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==STRUCTURE OF GALACTOCEREBROSIDASE FROM MOUSE==
==STRUCTURE OF GALACTOCEREBROSIDASE FROM MOUSE==
<StructureSection load='3zr5' size='340' side='right' caption='[[3zr5]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
<StructureSection load='3zr5' size='340' side='right'caption='[[3zr5]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[3zr5]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Lk3_transgenic_mice Lk3 transgenic mice]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3ZR5 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3ZR5 FirstGlance]. <br>
<table><tr><td colspan='2'>[[3zr5]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3ZR5 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3ZR5 FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1&#8491;</td></tr>
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3zr6|3zr6]]</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr>
<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Galactosylceramidase Galactosylceramidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.46 3.2.1.46] </span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3zr5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3zr5 OCA], [https://pdbe.org/3zr5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3zr5 RCSB], [https://www.ebi.ac.uk/pdbsum/3zr5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3zr5 ProSAT]</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=3zr5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3zr5 OCA], [http://pdbe.org/3zr5 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=3zr5 RCSB], [http://www.ebi.ac.uk/pdbsum/3zr5 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=3zr5 ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/GALC_MOUSE GALC_MOUSE]] Defects in Galc are the cause of the 'twitcher' phenotype; an autosomal recessive leukodystrophy similar to the human disease (Krabbe disease). This deficiency results in the insufficient catabolism of several galactolipids that are important in the production of normal myelin.  
[https://www.uniprot.org/uniprot/GALC_MOUSE GALC_MOUSE] Defects in Galc are the cause of the 'twitcher' phenotype; an autosomal recessive leukodystrophy similar to the human disease (Krabbe disease). This deficiency results in the insufficient catabolism of several galactolipids that are important in the production of normal myelin.
== Function ==
== Function ==
[[http://www.uniprot.org/uniprot/GALC_MOUSE GALC_MOUSE]] Hydrolyzes the galactose ester bonds of galactosylceramide, galactosylsphingosine, lactosylceramide, and monogalactosyldiglyceride. Enzyme with very low activity responsible for the lysosomal catabolism of galactosylceramide, a major lipid in myelin, kidney and epithelial cells of small intestine and colon.<ref>PMID:8769874</ref>
[https://www.uniprot.org/uniprot/GALC_MOUSE GALC_MOUSE] Hydrolyzes the galactose ester bonds of galactosylceramide, galactosylsphingosine, lactosylceramide, and monogalactosyldiglyceride. Enzyme with very low activity responsible for the lysosomal catabolism of galactosylceramide, a major lipid in myelin, kidney and epithelial cells of small intestine and colon.<ref>PMID:8769874</ref>  
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== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Galactosylceramidase]]
[[Category: Large Structures]]
[[Category: Lk3 transgenic mice]]
[[Category: Mus musculus]]
[[Category: Cachon-Gonzalez, M B]]
[[Category: Cachon-Gonzalez MB]]
[[Category: Cox, T M]]
[[Category: Cox TM]]
[[Category: Deane, J E]]
[[Category: Deane JE]]
[[Category: Graham, S C]]
[[Category: Graham SC]]
[[Category: Kim, N N]]
[[Category: Kim NN]]
[[Category: Mcnair, R]]
[[Category: Mcnair R]]
[[Category: Read, R J]]
[[Category: Read RJ]]
[[Category: Stein, P E]]
[[Category: Stein PE]]
[[Category: Galc]]
[[Category: Glycosyl hydrolase]]
[[Category: Hydrolase]]
[[Category: Krabbe disease]]
[[Category: Lectin domain]]
[[Category: Tim barrel]]

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