3fva

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{{STRUCTURE_3fva| PDB=3fva | SCENE= }}
 
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===NNQNTF segment from elk prion===
 
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{{ABSTRACT_PUBMED_19684598}}
 
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==Disease==
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==NNQNTF segment from elk prion==
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[[http://www.uniprot.org/uniprot/PRIO_CEREN PRIO_CEREN]] Note=PrP is found in high quantity in the brain of humans and animals infected with the degenerative neurological diseases kuru, Creutzfeldt-Jakob disease (CJD), Gerstmann-Straussler syndrome (GSS), scrapie, bovine spongiform encephalopathy (BSE), transmissible mink encephalopathy (TME), etc.
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<StructureSection load='3fva' size='340' side='right'caption='[[3fva]], [[Resolution|resolution]] 1.46&Aring;' scene=''>
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== Structural highlights ==
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==Function==
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<table><tr><td colspan='2'>[[3fva]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Cervus_canadensis_nelsoni Cervus canadensis nelsoni]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3FVA OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3FVA FirstGlance]. <br>
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[[http://www.uniprot.org/uniprot/PRIO_CEREN PRIO_CEREN]] May play a role in neuronal development and synaptic plasticity. May be required for neuronal myelin sheath maintenance. May play a role in iron uptake and iron homeostasis. Soluble oligomers are toxic to cultured neuroblastoma cells and induce apoptosis (in vitro). Association with GPC1 (via its heparan sulfate chains) targets PRNP to lipid rafts. Also provides Cu(2+) or ZN(2+) for the ascorbate-mediated GPC1 deaminase degradation of its heparan sulfate side chains (By similarity).
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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]] 1.458&#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=3fva FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3fva OCA], [https://pdbe.org/3fva PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3fva RCSB], [https://www.ebi.ac.uk/pdbsum/3fva PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3fva ProSAT]</span></td></tr>
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==About this Structure==
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</table>
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[[3fva]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3FVA OCA].
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== Disease ==
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[https://www.uniprot.org/uniprot/PRIO_CEREN PRIO_CEREN] Note=PrP is found in high quantity in the brain of humans and animals infected with the degenerative neurological diseases kuru, Creutzfeldt-Jakob disease (CJD), Gerstmann-Straussler syndrome (GSS), scrapie, bovine spongiform encephalopathy (BSE), transmissible mink encephalopathy (TME), etc.
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== Function ==
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[https://www.uniprot.org/uniprot/PRIO_CEREN PRIO_CEREN] May play a role in neuronal development and synaptic plasticity. May be required for neuronal myelin sheath maintenance. May play a role in iron uptake and iron homeostasis. Soluble oligomers are toxic to cultured neuroblastoma cells and induce apoptosis (in vitro). Association with GPC1 (via its heparan sulfate chains) targets PRNP to lipid rafts. Also provides Cu(2+) or ZN(2+) for the ascorbate-mediated GPC1 deaminase degradation of its heparan sulfate side chains (By similarity).
==See Also==
==See Also==
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*[[Prion|Prion]]
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*[[Prion 3D structures|Prion 3D structures]]
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__TOC__
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==Reference==
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</StructureSection>
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<ref group="xtra">PMID:019684598</ref><references group="xtra"/><references/>
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[[Category: Cervus canadensis nelsoni]]
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[[Category: Apostol, M I.]]
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[[Category: Large Structures]]
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[[Category: Eisenberg, D.]]
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[[Category: Apostol MI]]
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[[Category: Amyloid-like protofibril]]
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[[Category: Eisenberg D]]
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[[Category: Cell membrane]]
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[[Category: Glycoprotein]]
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[[Category: Golgi apparatus]]
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[[Category: Gpi-anchor]]
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[[Category: Lipoprotein]]
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[[Category: Membrane]]
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[[Category: Prion]]
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[[Category: Protein fibril]]
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Current revision

NNQNTF segment from elk prion

PDB ID 3fva

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