Difference between revisions of "Part:BBa K3338000"
Jonas Scholz (Talk | contribs) |
|||
Line 3: | Line 3: | ||
<partinfo>BBa_K3338000 short</partinfo> | <partinfo>BBa_K3338000 short</partinfo> | ||
− | MagA is a transmembrane iron transporter originating from the aquatic magnetotactic bacterium <i>Magnetospirillum magnetotacticum</i>. In the original host the protein is involved in the formation of intracellular magnetic particles of magnetite ( | + | MagA is a transmembrane iron transporter originating from the aquatic magnetotactic bacterium <i>Magnetospirillum magnetotacticum</i>. In the original host the protein is involved in the formation of intracellular magnetic particles of magnetite (Fe<sub>3</sub>O<sub>4</sub>). When expressed in procaryotic or eukaryotic cells it leads to the accumulation of intracellular iron that can be detected using magnetic resonance imaging (MRI) technique. This characteristic makes MagA ideal as an endogenous contrast agent for <i>in vitro</i> and <i>in vivo</i> applications. |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 13:53, 22 October 2020
Iron transporter MagA from Magnetospirillum magneticum
MagA is a transmembrane iron transporter originating from the aquatic magnetotactic bacterium Magnetospirillum magnetotacticum. In the original host the protein is involved in the formation of intracellular magnetic particles of magnetite (Fe3O4). When expressed in procaryotic or eukaryotic cells it leads to the accumulation of intracellular iron that can be detected using magnetic resonance imaging (MRI) technique. This characteristic makes MagA ideal as an endogenous contrast agent for in vitro and in vivo applications.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1182
Illegal BsaI.rc site found at 514
Illegal BsaI.rc site found at 1063
Illegal SapI site found at 204