9cee

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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 9cee is ON HOLD until Paper Publication
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==20S Proteasome core particle beta-T1A mutant auto-inhibited state (Frame 1)==
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<StructureSection load='9cee' size='340' side='right'caption='[[9cee]], [[Resolution|resolution]] 2.89&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9cee]] 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=9CEE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9CEE 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]] 2.89&#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=9cee FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9cee OCA], [https://pdbe.org/9cee PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9cee RCSB], [https://www.ebi.ac.uk/pdbsum/9cee PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9cee 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 beta-T1A mutant auto-inhibited state (Frame 1)

PDB ID 9cee

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