Difference between revisions of "Part:BBa K141002"

 
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<partinfo>BBa_K141002 short</partinfo>
 
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The uncoupling protein UCP 175 deleted is a proton carrier which is obtaines from the direct mugenesis  of the Ucp1 gene.
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Ucp 175 has a deletion in the triplet the encodes for the Glycine 175.
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The mutant shows a generation time and an heat up capacity higher than UCP1.
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UCP 175 deleted  uncouples the respiratory chain  of ATP production, converting the metabolic energy in heat.
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The mutant shows a generation time and an heat up capacity higher than UCP1.
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[[Image:Function.jpg]]
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UCP 175 deleted is a 33kd protein.
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The protein has a tripartite structure. The structure displays an around 100 residues region  which  is three times repeated. Each part encodes for two transmembrane segments and one long hydrophilic loop.The functional carrier unit is an homodimer.
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[[Image:Structure.jpg]]
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The main  difference between UCP 175 deleted and  most of the proteins with a nuclear codification is  the    lack of the importation targeting to the mitochondria in UCP 175 deleted proteins.
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The condition that determines the mitochondria as the protein target lays in the first loop which protudes in the mitochondrial matrix.
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The second loop of the matrix is essential for the insertion of the protein in the inner mitochondrial matrix.
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Purine nucleotides act as  inhibitors of protein activity and  esterificated fatty acids act as  inductors.
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Revision as of 15:22, 8 October 2008

Ucp 175 deleted

The uncoupling protein UCP 175 deleted is a proton carrier which is obtaines from the direct mugenesis of the Ucp1 gene. Ucp 175 has a deletion in the triplet the encodes for the Glycine 175. The mutant shows a generation time and an heat up capacity higher than UCP1. UCP 175 deleted uncouples the respiratory chain of ATP production, converting the metabolic energy in heat. The mutant shows a generation time and an heat up capacity higher than UCP1.

Function.jpg


UCP 175 deleted is a 33kd protein. The protein has a tripartite structure. The structure displays an around 100 residues region which is three times repeated. Each part encodes for two transmembrane segments and one long hydrophilic loop.The functional carrier unit is an homodimer.


Structure.jpg


The main difference between UCP 175 deleted and most of the proteins with a nuclear codification is the lack of the importation targeting to the mitochondria in UCP 175 deleted proteins.

The condition that determines the mitochondria as the protein target lays in the first loop which protudes in the mitochondrial matrix.

The second loop of the matrix is essential for the insertion of the protein in the inner mitochondrial matrix.

Purine nucleotides act as inhibitors of protein activity and esterificated fatty acids act as inductors.




Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 47
    Illegal BglII site found at 347
    Illegal BamHI site found at 832
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 58
  • 1000
    COMPATIBLE WITH RFC[1000]