HSD17B4

Hydroxysteroid (17-beta) dehydrogenase 4

PDB rendering based on 1ikt.

Available structures

Ortholog search: PDBe, RCSB

List of PDB id codes
1IKT, 1S9C, 1ZBQ

Identifiers

Symbols

HSD17B4 ; DBP; MFE-2; MPF-2; PRLTS1; SDR8C1

External IDs

OMIM: 601860 MGI: 105089 HomoloGene: 358 ChEMBL: 5814 GeneCards: HSD17B4 Gene

EC number

1.1.1.n12, 4.2.1.107, 4.2.1.119

Gene ontology
Molecular function	• 3-hydroxyacyl-CoA dehydrogenase activity • receptor binding • long-chain-enoyl-CoA hydratase activity • isomerase activity • 3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-enoyl-CoA hydratase activity • protein homodimerization activity • 17-beta-hydroxysteroid dehydrogenase (NAD+) activity
Cellular component	• mitochondrion • peroxisome • peroxisomal membrane • peroxisomal matrix • membrane • intracellular membrane-bounded organelle
Biological process	• very long-chain fatty acid metabolic process • osteoblast differentiation • fatty acid beta-oxidation • bile acid biosynthetic process • metabolic process • bile acid metabolic process • androgen metabolic process • estrogen metabolic process • fatty acid beta-oxidation using acyl-CoA oxidase • unsaturated fatty acid metabolic process • alpha-linolenic acid metabolic process • very long-chain fatty-acyl-CoA metabolic process • medium-chain fatty-acyl-CoA metabolic process • cellular lipid metabolic process • small molecule metabolic process • oxidation-reduction process • Sertoli cell development
Sources: Amigo / QuickGO

RNA expression pattern

More reference expression data

Orthologs

Species

Human

Mouse

RefSeq (mRNA)

RefSeq (protein)

Location (UCSC)

Chr 5:
118.79 – 118.97 Mb

Chr 18:
50.13 – 50.2 Mb

PubMed search

Peroxisomal multifunctional enzyme type 2 is a protein that in humans is encoded by the HSD17B4 gene.^[1]^[2]^[3]

The HSD17B4 gene encodes an enzyme involved in peroxisomal fatty acid beta-oxidation. It was first identified as a 17-beta-estradiol dehydrogenase (Leenders et al., 1996; van Grunsven et al., 1998). Peroxisomal beta-oxidation of fatty acids, originally described by Lazarow and de Duve (1976), is catalyzed by 3 enzymes: acyl-CoA oxidase (see, e.g., ACOX1, MIM 609751); the 'D-bifunctional enzyme,' with enoyl-CoA-hydratase and D-3-hydroxyacyl-CoA dehydrogenase activity, and 3-ketoacyl-CoA thiolase (MIM 604054).

See also the L-bifunctional peroxisomal protein (EHHADH; MIM 607037). The D- and L-bifunctional proteins have different substrate specificities. The D-bifunctional protein catalyzes the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids and also acts in shortening cholesterol for bile acid formation. In contrast, the L-specific bifunctional protein does not have the latter 2 activities (Jiang et al., 1997).[supplied by OMIM]^[3]

References

↑ Leenders F, Prescher G, Dolez V, Begue A, de Launoit Y, Adamski J (Mar 1997). "Assignment of human 17 beta-hydroxysteroid dehydrogenase IV to chromosome 5q2 by fluorescence in situ hybridization". Genomics 37 (3): 403–4. doi:10.1006/geno.1996.0578. PMID 8938456.
↑ Persson B, Kallberg Y, Bray JE, Bruford E, Dellaporta SL, Favia AD, Duarte RG, Jornvall H, Kavanagh KL, Kedishvili N, Kisiela M, Maser E, Mindnich R, Orchard S, Penning TM, Thornton JM, Adamski J, Oppermann U (Feb 2009). "The SDR (short-chain dehydrogenase/reductase and related enzymes) nomenclature initiative". Chem Biol Interact 178 (1-3): 94–8. doi:10.1016/j.cbi.2008.10.040. PMC 2896744. PMID 19027726.
↑ 3.0 3.1 "Entrez Gene: HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4".

de Launoit Y, Adamski J (1999). "Unique multifunctional HSD17B4 gene product: 17beta-hydroxysteroid dehydrogenase 4 and D-3-hydroxyacyl-coenzyme A dehydrogenase/hydratase involved in Zellweger syndrome.". J. Mol. Endocrinol. 22 (3): 227–40. doi:10.1677/jme.0.0220227. PMID 10343282.
Huyghe S, Mannaerts GP, Baes M, Van Veldhoven PP (2006). "Peroxisomal multifunctional protein-2: the enzyme, the patients and the knockout mouse model.". Biochim. Biophys. Acta 1761 (9): 973–94. doi:10.1016/j.bbalip.2006.04.006. PMID 16766224.
Palosaari PM, Hiltunen JK (1990). "Peroxisomal bifunctional protein from rat liver is a trifunctional enzyme possessing 2-enoyl-CoA hydratase, 3-hydroxyacyl-CoA dehydrogenase, and delta 3, delta 2-enoyl-CoA isomerase activities.". J. Biol. Chem. 265 (5): 2446–9. PMID 2303409.
Adamski J, Normand T, Leenders F et al. (1995). "Molecular cloning of a novel widely expressed human 80 kDa 17 beta-hydroxysteroid dehydrogenase IV.". Biochem. J. 311 (2): 437–43. PMC 1136019. PMID 7487879.
Markus M, Husen B, Adamski J (1996). "The subcellular localization of 17 beta-hydroxysteroid dehydrogenase type 4 and its interaction with actin.". J. Steroid Biochem. Mol. Biol. 55 (5-6): 617–21. doi:10.1016/0960-0760(95)00213-8. PMID 8547189.
Jiang LL, Kobayashi A, Matsuura H et al. (1997). "Purification and properties of human D-3-hydroxyacyl-CoA dehydratase: medium-chain enoyl-CoA hydratase is D-3-hydroxyacyl-CoA dehydratase.". J. Biochem. 120 (3): 624–32. doi:10.1093/oxfordjournals.jbchem.a021458. PMID 8902629.
Jiang LL, Miyazawa S, Souri M, Hashimoto T (1997). "Structure of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein.". J. Biochem. 121 (2): 364–9. doi:10.1093/oxfordjournals.jbchem.a021596. PMID 9089413.
Jiang LL, Kurosawa T, Sato M et al. (1997). "Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein.". J. Biochem. 121 (3): 506–13. doi:10.1093/oxfordjournals.jbchem.a021615. PMID 9133619.
Novikov D, Dieuaide-Noubhani M, Vermeesch JR et al. (1997). "The human peroxisomal multifunctional protein involved in bile acid synthesis: activity measurement, deficiency in Zellweger syndrome and chromosome mapping.". Biochim. Biophys. Acta 1360 (3): 229–40. doi:10.1016/s0925-4439(97)00003-3. PMID 9197465.
Suzuki Y, Jiang LL, Souri M et al. (1997). "D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.". Am. J. Hum. Genet. 61 (5): 1153–62. doi:10.1086/301599. PMC 1716023. PMID 9345094.
van Grunsven EG, van Berkel E, IJlst L et al. (1998). "Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency.". Proc. Natl. Acad. Sci. U.S.A. 95 (5): 2128–33. doi:10.1073/pnas.95.5.2128. PMC 19272. PMID 9482850.
Dong Y, Qiu QQ, Debear J et al. (1999). "17Beta-hydroxysteroid dehydrogenases in human bone cells.". J. Bone Miner. Res. 13 (10): 1539–46. doi:10.1359/jbmr.1998.13.10.1539. PMID 9783542.
Leenders F, Dolez V, Begue A et al. (1999). "Structure of the gene for the human 17beta-hydroxysteroid dehydrogenase type IV.". Mamm. Genome 9 (12): 1036–41. doi:10.1007/s003359900921. PMID 9880674.
Green VL, Speirs V, Landolt AM et al. (1999). "17Beta-hydroxysteroid dehydrogenase type 1, 2, 3, and 4 expression and enzyme activity in human anterior pituitary adenomas.". J. Clin. Endocrinol. Metab. 84 (4): 1340–5. doi:10.1210/jc.84.4.1340. PMID 10199776.
van Grunsven EG, Mooijer PA, Aubourg P, Wanders RJ (1999). "Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency.". Hum. Mol. Genet. 8 (8): 1509–16. doi:10.1093/hmg/8.8.1509. PMID 10400999.
Itoh M, Suzuki Y, Takashima S (1999). "A novel peroxisomal enzyme, D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein: its expression in the developing human brain.". Microsc. Res. Tech. 45 (6): 383–8. doi:10.1002/(SICI)1097-0029(19990615)45:6<383::AID-JEMT5>3.0.CO;2-7. PMID 10402265.
Möller G, Leenders F, van Grunsven EG et al. (1999). "Characterization of the HSD17B4 gene: D-specific multifunctional protein 2/17beta-hydroxysteroid dehydrogenase IV.". J. Steroid Biochem. Mol. Biol. 69 (1-6): 441–6. doi:10.1016/S0960-0760(99)00066-7. PMID 10419023.
Haapalainen AM, van Aalten DM, Meriläinen G et al. (2001). "Crystal structure of the liganded SCP-2-like domain of human peroxisomal multifunctional enzyme type 2 at 1.75 A resolution.". J. Mol. Biol. 313 (5): 1127–38. doi:10.1006/jmbi.2001.5084. PMID 11700068.

PDB gallery

1ikt: LIGANDED STEROL CARRIER PROTEIN TYPE 2 (SCP-2) LIKE DOMAIN OF HUMAN MULTIFUNCTIONAL ENZYME TYPE 2 (MFE-2)

1s9c: Crystal structure analysis of the 2-enoyl-CoA hydratase 2 domain of human peroxisomal multifunctional enzyme type 2

1zbq: Crystal Structure Of Human 17-Beta-Hydroxysteroid Dehydrogenase Type 4 In Complex With NAD

Peroxisomal and lysosomal proteins

Enzymes

Transporters

SLC27A2

Structure/Peroxin

LAMP

see also intermediates, disorders

Index of cells

Description	Structure nucleus chromosome genetics Organelles peroxisome cytoskeleton centrosome epithelia cilia mitochondria Membranes proteins cell adhesions Membrane transport ion channels vesicular transport solute carrier ABC transporters ATPase oxidoreduction-driven

Disease	Structural peroxisome cytoskeleton cilia mitochondria nucleus scleroprotein Membrane channelopathy solute carrier ATPase ABC transporters other extracellular ligands cell surface receptors intracellular signalling Vesicular transport Pore-forming toxins

HSD17B4

See also

References

Further reading