8sue: Difference between revisions
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==Human asparagine synthetase (apo-ASNS)== | |||
<StructureSection load='8sue' size='340' side='right'caption='[[8sue]], [[Resolution|resolution]] 3.50Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[8sue]] 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=8SUE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8SUE FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.5Å</td></tr> | |||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8sue FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8sue OCA], [https://pdbe.org/8sue PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8sue RCSB], [https://www.ebi.ac.uk/pdbsum/8sue PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8sue ProSAT]</span></td></tr> | ||
[[Category: | </table> | ||
[[Category: | == Disease == | ||
[[Category: | [https://www.uniprot.org/uniprot/ASNS_HUMAN ASNS_HUMAN] Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome. The disease is caused by mutations affecting the gene represented in this entry. | ||
[[Category: | == Function == | ||
[[Category: | [https://www.uniprot.org/uniprot/ASNS_HUMAN ASNS_HUMAN] | ||
[[Category: | __TOC__ | ||
[[Category: | </StructureSection> | ||
[[Category: Takagi | [[Category: Homo sapiens]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: Alcaro S]] | |||
[[Category: Chaptal V]] | |||
[[Category: Coricello A]] | |||
[[Category: Gratteri C]] | |||
[[Category: Lupia A]] | |||
[[Category: Richards N]] | |||
[[Category: Takagi Y]] | |||
[[Category: Vos M]] | |||
[[Category: Zhu W]] | |||
Revision as of 11:05, 22 May 2024
Human asparagine synthetase (apo-ASNS)Human asparagine synthetase (apo-ASNS)
Structural highlights
DiseaseASNS_HUMAN Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome. The disease is caused by mutations affecting the gene represented in this entry. Function |
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