AKR1C1

Protein-coding gene in the species Homo sapiens
AKR1C1
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

1MRQ, 3C3U, 3GUG, 3NTY, 4YVP

Identifiers
AliasesAKR1C1, 2-ALPHA-HSD, 20-ALPHA-HSD, C9, DD1, DD1/DD2, DDH, DDH1, H-37, HAKRC, HBAB, MBAB, aldo-keto reductase family 1, member C1, aldo-keto reductase family 1 member C1
External IDsOMIM: 600449; MGI: 1924587; HomoloGene: 134114; GeneCards: AKR1C1; OMA:AKR1C1 - orthologs
EC number1.1.1.112
Gene location (Human)
Chromosome 10 (human)
Chr.Chromosome 10 (human)[1]
Chromosome 10 (human)
Genomic location for AKR1C1
Genomic location for AKR1C1
Band10p15.1Start4,963,253 bp[1]
End4,983,283 bp[1]
Gene location (Mouse)
Chromosome 13 (mouse)
Chr.Chromosome 13 (mouse)[2]
Chromosome 13 (mouse)
Genomic location for AKR1C1
Genomic location for AKR1C1
Band13|13 A1Start4,624,074 bp[2]
End4,636,540 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • islet of Langerhans

  • gastric mucosa

  • right lobe of liver

  • right auricle

  • olfactory zone of nasal mucosa

  • body of stomach

  • left coronary artery

  • ascending aorta

  • Descending thoracic aorta

  • gallbladder
Top expressed in
  • right kidney

  • human kidney

  • proximal tubule

  • morula

  • embryo

  • primary oocyte

  • primary visual cortex

  • secondary oocyte

  • blastocyst

  • muscle of thigh
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
  • trans-1,2-dihydrobenzene-1,2-diol dehydrogenase activity
  • alditol:NADP+ 1-oxidoreductase activity
  • indanol dehydrogenase activity
  • aldo-keto reductase (NADP) activity
  • 17-alpha,20-alpha-dihydroxypregn-4-en-3-one dehydrogenase activity
  • androsterone dehydrogenase (B-specific) activity
  • phenanthrene 9,10-monooxygenase activity
  • oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor
  • bile acid binding
  • protein binding
  • carboxylic acid binding
  • oxidoreductase activity
  • ketosteroid monooxygenase activity
  • alcohol dehydrogenase (NADP+) activity
  • steroid dehydrogenase activity
Cellular component
  • cytoplasm
  • cytosol
  • extracellular exosome
Biological process
  • cellular response to jasmonic acid stimulus
  • epithelial cell differentiation
  • daunorubicin metabolic process
  • doxorubicin metabolic process
  • progesterone metabolic process
  • bile acid metabolic process
  • digestion
  • retinal metabolic process
  • retinoid metabolic process
  • response to organophosphorus
  • bile acid and bile salt transport
  • intestinal cholesterol absorption
  • xenobiotic metabolic process
  • cholesterol homeostasis
  • protein homooligomerization
  • steroid metabolic process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

1645

77337

Ensembl

ENSG00000187134

ENSMUSG00000021207

UniProt

Q04828

Q91WR5

RefSeq (mRNA)

NM_001353

NM_029901

RefSeq (protein)

NP_001344

NP_084177

Location (UCSC)Chr 10: 4.96 – 4.98 MbChr 13: 4.62 – 4.64 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Aldo-keto reductase family 1 member C1 also known as 20α-hydroxysteroid dehydrogenase, 3α-hydroxysteroid dehydrogenase, and dihydrodiol dehydrogenase 1/2 is an enzyme that in humans is encoded by the AKR1C1 gene.[5][6]

Superfamily of enzymes

This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols by utilizing NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This specific enzyme, AKR1C1, among other reactions, catalyzes the reduction of progesterone to the inactive form 20-alpha-hydroxy-progesterone. The AKR1C1 gene shares high sequence identity with three other gene members, and is clustered with those three genes at chromosome 10p15-p14.[6]

Isozymes of aldo-keto reductase family 1 member C

HGNC Gene Symbol Enzyme Name Aliases[7]
AKR1C1 aldo-keto reductase family 1 member C1; 20α-hydroxysteroid dehydrogenase
AKR1C2 aldo-keto reductase family 1 member C2; 3α-hydroxysteroid dehydrogenase type 3
AKR1C3 aldo-keto reductase family 1 member C3; 3α-hydroxysteroid dehydrogenase type 2; 17β-hydroxysteroid dehydrogenase type 5; HSD17B5
AKR1C4 aldo-keto reductase family 1 member C4; 3α-hydroxysteroid dehydrogenase type 1

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000187134 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000021207 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Ciaccio PJ, Tew KD (Jun 1994). "cDNA and deduced amino acid sequences of a human colon dihydrodiol dehydrogenase". Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1186 (1–2): 129–32. doi:10.1016/0005-2728(94)90144-9. PMID 8011662.
  6. ^ a b "Entrez Gene: AKR1C1 aldo-keto reductase family 1, member C1 (dihydrodiol dehydrogenase 1; 20-alpha (3-alpha)-hydroxysteroid dehydrogenase)".
  7. ^ Dufort I, Labrie F, Luu-The V (February 2001). "Human types 1 and 3 3 alpha-hydroxysteroid dehydrogenases: differential lability and tissue distribution". J Clin Endocrinol Metab. 86 (2): 841–6. doi:10.1210/jcem.86.2.7216. PMID 11158055. human types 1 and 3 3α-HSD, 20α-HSD, and type 5 17β-HSD were named AKR1C4, AKR1C2, AKR1C1, and AKR1C3, respectively

See also

External links

Further reading

  • Ciaccio PJ, Jaiswal AK, Tew KD (Jun 1994). "Regulation of human dihydrodiol dehydrogenase by Michael acceptor xenobiotics". The Journal of Biological Chemistry. 269 (22): 15558–62. doi:10.1016/S0021-9258(17)40716-2. PMID 7515059.
  • Khanna M, Qin KN, Cheng KC (Jun 1995). "Distribution of 3 alpha-hydroxysteroid dehydrogenase in rat brain and molecular cloning of multiple cDNAs encoding structurally related proteins in humans". The Journal of Steroid Biochemistry and Molecular Biology. 53 (1–6): 41–6. doi:10.1016/0960-0760(95)00019-V. PMID 7626489. S2CID 11316547.
  • Khanna M, Qin KN, Klisak I, Belkin S, Sparkes RS, Cheng KC (Jan 1995). "Localization of multiple human dihydrodiol dehydrogenase (DDH1 and DDH2) and chlordecone reductase (CHDR) genes in chromosome 10 by the polymerase chain reaction and fluorescence in situ hybridization". Genomics. 25 (2): 588–90. doi:10.1016/0888-7543(95)80066-U. PMID 7789999.
  • Lou H, Hammond L, Sharma V, Sparkes RS, Lusis AJ, Stolz A (Mar 1994). "Genomic organization and chromosomal localization of a novel human hepatic dihydrodiol dehydrogenase with high affinity bile acid binding". The Journal of Biological Chemistry. 269 (11): 8416–22. doi:10.1016/S0021-9258(17)37210-1. PMID 8132567.
  • Deyashiki Y, Ogasawara A, Nakayama T, Nakanishi M, Miyabe Y, Sato K, Hara A (Apr 1994). "Molecular cloning of two human liver 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase isoenzymes that are identical with chlordecone reductase and bile-acid binder". The Biochemical Journal. 299 (2): 545–52. doi:10.1042/bj2990545. PMC 1138306. PMID 8172617.
  • Qin KN, New MI, Cheng KC (Dec 1993). "Molecular cloning of multiple cDNAs encoding human enzymes structurally related to 3 alpha-hydroxysteroid dehydrogenase". The Journal of Steroid Biochemistry and Molecular Biology. 46 (6): 673–9. doi:10.1016/0960-0760(93)90308-J. PMID 8274401. S2CID 36210133.
  • Stolz A, Hammond L, Lou H, Takikawa H, Ronk M, Shively JE (May 1993). "cDNA cloning and expression of the human hepatic bile acid-binding protein. A member of the monomeric reductase gene family". The Journal of Biological Chemistry. 268 (14): 10448–57. doi:10.1016/S0021-9258(18)82220-7. PMID 8486699.
  • Hara A, Matsuura K, Tamada Y, Sato K, Miyabe Y, Deyashiki Y, Ishida N (Jan 1996). "Relationship of human liver dihydrodiol dehydrogenases to hepatic bile-acid-binding protein and an oxidoreductase of human colon cells". The Biochemical Journal. 313 (2): 373–6. doi:10.1042/bj3130373. PMC 1216918. PMID 8573067.
  • O'connor T, Ireland LS, Harrison DJ, Hayes JD (Oct 1999). "Major differences exist in the function and tissue-specific expression of human aflatoxin B1 aldehyde reductase and the principal human aldo-keto reductase AKR1 family members". The Biochemical Journal. 343 (2): 487–504. doi:10.1042/bj3430487. PMC 1220579. PMID 10510318.
  • Nishizawa M, Nakajima T, Yasuda K, Kanzaki H, Sasaguri Y, Watanabe K, Ito S (Feb 2000). "Close kinship of human 20alpha-hydroxysteroid dehydrogenase gene with three aldo-keto reductase genes". Genes to Cells. 5 (2): 111–25. doi:10.1046/j.1365-2443.2000.00310.x. PMID 10672042. S2CID 25136637.
  • Zhang Y, Dufort I, Rheault P, Luu-The V (Oct 2000). "Characterization of a human 20alpha-hydroxysteroid dehydrogenase". Journal of Molecular Endocrinology. 25 (2): 221–8. doi:10.1677/jme.0.0250221. PMID 11013348.
  • Nahoum V, Gangloff A, Legrand P, Zhu DW, Cantin L, Zhorov BS, Luu-The V, Labrie F, Breton R, Lin SX (Nov 2001). "Structure of the human 3alpha-hydroxysteroid dehydrogenase type 3 in complex with testosterone and NADP at 1.25-A resolution". The Journal of Biological Chemistry. 276 (45): 42091–8. doi:10.1074/jbc.M105610200. PMID 11514561.
  • Chen CY, Hsu CP, Hsu NY, Shih CS, Lin TY, Chow KC (2002). "Expression of dihydrodiol dehydrogenase in the resected stage I non-small cell lung cancer". Oncology Reports. 9 (3): 515–9. doi:10.3892/or.9.3.515. PMID 11956619.
  • Yang MD, Wu CC, Chiou SH, Chiu CF, Lin TY, Chiang IP, Chow KC (2003). "Reduction of dihydrodiol dehydrogenase expression in resected hepatocellular carcinoma". Oncology Reports. 10 (2): 271–6. doi:10.3892/or.10.2.271. PMID 12579257.
  • Nakajima T, Yasuda K, Nishizawa M, Okada H, Yoshimura T, Ito S, Kanzaki H (Feb 2003). "Expression of 20alpha-hydroxysteroid dehydrogenase mRNA in human endometrium and decidua". Endocrine Journal. 50 (1): 105–11. doi:10.1507/endocrj.50.105. PMID 12733716.
  • Couture JF, Legrand P, Cantin L, Luu-The V, Labrie F, Breton R (Aug 2003). "Human 20alpha-hydroxysteroid dehydrogenase: crystallographic and site-directed mutagenesis studies lead to the identification of an alternative binding site for C21-steroids". Journal of Molecular Biology. 331 (3): 593–604. doi:10.1016/S0022-2836(03)00762-9. PMID 12899831.
  • Agapova OA, Yang P, Wang WH, Lane DA, Clark AF, Weinstein BI, Hernandez MR (Oct 2003). "Altered expression of 3 alpha-hydroxysteroid dehydrogenases in human glaucomatous optic nerve head astrocytes". Neurobiology of Disease. 14 (1): 63–73. doi:10.1016/S0969-9961(03)00101-3. PMID 13678667. S2CID 21159141.
  • v
  • t
  • e
  • 1ihi: Crystal Structure of Human Type III 3-alpha-Hydroxysteroid Dehydrogenase/Bile Acid Binding Protein (AKR1C2) Complexed with NADP+ and Ursodeoxycholate
    1ihi: Crystal Structure of Human Type III 3-alpha-Hydroxysteroid Dehydrogenase/Bile Acid Binding Protein (AKR1C2) Complexed with NADP+ and Ursodeoxycholate
  • 1j96: Human 3alpha-HSD type 3 in Ternary Complex with NADP and Testosterone
    1j96: Human 3alpha-HSD type 3 in Ternary Complex with NADP and Testosterone
  • 1mrq: Crystal structure of human 20alpha-HSD in ternary complex with NADP and 20alpha-hydroxy-progesterone
    1mrq: Crystal structure of human 20alpha-HSD in ternary complex with NADP and 20alpha-hydroxy-progesterone
  • 1xjb: Crystal structure of human type 3 3alpha-hydroxysteroid dehydrogenase in complex with NADP(H), citrate and acetate molecules
    1xjb: Crystal structure of human type 3 3alpha-hydroxysteroid dehydrogenase in complex with NADP(H), citrate and acetate molecules
  • 2hdj: Crystal structure of human type 3 3alpha-hydroxysteroid dehydrogenase in complex with NADP(H)
    2hdj: Crystal structure of human type 3 3alpha-hydroxysteroid dehydrogenase in complex with NADP(H)
  • v
  • t
  • e
1.1.1: NAD/NADP acceptor
1.1.2: cytochrome acceptor
  • D-lactate dehydrogenase (cytochrome)
  • D-lactate dehydrogenase (cytochrome c-553)
  • Mannitol dehydrogenase (cytochrome)
1.1.3: oxygen acceptor
1.1.4: disulfide as acceptor
1.1.5: quinone/similar acceptor
1.1.99: other acceptors
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