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10.1016/j.pbiomolbio.2020.10.006 http://scihub22266oqcxt.onion/10.1016/j.pbiomolbio.2020.10.006 33137344!7604128!33137344     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=33137344&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Prog+Biophys+Mol+Biol 2021 ; 161 (ä): 39-53 Nephropedia Template TP {{tp|p=33137344|t=2021. Human coronavirus spike protein-host receptor recognition |pdf=|usr=}}{{33137344}} gab.com Text Human coronavirus spike protein-host receptor recognition JO: Prog Biophys Mol Biol http://www.kidney.de/pget.php?&tw=1&pmid=33137344 #FOAvip A variety of coronaviruses (CoVs) have infected humans and caused mild to severe respiratory diseases that could result in mortality. The human CoVs (HCoVs) belong to the genera of alpha- and beta-CoVs that originate in rodents and bats and are transmitted to humans via zoonotic contacts. The binding of viral spike proteins to the host cell receptors is essential for mediating fusion of viral and host cell membranes to cause infection. The SARS-CoV-2 originated in bats (RaTG13 SARS-CoV) and is transmitted to humans via pangolins. The presence of 'PRRA' sequence motif in SARS-CoV-2 spike proteins from human, dog, cat, mink, tiger and lion suggests a common viral entry mechanism into host cells. In this review, we discuss structural features of HCoV spike proteins and recognition of host protein and carbohydrate receptors. Twit Text FOAVip Human coronavirus spike protein-host receptor recognition ????Prog Biophys Mol Biol http://www.kidney.de/pget.php?&tw=1&pmid=33137344 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33137344 #FOAvip English Wikipedia <ref>{{Cite pmid|33137344}}</ref> Human coronavirus spike protein-host receptor recognition #MMPMID33137344 Guruprasad L Prog Biophys Mol Biol 2021[May]; 161 (ä): 39-53 PMID33137344show ga A variety of coronaviruses (CoVs) have infected humans and caused mild to severe respiratory diseases that could result in mortality. The human CoVs (HCoVs) belong to the genera of alpha- and beta-CoVs that originate in rodents and bats and are transmitted to humans via zoonotic contacts. The binding of viral spike proteins to the host cell receptors is essential for mediating fusion of viral and host cell membranes to cause infection. The SARS-CoV-2 originated in bats (RaTG13 SARS-CoV) and is transmitted to humans via pangolins. The presence of 'PRRA' sequence motif in SARS-CoV-2 spike proteins from human, dog, cat, mink, tiger and lion suggests a common viral entry mechanism into host cells. In this review, we discuss structural features of HCoV spike proteins and recognition of host protein and carbohydrate receptors. |Amino Acid Motifs[MESH] |Animals[MESH] |COVID-19/*immunology[MESH] |Carbohydrates/chemistry[MESH] |Chiroptera[MESH] |Cryoelectron Microscopy[MESH] |Databases, Protein[MESH] |Drug Repositioning[MESH] |Genome, Viral[MESH] |Humans[MESH] |Middle East Respiratory Syndrome Coronavirus[MESH] |Pangolins[MESH] |Phylogeny[MESH] |Protein Binding[MESH] |Protein Conformation[MESH] |Protein Interaction Mapping[MESH] |Receptors, Virus/*chemistry[MESH] |SARS-CoV-2[MESH] |Species Specificity[MESH]Human coronavirus spike protein-host receptor recognition (epmc).pdf DeepDyve Pubget Overpricing