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5lev
From Proteopedia
(Difference between revisions)
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1) (V264G mutant)== | |
| - | + | <StructureSection load='5lev' size='340' side='right' caption='[[5lev]], [[Resolution|resolution]] 3.20Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[5lev]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5LEV OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5LEV FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=UNL:UNKNOWN+LIGAND'>UNL</scene></td></tr> | |
| - | [[Category: | + | <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> |
| - | [[Category: | + | <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=5lev FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5lev OCA], [http://pdbe.org/5lev PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5lev RCSB], [http://www.ebi.ac.uk/pdbsum/5lev PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5lev ProSAT]</span></td></tr> |
| - | [[Category: | + | </table> |
| + | == Disease == | ||
| + | [[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. | ||
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/GPT_HUMAN GPT_HUMAN]] Catalyzes the initial step in the synthesis of dolichol-P-P-oligosaccharides. | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase]] | ||
| + | [[Category: Arrowsmith, C H]] | ||
| + | [[Category: Beeson, D]] | ||
| + | [[Category: Belaya, K]] | ||
| + | [[Category: Berridge, G]] | ||
| + | [[Category: Bountra, C]] | ||
[[Category: Burgess-Brown, N]] | [[Category: Burgess-Brown, N]] | ||
| - | [[Category: | + | [[Category: Carpenter, E P]] |
| + | [[Category: Chalk, R]] | ||
[[Category: Chu, A]] | [[Category: Chu, A]] | ||
| - | [[Category: | + | [[Category: Dong, L]] |
| - | [[Category: | + | [[Category: Dong, Y Y]] |
| - | [[Category: | + | [[Category: Edwards, A M]] |
| - | [[Category: | + | [[Category: Goubin, S]] |
[[Category: Kupinska, K]] | [[Category: Kupinska, K]] | ||
| - | [[Category: Dong, L]] | ||
| - | [[Category: Arrowsmith, C.H]] | ||
| - | [[Category: Chalk, R]] | ||
| - | [[Category: Dong, Y.Y]] | ||
[[Category: Mahajan, P]] | [[Category: Mahajan, P]] | ||
| + | [[Category: Mukhopadhyay, S]] | ||
| + | [[Category: Pike, A C.W]] | ||
| + | [[Category: Structural genomic]] | ||
[[Category: Tessitore, A]] | [[Category: Tessitore, A]] | ||
| - | [[Category: | + | [[Category: Wang, D]] |
| - | [[Category: | + | [[Category: Congenital myasthenic syndrome 13]] |
| - | [[Category: | + | [[Category: Integral membrane protein]] |
| - | [[Category: | + | [[Category: Protein glycosylation]] |
| + | [[Category: Sgc]] | ||
| + | [[Category: Transferase]] | ||
Revision as of 16:25, 2 January 2017
Crystal structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1) (V264G mutant)
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Categories: UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase | Arrowsmith, C H | Beeson, D | Belaya, K | Berridge, G | Bountra, C | Burgess-Brown, N | Carpenter, E P | Chalk, R | Chu, A | Dong, L | Dong, Y Y | Edwards, A M | Goubin, S | Kupinska, K | Mahajan, P | Mukhopadhyay, S | Pike, A C.W | Structural genomic | Tessitore, A | Wang, D | Congenital myasthenic syndrome 13 | Integral membrane protein | Protein glycosylation | Sgc | Transferase
