|
Contents
- 1 jmolSetTarget('1');jmolLink('delete $clickGreenLinkEcho; refresh;setL = \"setLoading();\"; javascript @setL; script /wiki/extensions/Proteopedia/spt/wipeFullLoadButton.spt; ~green = \"VesB\"; isosurface DELETE; scn = load(\"/wiki/scripts/79/799596/Cartoon_rotating_image/1.spt\"); scn = scn.replace(\'# initialize;\', \'# initialize;\nclearSceneScaleCmd = \"clearSceneScale();\"; javascript @clearSceneScaleCmd;\n\'); scn = scn.replace(\'_setSelectionState;\', \'_setSelectionState; message Scene_finished;\'); scn = scn.replace(\'_setState;\', \'_setState; setButtonsStartingState();\'); scn = scn.replace(\'DORESIZE\', \'\'); script inline scn;','VesB','VesB'); is found in Vibrio cholera. Its function is cleaving A subunit of cholera toxin, which plays an important role in activation of VesB and may contribute to intestinal growth or pathogenesis The substrate of VesB is any protein containing arginine (XXRXX) and the products after cleavage are (XXR+XX).
- 2 VesB has been shown to cause cholera. Cholera is a bacterial disease that is spread through contaminated food or water. Its symptoms include severe diarrhea and dehydration. Impoverished areas with lesser sanitation are most susceptible to cholera.
- 3 By studying VesB, improved treatment and prevention of cholera could be discovered. While it is not a major problem in the United States, lives could be improved and saved in areas such such as Africa, where cholera is more prevalent. This would allow more social interaction without concern of disease, which would be beneficial as many people are in close contact in these areas of contamination.
- 4 The primary jmolSetTarget('1');jmolLink('delete $clickGreenLinkEcho; refresh;setL = \"setLoading();\"; javascript @setL; script /wiki/extensions/Proteopedia/spt/wipeFullLoadButton.spt; ~green = \"secondary structure\"; isosurface DELETE; scn = load(\"/wiki/scripts/79/799596/Vesb_secondary_structure/1.spt\"); scn = scn.replace(\'# initialize;\', \'# initialize;\nclearSceneScaleCmd = \"clearSceneScale();\"; javascript @clearSceneScaleCmd;\n\'); scn = scn.replace(\'_setSelectionState;\', \'_setSelectionState; message Scene_finished;\'); scn = scn.replace(\'_setState;\', \'_setState; setButtonsStartingState();\'); scn = scn.replace(\'DORESIZE\', \'\'); script inline scn;','secondary structure','secondary structure'); of VesB is beta sheets, with some alpha helices and a few random coils. VesB has two jmolSetTarget('1');jmolLink('delete $clickGreenLinkEcho; refresh;setL = \"setLoading();\"; javascript @setL; script /wiki/extensions/Proteopedia/spt/wipeFullLoadButton.spt; ~green = \"disulfide bonds\"; isosurface DELETE; scn = load(\"/wiki/scripts/79/799596/Disulfide_bonds/1.spt\"); scn = scn.replace(\'# initialize;\', \'# initialize;\nclearSceneScaleCmd = \"clearSceneScale();\"; javascript @clearSceneScaleCmd;\n\'); scn = scn.replace(\'_setSelectionState;\', \'_setSelectionState; message Scene_finished;\'); scn = scn.replace(\'_setState;\', \'_setState; setButtonsStartingState();\'); scn = scn.replace(\'DORESIZE\', \'\'); script inline scn;','disulfide bonds','disulfide bonds'); and jmolSetTarget('1');jmolLink('delete $clickGreenLinkEcho; refresh;setL = \"setLoading();\"; javascript @setL; script /wiki/extensions/Proteopedia/spt/wipeFullLoadButton.spt; ~green = \"two domains\"; isosurface DELETE; scn = load(\"/wiki/scripts/79/799596/Domains/1.spt\"); scn = scn.replace(\'# initialize;\', \'# initialize;\nclearSceneScaleCmd = \"clearSceneScale();\"; javascript @clearSceneScaleCmd;\n\'); scn = scn.replace(\'_setSelectionState;\', \'_setSelectionState; message Scene_finished;\'); scn = scn.replace(\'_setState;\', \'_setState; setButtonsStartingState();\'); scn = scn.replace(\'DORESIZE\', \'\'); script inline scn;','two domains','two domains'); that make up its tertiary structure. There is an N-terminal protease domain with a trypsin/chymotrypsin fold and also a C-terminal Ig fold. jmolSetTarget('1');jmolLink('delete $clickGreenLinkEcho; refresh;setL = \"setLoading();\"; javascript @setL; script /wiki/extensions/Proteopedia/spt/wipeFullLoadButton.spt; ~green = \"VesB space-filling view\"; isosurface DELETE; scn = load(\"/wiki/scripts/79/799596/Spacefill/1.spt\"); scn = scn.replace(\'# initialize;\', \'# initialize;\nclearSceneScaleCmd = \"clearSceneScale();\"; javascript @clearSceneScaleCmd;\n\'); scn = scn.replace(\'_setSelectionState;\', \'_setSelectionState; message Scene_finished;\'); scn = scn.replace(\'_setState;\', \'_setState; setButtonsStartingState();\'); scn = scn.replace(\'DORESIZE\', \'\'); script inline scn;','VesB space-filling view','VesB space-filling view'); shows the size of the protein and the area each molecule occupies. There are both jmolSetTarget('1');jmolLink('delete $clickGreenLinkEcho; refresh;setL = \"setLoading();\"; javascript @setL; script /wiki/extensions/Proteopedia/spt/wipeFullLoadButton.spt; ~green = \"hydrophilic and hydrophobic\"; isosurface DELETE; scn = load(\"/wiki/scripts/79/799596/Hydrophobic_highlighted/1.spt\"); scn = scn.replace(\'# initialize;\', \'# initialize;\nclearSceneScaleCmd = \"clearSceneScale();\"; javascript @clearSceneScaleCmd;\n\'); scn = scn.replace(\'_setSelectionState;\', \'_setSelectionState; message Scene_finished;\'); scn = scn.replace(\'_setState;\', \'_setState; setButtonsStartingState();\'); scn = scn.replace(\'DORESIZE\', \'\'); script inline scn;','hydrophilic and hydrophobic','hydrophilic and hydrophobic'); sections of VesB. Its active site is hydrophobic, as is much of its surface. The alpha helices make up the majority of the hydrophilic areas, showing areas where water would be attracted to VesB. The crystal structure of VesB was solved without a ligand, however, any protein containing RX is a VesB ligand.
|
is found in Vibrio cholera. Its function is cleaving A subunit of cholera toxin, which plays an important role in activation of VesB and may contribute to intestinal growth or pathogenesis The substrate of VesB is any protein containing arginine (XXRXX) and the products after cleavage are (XXR+XX).
VesB has been shown to cause cholera. Cholera is a bacterial disease that is spread through contaminated food or water. Its symptoms include severe diarrhea and dehydration. Impoverished areas with lesser sanitation are most susceptible to cholera.
By studying VesB, improved treatment and prevention of cholera could be discovered. While it is not a major problem in the United States, lives could be improved and saved in areas such such as Africa, where cholera is more prevalent. This would allow more social interaction without concern of disease, which would be beneficial as many people are in close contact in these areas of contamination.
The primary of VesB is beta sheets, with some alpha helices and a few random coils. VesB has two and that make up its tertiary structure. There is an N-terminal protease domain with a trypsin/chymotrypsin fold and also a C-terminal Ig fold. shows the size of the protein and the area each molecule occupies. There are both sections of VesB. Its active site is hydrophobic, as is much of its surface. The alpha helices make up the majority of the hydrophilic areas, showing areas where water would be attracted to VesB. The crystal structure of VesB was solved without a ligand, however, any protein containing RX is a VesB ligand.
This is a sample scene created with SAT to by Group, and another to make of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.
|