4xwh
From Proteopedia
(Difference between revisions)
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| - | ''' | + | ==Crystal structure of the human N-acetyl-alpha-glucosaminidase== |
| - | + | <StructureSection load='4xwh' size='340' side='right' caption='[[4xwh]], [[Resolution|resolution]] 2.32Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[4xwh]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4XWH OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4XWH FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=XYL:D-XYLITOL'>XYL</scene></td></tr> | |
| - | + | <tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=NEP:N1-PHOSPHONOHISTIDINE'>NEP</scene></td></tr> | |
| - | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Alpha-N-acetylglucosaminidase Alpha-N-acetylglucosaminidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.50 3.2.1.50] </span></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=4xwh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4xwh OCA], [http://pdbe.org/4xwh PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4xwh RCSB], [http://www.ebi.ac.uk/pdbsum/4xwh PDBsum]</span></td></tr> |
| - | [[Category: | + | </table> |
| + | == Disease == | ||
| + | [[http://www.uniprot.org/uniprot/ANAG_HUMAN ANAG_HUMAN]] Sanfilippo syndrome type B. 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/ANAG_HUMAN ANAG_HUMAN]] Involved in the degradation of heparan sulfate. | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Alpha-N-acetylglucosaminidase]] | ||
[[Category: Birrane, G]] | [[Category: Birrane, G]] | ||
[[Category: Dassier, A]] | [[Category: Dassier, A]] | ||
| + | [[Category: Meiyappan, M]] | ||
| + | [[Category: Glycosidase]] | ||
| + | [[Category: Hydrolase]] | ||
Revision as of 15:50, 3 February 2016
Crystal structure of the human N-acetyl-alpha-glucosaminidase
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