1zz3: Difference between revisions

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[[Image:1zz3.gif|left|200px]]<br /><applet load="1zz3" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1zz3, resolution 1.76&Aring;" />
'''Crystal structure of a HDAC-like protein with CypX bound'''<br />


==Overview==
==Crystal structure of a HDAC-like protein with CypX bound==
Histone deacetylases (HDACs) are among the most promising targets in cancer therapy. However, structural information greatly enhancing the design of HDAC inhibitors as novel chemotherapeutics has not been available on class 2 HDACs so far. Here we present the structure of the bacterial FB188 HDAH (histone deacetylase-like amidohydrolase from Bordetella/Alcaligenes strain FB188) that reveals high sequential and functional homology to human class 2 HDACs. FB188 HDAH is capable to remove the acetyl moiety from acetylated histones. Several HDAC-specific inhibitors, which have been shown to inhibit tumor activity in both pre-clinical models and in clinical trials, also inhibit FB188 HDAH. We have determined the crystal structure of FB188 HDAH at a resolution of 1.6 angstroms in complex with the reaction product acetate, as well as in complex with the inhibitors suberoylanilide hydroxamic acid (SAHA) and cyclopentyle-propionyle hydroxamic acid (CypX) at a resolution of 1.57 angstroms and 1.75 angstroms, respectively. FB188 HDAH exhibits the canonical fold of class 1 HDACs and contains a catalytic zinc ion. The highest structural diversity compared to class 1 enzymes is found in loop regions especially in the area around the entrance of the active site, indicating significant differences among the acetylated proteins binding to class 1 and 2 HDACs, respectively.
<StructureSection load='1zz3' size='340' side='right'caption='[[1zz3]], [[Resolution|resolution]] 1.76&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1zz3]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Alcaligenaceae_bacterium_FB188 Alcaligenaceae bacterium FB188]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ZZ3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1ZZ3 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]] 1.76&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=3YP:3-CYCLOPENTYL-N-HYDROXYPROPANAMIDE'>3YP</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></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=1zz3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1zz3 OCA], [https://pdbe.org/1zz3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1zz3 RCSB], [https://www.ebi.ac.uk/pdbsum/1zz3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1zz3 ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/HDAH_ALCSD HDAH_ALCSD]
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/zz/1zz3_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1zz3 ConSurf].
<div style="clear:both"></div>


==About this Structure==
==See Also==
1ZZ3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bordetella_sp. Bordetella sp.] with <scene name='pdbligand=3YP:'>3YP</scene>, <scene name='pdbligand=ZN:'>ZN</scene> and <scene name='pdbligand=K:'>K</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ZZ3 OCA].
*[[Histone deacetylase 3D structures|Histone deacetylase 3D structures]]
 
__TOC__
==Reference==
</StructureSection>
Crystal structure of a bacterial class 2 histone deacetylase homologue., Nielsen TK, Hildmann C, Dickmanns A, Schwienhorst A, Ficner R, J Mol Biol. 2005 Nov 18;354(1):107-20. Epub 2005 Oct 7. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=16242151 16242151]
[[Category: Alcaligenaceae bacterium FB188]]
[[Category: Bordetella sp.]]
[[Category: Large Structures]]
[[Category: Single protein]]
[[Category: Dickmanns A]]
[[Category: Dickmanns, A.]]
[[Category: Ficner R]]
[[Category: Ficner, R.]]
[[Category: Hildmann C]]
[[Category: Hildmann, C.]]
[[Category: Nielsen TK]]
[[Category: Nielsen, T K.]]
[[Category: Schwienhorst A]]
[[Category: Schwienhorst, A.]]
[[Category: 3YP]]
[[Category: K]]
[[Category: ZN]]
[[Category: hydrolase]]
 
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