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EC 2.3.3.8 Details

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EC number

2.3.3.8

Accepted name

ATP citrate synthase

Reaction

ADP + phosphate + acetyl-CoA + oxaloacetate = ATP + citrate + CoA

Other name(s)

ATP-citric lyase, ATP:citrate oxaloacetate-lyase [(pro-S)-CH₂COO^-→acetyl-CoA] (ATP-dephosphorylating), acetyl-CoA:oxaloacetate acetyltransferase (isomerizing, ADP-phosphorylating), adenosine triphosphate citrate lyase, citrate cleavage enzyme, citrate-ATP lyase, citric cleavage enzyme, ATP citrate (pro-S)-lyase

Systematic name

acetyl-CoA:oxaloacetate C-acetyltransferase [(pro-S)-carboxymethyl-forming, ADP-phosphorylating]

CAS registry number

9027-95-6

Comment

The enzyme can be dissociated into components, two of which are identical with EC 4.1.3.34 (citryl-CoA lyase) and EC 6.2.1.18 (citrate—CoA ligase).

History

created 1965 as EC 4.1.3.8, modified 1986, transferred 2002 to EC 2.3.3.8

EC Tree

1 Oxidoreductases

1.1 Acting on the CH-OH group of donors

1.2 Acting on the aldehyde or oxo group of donors

1.3 Acting on the CH-CH group of donors

1.4 Acting on the CH-NH₂ group of donors

1.5 Acting on the CH-NH group of donors

1.6 Acting on NADH or NADPH

1.7 Acting on other nitrogenous compounds as donors

1.8 Acting on a sulfur group of donors

1.9 Acting on a heme group of donors

1.10 Acting on diphenols and related substances as donors

1.11 Acting on a peroxide as acceptor

1.12 Acting on hydrogen as donor

1.13 Acting on single donors with incorporation of molecular oxygen (oxygenases)

1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen

1.15 Acting on superoxide as acceptor

1.16 Oxidizing metal ions

1.17 Acting on CH or CH₂ groups

1.17.1 With NAD⁺ or NADP⁺ as acceptor

1.17.2 With a cytochrome as acceptor

1.17.3 With oxygen as acceptor

1.17.4 With a disulfide as acceptor

1.17.5 With a quinone or similar compound as acceptor

1.17.7 With an iron-sulfur protein as acceptor

1.17.8 With a flavin as acceptor

1.17.9 With a copper protein as acceptor

1.17.98 With other, known, physiological acceptors

1.17.99 With unknown physiological acceptors

1.18 Acting on iron-sulfur proteins as donors

1.19 Acting on reduced flavodoxin as donor

1.20 Acting on phosphorus or arsenic in donors

1.20.1 With NAD⁺ or NADP⁺ as acceptor

1.20.2 With a cytochrome as acceptor

1.20.4 With disulfide as acceptor

1.20.9 With a copper protein as acceptor

1.20.98 With other, known, physiological acceptors

1.20.99 With unknown physiological acceptors

1.20.99.1 arsenate reductase (donor)

1.21 Catalysing the reaction X-H + Y-H = X-Y

1.22 Acting on halogen in donors

1.23 Reducing C-O-C group as acceptor

1.97 Other oxidoreductases

1.98 Enzymes using H₂ as reductant (deleted subclass)

1.99 Other enzymes using O₂ as oxidant (deleted subclass)

2.1 Transferring one-carbon groups

2.2 Transferring aldehyde or ketonic groups

2.3 Acyltransferases

2.3.1 Transferring groups other than aminoacyl groups

2.3.2 Aminoacyltransferases

2.3.3 Acyl groups converted into alkyl groups on transfer

2.3.3.1 citrate (Si)-synthase

2.3.3.2 decylcitrate synthase

2.3.3.3 citrate (Re)-synthase

2.3.3.4 decylhomocitrate synthase

2.3.3.5 2-methylcitrate synthase

2.3.3.6 2-ethylmalate synthase

2.3.3.7 3-ethylmalate synthase

2.3.3.8 ATP citrate synthase

2.3.3.9 malate synthase

2.3.3.10 hydroxymethylglutaryl-CoA synthase

2.3.3.11 2-hydroxyglutarate synthase

2.3.3.12 3-propylmalate synthase

2.3.3.13 2-isopropylmalate synthase

2.3.3.14 homocitrate synthase

2.3.3.15 sulfoacetaldehyde acetyltransferase

2.3.3.16 citrate synthase (unknown stereospecificity)

2.3.3.17 methylthioalkylmalate synthase

2.3.3.18 2-phosphinomethylmalate synthase

2.3.3.19 2-phosphonomethylmalate synthase

2.3.3.20 acyl-CoA:acyl-CoA alkyltransferase

2.3.3.21 (R)-citramalate synthase

2.4 Glycosyltransferases

2.5 Transferring alkyl or aryl groups, other than methyl groups

2.6 Transferring nitrogenous groups

2.7 Transferring phosphorus-containing groups

2.8 Transferring sulfur-containing groups

2.9 Transferring selenium-containing groups

2.10 Transferring molybdenum- or tungsten-containing groups

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Release 2023.1 (January 2023)