[1]
|
Geiger, T. and Clarke, S. (1987) Deamidation, isomerization, and racemization at asparaginyl and aspartyl residues in peptides. Succinimide-linked reactions that contribute to protein degradation. Journal of Biological Chemistry, 262, 785-794. http://www.jbc.org/content/262/2/785.short
|
[2]
|
Stephenson, R.C. and Clarke, S. (1989) Succinimide formation from aspartyl and asparaginyl peptides as a model for the spontaneous degradation of proteins. Journal of Biological Chemistry, 264, 6164-6170. http://www.jbc.org/content/264/11/6164.short
|
[3]
|
Ritz-Timme, S. and Collins, M.J. (2002) Racemization of aspartic acid in human proteins. Ageing Research Reviews, 1, 43-59. http://dx.doi.org/10.1016/S0047-6374(01)00363-3
|
[4]
|
Fujii, N. (2005) D-Amino acid in elderly tissues. Biological & Pharmaceutical Bulletin, 28, 1585-1589. http://dx.doi.org/10.1248/bpb.28.1585
|
[5]
|
Motoie, R., Fujii, N., Tsunoda, S., Nagata, K., Shimo-oka, T., Kinouchi, T., Fujii, N., Saito, T. and Ono, K. (2009) Localization of D-β-aspartyl residue-containing proteins in various tissues. International Journal of Molecular Sciences, 10, 1999-2009. http://dx.doi.org/10.3390/ijms10051999
|
[6]
|
Radkiewicz, J.L., Zipse, H., Clarke, S. and Houk, K.N. (1996) Accelerated racemization of aspartic acid and asparagine residues via succinimide intermediates: An ab initio theoretical exploration of mechanism. Journal of the American Chemical Society, 118, 9148-9155. http://dx.doi.org/10.1021/ja953505b
|
[7]
|
Takahashi, O., Kobayashi, K. and Oda, A. (2010) Modeling the enolization of succinimide derivatives, a key step of racemization of aspartic acid residues: Importance of a two-H2O mechanism. Chemistry & Biodiversity, 7, 1349-1356. http://dx.doi.org/10.1002/cbdv.200900296
|
[8]
|
Takahashi, O., Kobayashi, K. and Oda, A. (2010) Computational insight into the mechanism of serine residue racemization. Chemistry & Biodiversity, 7, 1625-1629. http://dx.doi.org/10.1002/cbdv.200900297
|
[9]
|
Takahashi, O., Kobayashi, K. and Oda, A. (2010) Computational modeling of the enolization in a direct mechanism of racemization of the aspartic acid residue. Chemistry & Biodiversity, 7, 1630-1633. http://dx.doi.org/10.1002/cbdv.200900298
|
[10]
|
Takahashi, O. and Oda, A. (2012) Amide-iminol tautomerization of the C-terminal peptide groups of aspartic acid residues. Two-water-assisted mechanism, cyclization from the iminol tautomer leading to the tetrahedral intermediate of succinimide formation, and implication to peptide group hydrogen exchange. In: Jones, J.E. and Morano, D.M., Eds., Tyrosine and Aspartic Acid: Properties, Sources and Health Benefits, Nova Science Publishers, New York, 131-147. https://www.novapublishers.com/catalog/product_info.php?products_id=35660
|
[11]
|
Fujii, N., Momose, Y. and Harada, K. (1996) Kinetic study of racemization of aspartyl residues in model peptides of αA-crystallin. International Journal of Protein Research, 48, 118-122. http://dx.doi.org/10.1111/j.1399-3011.1996.tb00821.x
|
[12]
|
Kuge, K., Fujii, N., Miura, Y., Tajima, S. and Saito, T. (2004) Kinetic study of racemization of aspartyl residues in synthetic elastin peptides. Amino Acids, 27, 193-197. http://dx.doi.org/10.1007/s00726-004-0107-3
|