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6yl2
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Structural and DNA binding studies of the transcriptional repressor Rv2506 (BkaR) from Mycobacterium tuberculosis supports a role in L-Leucine catabolism== | |
| - | + | <StructureSection load='6yl2' size='340' side='right'caption='[[6yl2]], [[Resolution|resolution]] 3.15Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6yl2]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Mycobacterium_tuberculosis_H37Rv Mycobacterium tuberculosis H37Rv]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6YL2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6YL2 FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.15Å</td></tr> | |
| - | [[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6yl2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6yl2 OCA], [https://pdbe.org/6yl2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6yl2 RCSB], [https://www.ebi.ac.uk/pdbsum/6yl2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6yl2 ProSAT]</span></td></tr> |
| - | [[ | + | </table> |
| - | [[ | + | == Function == |
| - | [[Category: | + | [https://www.uniprot.org/uniprot/O06169_MYCTU O06169_MYCTU] |
| - | [[Category: | + | __TOC__ |
| - | [[Category: Keep | + | </StructureSection> |
| + | [[Category: Large Structures]] | ||
| + | [[Category: Mycobacterium tuberculosis H37Rv]] | ||
| + | [[Category: Cole AR]] | ||
| + | [[Category: Keep NH]] | ||
| + | [[Category: Kendall SL]] | ||
| + | [[Category: Pritchard JE]] | ||
| + | [[Category: Sula A]] | ||
Current revision
Structural and DNA binding studies of the transcriptional repressor Rv2506 (BkaR) from Mycobacterium tuberculosis supports a role in L-Leucine catabolism
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