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Search term: Golgi membrane

Results 1 - 100 of 125 > >>
EC Number
Localization
Commentary
GeneOntology No.
Reference
D-mannitol oxidase
; membrane-bound; smooth membrane; tentatively identified as Golgi or plasma membrane
D-mannitol oxidase
associated with inner wall surrounding the lumen; membrane-bound
D-mannitol oxidase
membrane-bound
procollagen-proline 4-dioxygenase
-
glucuronoxylan 4-O-methyltransferase
low and medium membrane
glutamate formimidoyltransferase
formiminotransferase cyclodeaminase, 58K, is a peripherically associated Golgi protein, binding is tight but not dependent on presence of intact microtubules, association is likely to be mediated by a protein, dynamic component of the Golgi, a proportion of FTCD molecules cycles between the Golgi and earlier compartments of the secretory pathway
glutamate formimidoyltransferase
formiminotransferase cyclodeaminase, 58K, is associated with the cytoplasmic surface of the Golgi apparatus in vivo, cytoplasmically oriented peripheral membrane protein of the Golgi membranes
glutamate formimidoyltransferase
localized on Golgi membranes as well as on some potentially Golgi complex-derived vesicular structures
protein S-acyltransferase
DHHC2 is present in at least some areas of the endoplasmic reticulum and Golgi
protein S-acyltransferase
HIP14 resides on the Golgi and can be observed on cytoplasmic vesicles
protein S-acyltransferase
isozymes DHHC-2, -3, -7, -8, and -21
1-acylglycerophosphocholine O-acyltransferase
associated
1-acylglycerophosphocholine O-acyltransferase
associated with, catalytic domain of the enzyme is exposed to the cytosol rather than to lumen of the Golgi cisternae
1-acylglycerophosphocholine O-acyltransferase
Golgi membrane tubule formation can result from increasing the content of lysophospholipids in membranes, either by stimulation of a phospholipase A2 or by inhibition of an lysophosphatidylcholine acyltransferase. The two opposing enzyme activities may help to coordinately regulate Golgi membrane shape and tubule formation
sphingosine N-acyltransferase
low enzyme level
lysine N-acetyltransferase
catalytic site facing the lumen of the endoplasmic reticulum/endoplasmic reticulum Goli intermediate compartment (ER/ERGIC)
N-acetylneuraminate 7-O(or 9-O)-acetyltransferase
the enzyme is a multimembrane spanning protein with 13 transmembrane segments, the SGNH-like domain of CASD1 faces the Golgi lumen. The enzyme shows cytosolic and luminal orientation of its N- and C-terminus, respectively
histone acetyltransferase
catalytic site facing the lumen of the endoplasmic reticulum/endoplasmic reticulum Goli intermediate compartment (ER/ERGIC)
1-acylglycerol-3-phosphate O-acyltransferase
integral enzyme
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
-
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
the enzyme is a Golgi-resident type-II membrane protein. The transmembrane domain of enzyme GnTI is the major determinant for its cis/medial-Golgi localization, while the stem region of GnTI contributes predominately to homomeric and heteromeric protein complex formation
GDP-Man:Man1GlcNAc2-PP-dolichol alpha-1,3-mannosyltransferase
-
GDP-Man:Man1GlcNAc2-PP-dolichol alpha-1,3-mannosyltransferase
; colocalizes with guanosine diphosphatase
-
GDP-Man:Man1GlcNAc2-PP-dolichol alpha-1,3-mannosyltransferase
colocalizes with guanosine diphosphatase
xylosylprotein 4-beta-galactosyltransferase
-
mannotetraose 2-alpha-N-acetylglucosaminyltransferase
catalytic reaction takes place in the lumen of Golgi vesicles
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase
-
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase
the enzyme possesses a cytoplasmic domain, a transmembrane domain, and a Golgi lumenal catalytic domain
xyloglucan 4-glucosyltransferase
-
glucuronosyltransferase
low activity
lactosylceramide beta-1,3-galactosyltransferase
-
high-mannose-oligosaccharide beta-1,4-N-acetylglucosaminyltransferase
integral membrane protein, at least the catalytic center is on the luminal site of the vesicles
initiation-specific alpha-1,6-mannosyltransferase
Mnn9p, type II Golgi membrane protein
initiation-specific alpha-1,6-mannosyltransferase
ScMnn9p enzyme is a type II membrane proteins, possessing a short cytosolic N-terminal domain followed by a transmembrane domain that is required for anchoring to the Golgi membrane
1,3-beta-glucan synthase
inactive, latent enzyme form
beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase
-
beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase
beta4Gal-T1 is a trans-Golgi glycosyltransferase, Glyco-T, with a type II membrane protein topology, a short N-terminal cytoplasmic domain, a membrane-spanning region, as well as a stem and a C-terminal catalytic domain facing the trans-Golgi-lumen
polypeptide N-acetylgalactosaminyltransferase
specifically localized in
polygalacturonate 4-alpha-galacturonosyltransferase
associated with galacturonosyltransferase1 in a complex
ganglioside galactosyltransferase
-
3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase
-
3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase
;
glycoprotein 6-alpha-L-fucosyltransferase
-
type 1 galactoside alpha-(1,2)-fucosyltransferase
-
glycosaminoglycan galactosyltransferase
-
ceramide glucosyltransferase
integral membrane protein
ceramide glucosyltransferase
orientation to the cytosolic side
N-acetyl-beta-D-glucosaminide beta-(1,3)-galactosyltransferase
-
xyloglucan 6-xylosyltransferase
-
xyloglucan 6-xylosyltransferase
complex formation in vivo and potential physical interactions among three xylosyltransferases, XXT1, XXT2, and XXT5, and a glucan synthase, CSLC4 is shown in the Golgi membrane in Arabidopsis cells; complex formation in vivo and potential physical interactions among three xylosyltransferases, XXT1, XXT2, and XXT5, and a glucan synthase, CSLC4 is shown in the Golgi membrane in Arabidopsis cells; complex formation in vivo and potential physical interactions among three xylosyltransferases, XXT1, XXT2, and XXT5, and a glucan synthase, CSLC4 is shown in the Golgi membrane in Arabidopsis cells
beta-galactoside alpha-(2,6)-sialyltransferase
the enzyme is a Golgi type II transmembrane glycosyltransferase
beta-galactoside alpha-(2,6)-sialyltransferase
the enzyme is a Golgi type II transmembrane glycosyltransferase; the enzyme is a Golgi type II transmembrane glycosyltransferase
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase
less than 4% of sialyltransferase activity
N-acetyllactosaminide alpha-2,3-sialyltransferase
-
N-acetyllactosaminide alpha-2,3-sialyltransferase
;
alpha-N-acetylneuraminyl-2,3-beta-galactosyl-1,3-N-acetylgalactosaminide 6-alpha-sialyltransferase
the enzyme is a Golgi type II transmembrane glycosyltransferase; the enzyme is a Golgi type II transmembrane glycosyltransferase; the enzyme is a Golgi type II transmembrane glycosyltransferase; the enzyme is a Golgi type II transmembrane glycosyltransferase
lactosylceramide alpha-2,3-sialyltransferase
-
1-phosphatidylinositol 4-kinase
-
1-phosphatidylinositol 4-kinase
isozyme PI4KIIIbeta
1-phosphatidylinositol 4-kinase
isozyme Pik1
non-specific serine/threonine protein kinase
coexpression of PAK4 and the constitutively active Cdc42HsV12 causes the redistribution of PAK4 to the brefeldin A-sensitive compartment of the Golgi membrane and the subsequent induction of filopodia and actin polymerization
Ca2+/calmodulin-dependent protein kinase
-
Ca2+/calmodulin-dependent protein kinase
anchored, perinuclear Golgi-like membranes
UTP-glucose-1-phosphate uridylyltransferase
-
UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase
integral membrane protein
sphingomyelin synthase
isozyme SMS1
sphingomyelin synthase
SMS1
ceramide ethanolamine phosphotransferase
the enzyme resides in the Golgi complex with its active site facing the lumen
galactosylceramide sulfotransferase
major part of the enzyme, the enzyme contains a transmembrane domain
protein-tyrosine sulfotransferase
trans-most subcompartment
protein-tyrosine sulfotransferase
type II transmembrane isozymes
phosphoinositide 5-phosphatase
cytoplasmic Golgi membrane
phosphatidate phosphatase
enzyme form Lpp1
diacylglycerol diphosphate phosphatase
-
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
a transmembrane enzyme
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
cis part
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
cis/medial golgi
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
mainly localized to the trans-Golgi network, cycles between the network and the plasma membrane, type I transmembrane glycoprotein, containing a 24-amino acid signal sequence, a luminal domain of 423 residues, a 27-residue transmembrane region and a 41-residue cytoplasmic tail
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
resides in the trans-Golgi network and cycles between the network and plasma membrane, type I membrane-spanning glycoprotein with a single 27-residue transmembrane domain and a 41-residue cytoplasmic tail
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
UCE is a type I homotetrameric transmembrane glycoprotein that is mainly localized to the trans-Golgi network. The signal sequence is excised in the endoplasmic reticulum and upon folding, the catalytically inactive protein is transported to the trans-Golgi network where it is activated by furin cleavage of the prosequence
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
with a transmembrane segment and a 41-residue cytoplasmic tail, resides primarily in the trans-Golgi network and cycles constitutively between the network and the plasma membrane, regulation of enzyme trafficking by multiple signals, e.g. the 486-YAYHPLQE-493 motif, which is recognized at several sorting sites and facilitates exit from the trans-Golgi network
mannosyl-oligosaccharide 1,2-alpha-mannosidase
-
mannosyl-oligosaccharide 1,2-alpha-mannosidase
cis-Golgi
mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase
alpha-mannosidase III, integral membrane glycoprotein with type II topology
mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase
integral membrane protein, hydrophilic catalytic domain is anchored to the lumenal face of Golgi membranes through an NH2-terminal hydrophobic membrane-anchoring domain
mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase
liver
mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase
topology study: integral membrane protein with lumenal orientation, hydrophilic catalytic domain is bound to an integral hydrophobic membrane anchoring domain through a proteolytically sensitive linkage
mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase
type II membrane protein, alpha-mannosidase II and IIx
mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase
type II transmembrane enzyme, subcompartmental localization, mainly over medial saccules of the Golgi stack
mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase
type II transmembrane protein with short cytoplasmic tail, single transmembrane domain and large C-terminal catalytic domain
glycoprotein endo-alpha-1,2-mannosidase
;
-
Results 1 - 100 of 125 > >>