The 17-residue transmembrane domain of beta-galactoside alpha 2,6-sialyltransferase is sufficient for Golgi retention.
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Golgi retention mechanism of beta-1,4-galactosyltransferase. Membrane-spanning domain-dependent homodimerization and association with alpha- and beta-tubulinsEndobrevin, a novel synaptobrevin/VAMP-like protein preferentially associated with the early endosomeLocalization of human heparan glucosaminyl N-deacetylase/N-sulphotransferase to the trans-Golgi networkMutational analysis of the human KDEL receptor: distinct structural requirements for Golgi retention, ligand binding and retrograde transportTwo independent targeting signals in the cytoplasmic domain determine trans-Golgi network localization and endosomal trafficking of the proprotein convertase furinAn investigation of the role of transmembrane domains in Golgi protein retentionThe single transmembrane segment of gp210 is sufficient for sorting to the pore membrane domain of the nuclear envelopeGS32, a novel Golgi SNARE of 32 kDa, interacts preferentially with syntaxin 6The amino-terminal domain of the lamin B receptor is a nuclear envelope targeting signalLocalization and targeting of the Saccharomyces cerevisiae Kre2p/Mnt1p alpha 1,2-mannosyltransferase to a medial-Golgi compartmentAltered Golgi localization of core 2 beta-1,6-N-acetylglucosaminyltransferase leads to decreased synthesis of branched O-glycansSyntaxin 7, a novel syntaxin member associated with the early endosomal compartmentConserved oligomeric Golgi complex specifically regulates the maintenance of Golgi glycosylation machinery.The Golgi localization of GOLPH2 (GP73/GOLM1) is determined by the transmembrane and cytoplamic sequences.GO-PROMTO illuminates protein membrane topologies of glycan biosynthetic enzymes in the Golgi apparatus of living tissues.Retrieval of human cytomegalovirus glycoprotein B from cell surface is not required for virus envelopment in astrocytoma cellsRetention of a cis Golgi protein requires polar residues on one face of a predicted alpha-helix in the transmembrane domain.Divergent fates of P- and E-selectins after their expression on the plasma membrane.Sorting of yeast alpha 1,3 mannosyltransferase is mediated by a lumenal domain interaction, and a transmembrane domain signal that can confer clathrin-dependent Golgi localization to a secreted protein.The first transmembrane domain of lipid phosphatase SAC1 promotes Golgi localization.Overlapping distribution of two glycosyltransferases in the Golgi apparatus of HeLa cellsOligomerization of a membrane protein correlates with its retention in the Golgi complexTargeting of protein ERGIC-53 to the ER/ERGIC/cis-Golgi recycling pathwaytrans-Golgi retention of a plasma membrane protein: mutations in the cytoplasmic domain of the asialoglycoprotein receptor subunit H1 result in trans-Golgi retention.Sorting signals in the MHC class II invariant chain cytoplasmic tail and transmembrane region determine trafficking to an endocytic processing compartment.Evolution of protein N-glycosylation process in Golgi apparatus which shapes diversity of protein N-glycan structures in plants, animals and fungiE5 oncoprotein retained in the endoplasmic reticulum/cis Golgi still induces PDGF receptor autophosphorylation but does not transform cellsIsolation and characterization of krp, a dibasic endopeptidase required for cell viability in the fission yeast Schizosaccharomyces pombe.Mechanisms of protein retention in the Golgi.Heterologous expression of WT and mutant photoreceptor peripherin/rds in Madin Darby canine kidney cells: an assessment of fusogenic function.Mutation of a tyrosine localization signal in the cytosolic tail of yeast Kex2 protease disrupts Golgi retention and results in default transport to the vacuole.Specificity and promiscuity in membrane helix interactions.Kin recognition between medial Golgi enzymes in HeLa cells.Kex2-dependent invertase secretion as a tool to study the targeting of transmembrane proteins which are involved in ER-->Golgi transport in yeastTGN38 is maintained in the trans-Golgi network by a tyrosine-containing motif in the cytoplasmic domainThe cytoplasmic, transmembrane, and stem regions of glycosyltransferases specify their in vivo functional sublocalization and stability in the Golgi.Oligomerization of a trans-Golgi/trans-Golgi network retained protein occurs in the Golgi complex and may be part of its retention.A signal for endoplasmic reticulum retention located at the carboxyl terminus of the plasma membrane Ca(2+)-ATPase isoform 4CI.Regulation of targeting signals in membrane proteins. [review]The first membrane spanning region of the lamin B receptor is sufficient for sorting to the inner nuclear membrane.
P2860
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P2860
The 17-residue transmembrane domain of beta-galactoside alpha 2,6-sialyltransferase is sufficient for Golgi retention.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
The 17-residue transmembrane d ...... ufficient for Golgi retention.
@ast
The 17-residue transmembrane d ...... ufficient for Golgi retention.
@en
type
label
The 17-residue transmembrane d ...... ufficient for Golgi retention.
@ast
The 17-residue transmembrane d ...... ufficient for Golgi retention.
@en
prefLabel
The 17-residue transmembrane d ...... ufficient for Golgi retention.
@ast
The 17-residue transmembrane d ...... ufficient for Golgi retention.
@en
P2093
P2860
P356
P1476
The 17-residue transmembrane d ...... ufficient for Golgi retention.
@en
P2093
P2860
P304
P356
10.1083/JCB.117.2.245
P407
P577
1992-04-01T00:00:00Z