8dda: Difference between revisions

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-'''Unreleased structure'''
-The entry 8dda is ON HOLD  until Paper Publication
+==Crystal structure of human aminoadipate semialdehyde synthase (AASS), lysine ketoglutarate reductase (LKR) domain==
+<StructureSection load='8dda' size='340' side='right'caption='[[8dda]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
-Authors: Muniz, J.R.C., Kopec, J., Rembeza, E., Burgess-Brown, N., Bountra, C., Yue, W.W.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[8dda]] is a 4 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=8DDA OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8DDA FirstGlance]. <br>
-Description: Crystal structure of human aminoadipate semialdehyde synthase (AASS), lysine ketoglutarate reductase (LKR) domain
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.4&#8491;</td></tr>
-[[Category: Unreleased Structures]]
+<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
-[[Category: Burgess-Brown, N]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8dda FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8dda OCA], [https://pdbe.org/8dda PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8dda RCSB], [https://www.ebi.ac.uk/pdbsum/8dda PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8dda ProSAT]</span></td></tr>
-[[Category: Yue, W.W]]
+</table>
-[[Category: Kopec, J]]
+== Disease ==
-[[Category: Rembeza, E]]
+[https://www.uniprot.org/uniprot/AASS_HUMAN AASS_HUMAN] Hyperlysinemia;Saccharopinuria. The disease is caused by mutations affecting the gene represented in this entry.  The protein represented in this entry is involved in disease pathogenesis. A selective decrease in mitochondrial NADP(H) levels due to NADK2 mutations causes a deficiency of NADPH-dependent mitochondrial enzymes, such as DECR1 and AASS.<ref>PMID:24847004</ref>
-[[Category: Muniz, J.R.C]]
+== Function ==
-[[Category: Bountra, C]]
+[https://www.uniprot.org/uniprot/AASS_HUMAN AASS_HUMAN] Bifunctional enzyme that catalyzes the first two steps in lysine degradation. The N-terminal and the C-terminal contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively.
+== References ==
+<references/>
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Bountra C]]
+[[Category: Burgess-Brown N]]
+[[Category: Kopec J]]
+[[Category: Muniz JRC]]
+[[Category: Rembeza E]]
+[[Category: Yue WW]]