6bgl

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m (Protected "6bgl" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6bgl is ON HOLD
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==Doubly PafE-capped 20S core particle in Mycobacterium tuberculosis==
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<SX load='6bgl' size='340' side='right' viewer='molstar' caption='[[6bgl]], [[Resolution|resolution]] 3.40&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6bgl]] is a 42 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=6BGL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6BGL 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">Electron Microscopy, [[Resolution|Resolution]] 3.4&#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=6bgl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6bgl OCA], [https://pdbe.org/6bgl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6bgl RCSB], [https://www.ebi.ac.uk/pdbsum/6bgl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6bgl 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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Authors: Li, H., Hu, K.
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==See Also==
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*[[Proteasome 3D structures|Proteasome 3D structures]]
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Description: Doubly PafE-capped 20S core particle in Mycobacterium tuberculosis
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: Li, H]]
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__TOC__
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[[Category: Hu, K]]
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</SX>
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[[Category: Large Structures]]
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[[Category: Mycobacterium tuberculosis]]
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[[Category: Hu K]]
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[[Category: Li H]]

Current revision

Doubly PafE-capped 20S core particle in Mycobacterium tuberculosis

6bgl, resolution 3.40Å

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