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Sandbox Reserved 1735
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| - | == Structural Highlights of HIV-1 | + | == Structural Highlights of HIV-1 protease== |
| - | ==Structural Highlights of HIV-2 | + | ==Structural Highlights of HIV-2 protease== |
| - | == HIV-1 | + | == HIV-1 Protease in Humans== |
HIV-1 is more transmissible than HIV-2 and is more likely to lead to AIDS in a patient. “HIV-1 protease (PR) is a virus-encoded proteolytic enzyme that is initially systemized as part of the GagPol polyprotein” (Huang et. al, 2013). HIV-1 protease belongs to Clan AA, family A2 of the aspartic proteases. Aspartic proteases are the smallest group of proteases found in humans (Huang et. al, 2013). | HIV-1 is more transmissible than HIV-2 and is more likely to lead to AIDS in a patient. “HIV-1 protease (PR) is a virus-encoded proteolytic enzyme that is initially systemized as part of the GagPol polyprotein” (Huang et. al, 2013). HIV-1 protease belongs to Clan AA, family A2 of the aspartic proteases. Aspartic proteases are the smallest group of proteases found in humans (Huang et. al, 2013). | ||
| - | ==HIV-2 | + | ==HIV-2 Protease in Humans== |
==The role of CD4+ T-cell== | ==The role of CD4+ T-cell== | ||
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==HIV Prevention== | ==HIV Prevention== | ||
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| - | This is a sample scene created with SAT to <scene name="/12/3456/Sample/1">color</scene> by Group, and another to make <scene name="/12/3456/Sample/2">a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes. | ||
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| - | </StructureSection> | ||
== References == | == References == | ||
| - | <references/> | ||
Revision as of 19:57, 14 November 2022
| This Sandbox is Reserved from August 30, 2022 through May 31, 2023 for use in the course Biochemistry I taught by Kimberly Lane at the Radford University, Radford, VA, USA. This reservation includes Sandbox Reserved 1730 through Sandbox Reserved 1749. |
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HIV-1 Protease
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