9ceg
From Proteopedia
(Difference between revisions)
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- | '''Unreleased structure''' | ||
- | + | ==20S Proteasome core particle beta-T1A mutant resting state (Frame 20)== | |
- | + | <StructureSection load='9ceg' size='340' side='right'caption='[[9ceg]], [[Resolution|resolution]] 2.86Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[9ceg]] 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=9CEG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9CEG FirstGlance]. <br> | |
- | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.86Å</td></tr> | |
- | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9ceg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9ceg OCA], [https://pdbe.org/9ceg PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9ceg RCSB], [https://www.ebi.ac.uk/pdbsum/9ceg PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9ceg ProSAT]</span></td></tr> |
+ | </table> | ||
+ | == Function == | ||
+ | [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> | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Mycobacterium tuberculosis]] | ||
+ | [[Category: Turner M]] | ||
+ | [[Category: Uday AB]] | ||
+ | [[Category: Vahidi S]] | ||
+ | [[Category: Zeytuni N]] |
Current revision
20S Proteasome core particle beta-T1A mutant resting state (Frame 20)
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