.
  Title
Identification of the Coenzyme A (CoA) Ester Intermediates and Genes Involved in  the Cleavage and Degradation of the Steroidal C-Ring by Comamonas testosteroni  TA441.
  Journal
Appl Environ Microbiol 87:e0110221 (2021)
DOI:10.1128/AEM.01102-21
Reference
  Authors
Horinouchi M, Hayashi T.
  Title
Comprehensive summary of steroid metabolism in Comamonas testosteroni TA441:  entire degradation process of basic four rings and removal of C12 hydroxyl group.
  Journal
Appl Environ Microbiol 89:e0014323 (2023)
DOI:10.1128/aem.00143-23
Reference
  Authors
Ouellet H, Johnston JB, de Montellano PR
  Title
Cholesterol catabolism as a therapeutic target in Mycobacterium tuberculosis.
  Journal
Trends Microbiol 19:530-9 (2011)
DOI:10.1016/j.tim.2011.07.009
Reference
  Authors
Van der Geize R, Yam K, Heuser T, Wilbrink MH, Hara H, Anderton MC, Sim E, Dijkhuizen L, Davies JE, Mohn WW, Eltis LD
  Title
A gene cluster encoding cholesterol catabolism in a soil actinomycete provides insight into Mycobacterium tuberculosis survival in macrophages.
  Journal
Proc Natl Acad Sci U S A 104:1947-52 (2007)
DOI:10.1073/pnas.0605728104
Reference
  Authors
Thomas ST, VanderVen BC, Sherman DR, Russell DG, Sampson NS
  Title
Pathway profiling in Mycobacterium tuberculosis: elucidation of cholesterol-derived catabolite and enzymes that catalyze its metabolism.
  Journal
J Biol Chem 286:43668-78 (2011)
DOI:10.1074/jbc.M111.313643
Reference
  Authors
Crowe AM, Casabon I, Brown KL, Liu J, Lian J, Rogalski JC, Hurst TE, Snieckus V, Foster LJ, Eltis LD.
  Title
Catabolism of the Last Two Steroid Rings in Mycobacterium tuberculosis and Other  Bacteria.
  Journal
mBio 8 (2017)
DOI:10.1128/mBio.00321-17
Reference
  Authors
Yuan T, Werman JM, Yin X, Yang M, Garcia-Diaz M, Sampson NS.
  Title
Enzymatic beta-Oxidation of the Cholesterol Side Chain in Mycobacterium tuberculosis  Bifurcates Stereospecifically at Hydration of 3-Oxo-cholest-4,22-dien-24-oyl-CoA.
  Journal
ACS Infect Dis 7:1739-1751 (2021)
DOI:10.1021/acsinfecdis.1c00069
Related
pathway
ko00010  Glycolysis / Gluconeogenesis
ko00020  Citrate cycle (TCA cycle)
ko00100  Steroid biosynthesis
ko00140  Steroid hormone biosynthesis
ko00640  Propanoate metabolism

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