6fm9

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m (Protected "6fm9" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6fm9 is ON HOLD
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==Crystal structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1)==
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<StructureSection load='6fm9' size='340' side='right' caption='[[6fm9]], [[Resolution|resolution]] 3.60&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6fm9]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6FM9 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6FM9 FirstGlance]. <br>
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Description:
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=P6L:(2S)-3-{[{[(2S)-2,3-DIHYDROXYPROPYL]OXY}(HYDROXY)PHOSPHORYL]OXY}-2-[(6E)-HEXADEC-6-ENOYLOXY]PROPYL+(8E)-OCTADEC-8-ENOATE'>P6L</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/UDP-N-acetylglucosamine--dolichyl-phosphate_N-acetylglucosaminephosphotransferase UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.8.15 2.7.8.15] </span></td></tr>
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<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=6fm9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6fm9 OCA], [http://pdbe.org/6fm9 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6fm9 RCSB], [http://www.ebi.ac.uk/pdbsum/6fm9 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6fm9 ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[[http://www.uniprot.org/uniprot/GPT_HUMAN GPT_HUMAN]] DPAGT1-CDG;Congenital myasthenic syndromes with glycosylation defect. 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.
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== Function ==
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[[http://www.uniprot.org/uniprot/GPT_HUMAN GPT_HUMAN]] Catalyzes the initial step in the synthesis of dolichol-P-P-oligosaccharides.
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__TOC__
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</StructureSection>
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[[Category: UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase]]
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[[Category: Arrowsmith, C H]]
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[[Category: Beeson, D]]
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[[Category: Belaya, K]]
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[[Category: Berridge, G]]
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[[Category: Bountra, C]]
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[[Category: Burgess-Brown, N]]
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[[Category: Carpenter, E P]]
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[[Category: Chalk, R]]
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[[Category: Chu, A]]
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[[Category: Dong, L]]
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[[Category: Dong, Y Y]]
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[[Category: Edwards, A M]]
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[[Category: Goubin, S]]
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[[Category: Kupinska, K]]
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[[Category: Mahajan, P]]
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[[Category: Mukhopadhyay, S]]
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[[Category: Pike, A C.W]]
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[[Category: Structural genomic]]
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[[Category: Tessitore, A]]
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[[Category: Wang, D]]
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[[Category: Congenital myasthenic syndrome 13]]
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[[Category: Integral membrane protein]]
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[[Category: Protein glycosylation]]
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[[Category: Sgc]]
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[[Category: Transferase]]

Revision as of 06:38, 28 February 2018

Crystal structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1)

6fm9, resolution 3.60Å

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