2trt

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[[Image:2trt.gif|left|200px]]
[[Image:2trt.gif|left|200px]]
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{{Structure
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The line below this paragraph, containing "STRUCTURE_2trt", creates the "Structure Box" on the page.
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|SITE=
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|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=TAC:TETRACYCLINE'>TAC</scene>
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{{STRUCTURE_2trt| PDB=2trt | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2trt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2trt OCA], [http://www.ebi.ac.uk/pdbsum/2trt PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2trt RCSB]</span>
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'''TETRACYCLINE REPRESSOR CLASS D'''
'''TETRACYCLINE REPRESSOR CLASS D'''
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==About this Structure==
==About this Structure==
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2TRT is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. This structure supersedes the now removed PDB entry 1TRT. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2TRT OCA].
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2TRT is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=1trt 1trt]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2TRT OCA].
==Reference==
==Reference==
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[[Category: Kisker, C.]]
[[Category: Kisker, C.]]
[[Category: Saenger, W.]]
[[Category: Saenger, W.]]
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[[Category: dna-binding]]
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[[Category: Dna-binding]]
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[[Category: repressor]]
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[[Category: Repressor]]
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[[Category: transcription regulation]]
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[[Category: Transcription regulation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 17:26:41 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 05:04:07 2008''
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Revision as of 14:26, 4 May 2008

Template:STRUCTURE 2trt

TETRACYCLINE REPRESSOR CLASS D


Overview

The most frequently occurring resistance of Gram-negative bacteria against tetracyclines is triggered by drug recognition of the Tet repressor. This causes dissociation of the repressor-operator DNA complex and enables expression of the resistance protein TetA, which is responsible for active efflux of tetracycline. The 2.5 angstrom resolution crystal structure of the homodimeric Tet repressor complexed with tetracycline-magnesium reveals detailed drug recognition. The orientation of the operator-binding helix-turn-helix motifs of the repressor is inverted in comparison with other DNA binding proteins. The repressor-drug complex is unable to interact with DNA because the separation of the DNA binding motifs is 5 angstroms wider than usually observed.

About this Structure

2TRT is a Single protein structure of sequence from Escherichia coli. This structure supersedes the now removed PDB entry 1trt. Full crystallographic information is available from OCA.

Reference

Structure of the Tet repressor-tetracycline complex and regulation of antibiotic resistance., Hinrichs W, Kisker C, Duvel M, Muller A, Tovar K, Hillen W, Saenger W, Science. 1994 Apr 15;264(5157):418-20. PMID:8153629 Page seeded by OCA on Sun May 4 17:26:41 2008

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