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Literature summary for 4.1.1.33 extracted from

  • Rothwell, C.; Lebreton, A.; Young Ng, C.; Lim, J.Y.; Liu, W.; Vasudevan, S.; Labow, M.; Gu, F.; Gaither, L.A.
    Cholesterol biosynthesis modulation regulates dengue viral replication (2009), Virology, 389, 8-19.
    View publication on PubMed

Application

Application Comment Organism
drug development siRNAs targeting mevalonate (diphospho) decarboxylase (MVD) are found to inhibit Dengue virus replication in a stable A549 subgenomic Renilla replicon cell line (Rluc-replicon) and in naive A549 cells after dengue type 2 (DEN-2) New Guinea C (NGC) live virus infection, knock down of mevalonate (diphospho) decarboxylase can inhibit dengue viral replication Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
ATP + 5-diphosphomevalonate Homo sapiens
-
ADP + phosphate + isopentenyl diphosphate + CO2
-
?

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
ATP + 5-diphosphomevalonate
-
Homo sapiens ADP + phosphate + isopentenyl diphosphate + CO2
-
?

Synonyms

Synonyms Comment Organism
mevalonate diphospho decarboxylase
-
Homo sapiens
MVD
-
Homo sapiens

General Information

General Information Comment Organism
physiological function investigation of the role of mevalonate diphospho decarboxylase in viral replication Homo sapiens