Characterization of Tannase Protein Sequences of Bacteria and Fungi: An In Silico Study

2012 ◽  
Vol 31 (4) ◽  
pp. 306-327 ◽  
Author(s):  
Amrita Banerjee ◽  
Arijit Jana ◽  
Bikash R. Pati ◽  
Keshab C. Mondal ◽  
Pradeep K. Das Mohapatra
2022 ◽  
Vol 146 ◽  
pp. 254-261
Author(s):  
Shahrbanou Ashrafian ◽  
Mahdi Moridi Farimani ◽  
Ali Sonboli ◽  
Hossein Ashrafian ◽  
Maryam Kabiri ◽  
...  
Keyword(s):  

2019 ◽  
Vol 90 ◽  
pp. 161-170 ◽  
Author(s):  
Neha Singh ◽  
Vikram Dalal ◽  
Vijay Kumar ◽  
Monica Sharma ◽  
Pravindra Kumar

2016 ◽  
Vol 64 ◽  
pp. 121-130 ◽  
Author(s):  
Simone Brogi ◽  
Simone Giovani ◽  
Margherita Brindisi ◽  
Sandra Gemma ◽  
Ettore Novellino ◽  
...  

Author(s):  
Mohammad Fahad Ullah ◽  
Tarig M.S. Alnoura ◽  
Elmutuz H. Elssaig ◽  
Eltayib H. Ahmed-Abakur

2021 ◽  
Vol 890 (1) ◽  
pp. 012017
Author(s):  
Dewi Syahidah

Abstract Some species of known pathogenic bacteria isolates in tropical aquaculture produces hemolysin. Hemolysin can be identified based on its ability to break down red blood cells in vitro. Some hemolysin is a pore-shaped poison that can damage cell membranes and kill host cells. The character of the 13 sequences of hemolysin protein in several pathogenic bacterial isolates in tropical aquaculture was analysed using the NCBI protein bioinformatics database. The phylogenetic tree was generated, and the analysis was conducted using the base character method (Maximum Parsimony) of Mega 6.06 software. The result showed that there are two big family of hemolysin from the known pathogenic bacteria. The closest characteristics of protein sequences were hemolysin of Streptococcus agalacticae and of S. iniae.


2021 ◽  
Vol 11 (4) ◽  
pp. 563-579
Author(s):  
Amrej Singh Yadav ◽  
Aishwarya Prabha ◽  
Divya Dornala ◽  
Debasish Swain ◽  
Dilep Kumar Sigalapalli ◽  
...  

2021 ◽  
Vol 31 (2) ◽  
Author(s):  
Hadi Sedigh Ebrahim-Saraie ◽  
Behzad Dehghani ◽  
Ali Mojtahedi ◽  
Mohammad Shenagari ◽  
Meysam Hasannejad-Bibalan

BACKGROUND፡ Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of the global outbreak of coronavirus disease 2019 (Covid-19), which has been considered as a pandemic by WHO. SARS-CoV-2 encodes four major structural proteins, among which spike protein has always been a main target for new vaccine studies. This in silico study aimed to investigate some physicochemical, functional, immunological, and structural features of spike protein using several bioinformatics tools.METHOD: We retrieved all SARS-CoV-2 spike protein sequences from different countries registered in NCBI GenBank. CLC Sequence Viewer was employed to translate and align the sequences, and several programs were utilized to predict B-cell epitopes. Modification sites such as phosphorylation, glycosylation, and disulfide bonds were defined. Secondary and tertiary structures of all sequences were further computed.RESULTS: Some mutations were determined, where only one (D614G) had a high prevalence. The mutations did not impact the B-cell and physicochemical properties of the spike protein. Seven disulfide bonds were specified and also predicted in several N-link glycosylation and phosphorylation sites. The results also indicated that spike protein is a non-allergen.CONCLUSION: In summary, our findings provided a deep understanding of spike protein, which can be valuable for future studies on SARS CoV-2 infections and design of new vaccines.


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