1rjw

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[[Image:1rjw.gif|left|200px]]<br /><applet load="1rjw" size="450" color="white" frame="true" align="right" spinBox="true"
 
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caption="1rjw, resolution 2.35&Aring;" />
 
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'''CRYSTAL STRUCTURE OF NAD(+)-DEPENDENT ALCOHOL DEHYDROGENASE FROM BACILLUS STEAROTHERMOPHILUS STRAIN LLD-R'''<br />
 
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==Overview==
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==CRYSTAL STRUCTURE OF NAD(+)-DEPENDENT ALCOHOL DEHYDROGENASE FROM BACILLUS STEAROTHERMOPHILUS STRAIN LLD-R==
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The crystal structure of NAD(+)-dependent alcohol dehydrogenase from, Bacillus stearothermophilus strain LLD-R (htADH) was determined using, X-ray diffraction data at a resolution of 2.35 A. The structure of, homotetrameric htADH is highly homologous to those of bacterial and, archaeal homotetrameric alcohol dehydrogenases (ADHs) and also to the, mammalian dimeric ADHs. There is one catalytic zinc atom and one, structural zinc atom per enzyme subunit. The enzyme was crystallized as a, binary complex lacking the nicotinamide adenine dinucleotide (NAD(+)), cofactor but including a zinc-coordinated substrate analogue, trifluoroethanol. The binary complex structure is in an open conformation, similar to ADH structures without the bound cofactor. Features important, for the thermostability of htADH are suggested by a comparison with a, homologous mesophilic enzyme (55% identity), NAD(+)-dependent alcohol, dehydrogenase from Escherichia coli. To gain insight into the, conformational change triggered by NAD(+) binding, amide, hydrogen-deuterium exchange of htADH, in the presence and absence of, NAD(+), was studied by HPLC-coupled electrospray mass spectrometry. When, the deuteron incorporation of the protein-derived peptides was analyzed, it was found that 9 of 21 peptides show some decrease in the level of, deuteron incorporation upon NAD(+) binding, and another 4 peptides display, slower exchange rates. With one exception (peptide number 8), none of the, peptides that are altered by bound NAD(+) are in contact with the, alcohol-substrate-binding pocket. Furthermore, peptides 5 and 8, which are, located outside the NAD(+)-binding pocket, are notable by displaying, changes upon NAD(+) binding. This suggests that the transition from the, open to the closed conformation caused by cofactor binding has some, long-range effects on the protein structure and dynamics.
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<StructureSection load='1rjw' size='340' side='right'caption='[[1rjw]], [[Resolution|resolution]] 2.35&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[1rjw]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Geobacillus_stearothermophilus Geobacillus stearothermophilus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RJW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1RJW FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.35&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ETF:TRIFLUOROETHANOL'>ETF</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1rjw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1rjw OCA], [https://pdbe.org/1rjw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1rjw RCSB], [https://www.ebi.ac.uk/pdbsum/1rjw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1rjw ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/ADH3_GEOSE ADH3_GEOSE] Thermophilic NAD(+)-dependent alcohol dehydrogenase. Bears mainly an ethanol-dehydrogenase activity.
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== Evolutionary Conservation ==
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[[Image:Consurf_key_small.gif|200px|right]]
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Check<jmol>
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<jmolCheckbox>
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/rj/1rjw_consurf.spt"</scriptWhenChecked>
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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<text>to colour the structure by Evolutionary Conservation</text>
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</jmolCheckbox>
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</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=1rjw ConSurf].
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<div style="clear:both"></div>
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==About this Structure==
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==See Also==
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1RJW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Geobacillus_stearothermophilus Geobacillus stearothermophilus] with ZN and ETF as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Alcohol_dehydrogenase Alcohol dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.1 1.1.1.1] Known structural/functional Site: <scene name='pdbsite=ZN8:Catalytic Zn Site, Chain D'>ZN8</scene>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1RJW OCA].
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*[[Alcohol dehydrogenase 3D structures|Alcohol dehydrogenase 3D structures]]
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__TOC__
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==Reference==
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</StructureSection>
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Crystal structure and amide H/D exchange of binary complexes of alcohol dehydrogenase from Bacillus stearothermophilus: insight into thermostability and cofactor binding., Ceccarelli C, Liang ZX, Strickler M, Prehna G, Goldstein BM, Klinman JP, Bahnson BJ, Biochemistry. 2004 May 11;43(18):5266-77. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15122892 15122892]
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[[Category: Alcohol dehydrogenase]]
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[[Category: Geobacillus stearothermophilus]]
[[Category: Geobacillus stearothermophilus]]
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[[Category: Single protein]]
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[[Category: Large Structures]]
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[[Category: Bahnson, B.J.]]
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[[Category: Bahnson BJ]]
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[[Category: Ceccarelli, C.]]
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[[Category: Ceccarelli C]]
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[[Category: ETF]]
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[[Category: ZN]]
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[[Category: alcohol]]
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[[Category: dehydrogenase]]
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[[Category: nad]]
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[[Category: oxidoreductase]]
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[[Category: tetramer]]
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[[Category: zinc]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Dec 18 17:59:23 2007''
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Current revision

CRYSTAL STRUCTURE OF NAD(+)-DEPENDENT ALCOHOL DEHYDROGENASE FROM BACILLUS STEAROTHERMOPHILUS STRAIN LLD-R

PDB ID 1rjw

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