Structure of the lectin mannose 6-phosphate receptor homology (MRH) domain of glucosidase II, an enzyme that regulates glycoprotein folding quality control in the endoplasmic reticulum

Journal of Biological Chemistry

Volumn 288, Issue 23, 2013, Pages 16460-16475

  Olson, Linda J ^a   Orsi, Ramiro ^b   Alculumbre, Solana G ^b   Peterson, Francis C ^a   Stigliano, Ivan D ^b   Parodi, Armando J ^b   D'Alessio, Cecilia ^b,c   Dahms, Nancy M ^a  

^a MEDICAL COLLEGE OF WISCONSIN   (United States)

^b FUNDACIÓN INSTITUTO LELOIR   (Argentina)

^c UNIVERSIDAD DE BUENOS AIRES   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING POCKETS; CONSERVED RESIDUES; ENDOPLASMIC RETICULUM; ENZYMATIC ACTIVITIES; GLUCOSE RESIDUES; GLUCOSYLTRANSFERASES; NASCENT PROTEIN; THREE-DIMENSIONAL STRUCTURE;

CELL MEMBRANES; GLUCOSE; GLYCOPROTEINS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; TRIMMING;

PROTEINS;

ALPHA GLUCOSIDASE AB; GLUCOSIDASE; GLUCOSIDASE II ALPHA; GLUCOSIDASE II BETA; GLYCAN; GLYCOPROTEIN; GLYCOSIDASE; LECTIN; MANNOSE; MANNOSE 6 PHOSPHATASE RECEPTOR HOMOLOGY; N GLYCAN; SOMATOMEDIN B RECEPTOR; UNCLASSIFIED DRUG; URIDINE DIPHOSPHATE;

ARTICLE; BINDING AFFINITY; BINDING SITE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME ASSAY; ENZYME LOCALIZATION; ENZYME REGULATION; ESCHERICHIA COLI; IN VIVO STUDY; MOLECULAR DYNAMICS; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN FOLDING; PROTEIN PROTEIN INTERACTION; QUALITY CONTROL; RESIDUE ANALYSIS; SCHIZOSACCHAROMYCES POMBE;

ENDOPLASMIC RETICULUM (ER); GLUCOSIDASE II Β; GLYCOBIOLOGY; GLYCOPROTEIN; MRH DOMAIN; N-GLYCAN; NMR; STRUCTURAL BIOLOGY;

ALPHA-GLUCOSIDASES; CRYSTALLOGRAPHY, X-RAY; ENDOPLASMIC RETICULUM; GLYCOPROTEINS; MANNOSE; PROTEIN FOLDING; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; SCHIZOSACCHAROMYCES; SCHIZOSACCHAROMYCES POMBE PROTEINS;

EID: 84878756888     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.450239     Document Type: Article

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