5ts0

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m (Protected "5ts0" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 5ts0 is ON HOLD
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==Structure of Mycobacterium tuberculosis proteasome in complex with N,C-capped dipeptide PKS2208==
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<StructureSection load='5ts0' size='340' side='right'caption='[[5ts0]], [[Resolution|resolution]] 2.85&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5ts0]] 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=5TS0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5TS0 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">X-ray diffraction, [[Resolution|Resolution]] 2.8467975&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=7J1:(2S)-N-{(2S)-3-METHOXY-1-[(NAPHTHALEN-1-YLMETHYL)AMINO]-1-OXOPROPAN-2-YL}-4-OXO-2-[(3-PHENYLPROPANOYL)AMINO]-4-(1H-PYRROL-1-YL)BUTANAMIDE+(NON-PREFERRED+NAME)'>7J1</scene></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=5ts0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ts0 OCA], [https://pdbe.org/5ts0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5ts0 RCSB], [https://www.ebi.ac.uk/pdbsum/5ts0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5ts0 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: Hao-Chi Hsu , Hao Fan, Pradeep K Singh , Rong Wang , George Sukenick , Carl Nathan , Gang Lin, Huilin Li
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==See Also==
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*[[Proteasome 3D structures|Proteasome 3D structures]]
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Description: Structure of Mycobacterium tuberculosis proteasome in complex with N,C-capped dipeptide PKS2208
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: Hao-Chi Hsu , Hao Fan, Pradeep K Singh , Rong Wang , George Sukenick , Carl Nathan , Gang Lin, Huilin Li]]
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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: Fan H]]
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[[Category: Hsu H-C]]
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[[Category: Li H]]
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[[Category: Lin G]]
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[[Category: Nathan C]]
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[[Category: Singh PK]]
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[[Category: Sukenick G]]
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[[Category: Wang R]]

Current revision

Structure of Mycobacterium tuberculosis proteasome in complex with N,C-capped dipeptide PKS2208

PDB ID 5ts0

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