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<< < Results 71 - 78 of 78
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
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 Homo sapiens ? - ?
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 Rattus norvegicus ? - ?
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 Mus musculus ? - ?
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 Rattus norvegicus ? - ?
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 Homo sapiens ? - ?
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 Homo sapiens ? - ?
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 Homo sapiens ? - ?
Show all pathways known for 1.3.1.21Display the word mapDisplay the reaction diagram Show all sequences 1.3.1.21more no substrates: 8-dehydrocholesterol or 20S-hydroxylumisterol Rattus norvegicus ? - -
<< < Results 71 - 78 of 78