9ud7: Difference between revisions
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==Crystal structure of human glutaminyl cyclase in complex with Inhibitor CL7== | |||
<StructureSection load='9ud7' size='340' side='right'caption='[[9ud7]], [[Resolution|resolution]] 2.49Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[9ud7]] is a 6 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=9UD7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9UD7 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]] 2.49Å</td></tr> | |||
[[Category: | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1EOY:6-[(5-methylimidazol-1-yl)methyl]-3-phenyl-1~{H}-pyridin-2-one'>A1EOY</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=TRS:2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL'>TRS</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></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=9ud7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9ud7 OCA], [https://pdbe.org/9ud7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9ud7 RCSB], [https://www.ebi.ac.uk/pdbsum/9ud7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9ud7 ProSAT]</span></td></tr> | ||
[[Category: Chen | </table> | ||
[[Category: Meng | == Function == | ||
[[Category: Ning | [https://www.uniprot.org/uniprot/QPCT_HUMAN QPCT_HUMAN] Responsible for the biosynthesis of pyroglutamyl peptides. Has a bias against acidic and tryptophan residues adjacent to the N-terminal glutaminyl residue and a lack of importance of chain length after the second residue. Also catalyzes N-terminal pyroglutamate formation. In vitro, catalyzes pyroglutamate formation of N-terminally truncated form of APP amyloid-beta peptides [Glu-3]-beta-amyloid. May be involved in the N-terminal pyroglutamate formation of several amyloid-related plaque-forming peptides.<ref>PMID:15063747</ref> <ref>PMID:18486145</ref> <ref>PMID:21288892</ref> | ||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Chen Y-T]] | |||
[[Category: Li G-B]] | |||
[[Category: Meng F-B]] | |||
[[Category: Ning X-L]] | |||
Latest revision as of 06:31, 8 April 2026
Crystal structure of human glutaminyl cyclase in complex with Inhibitor CL7
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