Ligand 2-aminoacrylate
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Basic Ligand Information
Molecular Structure
C3H5NO2
2-aminoacrylate
UQBOJOOOTLPNST-UHFFFAOYSA-N
2-aminoprop-2-enoate, alpha-aminoacrylate, aminoacrylate, dehydroalanine
MetaCyc
(Z)-butanethial-S-oxide biosynthesis,
(Z)-phenylmethanethial S-oxide biosynthesis,
alliin metabolism,
D-serine degradation,
ethiin metabolism, felinine and 3-methyl-3-sulfanylbutan-1-ol biosynthesis, glutathione-mediated detoxification I, glycine betaine degradation I, glycine betaine degradation III, L-cysteine degradation II, L-methionine biosynthesis II, L-serine degradation, L-tryptophan degradation II (via pyruvate), methiin metabolism, propanethial S-oxide biosynthesis, purine nucleobases degradation II (anaerobic), uracil degradation III 
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Roles as Enzyme Ligand
In Vivo Substrate in Enzyme-catalyzed Reactions (2 results)
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2-aminoacrylate + H2O = pyruvate + NH3
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2-aminoprop-2-enoate = 2-iminopropanoate
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In Vivo Product in Enzyme-catalyzed Reactions (6 results)
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ureidoacrylate + H2O = aminoacrylate + NH3 + CO2
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L-cystine = L-thiocysteine + 2-aminoprop-2-enoate
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(R)-S-(2-pyridyl)cysteine N-oxide = 2-sulfanylpyridine N-oxide + 2-aminoacrylate
(S)-(2-pyrrolyl)cysteine = 2-pyrrolesulfenic acid + 2-aminoacrylate
methiin = methanesulfenic acid + 2-aminoacrylate
S-(methylthiomethyl)cysteine 4-oxide = (methylthio)methane-sulfenic acid + 2-aminoacrylate
Substrate in Enzyme-catalyzed Reactions (3 results)
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2-aminoacrylate + 5-phospho-alpha-D-ribose 1-diphosphate = N-(5-phospho-D-ribosyl)-2-aminoacrylate + diphosphate
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2-aminoacrylate + H2O = pyruvate + NH3
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2-aminoprop-2-enoate = 2-iminopropanoate
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Product in Enzyme-catalyzed Reactions (9 results)
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O3-acetyl-L-serine = alpha-aminoacrylate
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ureidoacrylate + H2O = aminoacrylate + NH3 + CO2
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L-cystine = L-thiocysteine + 2-aminoprop-2-enoate
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(R)-S-(2-pyridyl)cysteine N-oxide = 2-sulfanylpyridine N-oxide + 2-aminoacrylate
(S)-(2-pyrrolyl)cysteine = 2-pyrrolesulfenic acid + 2-aminoacrylate
(S)-(2-pyrrolyl)cysteine S-oxide = 2-pyrrolesulfenic acid + 2-aminoacrylate
(S)-(3-pyrrolyl)cysteine S-oxide = 3-pyrrolesulfenic acid + 2-aminoacrylate
methiin = methanesulfenic acid + 2-aminoacrylate
S-(methylthiomethyl)cysteine 4-oxide = (methylthio)methane-sulfenic acid + 2-aminoacrylate
3D Structure of Enzyme-Ligand-Complex (PDB) (31 results)
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Enzyme Kinetic Parameters
References & Links
Literature References (3)
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The substrate capture mechanism of Mycobacterium tuberculosis anthranilate phosphoribosyltransferase provides a mode for inhibition
2013
Castell, A.; Short, F.L.; Evans, G.L.; Cookson, T.V.; Bulloch, E.M.; Joseph, D.D.; Lee, C.E.; Parker, E.J.; Baker, E.N.; Lott, J.S.
Biochemistry
52
1776-1787
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Rapid purification and characterization of cystine lyase b from broccoli inflorescence
1999
Ukai, K.; Sekiya, J.
Phytochemistry
51
853-859
Reactive enamines and imines in vivo lessons from the RidA paradigm
2019
Borchert, A.J.; Ernst, D.C.; Downs, D.M.
Trends Biochem. Sci.
44
849-860
Links to other databases for 2-aminoacrylate
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