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10.1002/jmv.25817 http://scihub22266oqcxt.onion/10.1002/jmv.25817 32239522!7228376!32239522     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Med+Virol 2020 ; 92 (9): 1649-1656 Nephropedia Template TP {{tp|p=32239522|t=2020. SARS-CoV-2 spike protein favors ACE2 from Bovidae and Cricetidae |pdf=|usr=}}{{32239522}} gab.com Text SARS-CoV-2 spike protein favors ACE2 from Bovidae and Cricetidae JO: J Med Virol http://www.kidney.de/pget.php?&tw=1&pmid=32239522 #FOAvip Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes the recent COVID-19 public health crisis. Bat is the widely believed original host of SARS-CoV-2. However, its intermediate host before transmitting to humans is not clear. Some studies proposed pangolin, snake, or turtle as the intermediate hosts. Angiotensin-converting enzyme 2 (ACE2) is the receptor for SARS-CoV-2, which determines the potential host range for SARS-CoV-2. On the basis of structural information of the complex of human ACE2 and SARS-CoV-2 receptor-binding domain (RBD), we analyzed the affinity to S protein of the 20 key residues in ACE2 from mammal, bird, turtle, and snake. Several ACE2 proteins from Primates, Bovidae, Cricetidae, and Cetacea maintained the majority of key residues in ACE2 for associating with SARS-CoV-2 RBD. The simulated structures indicated that ACE2 proteins from Bovidae and Cricetidae were able to associate with SARS-CoV-2 RBD. We found that nearly half of the key residues in turtle, snake, and bird were changed. The simulated structures showed several key contacts with SARS-CoV-2 RBD in turtle and snake ACE2 were abolished. This study demonstrated that neither snake nor turtle was the intermediate hosts for SARS-CoV-2, which further reinforced the concept that the reptiles are resistant against infection of coronavirus. This study suggested that Bovidae and Cricetidae should be included in the screening of intermediate hosts for SARS-CoV-2. Twit Text FOAVip SARS-CoV-2 spike protein favors ACE2 from Bovidae and Cricetidae ????J Med Virol http://www.kidney.de/pget.php?&tw=1&pmid=32239522 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32239522 #FOAvip English Wikipedia <ref>{{Cite pmid|32239522}}</ref> SARS-CoV-2 spike protein favors ACE2 from Bovidae and Cricetidae #MMPMID32239522 Luan J; Jin X; Lu Y; Zhang L J Med Virol 2020[Sep]; 92 (9): 1649-1656 PMID32239522show ga Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes the recent COVID-19 public health crisis. Bat is the widely believed original host of SARS-CoV-2. However, its intermediate host before transmitting to humans is not clear. Some studies proposed pangolin, snake, or turtle as the intermediate hosts. Angiotensin-converting enzyme 2 (ACE2) is the receptor for SARS-CoV-2, which determines the potential host range for SARS-CoV-2. On the basis of structural information of the complex of human ACE2 and SARS-CoV-2 receptor-binding domain (RBD), we analyzed the affinity to S protein of the 20 key residues in ACE2 from mammal, bird, turtle, and snake. Several ACE2 proteins from Primates, Bovidae, Cricetidae, and Cetacea maintained the majority of key residues in ACE2 for associating with SARS-CoV-2 RBD. The simulated structures indicated that ACE2 proteins from Bovidae and Cricetidae were able to associate with SARS-CoV-2 RBD. We found that nearly half of the key residues in turtle, snake, and bird were changed. The simulated structures showed several key contacts with SARS-CoV-2 RBD in turtle and snake ACE2 were abolished. This study demonstrated that neither snake nor turtle was the intermediate hosts for SARS-CoV-2, which further reinforced the concept that the reptiles are resistant against infection of coronavirus. This study suggested that Bovidae and Cricetidae should be included in the screening of intermediate hosts for SARS-CoV-2. |Amino Acid Sequence[MESH] |Angiotensin-Converting Enzyme 2/chemistry/*metabolism[MESH] |Animals[MESH] |Arvicolinae[MESH] |COVID-19/*metabolism/*virology[MESH] |Cattle[MESH] |Humans[MESH] |Models, Molecular[MESH] |Multiprotein Complexes/chemistry/metabolism[MESH] |Protein Binding[MESH] |Receptors, Virus/chemistry/*metabolism[MESH] |SARS-CoV-2/*physiology[MESH] |Sequence Alignment[MESH] |Spike Glycoprotein, Coronavirus/chemistry/genetics/*metabolism[MESH] |Structure-Activity Relationship[MESH]SARS-CoV-2 spike protein favors ACE2 from Bovidae and Cricetidae (epmc).pdf DeepDyve Pubget Overpricing