Glycosylasparaginase

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*AGA α+β subunits
*AGA α+β subunits
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**[[1ayy]], [[2gaw]] – EmAGA α+β subunits – ''Elizabethkingia meningoseptica''<br />
 
-
**[[5v2i]], [[6dey]] – EmAGA α+β (mutant) subunits <br />
 
**[[1apy]] – hAGA + Nag + β-mannose - human<br />
**[[1apy]] – hAGA + Nag + β-mannose - human<br />
**[[1apz]] – hAGA + Nag + β-mannose + Asp<br />
**[[1apz]] – hAGA + Nag + β-mannose + Asp<br />
 +
**[[1ayy]], [[2gaw]] – EmAGA α+β subunits – ''Elizabethkingia meningoseptica''<br />
 +
**[[5v2i]], [[6dey]] – EmAGA α+β (mutant) subunits <br />
**[[2gl9]] – EmAGA α+β (mutant) subunits + Nag + Asn<br />
**[[2gl9]] – EmAGA α+β (mutant) subunits + Nag + Asn<br />
 +
**[[4r4y]] – EmAGA α+β (mutant) subunits + hydroxyl-Asn<br />
 +
**[[1pgs]] – EmAGA α+β subunits – ''Flavobacterium meningoseptica''<br />
*AGA precursor
*AGA precursor

Current revision

Structure of glycosylated human glycosylasparaginase α (magenta and cyan) and β (green and yellow) subunits complex with asparagine (PDB code 2gl9).

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3D structures of glycosylasparaginase

Updated on 09-April-2023

References

  1. Qian X, Guan C, Guo HC. A dual role for an aspartic acid in glycosylasparaginase autoproteolysis. Structure. 2003 Aug;11(8):997-1003. PMID:12906830
  2. Ikonen E, Peltonen L. Mutations causing aspartylglucosaminuria (AGU): a lysosomal accumulation disease. Hum Mutat. 1992;1(5):361-5. PMID:1301945 doi:http://dx.doi.org/10.1002/humu.1380010503
  3. Wang Y, Guo HC. Crystallographic snapshot of a productive glycosylasparaginase-substrate complex. J Mol Biol. 2007 Feb 9;366(1):82-92. Epub 2006 Sep 26. PMID:17157318 doi:10.1016/j.jmb.2006.09.051

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky

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