9h6l
From Proteopedia
(Difference between revisions)
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| - | '''Unreleased structure''' | ||
| - | + | ==Human B4GALNT1 in Complex with UDP== | |
| - | + | <StructureSection load='9h6l' size='340' side='right'caption='[[9h6l]], [[Resolution|resolution]] 2.67Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[9h6l]] is a 2 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=9H6L OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9H6L FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.674Å</td></tr> | |
| - | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ACY:ACETIC+ACID'>ACY</scene>, <scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=MN:MANGANESE+(II)+ION'>MN</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=UDP:URIDINE-5-DIPHOSPHATE'>UDP</scene></td></tr> |
| - | [[Category: Deane | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9h6l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9h6l OCA], [https://pdbe.org/9h6l PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9h6l RCSB], [https://www.ebi.ac.uk/pdbsum/9h6l PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9h6l ProSAT]</span></td></tr> |
| - | [[Category: Welland | + | </table> |
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/B4GN1_HUMAN B4GN1_HUMAN] Autosomal recessive spastic paraplegia type 26. The disease is caused by variants affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/B4GN1_HUMAN B4GN1_HUMAN] Involved in the biosynthesis of gangliosides GM2, GD2, GT2 and GA2 from GM3, GD3, GT3 and GA3, respectively.<ref>PMID:1601877</ref> <ref>PMID:7487055</ref> <ref>PMID:7890749</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Deane JE]] | ||
| + | [[Category: Welland JWJ]] | ||
Current revision
Human B4GALNT1 in Complex with UDP
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