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Protein Page:
MGAT4C (human)

Overview
MGAT4C Glycosyltransferase that participates in the transfer of N-acetylglucosamine (GlcNAc) to the core mannose residues of N- linked glycans. Catalyzes the formation of the GlcNAcbeta1-4 branch on the GlcNAcbeta1-2Manalpha1-3 arm of the core structure of N-linked glycans. Essential for the production of tri- and tetra-antennary N-linked sugar chains. Does not catalyze the transfer of GlcNAc to the Manalpha1-6 arm to form GlcNAcBeta1-4Manalpha1-6 linkage ('GnT-VI' activity). Belongs to the glycosyltransferase 54 family. Note: This description may include information from UniProtKB.
Protein type: Membrane protein, integral; EC 2.4.1.145; Transferase
Cellular Component: Golgi membrane; integral to membrane
Molecular Function: alpha-1,3-mannosylglycoprotein 4-beta-N-acetylglucosaminyltransferase activity; metal ion binding
Biological Process: cellular protein metabolic process; protein amino acid N-linked glycosylation via asparagine; post-translational protein modification
Reference #:  Q9UBM8 (UniProtKB)
Alt. Names/Synonyms: Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C; GlcNAc-T IVc; GnT-IVc; GNTIVH; hGnT-IV-H; mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme C (putative); MGAT4C; MGT4C; N-acetylglucosaminyltransferase IV homolog; N-acetylglucosaminyltransferase IVc; N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase IVc; UDP-N-acetylglucosamine: alpha-1,3-D-mannoside beta-1,4-N-acetylglucosaminyltransferase IVc; UDP-N-acetylglucosamine:a-1,3-D-mannoside beta-1,4-N-acetylglucosaminyltransferase IV; UDP-N-acetylglucosamine:a-1,3-D-mannoside beta-1,4-N-acetylglucosaminyltransferase IV-homolog
Gene Symbols: MGAT4C
Molecular weight: 56,061 Da
Basal Isoelectric point: 8.28  Predict pI for various phosphorylation states
Select Structure to View Below

MGAT4C

Protein Structure Not Found.


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Modification Sites and Domains  

Modification Sites in Parent Protein, Orthologs, and Isoforms  
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 1 S77 VHTFKDLSNFsGAIN
0 2 S80-p FKDLSNFsGAINVTy
0 1 A82 DLSNFsGAINVTyRy
0 1 Y87-p sGAINVTyRyLAAtP
0 4 Y89-p AINVTyRyLAAtPLQ
0 3 T93-p TyRyLAAtPLQRKRY
0 1 Y178-p VIHAPEEyyPILDGL
0 1 Y179-p IHAPEEyyPILDGLK
0 1 T396-p IKKIKVNtGtEDRQN
0 1 T398-p KIKVNtGtEDRQNDI
  mouse

 
S77 VHTFKDLSNFSGTIN
S80 FKDLSNFSGTINVTY
T82 DLSNFSGTINVTYRY
Y87 SGTINVTYRYLAATP
Y89 TINVTYRYLAATPLQ
T93 TYRYLAATPLQRKRY
Y178 VIHAPEEYYPVLDGL
Y179 IHAPEEYYPVLDGLK
T396 IKKIKVNTGTEDRQN
T398 KIKVNTGTEDRQNDI
  rat

 
S92-p VHTFKDLsNFsGtIN
S95-p FKDLsNFsGtINVTY
T97-p DLsNFsGtINVTYRY
Y102 sGtINVTYRYLAAtP
Y104 tINVTYRYLAAtPLQ
T108-p TYRYLAAtPLQRKRY
Y193 VIHAPEEYYPVLDGL
Y194 IHAPEEYYPVLDGLK
T411 IKKIKVNTGTEDRQN
T413 KIKVNTGTEDRQNDI
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