Enzymes
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Reaction participants Show >> << Hide
- Name help_outline a phenolic steroid Identifier CHEBI:177917 Charge 0 Formula C18H23OR SMILEShelp_outline CC12CCC3C(CCC4=CC(O)=CC=C34)C1CCC2[*] 2D coordinates Mol file for the small molecule Search links Involved in 42 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline 3'-phosphoadenylyl sulfate Identifier CHEBI:58339 Charge -4 Formula C10H11N5O13P2S InChIKeyhelp_outline GACDQMDRPRGCTN-KQYNXXCUSA-J SMILEShelp_outline Nc1ncnc2n(cnc12)[C@@H]1O[C@H](COP([O-])(=O)OS([O-])(=O)=O)[C@@H](OP([O-])([O-])=O)[C@H]1O 2D coordinates Mol file for the small molecule Search links Involved in 108 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline a phenolic steroid 3-O-sulfate Identifier CHEBI:177918 Charge -1 Formula C18H22O4SR SMILEShelp_outline CC12CCC3C(CCC4=CC(OS([O-])(=O)=O)=CC=C34)C1CCC2[*] 2D coordinates Mol file for the small molecule Search links Involved in 1 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline adenosine 3',5'-bisphosphate Identifier CHEBI:58343 Charge -4 Formula C10H11N5O10P2 InChIKeyhelp_outline WHTCPDAXWFLDIH-KQYNXXCUSA-J SMILEShelp_outline Nc1ncnc2n(cnc12)[C@@H]1O[C@H](COP([O-])([O-])=O)[C@@H](OP([O-])([O-])=O)[C@H]1O 2D coordinates Mol file for the small molecule Search links Involved in 142 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline H+ Identifier CHEBI:15378 Charge 1 Formula H InChIKeyhelp_outline GPRLSGONYQIRFK-UHFFFAOYSA-N SMILEShelp_outline [H+] 2D coordinates Mol file for the small molecule Search links Involved in 9,717 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
| RHEA:68460 | RHEA:68461 | RHEA:68462 | RHEA:68463 | |
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| Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
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Publications
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Enzymic synthesis of steroid sulphates. XIII. Isolation and properties of dehydroepiandrosterone sulphotransferase from human foetal adrenals.
Adams J.B., McDonald D.
Human foetal adrenals have provided a rich source of steroid alcohol sulphotransferase (EC 2.8.2.-). The latter was isolated in pure form in one step by affinity chromatography on an (NH4)2SO4 cut derived from the cytosol fraction of the glands. The yield was 6-fold higher than that obtained from ... >> More
Human foetal adrenals have provided a rich source of steroid alcohol sulphotransferase (EC 2.8.2.-). The latter was isolated in pure form in one step by affinity chromatography on an (NH4)2SO4 cut derived from the cytosol fraction of the glands. The yield was 6-fold higher than that obtained from adult human adrenals. General properties of the enzyme are given and it appears to be identical to that obtained previously from adult human adrenals. << Less