9ce5

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Current revision (10:29, 12 March 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 9ce5 is ON HOLD until Paper Publication
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==20S Proteasome core particle==
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<StructureSection load='9ce5' size='340' side='right'caption='[[9ce5]], [[Resolution|resolution]] 2.66&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9ce5]] is a 28 chain structure with sequence from [https://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9CE5 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9CE5 FirstGlance]. <br>
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Description:
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.66&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=9ce5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9ce5 OCA], [https://pdbe.org/9ce5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9ce5 RCSB], [https://www.ebi.ac.uk/pdbsum/9ce5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9ce5 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/PSA_MYCTU PSA_MYCTU] Component of the proteasome core, a large protease complex with broad specificity involved in protein degradation. The M.tuberculosis proteasome is able to cleave oligopeptides not only after hydrophobic but also after basic, acidic and small neutral residues. Among the identified substrates of the M.tuberculosis proteasome are the pupylated FabD, PanB and Mpa proteins. One function of the proteasome is to contribute to M.tuberculosis ability to resist killing by host macrophages, since the core proteasome is essential for persistence of the pathogen during the chronic phase of infection in mice. The mechanism of protection against bactericidal chemistries of the host's immune response probably involves the degradation of proteins that are irreversibly oxidized, nitrated, or nitrosated.<ref>PMID:16468985</ref> <ref>PMID:18059281</ref>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Mycobacterium tuberculosis]]
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[[Category: Turner M]]
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[[Category: Uday AB]]
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[[Category: Vahidi S]]
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[[Category: Zeytuni N]]

Current revision

20S Proteasome core particle

PDB ID 9ce5

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