2.3.1.222: phosphate propanoyltransferase
This is an abbreviated version!
For detailed information about phosphate propanoyltransferase, go to the full flat file.
Word Map on EC 2.3.1.222
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2.3.1.222
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propionaldehyde
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reuteri
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3-hydroxypropionaldehyde
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propionate
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lactobacillus
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enterica
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1,2-propanediol
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3-hydroxypropionic
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propanediol
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biobased
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microcompartment
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biocatalytic
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encapsulate
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autotroph
- 2.3.1.222
- propionaldehyde
- reuteri
- 3-hydroxypropionaldehyde
- propionate
- lactobacillus
- enterica
- 1,2-propanediol
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3-hydroxypropionic
-
propanediol
-
biobased
-
microcompartment
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biocatalytic
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encapsulate
-
autotroph
Reaction
Synonyms
Moth_0864, Moth_1181, PduL, pduL1, pduL2, phosphotransacylase, PTAC
ECTree
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General Information
General Information on EC 2.3.1.222 - phosphate propanoyltransferase
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evolution
malfunction
metabolism
physiological function
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PduL is a phosphotransacylase, PTAC, required for 1,2-propanediol degradation
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PduL homologues are distributed among at least 49 bacterial species but are absent from the Archaea and Eukarya. Sequence analyses show that PduL is unrelated in amino acid sequence to known phosphotransacylase, PTAC, enzymes
evolution
the phosphotransacylase (PTAC) predominantly associated with metabolosomes (PduL) has no sequence homology to the PTAC ubiquitous among fermentative bacteria (Pta). PduL and Pta exemplify functional, but not structural, convergent evolution
evolution
the phosphotransacylase (PTAC) predominantly associated with metabolosomes (PduL) has no sequence homology to the PTAC ubiquitous among fermentative bacteria (Pta). PduL and Pta exemplify functional, but not structural, convergent evolution
evolution
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the phosphotransacylase (PTAC) predominantly associated with metabolosomes (PduL) has no sequence homology to the PTAC ubiquitous among fermentative bacteria (Pta). PduL and Pta exemplify functional, but not structural, convergent evolution
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pduL mutants are unable to ferment 1,2-propanediol and are also impaired for aerobic growth on this compound, overview. Ectopic expression of pduL corrects the growth defects of a pta mutant, the pta gene encodes another PTAC enzyme
malfunction
both pduL genes (pduL1 and pduL2) are associated with acetate formation via acetyl-coenzyme A (acetyl-CoA). Their disruption enables a shift in the homoacetic pathway to the genetically synthesized homolactic pathway via pyruvate
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PduL is required in the 1,2-propandiol degradation pathway, overview
metabolism
both pduL genes (pduL1 and pduL2) are associated with acetate formation via acetyl-coenzyme A (acetyl-CoA). Their disruption enables a shift in the homoacetic pathway to the genetically synthesized homolactic pathway via pyruvate
metabolism
the fact that PduL is confined almost exclusively to metabolosomes can be used to develop an inhibitor that blocks only PduL and not Pta as a way to selectively disrupt bacterial microcompartments(BMC)-based metabolism, while not affecting most commensal organisms that require phosphotransacylase (PTAC) activity
metabolism
the fact that PduL is confined almost exclusively to metabolosomes can be used to develop an inhibitor that blocks only PduL and not Pta as a way to selectively disrupt bacterial microcompartments(BMC)-based metabolism, while not affecting most commensal organisms that require phosphotransacylase (PTAC) activity
metabolism
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the fact that PduL is confined almost exclusively to metabolosomes can be used to develop an inhibitor that blocks only PduL and not Pta as a way to selectively disrupt bacterial microcompartments(BMC)-based metabolism, while not affecting most commensal organisms that require phosphotransacylase (PTAC) activity
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