EC Tree |
1. Oxidoreductases |
1.1 Acting on the CH-OH group of donors |
1.1.1 With NAD+ or NADP+ as acceptor |
ID: | 1.1.1.252 | ||
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Description: | Tetrahydroxynaphthalene reductase. | ||
Alternative Name: |
T4HN reductase. | ||
Prosite: | PDOC00060; | ||
PDB: |
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Cath: | 3.10.450.50; 3.40.50.720; |
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Note: Use your mouse to drag, rotate, and zoom in and out of the structure. Mouse-over to identify atoms and bonds. Mouse controls documentation.UniProtKB Enzyme Link: | UniProtKB 1.1.1.252 |
BRENDA Enzyme Link: | BRENDA 1.1.1.252 |
KEGG Enzyme Link: | KEGG1.1.1.252 |
BioCyc Enzyme Link: | BioCyc 1.1.1.252 |
ExPASy Enzyme Link: | ExPASy1.1.1.252 |
EC2PDB Enzyme Link: | EC2PDB 1.1.1.252 |
ExplorEnz Enzyme Link: | ExplorEnz 1.1.1.252 |
PRIAM enzyme-specific profiles Link: | PRIAM 1.1.1.252 |
IntEnz Enzyme Link: | IntEnz 1.1.1.252 |
MEDLINE Enzyme Link: | MEDLINE 1.1.1.252 |
MSA: | |
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Phylogenetic Tree: | |
Uniprot: | |
M-CSA: |
RHEA:21908 | NADP(+) + scytalone = H(+) + NADPH + naphthalene-1,3,6,8-tetrol |
RULE(radius=1) | [*:1]-[CH;+0:2]1-[CH2;+0:3]-[*:4]:[*:5]-[C;H0;+0:6](=[O;H0;+0:7])-[CH2;+0:8]-1.[*:9]-[n+;H0:10]1:[cH;+0:11]:[cH;+0:12]:[cH;+0:13]:[c;H0;+0:14](-[*:15]):[cH;+0:16]:1>>[*:9]-[N;H0;+0:10]1-[CH;+0:11]=[CH;+0:12]-[CH2;+0:13]-[C;H0;+0:14](-[*:15])=[CH;+0:16]-1.[*:1]-[c;H0;+0:2]1:[cH;+0:3]:[*:4]:[*:5]:[c;H0;+0:6](-[OH;+0:7]):[cH;+0:8]:1 |
Reaction | ![]() |
Core-to-Core | |
Core-to-Core |
Title | Authors | Date | PubMed ID |
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Trihydroxynaphthalene reductase from Magnaporthe grisea: realization of an active center inhibitor and elucidation of the kinetic mechanism. | Thompson JE, Basarab GS, Andersson A, Lindqvist Y, Jordan DB | 1997 Feb 18 | 9048570 |
Towards the first inhibitors of trihydroxynaphthalene reductase from Curvularia lunata: synthesis of artificial substrate, homology modelling and initial screening. | Brunskole M, Stefane B, Zorko K, Anderluh M, Stojan J, Lanisnik Rizner T, Gobec S | 2008 Jun 1 | 18482840 |
Structures of trihydroxynaphthalene reductase-fungicide complexes: implications for structure-based design and catalysis. | Liao D, Basarab GS, Gatenby AA, Valent B, Jordan DB | 2001 Jan 10 | 11342131 |