Molecular Diversity via Amino Acid Derived α-Amino Nitriles:  Synthesis of Spirocyclic 2,6-Dioxopiperazine Derivatives

2005 ◽  
Vol 70 (9) ◽  
pp. 3660-3666 ◽  
Author(s):  
Juan A. González-Vera ◽  
M. Teresa García-López ◽  
Rosario Herranz
2008 ◽  
Vol 5 (3) ◽  
pp. 209-221 ◽  
Author(s):  
Juan Gonzalez-Vera ◽  
M. Garcia-Lopez ◽  
Rosario Herranz

1997 ◽  
Vol 38 (17) ◽  
pp. 3085-3088 ◽  
Author(s):  
Suzanne J.E. Mulders ◽  
Arwin J. Brouwer ◽  
Rob M.J. Liskamp*

2021 ◽  
Vol 28 ◽  
Author(s):  
Márcio V. Ramos ◽  
Larissa B.N. Freitas ◽  
Emanuel A. Bezerra ◽  
Francimauro Sousa Morais ◽  
João P.M.S. Lima ◽  
...  

Background : The herbivores Danaus plexippus (Lepidoptera), Oncopeltus fasciatus and Aphis nerii (Hemiptera) are specialist insects that feed on Calotropis procera (Apocynaceae) (Sodom Apple). At least 35 chemically distinct cardenolides have been reported in C. procera. Objective We aimed to evaluate the interaction between cardenolides and Na+/K+ ATPases from herbivores. Methods : The Na+/K+ ATPases from these insects were modeled and docking studies were performed with cardenolides from C. procera. Results : The replacement of serine in sensitive Na+/K+ ATPase with histidine, phenylalanine and tyrosine in the structures examined suggests spatial impairment caused by interaction, probably making the herbivorous insects resistant against the cardenolides of C. procera. In addition, the ability of the insects to avoid cardenolide toxicity was not correlated with cardenolide polarity. Therefore, the plant fights predation through molecular diversity and the insects, regardless of their taxonomy, face this molecular diversity through amino acid replacements at key positions of the enzyme targeted by the cardenolides. Conclusions : The results show the arsenal of chemically distinct cardenolides synthesized by C. procera.


2005 ◽  
Vol 86 (10) ◽  
pp. 2897-2911 ◽  
Author(s):  
Audrey Schirmer ◽  
Didier Link ◽  
Valérie Cognat ◽  
Benoît Moury ◽  
Monique Beuve ◽  
...  

A study of molecular diversity was carried out on 136 sugar beets infected with Beet necrotic yellow vein virus (BNYVV, Benyvirus) collected worldwide. The nucleotide sequences of the RNA-2-encoded CP, RNA-3-encoded p25 and RNA-5-encoded p26 proteins were analysed. The resulting phylogenetic trees allowed BNYVV to be classified into groups that show correlations between the virus clusters and geographic origins. The selective constraints on these three sequences were measured by estimating the ratio between synonymous and non-synonymous substitution rates (ω) with maximum-likelihood models. The results suggest that selective constraints are exerted differently on the proteins. CP was the most conserved, with mean ω values ranging from 0·12 to 0·15, while p26 was less constrained, with mean ω values ranging from 0·20 to 0·33. Selection was detected in three amino acid positions of p26, with ω values of about 5·0. The p25 sequences presented the highest mean ω values (0·36–1·10), with strong positive selection (ω=4·7–54·7) acting on 14 amino acids, and particularly on amino acid 68, where the ω value was the highest so far encountered in plant viruses.


Marine Drugs ◽  
2019 ◽  
Vol 17 (6) ◽  
pp. 325 ◽  
Author(s):  
Bruno Madio ◽  
Glenn F. King ◽  
Eivind A. B. Undheim

Sea anemones produce venoms of exceptional molecular diversity, with at least 17 different molecular scaffolds reported to date. These venom components have traditionally been classified according to pharmacological activity and amino acid sequence. However, this classification system suffers from vulnerabilities due to functional convergence and functional promiscuity. Furthermore, for most known sea anemone toxins, the exact receptors they target are either unknown, or at best incomplete. In this review, we first provide an overview of the sea anemone venom system and then focus on the venom components. We have organised the venom components by distinguishing firstly between proteins and non-proteinaceous compounds, secondly between enzymes and other proteins without enzymatic activity, then according to the structural scaffold, and finally according to molecular target.


2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Aline S. Hora ◽  
Karen M. Asano ◽  
Juliana M. Guerra ◽  
Ramon G. Mesquita ◽  
Paulo Maiorka ◽  
...  

To evaluate the most controversial issue concerning current feline coronavirus (FCoV) virology, the coexisting hypotheses of the intrahost and interhost origins of feline infectious peritonitis virus (FIPV) in regard to the pathogenesis of feline infectious peritonitis (FIP), this study aimed to assess the molecular diversity of the membrane gene FCoVs in 190 samples from 10 cats with signs of FIP and in 5 faecal samples from cats without signs of FIP. All samples from the non-FIP cats and 25.26% of the samples from the FIP cats were positive for the FCoV membrane (M) gene. Mutations in this gene consisted of SNP changes randomly scattered among the sequences; few mutations resulted in amino acid changes. No geographic pattern was observed. Of the cats without FIP that harboured FECoV, the amino acid sequence identities for the M gene were 100% among cats (Cats 1–3) from the same cattery, and the overall sequence identity for the M gene was ≥91%. In one cat, two different lineages of FCoV, one enteric and one systemic, were found that segregated apart in the M gene tree. In conclusion, the in vivo mutation transition hypothesis and the circulating high virulent-low virulent FCoV hypothesis have been found to be plausible according to the results obtained from sequencing the M gene.


ChemInform ◽  
2009 ◽  
Vol 40 (28) ◽  
Author(s):  
Juan A. Gonzalez-Vera ◽  
M. Teresa Garcia-Lopez ◽  
Rosario Herranz

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