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Pathway · 4 proteins

Glyoxylate and dicarboxylate metabolism

Proteins of this group that KEGG places on its “Glyoxylate and dicarboxylate metabolism” map for Aquifex aeolicus.

How it works

This map covers two-carbon compounds such as glycolate and glyoxylate. The proteins here remove phosphoglycolate, a by-product of damaged sugar metabolism, oxidise glycolate and lactate, and activate acetate or propionate with coenzyme A.

Grouped by KEGG pathway map. The explanation above is the atlas’s own; the map itself covers more organisms than Aquifex.

Its proteins

ProteinECReaction (UniProt)Metal or clusterAmino acidsCertainty
Phosphoglycolate phosphatase3.1.3.182-phosphoglycolate + H2O = glycolate + phosphateMg(2+)213Unspecified
Glycolate oxidase iron-sulfur subunit1.1.99.14(R)-lactate + A = pyruvate + AH2[4Fe-4S] cluster395Unspecified
D-lactate dehydrogenase———482Unspecified
Propionate--CoA ligase—acetate + ATP + CoA = acetyl-CoA + AMP + diphosphate—510Unspecified

Also part of this pathway

These proteins are described under another pathway, but also take part here.

ProteinECReaction (UniProt)Metal or clusterAmino acidsCertainty
Malate dehydrogenase 1Home: Reductive TCA machinery1.1.1.37(S)-malate + NAD(+) = oxaloacetate + NADH + H(+)—335Step named
Aconitate hydratase AHome: Reductive TCA machinery4.2.1.3citrate = D-threo-isocitrate[4Fe-4S] cluster659Step named
Probable glycine dehydrogenase (decarboxylating) subunit 1Home: Folate-linked carbon transfer1.4.4.2N(6)-[(R)-lipoyl]-L-lysyl-[glycine-cleavage complex H protein] + glycine + H(+) = N(6)-[(R)-S(8)-aminomethyldihydrolipoyl]-L-lysyl-[glycine-cleavage complex H protein] + CO2—439Step named
Glutamine synthetaseHome: Nitrogen assimilation6.3.1.2L-glutamate + NH4(+) + ATP = L-glutamine + ADP + phosphate + H(+)Mg(2+)469Step named
AminomethyltransferaseHome: Folate-linked carbon transfer2.1.2.10N(6)-[(R)-S(8)-aminomethyldihydrolipoyl]-L-lysyl-[protein] + (6S)-5,6,7,8-tetrahydrofolate = N(6)-[(R)-dihydrolipoyl]-L-lysyl-[protein] + (6R)-5,10-methylene-5,6,7,8-tetrahydrofolate + NH4(+)—350Step named
Glycine cleavage system H protein 1Home: Glycine, serine and threonine metabolism———143Step named
Formyltetrahydrofolate deformylaseHome: Folate and pterin chemistry3.5.1.10(6R)-10-formyltetrahydrofolate + H2O = (6S)-5,6,7,8-tetrahydrofolate + formate + H(+)—283Step named
Probable glycine dehydrogenase (decarboxylating) subunit 2Home: Folate-linked carbon transfer1.4.4.2N(6)-[(R)-lipoyl]-L-lysyl-[glycine-cleavage complex H protein] + glycine + H(+) = N(6)-[(R)-S(8)-aminomethyldihydrolipoyl]-L-lysyl-[glycine-cleavage complex H protein] + CO2—482Step named
Serine hydroxymethyltransferaseHome: Amino-acid connections2.1.2.1(6R)-5,10-methylene-5,6,7,8-tetrahydrofolate + glycine + H2O = (6S)-5,6,7,8-tetrahydrofolate + L-serine—428Step named
Dihydrolipoyl dehydrogenaseHome: Glycine, serine and threonine metabolism1.8.1.4N(6)-[(R)-dihydrolipoyl]-L-lysyl-[protein] + NAD(+) = N(6)-[(R)-lipoyl]-L-lysyl-[protein] + NADH + H(+)—465Step named

Origins

Why would the first cell need enzymes that clear by-products?

Naturalistic proposal

None of the books searched discusses these reactions in an origins context.

Design analysis

Some reactions make unwanted side products. When rubisco adds oxygen instead of carbon dioxide, it produces phosphoglycolate, which cells must remove. Clearing such by-products is part of making chemistry work in a cell, and four proteins in this pathway do it.

From the books: Brooker, Biology, p. 178.

The wider question for this part of the cell: origins for conserved, but we cannot say what they do.

Sources

Other pathways in this group: tRNA charging · Nutrient and metabolic state · Biosynthesis of various nucleotide sugars · Purine metabolism · Bacterial secretion system · Starch and sucrose metabolism · Homologous recombination · Fructose and mannose metabolism · Streptomycin biosynthesis · Other carbon fixation pathways · Nicotinate and nicotinamide metabolism · Not yet placed in a pathway