6i34: Difference between revisions

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New page: '''Unreleased structure''' The entry 6i34 is ON HOLD Authors: Van Laer, B., Kapp, U., Leonard, G., Mueller-Dieckmann, C. Description: Crystal structure of Neanderthal glycine decarboxy...
 
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'''Unreleased structure'''


The entry 6i34 is ON HOLD
==Crystal structure of Neanderthal glycine decarboxylase (P-protein)==
 
<StructureSection load='6i34' size='340' side='right'caption='[[6i34]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
Authors: Van Laer, B., Kapp, U., Leonard, G., Mueller-Dieckmann, C.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[6i34]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens_neanderthalensis Homo sapiens neanderthalensis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6I34 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6I34 FirstGlance]. <br>
Description: Crystal structure of Neanderthal glycine decarboxylase (P-protein)
</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>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene>, <scene name='pdbligand=PLP:PYRIDOXAL-5-PHOSPHATE'>PLP</scene></td></tr>
[[Category: Kapp, U]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6i34 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6i34 OCA], [https://pdbe.org/6i34 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6i34 RCSB], [https://www.ebi.ac.uk/pdbsum/6i34 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6i34 ProSAT]</span></td></tr>
[[Category: Van Laer, B]]
</table>
[[Category: Mueller-Dieckmann, C]]
== Disease ==
[[Category: Leonard, G]]
[https://www.uniprot.org/uniprot/GCSP_HUMAN GCSP_HUMAN] Atypical glycine encephalopathy;Infantile glycine encephalopathy;Neonatal glycine encephalopathy. The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/GCSP_HUMAN GCSP_HUMAN] The glycine cleavage system catalyzes the degradation of glycine. The P protein (GLDC) binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein (GCSH).<ref>PMID:1993704</ref> <ref>PMID:1996985</ref> <ref>PMID:28244183</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens neanderthalensis]]
[[Category: Large Structures]]
[[Category: Kapp U]]
[[Category: Leonard G]]
[[Category: Mueller-Dieckmann C]]
[[Category: Van Laer B]]