EC: 1.1.1.209

3(or 17)alpha-hydroxysteroid dehydrogenase (3(or 17)alpha-hydroxysteroid:NAD(P)+ oxidoreductase)

enzyme lambda metabolic reaction experiment

Pathways

pathway id name
BioCyc:HUMAN_PWY-7455 allopregnanolone biosynthesis
BioCyc:HUMAN_PWY-6872 retinoate biosynthesis I
BioCyc:META_PWY-6872 retinoate biosynthesis I
BioCyc:META_PWY-6861 the visual cycle I (vertebrates)
BioCyc:META_PWY-6857 retinol biosynthesis
BioCyc:HUMAN_PWY-6857 retinol biosynthesis
BioCyc:HUMAN_PWY-6861 the visual cycle I (vertebrates)
BioCyc:META_PWY-7455 allopregnanolone biosynthesis
Reactome:R-HSA-9757110 Prednisone ADME
Reactome:R-HSA-9748784 Drug ADME
WikiPathways:WP5188 Retinol metabolism
WikiPathways:WP5280 Glucocorticoid biosynthesis
WikiPathways:WP5176 Disorders of bile acid synthesis and biliary transport
WikiPathways:WP4524 Alternative pathway of fetal androgen synthesis
PathBank:SMP0030406 Androstenedione Metabolism
PathBank:SMP0000373 Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
PathBank:SMP0000318 Congenital Bile Acid Synthesis Defect Type III
PathBank:SMP0000576 21-Hydroxylase Deficiency (CYP21)
PathBank:SMP0000718 3-beta-Hydroxysteroid Dehydrogenase Deficiency
PathBank:SMP0000035 Bile Acid Biosynthesis
PathBank:SMP0000314 Congenital Bile Acid Synthesis Defect Type II
PathBank:SMP0000315 Cerebrotendinous Xanthomatosis (CTX)
PathBank:SMP0000575 11-beta-Hydroxylase Deficiency (CYP11B1)
PathBank:SMP0000717 Apparent Mineralocorticoid Excess Syndrome
PathBank:SMP0087353 Retinol Metabolism
PathBank:SMP0120720 Vitamin A Deficiency
PathBank:SMP0000130 Steroidogenesis
PathBank:SMP0000074 Retinol Metabolism
PathBank:SMP0000371 Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH
PathBank:SMP0000317 Familial Hypercholanemia (FHCA)
PathBank:SMP0000336 Vitamin A Deficiency
PathBank:SMP0000577 Corticosterone Methyl Oxidase I Deficiency (CMO I)
PathBank:SMP0087260 Retinol Metabolism
PathBank:SMP0000372 Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency
PathBank:SMP0000316 Zellweger Syndrome
PathBank:SMP0000566 17-alpha-Hydroxylase Deficiency (CYP17)
PathBank:SMP0000578 Corticosterone Methyl Oxidase II Deficiency (CMO II)
PathBank:SMP0000720 27-Hydroxylase Deficiency