DB code: S00229
CATH domain | 3.20.20.100 : TIM Barrel | Catalytic domain |
---|---|---|
E.C. | 1.1.1.213 | |
CSA | ||
M-CSA | ||
MACiE |
CATH domain | Related DB codes (homologues) |
---|---|
3.20.20.100 : TIM Barrel | S00227 S00228 |
Uniprot Enzyme Name | UniprotKB | Protein name | Synonyms | RefSeq | Pfam |
---|---|---|---|---|
P23457 |
3-alpha-hydroxysteroid dehydrogenase
|
3-alpha-HSD
EC 1.1.1.213 Hydroxyprostaglandin dehydrogenase |
NP_612556.1
(Protein)
NM_138547.2 (DNA/RNA sequence) |
PF00248
(Aldo_ket_red)
[Graphical View] |
KEGG enzyme name |
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3alpha-hydroxysteroid dehydrogenase (A-specific)
|
UniprotKB: Accession Number | Entry name | Activity | Subunit | Subcellular location | Cofactor |
---|---|---|---|---|---|
P23457 | DIDH_RAT | Androsterone + NAD(P)(+) = 5-alpha-androstane- 3,17-dione + NAD(P)H. | Monomer. | Cytoplasm. |
KEGG Pathways | Map code | Pathways | E.C. |
---|
Compound table | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Substrates | Products | Intermediates | |||||||||||
KEGG-id | C00523 | C00003 | C00006 | C00674 | C00004 | C00005 | C00080 | ||||||
E.C. | |||||||||||||
Compound | Androsterone | NAD+ | NADP+ | 5alpha-Androstane-3,17-dione | NADH | NADPH | H+ | ||||||
Type | carbohydrate,steroid | amide group,amine group,nucleotide | amide group,amine group,nucleotide | carbohydrate,steroid | amide group,amine group,nucleotide | amide group,amine group,nucleotide | others | ||||||
ChEBI |
16032 16032 |
15846 15846 |
18009 18009 |
15994 15994 |
16908 16908 |
16474 16474 |
15378 15378 |
||||||
PubChem |
5879 5879 |
5893 5893 |
5886 5886 |
222865 439289 222865 439289 |
439153 439153 |
5884 5884 |
1038 1038 |
||||||
1afsA | Unbound | Unbound | Bound:NAP | Analogue:TES | Unbound | Unbound | |||||||
1afsB | Unbound | Unbound | Bound:NAP | Analogue:TES | Unbound | Unbound | |||||||
1lwiA | Unbound | Unbound | Bound:NAP | Unbound | Unbound | Unbound | |||||||
1lwiB | Unbound | Unbound | Bound:NAP | Unbound | Unbound | Unbound | |||||||
1ralA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound |
Reference for Active-site residues | ||
---|---|---|
resource | references | E.C. |
Swiss-prot;P23457 & literature [16] & [19] |
Active-site residues | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
PDB | Catalytic residues | Cofactor-binding residues | Modified residues | Main-chain involved in catalysis | Comment | |||||
1afsA | ASP 50;TYR 55;LYS 84;HIS 117 | |||||||||
1afsB | ASP 50;TYR 55;LYS 84;HIS 117 | |||||||||
1lwiA | ASP 50;TYR 55;LYS 84;HIS 117 | |||||||||
1lwiB | ASP 50;TYR 55;LYS 84;HIS 117 | |||||||||
1ralA | ASP 50;TYR 55;LYS 84;HIS 117 |
References for Catalytic Mechanism | ||
---|---|---|
References | Sections | No. of steps in catalysis |
[6]
|
Scheme II, p.13509 | 1 |
[7]
|
Fig.4, p.2519 | 1 |
[9]
|
p.10710 | |
[10]
|
Fig.6, p.S178-S181 | |
[11]
|
Fig.7, Fig.8, Fig.10, p.513 | |
[13]
|
Fig.3, p.477-481 | |
[14]
|
Fig.2, Fig.5, Fig.6, p.104-105 | |
[15]
|
p.804-806 | |
[16]
|
Fig.6, p.9700-9702 | |
[17]
|
Fig.4, p.11009-11011 | |
[19]
|
Fig.4, p.215-218 | |
[18]
|
Fig. 7, p.218 | |
[23]
|
Fig. 6, p.666 |
References | |
---|---|
[1] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 3006670 |
Journal | Biochem J |
Year | 1986 |
Volume | 233 |
Pages | 493-7 |
Authors | Kim HS, Minard P, Legoy MD, Thomas D |
Title |
Inactivation of 3 alpha-hydroxysteroid dehydrogenase by superoxide radicals. |
Related PDB | |
Related UniProtKB | |
[2] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1793046 |
Journal | Agents Actions |
Year | 1991 |
Volume | 34 |
Pages | 289-93 |
Authors | Pawlowski J, Huizinga M, Penning TM |
Title | Isolation and partial characterization of a full-length cDNA clone for 3 alpha-hydroxysteroid dehydrogenase: a potential target enzyme for nonsteroidal anti-inflammatory drugs. |
Related PDB | |
Related UniProtKB | |
[3] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1747374 |
Journal | Biochemistry |
Year | 1991 |
Volume | 30 |
Pages | 11553-60 |
Authors | Askonas LJ, Penning TM |
Title | Development of affinity labeling agents based on nonsteroidal anti-inflammatory drugs: labeling of the nonsteroidal anti-inflammatory drug binding site of 3 alpha-hydroxysteroid dehydrogenase. |
Related PDB | |
Related UniProtKB | |
[4] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1788860 |
Journal | Steroids |
Year | 1991 |
Volume | 56 |
Pages | 420-7 |
Authors | Penning TM, Thronton R, Ricigliano JW |
Title | Clues to the development of mechanism-based inactivators of 3 alpha-hydroxysteroid dehydrogenase: comparison of steroidal and nonsteroidal Michael acceptors and epoxides. |
Related PDB | |
Related UniProtKB | |
[5] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7945717 |
Journal | Farmaco |
Year | 1994 |
Volume | 49 |
Pages | 505-7 |
Authors | Plescia S, Raffa D, Daidone G, Schillaci D, Maggio B |
Title | 3 alpha-hydroxysteroid dehydrogenase inhibitory activity of some N(3)-(1-R-4-carboxypyrazol-5-yl)-1,2,3-benzotriazin-4(3H)-one and quinazolin-4(3H)-one acids. |
Related PDB | |
Related UniProtKB | |
[6] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8175784 |
Journal | J Biol Chem |
Year | 1994 |
Volume | 269 |
Pages | 13502-10 |
Authors | Pawlowski JE, Penning TM |
Title |
Overexpression and mutagenesis of the cDNA for rat liver 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase. |
Related PDB | |
Related UniProtKB | |
[7] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (3.0 ANGSTROMS) |
Medline ID | 94195773 |
PubMed ID | 8146147 |
Journal | Proc Natl Acad Sci U S A |
Year | 1994 |
Volume | 91 |
Pages | 2517-21 |
Authors | Hoog SS, Pawlowski JE, Alzari PM, Penning TM, Lewis M |
Title | Three-dimensional structure of rat liver 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase: a member of the aldo-keto reductase superfamily. |
Related PDB | 1ral |
Related UniProtKB | P23457 |
[8] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7676484 |
Journal | Steroids |
Year | 1995 |
Volume | 60 |
Pages | 491-6 |
Authors | Hu Y, Sherwin PF, Covey DF |
Title |
Synthesis of (17R)- and (17S)-17-hydroxy-14, |
Related PDB | |
Related UniProtKB | |
[9] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (2.7 ANGSTROMS) |
Medline ID | 96346063 |
PubMed ID | 8718859 |
Journal | Biochemistry |
Year | 1996 |
Volume | 35 |
Pages | 10702-11 |
Authors | Bennett MJ, Schlegel BP, Jez JM, Penning TM, Lewis M |
Title | Structure of 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase complexed with NADP+. |
Related PDB | 1lwi |
Related UniProtKB | P23457 |
[10] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8943801 |
Journal | J Endocrinol |
Year | 1996 |
Volume | 150 Suppl |
Pages | S175-87 |
Authors | Penning TM |
Title | 3 alpha-hydroxysteroid dehydrogenase: three dimensional structure and gene regulation. |
Related PDB | |
Related UniProtKB | |
[11] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8883217 |
Journal | Steroids |
Year | 1996 |
Volume | 61 |
Pages | 508-23 |
Authors | Penning TM, Pawlowski JE, Schlegel BP, Jez JM, Lin HK, Hoog SS, Bennett MJ, Lewis M |
Title | Mammalian 3 alpha-hydroxysteroid dehydrogenases. |
Related PDB | |
Related UniProtKB | |
[12] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9059665 |
Journal | Adv Exp Med Biol |
Year | 1997 |
Volume | 414 |
Pages | 579-600 |
Authors | Jez JM, Flynn TG, Penning TM |
Title | A nomenclature system for the aldo-keto reductase superfamily. |
Related PDB | |
Related UniProtKB | |
[13] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9059653 |
Journal | Adv Exp Med Biol |
Year | 1997 |
Volume | 414 |
Pages | 475-90 |
Authors | Penning TM |
Title |
Hydroxysteroid dehydrogenases. |
Related PDB | |
Related UniProtKB | |
[14] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9029723 |
Journal | Steroids |
Year | 1997 |
Volume | 62 |
Pages | 101-11 |
Authors | Penning TM, Bennett MJ, Smith-Hoog S, Schlegel BP, Jez JM, Lewis M |
Title | Structure and function of 3 alpha-hydroxysteroid dehydrogenase. |
Related PDB | |
Related UniProtKB | |
[15] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 9261071 |
Journal | Structure |
Year | 1997 |
Volume | 5 |
Pages | 799-812 |
Authors | Bennett MJ, Albert RH, Jez JM, Ma H, Penning TM, Lewis M |
Title | Steroid recognition and regulation of hormone action: crystal structure of testosterone and NADP+ bound to 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase. |
Related PDB | 1afs |
Related UniProtKB | |
[16] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9657682 |
Journal | Biochemistry |
Year | 1998 |
Volume | 37 |
Pages | 9695-703 |
Authors | Jez JM, Penning TM |
Title | Engineering steroid 5 beta-reductase activity into rat liver 3 alpha-hydroxysteroid dehydrogenase. |
Related PDB | |
Related UniProtKB | |
[17] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9692994 |
Journal | Biochemistry |
Year | 1998 |
Volume | 37 |
Pages | 11003-11 |
Authors | Schlegel BP, Ratnam K, Penning TM |
Title | Retention of NADPH-linked quinone reductase activity in an aldo-keto reductase following mutation of the catalytic tyrosine. |
Related PDB | |
Related UniProtKB | |
[18] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10549852 |
Journal | Biol Pharm Bull |
Year | 1999 |
Volume | 22 |
Pages | 1038-46 |
Authors | Yamano S, Ichinose F, Todaka T, Toki S |
Title |
Purification and characterization of two major forms of naloxone reductase from rabbit liver cytosol, |
Related PDB | |
Related UniProtKB | |
[19] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10418995 |
Journal | J Steroid Biochem Mol Biol |
Year | 1999 |
Volume | 69 |
Pages | 211-25 |
Authors | Penning TM |
Title |
Molecular determinants of steroid recognition and catalysis in aldo-keto reductases. |
Related PDB | |
Related UniProtKB | |
[20] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10500147 |
Journal | Proc Natl Acad Sci U S A |
Year | 1999 |
Volume | 96 |
Pages | 11161-6 |
Authors | Ma H, Penning TM |
Title | Conversion of mammalian 3alpha-hydroxysteroid dehydrogenase to 20alpha-hydroxysteroid dehydrogenase using loop chimeras: changing specificity from androgens to progestins. |
Related PDB | |
Related UniProtKB | |
[21] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10998348 |
Journal | Biochem J |
Year | 2000 |
Volume | 351 |
Pages | 67-77 |
Authors | Penning TM, Burczynski ME, Jez JM, Hung CF, Lin HK, Ma H, Moore M, Palackal N, Ratnam K |
Title | Human 3alpha-hydroxysteroid dehydrogenase isoforms (AKR1C1-AKR1C4) of the aldo-keto reductase superfamily: functional plasticity and tissue distribution reveals roles in the inactivation and formation of male and female sex hormones. |
Related PDB | |
Related UniProtKB | |
[22] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10876166 |
Journal | J Biochem (Tokyo) |
Year | 2000 |
Volume | 128 |
Pages | 121-8 |
Authors | Yamamoto T, Nozaki A, Shintani S, Ishikura S, Katagiri Y, Hara A |
Title | Structure-specific effects of thyroxine analogs on human liver 3 alpha-hydroxysteroid dehydrogenase. |
Related PDB | |
Related UniProtKB | |
[23] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11306084 |
Journal | Chem Biol Interact |
Year | 2001 |
Volume | 130-132 |
Pages | 659-71 |
Authors | Penning TM, Ma H, Jez JM |
Title | Engineering steroid hormone specificity into aldo-keto reductases. |
Related PDB | |
Related UniProtKB | |
[24] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11165022 |
Journal | Mol Cell Endocrinol |
Year | 2001 |
Volume | 171 |
Pages | 137-49 |
Authors | Penning TM, Burczynski ME, Jez JM, Lin HK, Ma H, Moore M, Ratnam K, Palackal N |
Title | Structure-function aspects and inhibitor design of type 5 17beta-hydroxysteroid dehydrogenase (AKR1C3). |
Related PDB | |
Related UniProtKB | |
[25] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 12943710 |
Journal | J Steroid Biochem Mol Biol |
Year | 2003 |
Volume | 85 |
Pages | 247-55 |
Authors | Penning TM, Jin Y, Heredia VV, Lewis M |
Title | Structure-function relationships in 3alpha-hydroxysteroid dehydrogenases: a comparison of the rat and human isoforms. |
Related PDB | |
Related UniProtKB |
Comments |
---|
This enzyme has been transferred from E.C.1.1.1.50 (B-specific) to E.C.1.1.1.213 (A-specific) (see [9]).
|
Created | Updated |
---|---|
2004-02-02 | 2009-02-26 |