DB code: S00522
CATH domain | 3.40.50.360 : Rossmann fold | Catalytic domain |
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E.C. | 1.10.99.2 | |
CSA | ||
M-CSA | ||
MACiE |
CATH domain | Related DB codes (homologues) |
---|---|
3.40.50.360 : Rossmann fold | S00343 M00006 M00154 |
Uniprot Enzyme Name | UniprotKB | Protein name | Synonyms | RefSeq | Pfam |
---|---|---|---|---|
P16083 |
Ribosyldihydronicotinamide dehydrogenase {quinone}
|
EC
1.10.99.2
NRH dehydrogenase {quinone} 2 NRH:quinone oxidoreductase 2 Quinone reductase 2 QR2 |
NP_000895.2
(Protein)
NM_000904.3 (DNA/RNA sequence) |
PF02525
(Flavodoxin_2)
[Graphical View] |
KEGG enzyme name |
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ribosyldihydronicotinamide dehydrogenase (quinone)
NRH:quinone oxidoreductase 2 NQO2 NQO2 NAD(P)H:quinone oxidoreductase-2 (misleading) QR2 quinone reductase 2 N-ribosyldihydronicotinamide dehydrogenase (quinone) NAD(P)H:quinone oxidoreductase2 (misleading) |
UniprotKB: Accession Number | Entry name | Activity | Subunit | Subcellular location | Cofactor |
---|---|---|---|---|---|
P16083 | NQO2_HUMAN | 1-(beta-D-ribofuranosyl)-1,4- dihydronicotinamide + a quinone = 1-(beta-D- ribofuranosyl)nicotinamide + a hydroquinone. | Homodimer. | Cytoplasm. | Binds 1 zinc ion per subunit. FAD. |
KEGG Pathways | Map code | Pathways | E.C. |
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Compound table | |||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cofactors | Substrates | Products | Intermediates | ||||||||||||
KEGG-id | C00016 | C00038 | C00005 | C00004 | C00080 | C01628 | C00006 | C00003 | C05850 | ||||||
E.C. | |||||||||||||||
Compound | FAD | Zinc | NADPH | NADH | H+ | Vitamin K | NADP+ | NAD+ | Reduced Vitamin K | ||||||
Type | amide group,amine group,aromatic ring (only carbon atom),aromatic ring (with nitrogen atoms),carbohydrate,nucleotide | heavy metal | amide group,amine group,nucleotide | amide group,amine group,nucleotide | others | aromatic ring (only carbon atom),carbohydrate,lipid | amide group,amine group,nucleotide | amide group,amine group,nucleotide | aromatic ring (only carbon atom),carbohydrate,lipid | ||||||
ChEBI |
16238 16238 |
29105 29105 |
16474 16474 |
16908 16908 |
15378 15378 |
18009 18009 |
15846 15846 |
||||||||
PubChem |
643975 643975 |
32051 32051 |
5884 5884 |
439153 439153 |
1038 1038 |
5886 5886 |
5893 5893 |
||||||||
1qr2A | Bound:FAD | Bound:_ZN | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1qr2B | Bound:FAD | Bound:_ZN | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
2qr2A | Bound:FAD | Bound:_ZN | Unbound | Unbound | Bound:VK3 | Unbound | Unbound | Unbound | |||||||
2qr2B | Bound:FAD | Bound:_ZN | Unbound | Unbound | Bound:VK3 | Unbound | Unbound | Unbound |
Reference for Active-site residues | ||
---|---|---|
resource | references | E.C. |
Swiss-prot;P16083 & literature [7] |
Active-site residues | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
PDB | Catalytic residues | Cofactor-binding residues | Modified residues | Main-chain involved in catalysis | Comment | |||||
1qr2A | GLY 149;TYR 155 | HIS 173;HIS 177;CYS 222(Zinc binding) | ||||||||
1qr2B | GLY 149;TYR 155 | HIS 173;HIS 177;CYS 222(Zinc binding) | ||||||||
2qr2A | GLY 149;TYR 155 | HIS 173;HIS 177;CYS 222(Zinc binding) | ||||||||
2qr2B | GLY 149;TYR 155 | HIS 173;HIS 177;CYS 222(Zinc binding) |
References for Catalytic Mechanism | ||
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References | Sections | No. of steps in catalysis |
[3]
|
Fig.8, p.8849-8850 | |
[6]
|
p.612-614 | |
[7]
|
p.9985-9986 | |
[10]
|
p.278-279 | |
[13]
|
Fig.1, Fig.4, p.130-131 | |
[14]
|
p.244 | |
[15]
|
p.664-665 | |
[19]
|
Fig.8 |
References | |
---|---|
[1] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1510975 |
Journal | Biochemistry |
Year | 1992 |
Volume | 31 |
Pages | 7879-85 |
Authors | Siegel D, Beall H, Senekowitsch C, Kasai M, Arai H, Gibson NW, Ross D |
Title | Bioreductive activation of mitomycin C by DT-diaphorase. |
Related PDB | |
Related UniProtKB | |
[2] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7530954 |
Journal | Biochem Pharmacol |
Year | 1995 |
Volume | 49 |
Pages | 127-40 |
Authors | Cadenas E |
Title | Antioxidant and prooxidant functions of DT-diaphorase in quinone metabolism. |
Related PDB | |
Related UniProtKB | |
[3] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 7568029 |
Journal | Proc Natl Acad Sci U S A |
Year | 1995 |
Volume | 92 |
Pages | 8846-50 |
Authors | Li R, Bianchet MA, Talalay P, Amzel LM |
Title |
The three-dimensional structure of NAD(P)H:quinone reductase, |
Related PDB | 1qrd |
Related UniProtKB | |
[4] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8999809 |
Journal | J Biol Chem |
Year | 1997 |
Volume | 272 |
Pages | 1437-9 |
Authors | Chen S, Knox R, Wu K, Deng PS, Zhou D, Bianchet MA, Amzel LM |
Title |
Molecular basis of the catalytic differences among DT-diaphorase of human, |
Related PDB | |
Related UniProtKB | |
[5] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9050836 |
Journal | Proc Natl Acad Sci U S A |
Year | 1997 |
Volume | 94 |
Pages | 1669-74 |
Authors | Zhao Q, Yang XL, Holtzclaw WD, Talalay P |
Title | Unexpected genetic and structural relationships of a long-forgotten flavoenzyme to NAD(P)H:quinone reductase (DT-diaphorase). |
Related PDB | |
Related UniProtKB | |
[6] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10917652 |
Journal | Biochem Soc Trans |
Year | 1999 |
Volume | 27 |
Pages | 610-5 |
Authors | Bianchet MA, Foster C, Faig M, Talalay P, Amzel LM |
Title | Structure and mechanism of cytosolic quinone reductases. |
Related PDB | |
Related UniProtKB | |
[7] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10433694 |
Journal | Biochemistry |
Year | 1999 |
Volume | 38 |
Pages | 9881-6 |
Authors | Foster CE, Bianchet MA, Talalay P, Zhao Q, Amzel LM |
Title |
Crystal structure of human quinone reductase type 2, |
Related PDB | 1qr2 2qr2 |
Related UniProtKB | |
[8] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10543876 |
Journal | J Med Chem |
Year | 1999 |
Volume | 42 |
Pages | 4325-30 |
Authors | Skelly JV, Sanderson MR, Suter DA, Baumann U, Read MA, Gregory DS, Bennett M, Hobbs SM, Neidle S |
Title | Crystal structure of human DT-diaphorase: a model for interaction with the cytotoxic prodrug 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB1954). |
Related PDB | 1qbg |
Related UniProtKB | |
[9] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10419545 |
Journal | Mol Pharmacol |
Year | 1999 |
Volume | 56 |
Pages | 272-8 |
Authors | Chen S, Wu K, Zhang D, Sherman M, Knox R, Yang CS |
Title |
Molecular characterization of binding of substrates and inhibitors to DT-diaphorase: combined approach involving site-directed mutagenesis, |
Related PDB | |
Related UniProtKB | |
[10] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11035256 |
Journal | Free Radic Biol Med |
Year | 2000 |
Volume | 29 |
Pages | 276-84 |
Authors | Chen S, Wu K, Knox R |
Title | Structure-function studies of DT-diaphorase (NQO1) and NRH: quinone oxidoreductase (NQO2). |
Related PDB | |
Related UniProtKB | |
[11] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10877993 |
Journal | Front Biosci |
Year | 2000 |
Volume | 5 |
Pages | D639-48 |
Authors | Beall HD, Winski SI |
Title |
Mechanisms of action of quinone-containing alkylating agents. |
Related PDB | |
Related UniProtKB | |
[12] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (2.5 ANGSTROMS). |
Medline ID | 20202608 |
PubMed ID | 10706635 |
Journal | Proc Natl Acad Sci U S A |
Year | 2000 |
Volume | 97 |
Pages | 3177-82 |
Authors | Faig M, Bianchet MA, Talalay P, Chen S, Winski S, Ross D, Amzel LM |
Title | Structures of recombinant human and mouse NAD(P)H:quinone oxidoreductases: species comparison and structural changes with substrate binding and release. |
Related PDB | 1d4a 1dxo 1dxq |
Related UniProtKB | P15559 |
[13] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10694883 |
Journal | Trends Biochem Sci |
Year | 2000 |
Volume | 25 |
Pages | 126-32 |
Authors | Fraaije MW, Mattevi A |
Title | Flavoenzymes: diverse catalysts with recurrent features. |
Related PDB | |
Related UniProtKB | |
[14] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11035252 |
Journal | Free Radic Biol Med |
Year | 2000 |
Volume | 29 |
Pages | 241-5 |
Authors | Foster CE, Bianchet MA, Talalay P, Faig M, Amzel LM |
Title | Structures of mammalian cytosolic quinone reductases. |
Related PDB | |
Related UniProtKB | |
[15] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 11587640 |
Journal | Structure (Camb) |
Year | 2001 |
Volume | 9 |
Pages | 659-67 |
Authors | Faig M, Bianchet MA, Winski S, Hargreaves R, Moody CJ, Hudnott AR, Ross D, Amzel LM |
Title | Structure-based development of anticancer drugs: complexes of NAD(P)H:quinone oxidoreductase 1 with chemotherapeutic quinones. |
Related PDB | 1gg5 1h66 1h69 |
Related UniProtKB | |
[16] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 11735396 |
Journal | Biochemistry |
Year | 2001 |
Volume | 40 |
Pages | 15135-42 |
Authors | Winski SL, Faig M, Bianchet MA, Siegel D, Swann E, Fung K, Duncan MW, Moody CJ, Amzel LM, Ross D |
Title |
Characterization of a mechanism-based inhibitor of NAD(P)H:quinone oxidoreductase 1 by biochemical, |
Related PDB | 1kbo 1kbq |
Related UniProtKB | |
[17] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11340659 |
Journal | Proteins |
Year | 2001 |
Volume | 43 |
Pages | 420-32 |
Authors | Cavelier G, Amzel LM |
Title | Mechanism of NAD(P)H:quinone reductase: Ab initio studies of reduced flavin. |
Related PDB | |
Related UniProtKB | |
[18] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 12147263 |
Journal | Arch Biochem Biophys |
Year | 2002 |
Volume | 404 |
Pages | 254-62 |
Authors | Anusevicius Z, Sarlauskas J, Cenas N |
Title | Two-electron reduction of quinones by rat liver NAD(P)H:quinone oxidoreductase: quantitative structure-activity relationships. |
Related PDB | |
Related UniProtKB | |
[19] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 15078100 |
Journal | Biochemistry |
Year | 2004 |
Volume | 43 |
Pages | 4538-47 |
Authors | Kwiek JJ, Haystead TA, Rudolph J |
Title | Kinetic mechanism of quinone oxidoreductase 2 and its inhibition by the antimalarial quinolines. |
Related PDB | |
Related UniProtKB |
Comments |
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This enzyme has a similar catalytic mechanism to that of QR1 (S00343 in EzCatDB), |
Created | Updated |
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2004-10-26 | 2009-02-26 |