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congenital disorder of glycosylation, type iv
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NGLY1
A complex between peptide:N-glycanase and two proteasome-linked proteins suggests a mechanism for the degradation of misfolded glycoproteins
The retrotranslocation protein Derlin-1 binds peptide:N-glycanase to the endoplasmic reticulum
Multiple modes of interaction of the deglycosylation enzyme, mouse peptide N-glycanase, with the proteasome
The AAA ATPase p97 links peptide N-glycanase to the endoplasmic reticulum-associated E3 ligase autocrine motility factor receptor
Hypothesis: a glycoprotein-degradation complex formed by protein-protein interaction involves cytoplasmic peptide:N-glycanase
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