2n6d

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m (Protected "2n6d" [edit=sysop:move=sysop])
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'''Unreleased structure'''
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==NMR structure of the 140-315 fragment of the N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits==
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<StructureSection load='2n6d' size='340' side='right' caption='[[2n6d]], [[NMR_Ensembles_of_Models | 19 NMR models]]' scene=''>
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The entry 2n6d is ON HOLD
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== Structural highlights ==
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<table><tr><td colspan='2'>[[2n6d]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2N6D OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2N6D FirstGlance]. <br>
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Authors: Serrano, P., Geralt, M., Wuthrich, K., Joint Center for Structural Genomics (JCSG)
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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=2n6d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2n6d OCA], [http://pdbe.org/2n6d PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2n6d RCSB], [http://www.ebi.ac.uk/pdbsum/2n6d PDBsum]</span></td></tr>
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</table>
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Description: NMR structure of the 140-315 fragment of the N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
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== Disease ==
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[[Category: Unreleased Structures]]
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[[http://www.uniprot.org/uniprot/GNPTA_HUMAN GNPTA_HUMAN]] Mucolipidosis type 2;Mucolipidosis type 3. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. Defects in GNPTAB have been suggested to play a role in susceptibility to persistent stuttering. Stuttering is a common speech disorder characterized by repetitions, prolongations, and interruptions in the flow of speech.<ref>PMID:20147709</ref>
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[[Category: Wuthrich, K]]
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== Function ==
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[[Category: Serrano, P]]
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[[http://www.uniprot.org/uniprot/GNPTA_HUMAN GNPTA_HUMAN]] Catalyzes the formation of mannose 6-phosphate (M6P) markers on high mannose type oligosaccharides in the Golgi apparatus. M6P residues are required to bind to the M6P receptors (MPR), which mediate the vesicular transport of lysosomal enzymes to the endosomal/prelysosomal compartment.<ref>PMID:19955174</ref> <ref>PMID:23733939</ref>
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[[Category: Joint Center For Structural Genomics (Jcsg)]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Geralt, M]]
[[Category: Geralt, M]]
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[[Category: Structural genomic]]
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[[Category: Serrano, P]]
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[[Category: Wuthrich, K]]
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[[Category: N-acetylglucosamine-1-phosphate transferase]]
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[[Category: Psi-biology]]
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[[Category: Transferase]]

Revision as of 04:00, 16 October 2015

NMR structure of the 140-315 fragment of the N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits

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