Enzymes
UniProtKB help_outline | 1 proteins |
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- Name help_outline 1ʼ-[1,2-di-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phospho]-3ʼ-[1-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phospho]-glycerol Identifier CHEBI:83580 Charge -2 Formula C63H110O16P2 InChIKeyhelp_outline XGVZPSSAPUZKKQ-GJZMZSJTSA-L SMILEShelp_outline CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC[C@@H](O)COP([O-])(=O)OCC(O)COP([O-])(=O)OC[C@@H](COC(=O)CCCCCCC\C=C/C\C=C/CCCCC)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC 2D coordinates Mol file for the small molecule Search links Involved in 11 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline 1,2-di-(9Z-octadecenoyl)-sn-glycero-3-phosphocholine Identifier CHEBI:74669 (CAS: 4235-95-4) help_outline Charge 0 Formula C44H84NO8P InChIKeyhelp_outline SNKAWJBJQDLSFF-NVKMUCNASA-N SMILEShelp_outline CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/CCCCCCCC 2D coordinates Mol file for the small molecule Search links Involved in 30 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline 1ʼ-[1,2-di-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phospho]-3ʼ-[1-(9Z,12Z-octadecadienoyl)-2-(9Z-octadecenoyl)-sn-glycero-3-phospho]-glycerol Identifier CHEBI:83582 Charge -2 Formula C81H142O17P2 InChIKeyhelp_outline WSEKMBMSQDAXBT-NBWTYSCASA-L SMILEShelp_outline CCCCCCCC\C=C/CCCCCCCC(=O)O[C@H](COC(=O)CCCCCCC\C=C/C\C=C/CCCCC)COP([O-])(=O)OCC(O)COP([O-])(=O)OC[C@@H](COC(=O)CCCCCCC\C=C/C\C=C/CCCCC)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC 2D coordinates Mol file for the small molecule Search links Involved in 3 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline 1-(9Z-octadecenoyl)-sn-glycero-3-phosphocholine Identifier CHEBI:28610 (CAS: 3542-29-8) help_outline Charge 0 Formula C26H52NO7P InChIKeyhelp_outline YAMUFBLWGFFICM-PTGWMXDISA-N SMILEShelp_outline O(C[C@H](O)COC(CCCCCCC/C=C\CCCCCCCC)=O)P(OCC[N+](C)(C)C)(=O)[O-] 2D coordinates Mol file for the small molecule Search links Involved in 29 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
RHEA:67836 | RHEA:67837 | RHEA:67838 | RHEA:67839 | |
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Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
UniProtKB help_outline |
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Related reactions help_outline
More general form(s) of this reaction
Publications
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The Basis for Acyl Specificity in the Tafazzin Reaction.
Schlame M., Xu Y., Ren M.
Tafazzin is a mitochondrial enzyme that transfers fatty acids from phospholipids to lysophospholipids. Mutations in tafazzin cause abnormal molecular species of cardiolipin and the clinical phenotype of Barth syndrome. However, the mechanism by which tafazzin creates acyl specificity has been cont ... >> More
Tafazzin is a mitochondrial enzyme that transfers fatty acids from phospholipids to lysophospholipids. Mutations in tafazzin cause abnormal molecular species of cardiolipin and the clinical phenotype of Barth syndrome. However, the mechanism by which tafazzin creates acyl specificity has been controversial. We have shown that the lipid phase state can produce acyl specificity in the tafazzin reaction, but others have reported that tafazzin itself carries enzymatic specificity. To resolve this issue, we replicated and expanded the controversial experiments, <i>i.e.</i> the transfer of different acyl groups from phosphatidylcholine to monolysocardiolipin by yeast tafazzin. Our data show that this reaction requires the presence of detergent and does not take place in liposomes but in mixed micelles. To separate thermodynamic (lipid-dependent) from kinetic (enzyme-dependent) parameters, we followed the accumulation of cardiolipin during the reaction from the initial state to the equilibrium state. The transacylation rates of different acyl groups varied over 2 orders of magnitude and correlated tightly with the concentration of cardiolipin in the equilibrium state (lipid-dependent parameter). In contrast, the rates by which different transacylations approached the equilibrium state were very similar (enzyme-dependent parameter). Furthermore, we found that tafazzin catalyzes the remodeling of cardiolipin by combinations of forward and reverse transacylations, essentially creating an equilibrium distribution of acyl groups. These data strongly support the idea that the acyl specificity of the tafazzin reaction results from the physical properties of lipids. << Less
J. Biol. Chem. 292:5499-5506(2017) [PubMed] [EuropePMC]
This publication is cited by 1 other entry.