6bsc

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'''Unreleased structure'''
 
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The entry 6bsc is ON HOLD until Paper Publication
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==Crystal structure of the Mucin-1 SEA domain==
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<StructureSection load='6bsc' size='340' side='right' caption='[[6bsc]], [[Resolution|resolution]] 1.30&Aring;' scene=''>
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Authors: Noguera, M.E., Jakoncic, J., Ermacora, M.R.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6bsc]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6BSC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6BSC FirstGlance]. <br>
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Description: Crystal structure of the Mucin-1 SEA domain
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6bsc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6bsc OCA], [http://pdbe.org/6bsc PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6bsc RCSB], [http://www.ebi.ac.uk/pdbsum/6bsc PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6bsc ProSAT]</span></td></tr>
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[[Category: Unreleased Structures]]
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</table>
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[[Category: Ermacora, M.R]]
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== Disease ==
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[[Category: Noguera, M.E]]
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[[http://www.uniprot.org/uniprot/MUC1_HUMAN MUC1_HUMAN]] Note=MUC1/CA 15-3 is used as a serological clinical marker of breast cancer to monitor response to breast cancer treatment and disease recurrence (PubMed:20816948). Decreased levels over time may be indicative of a positive response to treatment. Conversely, increased levels may indicate disease progression. At an early stage disease, only 21% of patients exhibit high MUC1/CA 15-3 levels, that is why CA 15-3 is not a useful screening test. Most antibodies target the highly immunodominant core peptide domain of 20 amino acid (APDTRPAPGSTAPPAHGVTS) tandem repeats. Some antibodies recognize glycosylated epitopes.
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== Function ==
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[[http://www.uniprot.org/uniprot/MUC1_HUMAN MUC1_HUMAN]] The alpha subunit has cell adhesive properties. Can act both as an adhesion and an anti-adhesion protein. May provide a protective layer on epithelial cells against bacterial and enzyme attack.<ref>PMID:9139698</ref> <ref>PMID:11877440</ref> <ref>PMID:14688481</ref> <ref>PMID:15710329</ref> <ref>PMID:16288032</ref> <ref>PMID:15513966</ref> <ref>PMID:17524503</ref> <ref>PMID:17308127</ref> <ref>PMID:16983337</ref> The beta subunit contains a C-terminal domain which is involved in cell signaling, through phosphorylations and protein-protein interactions. Modulates signaling in ERK, SRC and NF-kappa-B pathways. In activated T-cells, influences directly or indirectly the Ras/MAPK pathway. Promotes tumor progression. Regulates TP53-mediated transcription and determines cell fate in the genotoxic stress response. Binds, together with KLF4, the PE21 promoter element of TP53 and represses TP53 activity.<ref>PMID:9139698</ref> <ref>PMID:11877440</ref> <ref>PMID:14688481</ref> <ref>PMID:15710329</ref> <ref>PMID:16288032</ref> <ref>PMID:15513966</ref> <ref>PMID:17524503</ref> <ref>PMID:17308127</ref> <ref>PMID:16983337</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: Ermacora, M R]]
[[Category: Jakoncic, J]]
[[Category: Jakoncic, J]]
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[[Category: Noguera, M E]]
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[[Category: Sea domain autoproteolysis muc1]]
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[[Category: Structural protein]]

Revision as of 06:32, 5 December 2018

Crystal structure of the Mucin-1 SEA domain

6bsc, resolution 1.30Å

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