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4v2f
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(Difference between revisions)
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4v2f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4v2f OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4v2f RCSB], [http://www.ebi.ac.uk/pdbsum/4v2f PDBsum]</span></td></tr> | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4v2f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4v2f OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4v2f RCSB], [http://www.ebi.ac.uk/pdbsum/4v2f PDBsum]</span></td></tr> | ||
</table> | </table> | ||
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/TETR4_ECOLX TETR4_ECOLX]] TetR is the repressor of the tetracycline resistance element; its N-terminal region forms a helix-turn-helix structure and binds DNA. Binding of tetracycline to TetR reduces the repressor affinity for the tetracycline resistance gene (tetA) promoter operator sites. | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
Revision as of 18:56, 24 December 2014
Tetracycline repressor TetR(D), unliganded
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