5k4f
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==CAL PDZ mutant C319A with a peptide== | |
- | + | <StructureSection load='5k4f' size='340' side='right' caption='[[5k4f]], [[Resolution|resolution]] 1.36Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[5k4f]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5K4F OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5K4F FirstGlance]. <br> | |
- | + | </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=5k4f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5k4f OCA], [http://pdbe.org/5k4f PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5k4f RCSB], [http://www.ebi.ac.uk/pdbsum/5k4f PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5k4f ProSAT]</span></td></tr> | |
- | [[Category: | + | </table> |
+ | == Disease == | ||
+ | [[http://www.uniprot.org/uniprot/GOPC_HUMAN GOPC_HUMAN]] Note=A chromosomal aberration involving GOPC is found in a glioblastoma multiforme sample. An intra-chromosomal deletion del(6)(q21q21) is responsible for the formation of GOPC-ROS1 chimeric protein which has a constitutive receptor tyrosine kinase activity.<ref>PMID:12661006</ref> | ||
+ | == Function == | ||
+ | [[http://www.uniprot.org/uniprot/GOPC_HUMAN GOPC_HUMAN]] Plays a role in intracellular protein trafficking and degradation. May regulate CFTR chloride currents and acid-induced ASIC3 currents by modulating cell surface expression of both channels. May also regulate the intracellular trafficking of the ADR1B receptor. May play a role in autophagy. Overexpression results in CFTR intracellular retention and degradation in the lysosomes.<ref>PMID:11707463</ref> <ref>PMID:14570915</ref> <ref>PMID:15358775</ref> [[http://www.uniprot.org/uniprot/VE6_HPV18 VE6_HPV18]] Transcriptional transactivator. Binds double stranded DNA (By similarity). Has transforming activity. Inactivates, with E6-AP ubiquitin-protein ligase, the human p53/TP53 tumor suppressor protein by targeting it to degradation. Binds and targets human MUPP1/MPDZ protein to degradation. Those two functions presumably contribute to transforming activity. Interaction with human FBLN1 protein also seems to be linked to cell transformation. | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Madden, D R]] | ||
[[Category: Zhao, Y]] | [[Category: Zhao, Y]] | ||
- | [[Category: | + | [[Category: C319a]] |
+ | [[Category: Cal pdz mutant]] | ||
+ | [[Category: Peptide binding protein]] |
Revision as of 07:27, 6 October 2017
CAL PDZ mutant C319A with a peptide
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