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Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 J+Med+Virol 2021 ; 93 (3): 1581-1588 Nephropedia Template TP
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The emerging SARS-CoV-2 papain-like protease: Its relationship with recent coronavirus epidemics #MMPMID32902889
Kandeel M; Kitade Y; Fayez M; Venugopala KN; Ibrahim A
J Med Virol 2021[Mar]; 93 (3): 1581-1588 PMID32902889show ga
The papain-like protease (PL(pro) ) is an important enzyme for coronavirus polyprotein processing, as well as for virus-host immune suppression. Previous studies reveal that a molecular analysis of PL(pro) indicates the catalytic activity of viral PL(pro) and its interactions with ubiquitin. By using sequence comparisons, molecular models, and protein-protein interaction maps, PL(pro) was compared in the three recorded fatal CoV epidemics, which involved severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), severe acute respiratory syndrome CoV (SARS-CoV), and Middle East respiratory syndrome coronavirus (MERS-CoV). The pairwise sequence comparison of SARS-CoV-2 PL(pro) indicated similarity percentages of 82.59% and 30.06% with SARS-CoV PL(pro) and MERS-CoV PL(pro) , respectively. In comparison with SARS-CoV PL(pro) , in SARS-CoV-2, the PL(pro) had a conserved catalytic triad of C111, H278, and D293, with a slightly lower number of polar interface residues and of hydrogen bonds, a higher number of buried interface sizes, and a lower number of residues that interact with ubiquitin and PL(pro) . These features might contribute to a similar or slightly lower level of deubiquitinating activity in SARS-CoV-2 PLpro. It was, however, a much higher level compared to MERS-CoV, which contained amino acid mutations and a low number of polar interfaces. SARS-CoV-2 PL(pro) and SARS-CoV PL(pro) showed almost the same catalytic site profiles, interface area compositions and polarities, suggesting a general similarity in deubiquitination activity. Compared with MERS-CoV, SARS-CoV-2 had a higher potential for binding interactions with ubiquitin. These estimated parameters contribute to the knowledge gap in understanding how the new virus interacts with the immune system.
J+Med+Virol 2021 ; 93 (3): 1581-1588
