1jty

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
[[Image:1jty.gif|left|200px]]
[[Image:1jty.gif|left|200px]]
-
{{Structure
+
<!--
-
|PDB= 1jty |SIZE=350|CAPTION= <scene name='initialview01'>1jty</scene>, resolution 2.97&Aring;
+
The line below this paragraph, containing "STRUCTURE_1jty", creates the "Structure Box" on the page.
-
|SITE=
+
You may change the PDB parameter (which sets the PDB file loaded into the applet)
-
|LIGAND= <scene name='pdbligand=ET:ETHIDIUM'>ET</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>
+
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
-
|ACTIVITY=
+
or leave the SCENE parameter empty for the default display.
-
|GENE=
+
-->
-
|DOMAIN=
+
{{STRUCTURE_1jty| PDB=1jty | SCENE= }}
-
|RELATEDENTRY=[[1jt0|1JT0]], [[1jt6|1JT6]], [[1jtx|1JTX]], [[1jum|1JUM]], [[1jup|1JUP]], [[1jus|1JUS]]
+
-
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1jty FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1jty OCA], [http://www.ebi.ac.uk/pdbsum/1jty PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1jty RCSB]</span>
+
-
}}
+
'''Crystal structure of the multidrug binding transcriptional regulator QacR bound to ethidium'''
'''Crystal structure of the multidrug binding transcriptional regulator QacR bound to ethidium'''
Line 31: Line 28:
[[Category: Schumacher, M A.]]
[[Category: Schumacher, M A.]]
[[Category: Skurray, R A.]]
[[Category: Skurray, R A.]]
-
[[Category: cationic lipophilic drug]]
+
[[Category: Cationic lipophilic drug]]
-
[[Category: multidrug binding]]
+
[[Category: Multidrug binding]]
-
[[Category: multidrug recognition mechanism]]
+
[[Category: Multidrug recognition mechanism]]
-
[[Category: qaca]]
+
[[Category: Qaca]]
-
[[Category: qacr]]
+
[[Category: Qacr]]
-
[[Category: repressor]]
+
[[Category: Repressor]]
-
[[Category: transcription]]
+
[[Category: Transcription]]
-
 
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 21:55:10 2008''
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:38:59 2008''
+

Revision as of 18:55, 2 May 2008

Template:STRUCTURE 1jty

Crystal structure of the multidrug binding transcriptional regulator QacR bound to ethidium


Overview

The Staphylococcus aureus multidrug binding protein QacR represses transcription of the qacA multidrug transporter gene and is induced by structurally diverse cationic lipophilic drugs. Here, we report the crystal structures of six QacR-drug complexes. Compared to the DNA bound structure, drug binding elicits a coil-to-helix transition that causes induction and creates an expansive multidrug-binding pocket, containing four glutamates and multiple aromatic and polar residues. These structures indicate the presence of separate but linked drug-binding sites within a single protein. This multisite drug-binding mechanism is consonant with studies on multidrug resistance transporters.

About this Structure

1JTY is a Single protein structure of sequence from Staphylococcus aureus. Full crystallographic information is available from OCA.

Reference

Structural mechanisms of QacR induction and multidrug recognition., Schumacher MA, Miller MC, Grkovic S, Brown MH, Skurray RA, Brennan RG, Science. 2001 Dec 7;294(5549):2158-63. PMID:11739955 Page seeded by OCA on Fri May 2 21:55:10 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools