<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zimbres FM</submitter><funding>NIH HHS</funding><pagination>178</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10780415</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(1)</volume><pubmed_abstract>Dolichols are isoprenoid end-products of the mevalonate and 2&lt;i>C&lt;/i>-methyl-D-erythritol-4-phosphate pathways. The synthesis of dolichols is initiated with the addition of several molecules of isopentenyl diphosphate to farnesyl diphosphate. This reaction is catalyzed by a &lt;i>cis&lt;/i>-prenyltransferase and leads to the formation of polyprenyl diphosphate. Subsequent steps involve the dephosphorylation and reduction of the α-isoprene unit by a polyprenol reductase, resulting in the generation of dolichol. The size of the dolichol varies, depending on the number of isoprene units incorporated. In eukaryotes, dolichols are synthesized as a mixture of four or more different lengths. Their biosynthesis is predicted to occur in the endoplasmic reticulum, where dolichols play an essential role in</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Aptamer-Based Imaging of Polyisoprenoids in the Malaria Parasite.</pubmed_title><pmcid>PMC10780415</pmcid><funding_grant_id>AI108819</funding_grant_id><funding_grant_id>T32-AI060546</funding_grant_id><pubmed_authors>Merino EF</pubmed_authors><pubmed_authors>Butschek GJ</pubmed_authors><pubmed_authors>Zimbres FM</pubmed_authors><pubmed_authors>Butler JH</pubmed_authors><pubmed_authors>Cassera MB</pubmed_authors><pubmed_authors>Duconge F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aptamer-Based Imaging of Polyisoprenoids in the Malaria Parasite.</name><description>Dolichols are isoprenoid end-products of the mevalonate and 2&lt;i>C&lt;/i>-methyl-D-erythritol-4-phosphate pathways. The synthesis of dolichols is initiated with the addition of several molecules of isopentenyl diphosphate to farnesyl diphosphate. This reaction is catalyzed by a &lt;i>cis&lt;/i>-prenyltransferase and leads to the formation of polyprenyl diphosphate. Subsequent steps involve the dephosphorylation and reduction of the α-isoprene unit by a polyprenol reductase, resulting in the generation of dolichol. The size of the dolichol varies, depending on the number of isoprene units incorporated. In eukaryotes, dolichols are synthesized as a mixture of four or more different lengths. Their biosynthesis is predicted to occur in the endoplasmic reticulum, where dolichols play an essential role in</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2025-04-04T13:59:50.779Z</modification><creation>2025-04-04T13:59:50.779Z</creation></dates><accession>S-EPMC10780415</accession><cross_references><pubmed>38202761</pubmed><doi>10.3390/molecules29010178</doi></cross_references></HashMap>