Difference between revisions of "Team:LambertGA/Basic Part"
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<header> | <header> | ||
<div id="headerLinks"> | <div id="headerLinks"> | ||
| − | < | + | <a href="https://2016.igem.org/Team:LambertGA" class="dropbtn">Home</a><!-- |
| − | <li class="dropdown"> | + | --><li class="dropdown" > |
| + | <a href="https://2016.igem.org/Team:LambertGA/Team" class="dropbtn">Team</a> | ||
| + | <div class="dropdown-content"> | ||
| + | <a href="https://2016.igem.org/Team:LambertGA/Collaborations">Collaborations</a> | ||
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| + | </li><!-- | ||
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<a href="https://2016.igem.org/Team:LambertGA/Description" class="dropbtn">Project</a> | <a href="https://2016.igem.org/Team:LambertGA/Description" class="dropbtn">Project</a> | ||
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<a href="https://2016.igem.org/Team:LambertGA/Proof">Proof of Concept</a> | <a href="https://2016.igem.org/Team:LambertGA/Proof">Proof of Concept</a> | ||
<a href="https://2016.igem.org/Team:LambertGA/Demonstrate">Demonstrate</a> | <a href="https://2016.igem.org/Team:LambertGA/Demonstrate">Demonstrate</a> | ||
| + | <a href="https://2016.igem.org/Team:LambertGA/Results">Results</a> | ||
| + | <a href="https://2016.igem.org/Team:LambertGA/Notebook">Notebook</a> | ||
</div> | </div> | ||
</li><!-- | </li><!-- | ||
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<a href="https://2016.igem.org/Team:LambertGA/Basic_Part">Basic Parts</a> | <a href="https://2016.igem.org/Team:LambertGA/Basic_Part">Basic Parts</a> | ||
<a href="https://2016.igem.org/Team:LambertGA/Composite_Part">Composite Parts</a> | <a href="https://2016.igem.org/Team:LambertGA/Composite_Part">Composite Parts</a> | ||
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<a href="https://2016.igem.org/Team:LambertGA/Awards" class="dropbtn">Awards</a> | <a href="https://2016.igem.org/Team:LambertGA/Awards" class="dropbtn">Awards</a> | ||
<div class="dropdown-content"> | <div class="dropdown-content"> | ||
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<a href="https://2016.igem.org/Team:LambertGA/Hardware">Hardware</a> | <a href="https://2016.igem.org/Team:LambertGA/Hardware">Hardware</a> | ||
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<a href="https://2016.igem.org/Team:LambertGA/Measurement">Measurement</a> | <a href="https://2016.igem.org/Team:LambertGA/Measurement">Measurement</a> | ||
<a href="https://2016.igem.org/Team:LambertGA/Model">Model</a> | <a href="https://2016.igem.org/Team:LambertGA/Model">Model</a> | ||
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<center> <h1 id="MainTitle"><b> Basic Part </b></h1> </center> | <center> <h1 id="MainTitle"><b> Basic Part </b></h1> </center> | ||
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| − | <a href="http://www.forsyth.k12.ga.us/lhs"><img src="https://static.igem.org/mediawiki/ | + | <a href="http://www.forsyth.k12.ga.us/lhs"><img src="https://static.igem.org/mediawiki/2016/9/9e/T--LambertGA--longhorn_iGEM_logo.png" class="transparent" style="height:100px;padding:20px;"></a> |
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Revision as of 03:01, 14 October 2016
Basic Part
BBa_K1911002: ClpP
The ClpP gene codes for the ClpP subunit protein which works together with the ClpX subunit to break down proteins that are tagged with degradation tags. The ClpXP system identifies tagged proteins and proceeds to unfold the protein and break it down into individual amino acids. The ClpXP system along with degradation tags can be used to break down certain proteins which are produced by certain genes of interest and it has a range of applications such as measuring how fast a certain protein can be degraded in a cell.The ClpP sequence which was pulled from the E. coli genome contained illegal restriction enzyme sites. In order to remove these illegal sites, wobbles were introduced into the ClpP sequence so that the gene is not cut anywhere and is allowed to function properly.ClpP is a naturally present gene in the E. coli genome.
BBa_K1911003: ClpX
ClpX is part of the protein-degradation system called ClpXP. It works in unison with another protein called ClpXP so that it can de-linearize and unfold proteins into amino acids which can then be recycled by the cells. In E. coli cells, ClpXP focuses on degrading incorrect proteins and reducing them down into amino acids which can be recycled by the cells. ClpXP recognizes the incorrect proteins by certain SsrA-tags which are attached at the ends of incorrect proteins. ClpX in unison with ClpP can be used to degrade unwanted proteins and can be used in future projects in conjunction with certain degradation tags.There were illegal restriction sites which cut the ClpX gene into smaller sequences, rendering it obsolete. So we had to introduce wobbles to eliminate these illegal restriction sites so that ClpX may be expressed and allowed to function as a complete protein.ClpX is found naturally in the E. coli genome.
The ClpP gene codes for the ClpP subunit protein which works together with the ClpX subunit to break down proteins that are tagged with degradation tags. The ClpXP system identifies tagged proteins and proceeds to unfold the protein and break it down into individual amino acids. The ClpXP system along with degradation tags can be used to break down certain proteins which are produced by certain genes of interest and it has a range of applications such as measuring how fast a certain protein can be degraded in a cell.The ClpP sequence which was pulled from the E. coli genome contained illegal restriction enzyme sites. In order to remove these illegal sites, wobbles were introduced into the ClpP sequence so that the gene is not cut anywhere and is allowed to function properly.ClpP is a naturally present gene in the E. coli genome.
BBa_K1911003: ClpX
ClpX is part of the protein-degradation system called ClpXP. It works in unison with another protein called ClpXP so that it can de-linearize and unfold proteins into amino acids which can then be recycled by the cells. In E. coli cells, ClpXP focuses on degrading incorrect proteins and reducing them down into amino acids which can be recycled by the cells. ClpXP recognizes the incorrect proteins by certain SsrA-tags which are attached at the ends of incorrect proteins. ClpX in unison with ClpP can be used to degrade unwanted proteins and can be used in future projects in conjunction with certain degradation tags.There were illegal restriction sites which cut the ClpX gene into smaller sequences, rendering it obsolete. So we had to introduce wobbles to eliminate these illegal restriction sites so that ClpX may be expressed and allowed to function as a complete protein.ClpX is found naturally in the E. coli genome.
