6qh4: Difference between revisions
No edit summary |
No edit summary |
||
Line 3: | Line 3: | ||
<StructureSection load='6qh4' size='340' side='right'caption='[[6qh4]], [[Resolution|resolution]] 1.92Å' scene=''> | <StructureSection load='6qh4' size='340' side='right'caption='[[6qh4]], [[Resolution|resolution]] 1.92Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6qh4]] is a 4 chain structure with sequence from [ | <table><tr><td colspan='2'>[[6qh4]] 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=6QH4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6QH4 FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.922Å</td></tr> | ||
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CO:COBALT+(II)+ION'>CO</scene></td></tr> | |||
<tr id=' | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6qh4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6qh4 OCA], [https://pdbe.org/6qh4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6qh4 RCSB], [https://www.ebi.ac.uk/pdbsum/6qh4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6qh4 ProSAT]</span></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[ | [https://www.uniprot.org/uniprot/MCEE_HUMAN MCEE_HUMAN] Vitamin B12-unresponsive methylmalonic acidemia. Methylmalonyl-CoA epimerase deficiency (MCEED) [MIM:[https://omim.org/entry/251120 251120]: Autosomal recessive inborn error of amino acid metabolism, involving valine, threonine, isoleucine and methionine. This organic aciduria may present in the neonatal period with life-threatening metabolic acidosis, hyperammonemia, feeding difficulties, pancytopenia and coma. Note=The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:16752391</ref> | ||
== Function == | |||
[https://www.uniprot.org/uniprot/MCEE_HUMAN MCEE_HUMAN] | |||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Bailey HJ]] | |||
[[Category: Bailey | [[Category: Bountra C]] | ||
[[Category: Bountra | [[Category: Chaikuid A]] | ||
[[Category: Chaikuid | [[Category: Diaz-Saez L]] | ||
[[Category: Diaz-Saez | [[Category: Edwards AM]] | ||
[[Category: Edwards | [[Category: Froese DS]] | ||
[[Category: Froese | [[Category: Kennedy E]] | ||
[[Category: Kennedy | [[Category: Krysztofinska E]] | ||
[[Category: Krysztofinska | [[Category: Sorrell FJ]] | ||
[[Category: Sorrell | [[Category: Yue WW]] | ||
[[Category: Yue | |||