DB code: S00331
RLCP classification | 9.5010.536200.8010 : Hydride transfer | |
---|---|---|
CATH domain | 3.40.50.720 : Rossmann fold | Catalytic domain |
E.C. | 1.1.1.184 | |
CSA | ||
M-CSA | ||
MACiE |
CATH domain | Related DB codes (homologues) |
---|---|
3.40.50.720 : Rossmann fold | S00543 S00551 S00552 S00553 S00602 S00604 S00605 S00608 S00610 S00625 S00319 S00328 S00329 S00330 S00332 D00456 D00457 D00458 S00324 S00320 S00325 S00326 S00327 D00459 S00335 S00336 S00334 T00219 S00339 D00513 D00001 D00002 D00003 D00005 D00007 D00008 D00010 D00012 D00017 D00018 D00023 D00027 D00028 D00031 D00032 D00033 D00034 D00035 D00037 D00048 D00071 D00476 D00481 D00482 D00490 D00492 D00494 D00545 D00601 D00603 D00604 D00605 D00615 D00845 D00857 D00858 M00161 M00171 M00210 T00002 T00010 T00011 T00015 T00227 T00247 T00408 T00414 D00827 D00262 D00274 D00275 M00035 T00109 |
Uniprot Enzyme Name | UniprotKB | Protein name | Synonyms | RefSeq | Pfam |
---|---|---|---|---|
Q9W3H4 |
|
Sniffer
EC 1.1.1.184 LD36273p |
NP_572466.1
(Protein)
NM_132238.3 (DNA/RNA sequence) |
PF00106
(adh_short)
[Graphical View] |
P08074 |
Carbonyl reductase {NADPH} 2
|
EC
1.1.1.184
NADPH-dependent carbonyl reductase 2 Lung carbonyl reductase LCR Adipocyte protein P27 AP27 |
NP_031647.1
(Protein)
NM_007621.2 (DNA/RNA sequence) |
PF00106
(adh_short)
[Graphical View] |
Q8WNV7 |
Dehydrogenase/reductase SDR family member 4
|
EC
1.1.1.184
NADPH-dependent carbonyl reductase/NADP-retinol dehydrogenase PHCR CR Peroxisomal short-chain alcohol dehydrogenase NADPH-dependent retinol dehydrogenase/reductase NDRD |
NP_999184.1
(Protein)
NM_214019.1 (DNA/RNA sequence) |
[Graphical View] |
Q9BTZ2 |
Dehydrogenase/reductase SDR family member 4
|
EC
1.1.1.184
Short-chain dehydrogenase/reductase family member 4 NADPH-dependent carbonyl reductase/NADP-retinol dehydrogenase PHCR CR Peroxisomal short-chain alcohol dehydrogenase PSCD NADPH-dependent retinol dehydrogenase/reductase NRDR humNRDR SCAD-SRL |
NP_066284.2
(Protein)
NM_021004.2 (DNA/RNA sequence) |
[Graphical View] |
O75828 |
Carbonyl reductase {NADPH} 3
|
EC
1.1.1.184
NADPH-dependent carbonyl reductase 3 |
NP_001227.1
(Protein)
NM_001236.3 (DNA/RNA sequence) |
PF00106
(adh_short)
[Graphical View] |
KEGG enzyme name |
---|
carbonyl reductase (NADPH)
aldehyde reductase 1 prostaglandin 9-ketoreductase xenobiotic ketone reductase NADPH-dependent carbonyl reductase ALR3 carbonyl reductase nonspecific NADPH-dependent carbonyl reductase aldehyde reductase 1 carbonyl reductase (NADPH) |
UniprotKB: Accession Number | Entry name | Activity | Subunit | Subcellular location | Cofactor |
---|---|---|---|---|---|
Q9W3H4 | Q9W3H4_DROME | ||||
P08074 | CBR2_MOUSE | R-CHOH-R' + NADP(+) = R-CO-R' + NADPH. | Homotetramer. | Mitochondrion matrix. | |
Q8WNV7 | DHRS4_PIG | R-CHOH-R' + NADP(+) = R-CO-R' + NADPH. | Homotetramer. | Peroxisome. | |
Q9BTZ2 | DHRS4_HUMAN | R-CHOH-R' + NADP(+) = R-CO-R' + NADPH. | Homotetramer (By similarity). | Peroxisome. Note=Isoform 1 is peroxisomal, while isoform 4 is not. | |
O75828 | CBR3_HUMAN | R-CHOH-R' + NADP(+) = R-CO-R' + NADPH. | Cytoplasm. |
KEGG Pathways | Map code | Pathways | E.C. |
---|---|---|
MAP00590 | Arachidonic acid metabolism |
Compound table | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Substrates | Products | Intermediates | |||||||||
KEGG-id | C00005 | C01450 | C00080 | C00006 | C01612 | ||||||
E.C. | |||||||||||
Compound | NADPH | R-CO-R' | H+ | NADP+ | R-CHOH-R' | ||||||
Type | amide group,amine group,nucleotide | carbohydrate | others | amide group,amine group,nucleotide | carbohydrate | ||||||
ChEBI |
16474 16474 |
15378 15378 |
18009 18009 |
||||||||
PubChem |
5884 5884 |
1038 1038 |
5886 5886 |
||||||||
1snyA | Unbound | Unbound | Bound:NAP | Unbound | |||||||
1cydA | Unbound | Unbound | Bound:NAP | Bound:IPA | |||||||
1cydB | Unbound | Unbound | Bound:NAP | Bound:IPA | |||||||
1cydC | Unbound | Unbound | Bound:NAP | Bound:IPA | |||||||
1cydD | Unbound | Unbound | Bound:NAP | Bound:IPA | |||||||
2zatA | Unbound | Unbound | Bound:NAP | Unbound | |||||||
2zatB | Unbound | Unbound | Bound:NAP | Unbound | |||||||
2zatC | Unbound | Unbound | Bound:NAP | Unbound | |||||||
2zatD | Unbound | Unbound | Bound:NAP | Unbound | |||||||
3o4rA | Unbound | Unbound | Bound:NAP | Unbound | |||||||
3o4rB | Unbound | Unbound | Bound:NAP | Bound:GOL | |||||||
3o4rC | Unbound | Unbound | Bound:NAP | Bound:GOL | |||||||
3o4rD | Unbound | Unbound | Bound:NAP | Unbound | |||||||
2hrbA | Unbound | Unbound | Bound:NAP | Unbound |
Reference for Active-site residues | ||
---|---|---|
resource | references | E.C. |
Swiss-prot;P08074 & literature [10] |
Active-site residues | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
PDB | Catalytic residues | Cofactor-binding residues | Modified residues | Main-chain involved in catalysis | Comment | |||||
1snyA | SER 154;TYR 170;LYS 174 | |||||||||
1cydA | SER 136;TYR 149;LYS 153 | |||||||||
1cydB | SER 136;TYR 149;LYS 153 | |||||||||
1cydC | SER 136;TYR 149;LYS 153 | |||||||||
1cydD | SER 136;TYR 149;LYS 153 | |||||||||
2zatA | SER 151;TYR 164;LYS 168 | |||||||||
2zatB | SER 151;TYR 164;LYS 168 | |||||||||
2zatC | SER 151;TYR 164;LYS 168 | |||||||||
2zatD | SER 151;TYR 164;LYS 168 | |||||||||
3o4rA | SER 169;TYR 182;LYS 186 | |||||||||
3o4rB | SER 169;TYR 182;LYS 186 | |||||||||
3o4rC | SER 169;TYR 182;LYS 186 | |||||||||
3o4rD | SER 169;TYR 182;LYS 186 | |||||||||
2hrbA | SER 140;TYR 194;LYS 198 |
References for Catalytic Mechanism | ||
---|---|---|
References | Sections | No. of steps in catalysis |
[10]
|
p.42 | |
[12]
|
p.559-560 | |
[17]
|
p.1617 | |
[18]
|
p.392 |
References | |
---|---|
[1] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 3511844 |
Journal | Arch Biochem Biophys |
Year | 1986 |
Volume | 244 |
Pages | 238-47 |
Authors | Hara A, Nakayama T, Deyashiki Y, Kariya K, Sawada H |
Title |
Carbonyl reductase of dog liver: purification, |
Related PDB | |
Related UniProtKB | |
[2] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 2388711 |
Journal | Neurochem Res |
Year | 1990 |
Volume | 15 |
Pages | 385-92 |
Authors | Hayashi H, Fujii Y, Watanabe K, Hayaishi O |
Title | Enzymatic formation of prostaglandin F2 alpha in human brain. |
Related PDB | |
Related UniProtKB | |
[3] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1449827 |
Journal | Eicosanoids |
Year | 1992 |
Volume | 5 Suppl |
Pages | S37-8 |
Authors | Schieber A, Ghisla S |
Title |
Prostaglandin 9-ketoreductase from pig and human kidney: purification, |
Related PDB | |
Related UniProtKB | |
[4] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1576998 |
Journal | Eur J Biochem |
Year | 1992 |
Volume | 205 |
Pages | 1155-62 |
Authors | Klein J, Thomas H, Post K, Worner W, Oesch F |
Title | Dihydrodiol dehydrogenase activities of rabbit liver are associated with hydroxysteroid dehydrogenases and aldo-keto reductases. |
Related PDB | |
Related UniProtKB | |
[5] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1597188 |
Journal | Eur J Biochem |
Year | 1992 |
Volume | 206 |
Pages | 491-502 |
Authors | Schieber A, Frank RW, Ghisla S |
Title |
Purification and properties of prostaglandin 9-ketoreductase from pig and human kidney. |
Related PDB | |
Related UniProtKB | |
[6] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8421682 |
Journal | Proc Natl Acad Sci U S A |
Year | 1993 |
Volume | 90 |
Pages | 502-6 |
Authors | Krook M, Ghosh D, Stromberg R, Carlquist M, Jornvall H |
Title | Carboxyethyllysine in a protein: native carbonyl reductase/NADP(+)-dependent prostaglandin dehydrogenase. |
Related PDB | |
Related UniProtKB | |
[7] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7990149 |
Journal | J Mol Biol |
Year | 1994 |
Volume | 244 |
Pages | 659-64 |
Authors | Bohren KM, Wermuth B, Harrison D, Ringe D, Petsko GA, Gabbay KH |
Title |
Expression, |
Related PDB | |
Related UniProtKB | |
[8] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7981120 |
Journal | J Steroid Biochem Mol Biol |
Year | 1994 |
Volume | 51 |
Pages | 125-30 |
Authors | Krozowski Z |
Title | The short-chain alcohol dehydrogenase superfamily: variations on a common theme. |
Related PDB | |
Related UniProtKB | |
[9] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8889808 |
Journal | J Biochem (Tokyo) |
Year | 1996 |
Volume | 120 |
Pages | 257-63 |
Authors | Nakanishi M, Kakumoto M, Matsuura K, Deyashiki Y, Tanaka N, Nonaka T, Mitsui Y, Hara A |
Title | Involvement of two basic residues (Lys-17 and Arg-39) of mouse lung carbonyl reductase in NADP(H)-binding and fatty acid activation: site-directed mutagenesis and kinetic analyses. |
Related PDB | |
Related UniProtKB | |
[10] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (1.8 ANGSTROMS) IN COMPLEX WITH NADPH. |
Medline ID | |
PubMed ID | 8805511 |
Journal | Structure |
Year | 1996 |
Volume | 4 |
Pages | 33-45 |
Authors | Tanaka N, Nonaka T, Nakanishi M, Deyashiki Y, Hara A, Mitsui Y |
Title | Crystal structure of the ternary complex of mouse lung carbonyl reductase at 1.8 A resolution: the structural origin of coenzyme specificity in the short-chain dehydrogenase/reductase family. |
Related PDB | 1cyd |
Related UniProtKB | P08074 |
[11] | |
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 | |
[12] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9059662 |
Journal | Adv Exp Med Biol |
Year | 1997 |
Volume | 414 |
Pages | 555-61 |
Authors | Nakanishi M, Kaibe H, Matsuura K, Kakumoto M, Tanaka N, Nonaka T, Mitsui Y, Hara A |
Title | Site-directed mutagenesis of residues in coenzyme-binding domain and active site of mouse lung carbonyl reductase. |
Related PDB | |
Related UniProtKB | |
[13] | |
Resource | |
Comments |
MUTAGENESIS OF THR-38, |
Medline ID | |
PubMed ID | 8999926 |
Journal | J Biol Chem |
Year | 1997 |
Volume | 272 |
Pages | 2218-22 |
Authors | Nakanishi M, Matsuura K, Kaibe H, Tanaka N, Nonaka T, Mitsui Y, Hara A |
Title | Switch of coenzyme specificity of mouse lung carbonyl reductase by substitution of threonine 38 with aspartic acid. |
Related PDB | |
Related UniProtKB | P08074 |
[14] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9729461 |
Journal | Biochem J |
Year | 1998 |
Volume | 334 |
Pages | 553-7 |
Authors | Nakajin S, Takase N, Ohno S, Toyoshima S, Baker ME |
Title | Mutation of tyrosine-194 and lysine-198 in the catalytic site of pig 3alpha/beta,20beta-hydroxysteroid dehydrogenase. |
Related PDB | |
Related UniProtKB | |
[15] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9880795 |
Journal | J Biochem (Tokyo) |
Year | 1999 |
Volume | 125 |
Pages | 41-7 |
Authors | Imamura Y, Migita T, Otagiri M, Choshi T, Hibino S |
Title | Purification and catalytic properties of a tetrameric carbonyl reductase from rabbit heart. |
Related PDB | |
Related UniProtKB | |
[16] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11279087 |
Journal | J Biol Chem |
Year | 2001 |
Volume | 276 |
Pages | 18457-63 |
Authors | Ghosh D, Sawicki M, Pletnev V, Erman M, Ohno S, Nakajin S, Duax WL |
Title |
Porcine carbonyl reductase. |
Related PDB | 1hu4 1n5d |
Related UniProtKB | |
[17] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 15364585 |
Journal | J Mol Biol |
Year | 2004 |
Volume | 342 |
Pages | 1613-24 |
Authors | Sgraja T, Ulschmid J, Becker K, Schneuwly S, Klebe G, Reuter K, Heine A |
Title | Structural insights into the neuroprotective-acting carbonyl reductase Sniffer of Drosophila melanogaster. |
Related PDB | 1sny |
Related UniProtKB | |
[18] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 18334214 |
Journal | Structure |
Year | 2008 |
Volume | 16 |
Pages | 388-97 |
Authors | Tanaka N, Aoki K, Ishikura S, Nagano M, Imamura Y, Hara A, Nakamura KT |
Title | Molecular basis for peroxisomal localization of tetrameric carbonyl reductase. |
Related PDB | 2zat |
Related UniProtKB | |
[19] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 19056333 |
Journal | Arch Biochem Biophys |
Year | 2009 |
Volume | 481 |
Pages | 183-90 |
Authors | Endo S, Maeda S, Matsunaga T, Dhagat U, El-Kabbani O, Tanaka N, Nakamura KT, Tajima K, Hara A |
Title | Molecular determinants for the stereospecific reduction of 3-ketosteroids and reactivity towards all-trans-retinal of a short-chain dehydrogenase/reductase (DHRS4). |
Related PDB | |
Related UniProtKB |
Comments |
---|
This enzyme belongs to the short-chain dehydrogenase/reductase (SDR) superfamily, This enzyme seems to catalyze the reduction of a variety of carbonyl compounds. |
Created | Updated |
---|---|
2005-01-24 | 2011-06-30 |