1yuo: Difference between revisions
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<StructureSection load='1yuo' size='340' side='right'caption='[[1yuo]], [[Resolution|resolution]] 1.95Å' scene=''> | <StructureSection load='1yuo' size='340' side='right'caption='[[1yuo]], [[Resolution|resolution]] 1.95Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1yuo]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[1yuo]] 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=1YUO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1YUO 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]] 1.95Å</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=1yuo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1yuo OCA], [https://pdbe.org/1yuo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1yuo RCSB], [https://www.ebi.ac.uk/pdbsum/1yuo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1yuo ProSAT]</span></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=1yuo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1yuo OCA], [https://pdbe.org/1yuo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1yuo RCSB], [https://www.ebi.ac.uk/pdbsum/1yuo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1yuo ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/UNG_HUMAN UNG_HUMAN] Defects in UNG are a cause of immunodeficiency with hyper-IgM type 5 (HIGM5) [MIM:[https://omim.org/entry/608106 608106]. A rare immunodeficiency syndrome characterized by normal or elevated serum IgM levels with absence of IgG, IgA, and IgE. It results in a profound susceptibility to bacterial infections.<ref>PMID:12958596</ref> <ref>PMID:15967827</ref> | |||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/UNG_HUMAN UNG_HUMAN] Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine. | |||
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Lanes O]] | |||
[[Category: Lanes | [[Category: Leiros I]] | ||
[[Category: Leiros | [[Category: Moe E]] | ||
[[Category: Moe | [[Category: Olufsen M]] | ||
[[Category: Olufsen | [[Category: Riise EK]] | ||
[[Category: Riise | [[Category: Smalas AO]] | ||
[[Category: Smalas | [[Category: Willassen NP]] | ||
[[Category: Willassen | |||