7bqi

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==Crystal structure of FYCO1 RUN domain==
==Crystal structure of FYCO1 RUN domain==
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<StructureSection load='7bqi' size='340' side='right'caption='[[7bqi]]' scene=''>
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<StructureSection load='7bqi' size='340' side='right'caption='[[7bqi]], [[Resolution|resolution]] 1.30&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7BQI OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=7BQI FirstGlance]. <br>
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<table><tr><td colspan='2'>[[7bqi]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7BQI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7BQI FirstGlance]. <br>
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=7bqi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7bqi OCA], [http://pdbe.org/7bqi PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=7bqi RCSB], [http://www.ebi.ac.uk/pdbsum/7bqi PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=7bqi ProSAT]</span></td></tr>
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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]] 1.3&#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=7bqi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7bqi OCA], [https://pdbe.org/7bqi PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7bqi RCSB], [https://www.ebi.ac.uk/pdbsum/7bqi PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7bqi ProSAT]</span></td></tr>
</table>
</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/FYCO1_HUMAN FYCO1_HUMAN] Nuclear cataract. The disease is caused by mutations affecting the gene represented in this entry. Pathogenic mutations in FYCO1 can affect intracellular transport of autophagocytic vesicles from the perinuclear area to the periphery, leading to an accumulation of large numbers of vesicles and hence loss of lens transparency (PubMed:21636066).<ref>PMID:21636066</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/FYCO1_HUMAN FYCO1_HUMAN] May mediate microtubule plus end-directed vesicle transport.<ref>PMID:20100911</ref>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Ohto U]]
[[Category: Ohto U]]
[[Category: Sakurai S]]
[[Category: Sakurai S]]
[[Category: Shimizu T]]
[[Category: Shimizu T]]

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Crystal structure of FYCO1 RUN domain

PDB ID 7bqi

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