scholarly journals Proposal of the Annotation of Phosphorylated Amino Acids and Peptides Using Biological and Chemical Codes

Molecules ◽  
2021 ◽  
Vol 26 (3) ◽  
pp. 712
Author(s):  
Piotr Minkiewicz ◽  
Małgorzata Darewicz ◽  
Anna Iwaniak ◽  
Marta Turło

Phosphorylation represents one of the most important modifications of amino acids, peptides, and proteins. By modifying the latter, it is useful in improving the functional properties of foods. Although all these substances are broadly annotated in internet databases, there is no unified code for their annotation. The present publication aims to describe a simple code for the annotation of phosphopeptide sequences. The proposed code describes the location of phosphate residues in amino acid side chains (including new rules of atom numbering in amino acids) and the diversity of phosphate residues (e.g., di- and triphosphate residues and phosphate amidation). This article also includes translating the proposed biological code into SMILES, being the most commonly used chemical code. Finally, it discusses possible errors associated with applying the proposed code and in the resulting SMILES representations of phosphopeptides. The proposed code can be extended to describe other modifications in the future.

ChemInform ◽  
2008 ◽  
Vol 39 (11) ◽  
Author(s):  
Stefania Capone ◽  
Silvana Pedatella ◽  
Annalisa Guaragna ◽  
Mauro De Nisco ◽  
Giovanni Palumbo

2017 ◽  
Vol 15 (45) ◽  
pp. 9685-9695 ◽  
Author(s):  
H. Mukherjee ◽  
J. Debreczeni ◽  
J. Breed ◽  
S. Tentarelli ◽  
B. Aquila ◽  
...  

Profiling the reactivity and stability of SVI–F warheads towards nucleophilic amino acids for the development of biochemical probe compounds.


2016 ◽  
Vol 113 (46) ◽  
pp. 12946-12951 ◽  
Author(s):  
Chongqin Zhu ◽  
Yurui Gao ◽  
Hui Li ◽  
Sheng Meng ◽  
Lei Li ◽  
...  

Hydrophobicity of macroscopic planar surface is conventionally characterized by the contact angle of water droplets. However, this engineering measurement cannot be directly extended to surfaces of proteins, due to the nanometer scale of amino acids and inherent nonplanar structures. To measure the hydrophobicity of side chains of proteins quantitatively, numerous parameters were developed to characterize behavior of hydrophobic solvation. However, consistency among these parameters is not always apparent. Herein, we demonstrate an alternative way of characterizing hydrophobicity of amino acid side chains in a protein environment by constructing a monolayer of amino acids (i.e., artificial planar peptide network) according to the primary and the β-sheet secondary structures of protein so that the conventional engineering measurement of the contact angle of a water droplet can be brought to bear. Using molecular dynamics simulations, contact angles θ of a water nanodroplet on the planar peptide network, together with excess chemical potentials of purely repulsive methane-sized Weeks−Chandler−Andersen solute, are computed. All of the 20 types of amino acids and the corresponding planar peptide networks are studied. Expectedly, all of the planar peptide networks with nonpolar amino acids are hydrophobic due to θ> 90°, whereas all of the planar peptide networks of the polar and charged amino acids are hydrophilic due to θ< 90°. Planar peptide networks of the charged amino acids exhibit complete-wetting behavior due to θ= 0°. This computational approach for characterization of hydrophobicity can be extended to artificial planar networks of other soft matter.


Tetrahedron ◽  
2007 ◽  
Vol 63 (49) ◽  
pp. 12202-12206 ◽  
Author(s):  
Stefania Capone ◽  
Silvana Pedatella ◽  
Annalisa Guaragna ◽  
Mauro De Nisco ◽  
Giovanni Palumbo

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