scholarly journals Chemistry of Homocysteine Thiolactone in A Prebiotic Perspective

Life ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 40 ◽  
Author(s):  
Ibrahim Shalayel ◽  
Yannick Vallée

Homocysteine is a non-proteinogenic sulfur-containing amino acid. Like cysteine, it can form disulfide bridges and complex metallic cations. It is also closely related to methionine, the first amino acid in the synthesis of all contemporary proteins. Furthermore, its cyclized form, a five-membered ring thiolactone, is stable in acidic and neutral water. Here, we demonstrate that this thiolactone may have been formed in the primitive ocean directly from the Strecker precursor of homocysteine, an aminonitrile. Even though it is poorly reactive, this thiolactone may be open by some amines, yielding amides which, in turn, could be the precursors of longer peptides.

2018 ◽  
Vol 20 (24) ◽  
pp. 7830-7834 ◽  
Author(s):  
Yurie Koba ◽  
Atsushi Ueda ◽  
Makoto Oba ◽  
Mitsunobu Doi ◽  
Takuma Kato ◽  
...  

1993 ◽  
Vol 30 (1) ◽  
pp. 31-39 ◽  
Author(s):  
Kazuyuki KOIDE ◽  
Yoshiyuki OHTA ◽  
Michiaki ITO ◽  
Emiko WATANABE ◽  
Masaaki TOYOMIZU ◽  
...  

1971 ◽  
Vol 19 (6) ◽  
pp. 1151-1154 ◽  
Author(s):  
Michiko. Yamashita ◽  
Soichi. Arai ◽  
Shun-Jen. Tsai ◽  
Masao. Fujimaki

2000 ◽  
Vol 74 (19) ◽  
pp. 9313-9316 ◽  
Author(s):  
Brett S. Phinney ◽  
Dennis T. Brown

ABSTRACT The E1 membrane glycoprotein of Sindbis virus contains structural and functional domains, which are conformationally dependent on the presence of intramolecular disulfide bridges (B. A. Abell and D. T. Brown, J. Virol. 67:5496–5501, 1993; R. P. Anthony, A. M. Paredes, and D. T. Brown, Virology 190:330–336, 1992). We have examined the disulfide bonds in E1 and have determined that the E1 membrane glycoprotein contains two separate sets of interconnecting disulfide linkages, which divide the protein into two domains at amino acid 129. These separate sets of disulfides may stabilize and define the structural and functional regions of the E1 protein.


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