Literature summary extracted from
Matsuura, K.; Hara, A.; Deyashiki, Y.; Iwasa, H.; Kume, T.; Ishikura, S.; Shiraishi, H.; Katagiri, Y.
Roles of the C-terminal domains of human dihydrodiol dehydrogenase isoforms in the binding of substrates and modulators: probing with chimeric enzymes (1998), Biochem. J., 336, 429-436.
Activating Compound
EC Number |
Activating Compound |
Comment |
Organism |
Structure |
---|
1.3.1.20 |
bezafibric acid |
DD4 |
Homo sapiens |
|
1.3.1.20 |
Clofibric acid |
DD4, CDD4-1 |
Homo sapiens |
|
1.3.1.20 |
fenofibric acid |
DD4, CDD4-1 |
Homo sapiens |
|
1.3.1.20 |
Sulfobromophthalein |
DD4, CDD4-1 |
Homo sapiens |
|
Cloned(Commentary)
EC Number |
Cloned (Comment) |
Organism |
---|
1.3.1.20 |
DD1, DD4, CDD1-4, CDD4-1, all expressed in Escherichia coli |
Homo sapiens |
Protein Variants
EC Number |
Protein Variants |
Comment |
Organism |
---|
1.3.1.20 |
C87S |
DD1 mutant |
Homo sapiens |
1.3.1.20 |
L54V |
DD1 mutant, increase in activity towards (S)-indan-1-ol and bile-acids, increased Km for trans-benzene dihydrodiol |
Homo sapiens |
1.3.1.20 |
additional information |
CDD1-4 mutant consisting of DD1 with C-terminal end of DD4 shows 10-37fold increase in Km for indan-1-ol and 1,2,3,4-tetrahydronaphth-1-ol and significantly decreased activity towards androstanes, higher activity with bile-acids and 5beta-steroid than DD1 |
Homo sapiens |
1.3.1.20 |
additional information |
CDD4-1 mutant consisting of DD4 with C-terminal end of DD1shows new stereospecificity toward indan-1-ol stereomers and increased Km-values with bile acids and 3-hydroxysteroids compared to DD4 |
Homo sapiens |
1.3.1.20 |
Q172L |
DD1 mutant |
Homo sapiens |
1.3.1.20 |
R170H |
DD1 mutant |
Homo sapiens |
1.3.1.20 |
R47H |
DD1 mutant |
Homo sapiens |
1.3.1.20 |
T38V |
DD1 mutant |
Homo sapiens |
1.3.1.20 |
V151M |
DD1 mutant |
Homo sapiens |
Inhibitors
EC Number |
Inhibitors |
Comment |
Organism |
Structure |
---|
1.3.1.20 |
1,10-phenanthroline |
recombinant: DD1, DD4, CDD1-4, CDD4-1 |
Homo sapiens |
|
1.3.1.20 |
Betamethasone |
recombinant: DD1, DD4, CDD1-4, CDD4-1 |
Homo sapiens |
|
1.3.1.20 |
Flufenamic acid |
recombinant: DD1, DD4, CDD1-4, CDD4-1 |
Homo sapiens |
|
1.3.1.20 |
Hexestrol |
recombinant: DD1, DD4, CDD1-4, CDD4-1 |
Homo sapiens |
|
1.3.1.20 |
indomethacin |
recombinant: DD1, DD4, CDD1-4, CDD4-1 |
Homo sapiens |
|
1.3.1.20 |
Medroxyprogesterone acetate |
recombinant: DD1, DD4, CDD1-4, CDD4-1 |
Homo sapiens |
|
1.3.1.20 |
Phenolphthalein |
recombinant: DD1, DD4, CDD1-4, CDD4-1 |
Homo sapiens |
|
Organism
EC Number |
Organism |
UniProt |
Comment |
Textmining |
---|
1.3.1.20 |
Homo sapiens |
- |
DD1, DD4 |
- |
Purification (Commentary)
EC Number |
Purification (Comment) |
Organism |
---|
1.3.1.20 |
DD1, DD4, CDD1-4, CDD4-1, all recombinant from Escherichia coli |
Homo sapiens |
Source Tissue
EC Number |
Source Tissue |
Comment |
Organism |
Textmining |
---|
1.3.1.20 |
liver |
- |
Homo sapiens |
- |
Substrates and Products (Substrate)
EC Number |
Substrates |
Comment Substrates |
Organism |
Products |
Comment (Products) |
Rev. |
Reac. |
---|
1.3.1.20 |
(S)-indan-1-ol + NADP+ |
DD1, DD4, mutant CDD1-4, mutant CDD4-1 |
Homo sapiens |
? |
- |
? |
|
Cofactor
EC Number |
Cofactor |
Comment |
Organism |
Structure |
---|
1.3.1.20 |
NADP+ |
- |
Homo sapiens |
|