Any feedback?
Please rate this page
(search_result.php)
(0/150)

BRENDA support

Refine search

Search Natural Substrates/ Products (Substrates)

show results
Don't show organism specific information (fast!)
Search organism in taxonomic tree (slow, choose "exact" as search mode, e.g. "mammalia" for rat,human,monkey,...)
(Not possible to combine with the first option)
Refine your search
Search for synonyms (with exact matching search term)

Search term:

<< < Results 21 - 27 of 27
EC Number Natural Substrates Commentary (Nat. Sub.)
Show all pathways known for 1.3.1.21Display the word mapDisplay the reaction diagram Show all sequences 1.3.1.21more a mutational enzyme defect causes the Smith-Lemli-Opitz syndrome, a severe developmental disorder associated with multiple congenital anomalies, with low cholesterol and high precurosor 7-hydrocholesterol contents in plasma and tissues, clinical symptoms, overview
Show all pathways known for 1.3.1.21Display the word mapDisplay the reaction diagram Show all sequences 1.3.1.21more enzyme is essential for steroidogenesis, enzyme is not regulated by the luteinizing hormone LH
Show all pathways known for 1.3.1.21Display the word mapDisplay the reaction diagram Show all sequences 1.3.1.21more enzyme is regulated through tissue-specific transcription and differential alternative splicing
Show all pathways known for 1.3.1.21Display the word mapDisplay the reaction diagram Show all sequences 1.3.1.21more enzyme is regulated through tissue-specific transcription and differential alternative splicing, enzyme is induced when sterols are depleted both in vivo and in vitro
Show all pathways known for 1.3.1.21Display the word mapDisplay the reaction diagram Show all sequences 1.3.1.21more over 92% reduced enzyme activity, due to autosomal recessive mutational disorder, leads to the Smith-Lemli-Opitz syndrome in multiple cell types
Show all pathways known for 1.3.1.21Display the word mapDisplay the reaction diagram Show all sequences 1.3.1.21more reduced enzyme activity due to mutation leads to holoprosencephaly in vivo, phenotype
Show all pathways known for 1.3.1.21Display the word mapDisplay the reaction diagram Show all sequences 1.3.1.21more several enzyme mutational defects cause the Smith-Lemli-Opitz syndrome, a severe developmental disorder associated with multiple congenital malformations and mental retardation, or desmosterolosis and lathosterolosis, rare autosomal recessive disorders, defect cholesterol synthesis, clinical symptoms, overview
<< < Results 21 - 27 of 27