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{{STRUCTURE_3tkb|  PDB=3tkb  |  SCENE=  }}
===crystal structure of human uracil-DNA glycosylase D183G/K302R mutant===
{{ABSTRACT_PUBMED_21959147}}


==Disease==
==crystal structure of human uracil-DNA glycosylase D183G/K302R mutant==
[[http://www.uniprot.org/uniprot/UNG_HUMAN UNG_HUMAN]] Defects in UNG are a cause of immunodeficiency with hyper-IgM type 5 (HIGM5) [MIM:[http://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>  
<StructureSection load='3tkb' size='340' side='right'caption='[[3tkb]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[3tkb]] 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=3TKB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3TKB FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.5&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=IMD:IMIDAZOLE'>IMD</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=3tkb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3tkb OCA], [https://pdbe.org/3tkb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3tkb RCSB], [https://www.ebi.ac.uk/pdbsum/3tkb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3tkb ProSAT]</span></td></tr>
</table>
== 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 ==
[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.


==Function==
==See Also==
[[http://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.
*[[DNA glycosylase 3D structures|DNA glycosylase 3D structures]]
 
== References ==
==About this Structure==
<references/>
[[3tkb]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3TKB OCA].
__TOC__
 
</StructureSection>
==Reference==
<ref group="xtra">PMID:021959147</ref><references group="xtra"/><references/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Uracil-DNA glycosylase]]
[[Category: Large Structures]]
[[Category: Assefa, N G.]]
[[Category: Assefa NG]]
[[Category: Moe, E.]]
[[Category: Moe E]]
[[Category: Niiranen, L.]]
[[Category: Niiranen L]]
[[Category: Smalas, A O.]]
[[Category: Smalas AO]]
[[Category: Willassen, N P.]]
[[Category: Willassen NP]]
[[Category: Alpha/beta protein]]
[[Category: Glycosidase]]
[[Category: Hydrolase]]

Latest revision as of 13:31, 14 March 2024

crystal structure of human uracil-DNA glycosylase D183G/K302R mutant

3tkb, resolution 1.50Å

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