9bum
From Proteopedia
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			 (New page: '''Unreleased structure'''  The entry 9bum is ON HOLD   Authors:   Description:  Category: Unreleased Structures)  | 
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| - | '''Unreleased structure'''  | ||
| - | The entry   | + | ==Structure of r-glutamyl carboxylase (GGCX)==  | 
| - | + | <StructureSection load='9bum' size='340' side='right'caption='[[9bum]], [[Resolution|resolution]] 3.63Å' scene=''>  | |
| - | + | == Structural highlights ==  | |
| - | + | <table><tr><td colspan='2'>[[9bum]] is a 1 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=9BUM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9BUM 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]] 3.63Å</td></tr>  | |
| - | [[Category:   | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CLR:CHOLESTEROL'>CLR</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></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=9bum FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9bum OCA], [https://pdbe.org/9bum PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9bum RCSB], [https://www.ebi.ac.uk/pdbsum/9bum PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9bum ProSAT]</span></td></tr>  | ||
| + | </table>  | ||
| + | == Disease ==  | ||
| + | [https://www.uniprot.org/uniprot/VKGC_HUMAN VKGC_HUMAN] Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa;Hereditary combined deficiency of vitamin K-dependent clotting factors;Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency. The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  | ||
| + | == Function ==  | ||
| + | [https://www.uniprot.org/uniprot/VKGC_HUMAN VKGC_HUMAN] Mediates the vitamin K-dependent carboxylation of glutamate residues to calcium-binding gamma-carboxyglutamate (Gla) residues with the concomitant conversion of the reduced hydroquinone form of vitamin K to vitamin K epoxide (PubMed:17073445). Catalyzes gamma-carboxylation of various proteins, such as blood coagulation factors (F2, F7, F9 and F10), osteocalcin (BGLAP) or matrix Gla protein (MGP) (PubMed:17073445).<ref>PMID:17073445</ref>   | ||
| + | == References ==  | ||
| + | <references/>  | ||
| + | __TOC__  | ||
| + | </StructureSection>  | ||
| + | [[Category: Homo sapiens]]  | ||
| + | [[Category: Large Structures]]  | ||
| + | [[Category: Qi X]]  | ||
| + | [[Category: Wang R]]  | ||
Current revision
Structure of r-glutamyl carboxylase (GGCX)
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