Team:UST-Beijing/Parts

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    <td width="785"><img src="https://static.igem.org/mediawiki/igem.org/0/0d/USTBpart.JPG" width="794" height="763"></td>
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You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2008.igem.org/Help:Template/Examples">HERE</a>.
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    <td>PR, an abbreviation for proteorhodopsin, is a transmembrane protein which was discovered in 2000 through shortgun genome sequencing of unculturable bacteria isolated from the seawater off the coast of California. PR is a light-activated proton pump and generates a pmf which is short for proton motive force. This part, K603000 designed by Danyang Wang, was constructed as below: We replaced the PR's precusor sequence with the leader peptide of human cytochrome oxidase subunit 4 isoform 1, targeting it to mitochondrial inner membrane. Meanwhile, all the codons were re-designed according to codon usage bias for Homo sapiens.</td>
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You <strong>MUST</strong> have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page.  PLEASE keep all of your pages within your teams namespace. 
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    <td>&nbsp;</td>
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<p>Part：BBa-K603000
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   Designed by Dan yang Wang    Team: UST-Beijing &nbsp;&nbsp;
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<a href="https://static.igem.org/mediawiki/2011/6/62/PSB1AC3.jpg">selected sequence </a>
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  PR, a abbreviation of proteorhodopsin,is a kind of membrane protein </p>
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<p>which was discovered in 2000 through shortgun sequencing of seawater off the coast of California. PR is a light-activated proton pump and generates </p>
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<p>a pmf which is short for proton motive force. The part is constructed as below: We replace the PR’s precusor sequence with cytochrome</p>
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<p> cxidase subunit 4 isoform 1, mitochondrial precursor (Homo sapiens). Meanwhile, all the codons are redesigned according to codon usage </p>
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<p>bias for Homo sspiens.</p>
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|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
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|[[Image:UST-Beijing_logo.png|200px|right|frame]]
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''Tell us more about your project.  Give us background.  Use this is the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
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|align="center"|[[Team:UST-Beijing | Team Example]]
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{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
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!align="center"|[[Team:UST-Beijing|Home]]
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!align="center"|[[Team:UST-Beijing/Team|Team]]
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!align="center"|[https://igem.org/Team.cgi?year=2010&team_name=UST-Beijing Official Team Profile]
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!align="center"|[[Team:UST-Beijing/Project|Project]]
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!align="center"|[[Team:UST-Beijing/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:UST-Beijing/Modeling|Modeling]]
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!align="center"|[[Team:UST-Beijing/Notebook|Notebook]]
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!align="center"|[[Team:UST-Beijing/Safety|Safety]]
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!align="center"|[[Team:UST-Beijing/Attributions|Attributions]]
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Latest revision as of 02:16, 13 September 2011

 

 
https://static.igem.org/mediawiki/2011/6/62/PSB1AC3.jpg PR, an abbreviation for proteorhodopsin, is a transmembrane protein which was discovered in 2000 through shortgun genome sequencing of unculturable bacteria isolated from the seawater off the coast of California. PR is a light-activated proton pump and generates a pmf which is short for proton motive force. This part, K603000 designed by Danyang Wang, was constructed as below: We replaced the PR's precusor sequence with the leader peptide of human cytochrome oxidase subunit 4 isoform 1, targeting it to mitochondrial inner membrane. Meanwhile, all the codons were re-designed according to codon usage bias for Homo sapiens.
   

 

 

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