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Evolutionary relationships among pyridoxal‐5′‐phosphate‐dependent enzymes: Regio‐specific α, β and γ families
Abstract
Pyridoxal‐5′‐phosphate‐dependent enzymes catalyze manifold reactions in the metabolism of amino acids. A comprehensive comparison of amino acid sequences has shown that most of these enzymes can be assigned to one of three different families of homologous proteins. The sequences of the enzymes of each family were aligned and their homology confirmed by profile analysis. Scrutiny of the reactions catalyzed by the enzymes showed that their affiliation with one of the three structurally defined families correlates in most cases with their regio‐specificity. In the largest family, the covalency changes of the substrate occur at the same carbon atom that carries the amino group forming the imine linkage with the coenzyme. This family was thus named α family. It comprises glycine hydroxymethyltransferase, glycine C‐acetyltransferase, 5‐aminolevulinate synthase, 8‐amino‐7‐oxononanoate synthase, all aminotransferases (with the possible exception of subgroup III), a number of other enzymes relatively closely related with the aminotransferases and very likely a certain group of amino acid decarboxylases as well as tryptophanase and tyrosine phenol‐lyase which, however, catalyze β‐elimination reactions. The β family includes L‐ and D‐serine dehydratase, threonine dehydratase, the β subunit of tryptophan synthase, threonine synthase and cysteine synthase. These enzymes catalyze β‐replacement or β‐elimination reactions. The γ family incorporates O‐succinylhomoserine (thiol)‐lyase, O‐acetylhomoserine (thiol)‐lyase, and cystathionine γ‐lyase, which catalyze γ‐replacement or γ‐elimination reactions, as well as cystathionine β‐lyase. The α and γ family might be distantly related with one another, but are clearly not homologous with the β family. Apparently, the primordial pyridoxal‐5′‐phosphate‐dependent enzymes were regio‐specific catalysts, which first specialized for reaction specificity and then for substrate specificity. The following pyridoxal‐5′‐phosphate‐dependent enzymes seem to be unrelated with the α, β or γ family by the criterion of profile analysis: alanine racemase, selenocysteine synthase, and many amino acid decarboxylases. These enzymes may represent yet other families of B 6 enzymes.
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Citations
Cited by
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Filipovic, M. R., Zivanovic, J., Alvarez, B., & Banerjee, R. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00205 · Cited by 1,046
Neurotoxic Alkaloids: Saxitoxin and Its Analogs
Wiese, M., D’Agostino, P. M., Mihali, T. K., Moffitt, M. C., & Neilan, B. A. (2010) · Marine Drugs · doi:10.3390/md8072185 · Cited by 769
Structure, evolution and action of vitamin B6-dependent enzymes
Jansonius, J. N. (1998) · Current Opinion in Structural Biology · doi:10.1016/s0959-440x(98)80096-1 · Cited by 390
The manifold of vitamin B6 dependent enzymes
Schneider, G., Käck, H., & Lindqvist, Y. (2000) · Structure · doi:10.1016/s0969-2126(00)00085-x · Cited by 385
Pyridoxal phosphate-dependent enzymes
John, R. A. (1995) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/0167-4838(95)00025-p · Cited by 356
Metadata
- Authors
- ALEXANDER, F. W., SANDMEIER, E., MEHTA, P. K., & CHRISTEN, P.
- Venue
- European Journal of Biochemistry
- Publisher
- Wiley
- Published
- 1994-02
- Volume
- 219
- Issue
- 3
- Pages
- 953-960
- ISSN
- 0014-2956 (ISSN-L)
- 1432-1033
- OpenAlex
- W1861199552
- Cited by
- 373
- References
- 0
- FWCI
- 8.99
- Type
- journal article
- Language
- en
- Open access
- closed
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- ALEXANDER, F. W., SANDMEIER, E., MEHTA, P. K., & CHRISTEN, P. (1994). Evolutionary relationships among pyridoxal‐5′‐phosphate‐dependent enzymes: Regio‐specific α, β and γ families. European Journal of Biochemistry. https://doi.org/10.1111/j.1432-1033.1994.tb18577.x
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