Enzymes
| UniProtKB help_outline | 1,724 proteins |
| Enzyme class help_outline |
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- Name help_outline all-trans-heptaprenyl diphosphate Identifier CHEBI:58206 Charge -3 Formula C35H57O7P2 InChIKeyhelp_outline LSJLEXWXRKTZAJ-YUIIPXGZSA-K SMILEShelp_outline CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\COP([O-])(=O)OP([O-])([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 7 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline sn-glycerol 1-phosphate Identifier CHEBI:57685 (Beilstein: 3543395) help_outline Charge -2 Formula C3H7O6P InChIKeyhelp_outline AWUCVROLDVIAJX-VKHMYHEASA-L SMILEShelp_outline OC[C@H](O)COP([O-])([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 7 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline 3-heptaprenyl-sn-glycero-1-phosphate Identifier CHEBI:64781 Charge -2 Formula C38H63O6P InChIKeyhelp_outline CVJYKALOCTYTRR-HNNRUBMXSA-L SMILEShelp_outline CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\COC[C@H](O)COP([O-])([O-])=O 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 diphosphate Identifier CHEBI:33019 (Beilstein: 185088) help_outline Charge -3 Formula HO7P2 InChIKeyhelp_outline XPPKVPWEQAFLFU-UHFFFAOYSA-K SMILEShelp_outline OP([O-])(=O)OP([O-])([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 1,129 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
| RHEA:33495 | RHEA:33496 | RHEA:33497 | RHEA:33498 | |
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| Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
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| EC numbers help_outline |
Publications
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Functional assignment of an enzyme that catalyzes the synthesis of an archaea-type ether lipid in bacteria.
Guldan H., Matysik F.M., Bocola M., Sterner R., Babinger P.
An archaea-type ether lipid in bacteria: PcrB, the bacterial homologue of the archaea-specific geranylgeranylglyceryl phosphate synthase, produces heptaprenylglyceryl phosphate in bacillales. The product becomes dephosphorylated and acetylated in vivo.
Angew. Chem. Int. Ed. Engl. 50:8188-8191(2011) [PubMed] [EuropePMC]
This publication is cited by 1 other entry.