<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Glisic S</submitter><funding>Ministry of Education, Science and Technological Development of the Republic of Serbia</funding><pagination>139</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4802633</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The pathophysiological overlapping between Sjorgen's Syndrome (SS) and HCV, presence of anti- muscarinic receptor type 3 (M3R) antibodies in SS, the role that M3R plays in the regulation of the heart rate, has led to the assumption that cardiovagal dysfunction in HCV patients is caused by anti-M3R antibodies elicited by HCV proteins or by their direct interaction with M3R.&lt;h4>Results&lt;/h4>To identify HCV protein which possibly is crossreactive with M3R or which binds to this receptor, we performed the Informational Spectrum Method (ISM) analysis of the HCV proteome. This analysis revealed that NS5A protein represents the most probable interactor of M3R or that this viral protein could elicit antibodies which modulate function of this receptor. Further detailed structure/f</pubmed_abstract><journal>BMC bioinformatics</journal><pubmed_title>Common molecular mechanism of the hepatic lesion and the cardiac parasympathetic regulation in chronic hepatitis C infection: a critical role for the muscarinic receptor type 3.</pubmed_title><pmcid>PMC4802633</pmcid><funding_grant_id>OI 173001</funding_grant_id><pubmed_authors>Chittur KK</pubmed_authors><pubmed_authors>Bojic T</pubmed_authors><pubmed_authors>Sencanski M</pubmed_authors><pubmed_authors>Glisic S</pubmed_authors><pubmed_authors>Cavanaugh DP</pubmed_authors><pubmed_authors>Perovic V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Common molecular mechanism of the hepatic lesion and the cardiac parasympathetic regulation in chronic hepatitis C infection: a critical role for the muscarinic receptor type 3.</name><description>&lt;h4>Background&lt;/h4>The pathophysiological overlapping between Sjorgen's Syndrome (SS) and HCV, presence of anti- muscarinic receptor type 3 (M3R) antibodies in SS, the role that M3R plays in the regulation of the heart rate, has led to the assumption that cardiovagal dysfunction in HCV patients is caused by anti-M3R antibodies elicited by HCV proteins or by their direct interaction with M3R.&lt;h4>Results&lt;/h4>To identify HCV protein which possibly is crossreactive with M3R or which binds to this receptor, we performed the Informational Spectrum Method (ISM) analysis of the HCV proteome. This analysis revealed that NS5A protein represents the most probable interactor of M3R or that this viral protein could elicit antibodies which modulate function of this receptor. Further detailed structure/f</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2025-05-29T21:25:16.392Z</modification><creation>2019-03-27T03:10:03Z</creation></dates><accession>S-EPMC4802633</accession><cross_references><pubmed>27000565</pubmed><doi>10.1186/s12859-016-0988-7</doi></cross_references></HashMap>