Application | Comment | Organism |
---|---|---|
pharmacology | covalent docking plus MD refinement of a representative set of known SARS-CoV inhibitors into OTUB2, OTUB1, and the PLpro from SARS-CoV-2 to probe their inhibitor binding and rationalize a deubiquitinase selectivity. It is pointed out that the structural differences in cellular deubiquitinases suggest that these enzymes may be different enough to be selectively targeted | Homo sapiens |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
additional information | the binding of SARS-CoV covalent and non-covalent inhibitors to the SARS-CoV-2 papain-like protease and ovarian tumor domain deubiquitinases (OTUB1 and OTUB2) is studied; the binding of SARS-CoV covalent and non-covalent inhibitors to the SARS-CoV-2 papain-like protease and ovarian tumor domain deubiquitinases (OTUB1 and OTUB2) is studied | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | Q96DC9 | - |
- |
Homo sapiens | Q96FW1 | - |
- |
Synonyms | Comment | Organism |
---|---|---|
OTUB1 | - |
Homo sapiens |
OTUB2 | - |
Homo sapiens |
Otubain-1 | - |
Homo sapiens |
Otubain-2 | - |
Homo sapiens |
General Information | Comment | Organism |
---|---|---|
physiological function | the enzyme is essential for viral replication | Homo sapiens |