Two N-glycosylation sites in the GluN1 subunit are essential for releasing N-methyl-D-aspartate (NMDA) receptors from the endoplasmic reticulum

Journal of Biological Chemistry

Volumn 290, Issue 30, 2015, Pages 18379-18390

  Lichnerova, Katarina ^a,b   Kaniakova, Martina ^a   Park, Seung Pyo ^c   Skrenkova, Kristyna ^a   Wang, Ya Xian ^d   Petralia, Ronald S ^d   Suh, Young Ho ^c   Horak, Martin ^a  

^a INSTITUTE OF PHYSIOLOGY   (Czech Republic)

^b CHARLES UNIVERSITY   (Czech Republic)

^c Seoul National University College of Medicine   (South Korea)

^d NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; ELECTROPHYSIOLOGY;

ASPARAGINE RESIDUE; ENDOPLASMIC RETICULUM; INTRACELLULAR TRAFFICKING; MOLECULAR REPLACEMENTS; N-GLYCOSYLATION SITES; N-METHYL-D-ASPARTATE; POST-TRANSLATIONAL MODIFICATIONS; SURFACE EXPRESSION;

GLYCOSYLATION;

ASPARAGINE; CELL PROTEIN; GLUN1 PROTEIN; GLUTAMIC ACID; LENTIVIRUS VECTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; UNCLASSIFIED DRUG; N METHYLASPARTIC ACID; POLYSACCHARIDE;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CONFOCAL MICROSCOPY; ELECTRON MICROSCOPY; ELECTROPHYSIOLOGICAL PROCEDURES; ENDOPLASMIC RETICULUM; HUMAN; HUMAN CELL; NERVE CELL; NONHUMAN; POSTSYNAPTIC MEMBRANE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN GLYCOSYLATION; PROTEIN SECRETION; PROTEIN SUBUNIT; PROTEIN TRANSPORT; RAT; RECEPTOR AFFINITY; RECEPTOR UPREGULATION; REGULATORY MECHANISM; ANIMAL; CHEMISTRY; CHLOROCEBUS AETHIOPS; COS 1 CELL LINE; GLYCOSYLATION; GOLGI COMPLEX; HEK293 CELL LINE; METABOLISM; SYNAPSE; SYNAPTIC TRANSMISSION;

LENTIVIRUS;

ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; ENDOPLASMIC RETICULUM; GLYCOSYLATION; GOLGI APPARATUS; HEK293 CELLS; HUMANS; N-METHYLASPARTATE; NEURONS; POLYSACCHARIDES; RATS; RECEPTORS, N-METHYL-D-ASPARTATE; SYNAPSES; SYNAPTIC TRANSMISSION;

EID: 84937684236     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M115.656546     Document Type: Article

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