1sev

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[[Image:1sev.gif|left|200px]]
 
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==Mature and translocatable forms of glyoxysomal malate dehydrogenase have different activities and stabilities but similar crystal structures==
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The line below this paragraph, containing "STRUCTURE_1sev", creates the "Structure Box" on the page.
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<StructureSection load='1sev' size='340' side='right'caption='[[1sev]], [[Resolution|resolution]] 2.55&Aring;' scene=''>
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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== Structural highlights ==
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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<table><tr><td colspan='2'>[[1sev]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Citrullus_lanatus Citrullus lanatus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SEV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1SEV FirstGlance]. <br>
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or leave the SCENE parameter empty for the default display.
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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]] 2.55&#8491;</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=1sev FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1sev OCA], [https://pdbe.org/1sev PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1sev RCSB], [https://www.ebi.ac.uk/pdbsum/1sev PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1sev ProSAT]</span></td></tr>
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{{STRUCTURE_1sev| PDB=1sev | SCENE= }}
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/MDHG_CITLA MDHG_CITLA]
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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/se/1sev_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=1sev ConSurf].
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<div style="clear:both"></div>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Many organelle enzymes coded for by nuclear genes have N-terminal sequences, which directs them into the organelle (precursor) and are removed upon import (mature). The experiments described below characterize the differences between the precursor and mature forms of watermelon glyoxysomal malate dehydrogenase. Using recombinant protein methods, the precursor (p-gMDH) and mature (gMDH) forms were purified to homogeneity using Ni2+-NTA affinity chromatography. Gel filtration and dynamic light scattering have shown both gMDH and p-gMDH to be dimers in solution with p-gMDH having a correspondingly higher molecular weight. p-gMDH also exhibited a smaller translational diffusion coefficient (D(t)) at temperatures between 4 and 32 degrees C resulting from the extra amino acids on the N-terminal. Differential scanning calorimetry described marked differences in the unfolding properties of the two proteins with p-gMDH showing additional temperature dependent transitions. In addition, some differences were found in the steady state kinetic constants and the pH dependence of the K(m) for oxaloacetate. Both the organelle-precursor and the mature form of this glyoxysomal enzyme were crystallized under identical conditions. The crystal structure of p-gMDH, the first structure of a cleavable and translocatable protein, was solved to a resolution of 2.55 A. GMDH is the first glyoxysomal MDH structure and was solved to a resolution of 2.50 A. A comparison of the two structures shows that there are few visible tertiary or quaternary structural differences between corresponding elements of p-gMDH, gMDH and other MDHs. Maps from both the mature and translocatable proteins lack significant electron density prior to G44. While no portion of the translocation sequences from either monomer in the biological dimer was visible, all of the other solution properties indicated measurable effects of the additional residues at the N-terminal.
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'''Mature and translocatable forms of glyoxysomal malate dehydrogenase have different activities and stabilities but similar crystal structures'''
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Organelle and translocatable forms of glyoxysomal malate dehydrogenase. The effect of the N-terminal presequence.,Cox B, Chit MM, Weaver T, Gietl C, Bailey J, Bell E, Banaszak L FEBS J. 2005 Feb;272(3):643-54. PMID:15670147<ref>PMID:15670147</ref>
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==Overview==
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Many organelle enzymes coded for by nuclear genes have N-terminal sequences, which directs them into the organelle (precursor) and are removed upon import (mature). The experiments described below characterize the differences between the precursor and mature forms of watermelon glyoxysomal malate dehydrogenase. Using recombinant protein methods, the precursor (p-gMDH) and mature (gMDH) forms were purified to homogeneity using Ni2+-NTA affinity chromatography. Gel filtration and dynamic light scattering have shown both gMDH and p-gMDH to be dimers in solution with p-gMDH having a correspondingly higher molecular weight. p-gMDH also exhibited a smaller translational diffusion coefficient (D(t)) at temperatures between 4 and 32 degrees C resulting from the extra amino acids on the N-terminal. Differential scanning calorimetry described marked differences in the unfolding properties of the two proteins with p-gMDH showing additional temperature dependent transitions. In addition, some differences were found in the steady state kinetic constants and the pH dependence of the K(m) for oxaloacetate. Both the organelle-precursor and the mature form of this glyoxysomal enzyme were crystallized under identical conditions. The crystal structure of p-gMDH, the first structure of a cleavable and translocatable protein, was solved to a resolution of 2.55 A. GMDH is the first glyoxysomal MDH structure and was solved to a resolution of 2.50 A. A comparison of the two structures shows that there are few visible tertiary or quaternary structural differences between corresponding elements of p-gMDH, gMDH and other MDHs. Maps from both the mature and translocatable proteins lack significant electron density prior to G44. While no portion of the translocation sequences from either monomer in the biological dimer was visible, all of the other solution properties indicated measurable effects of the additional residues at the N-terminal.
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==About this Structure==
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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1SEV is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Citrullus_lanatus Citrullus lanatus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SEV OCA].
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</div>
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<div class="pdbe-citations 1sev" style="background-color:#fffaf0;"></div>
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==Reference==
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==See Also==
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Organelle and translocatable forms of glyoxysomal malate dehydrogenase. The effect of the N-terminal presequence., Cox B, Chit MM, Weaver T, Gietl C, Bailey J, Bell E, Banaszak L, FEBS J. 2005 Feb;272(3):643-54. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15670147 15670147]
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*[[Malate Dehydrogenase 3D structures|Malate Dehydrogenase 3D structures]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Citrullus lanatus]]
[[Category: Citrullus lanatus]]
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[[Category: Malate dehydrogenase]]
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[[Category: Large Structures]]
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[[Category: Single protein]]
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[[Category: Bailey J]]
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[[Category: Bailey, J.]]
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[[Category: Banaszak LJ]]
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[[Category: Banaszak, L J.]]
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[[Category: Bell E]]
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[[Category: Bell, E.]]
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[[Category: Chit MM]]
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[[Category: Chit, M M.]]
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[[Category: Cox BR]]
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[[Category: Cox, B R.]]
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[[Category: Gietl C]]
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[[Category: Gietl, C.]]
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[[Category: Weaver TM]]
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[[Category: Weaver, T M.]]
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[[Category: Oxidoreductase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 08:37:13 2008''
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Mature and translocatable forms of glyoxysomal malate dehydrogenase have different activities and stabilities but similar crystal structures

PDB ID 1sev

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