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Protein Page:
GLUT11 (human)
p Phosphorylation
ac Acetylation
me Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
ub Ubiquitination
sm Sumoylation
ne Neddylation
gl O-GlcNAc
ga O-GalNAc
pa Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage
sc Succinylation

Overview
GLUT11 an integral membrane facilitative glucose transporter. One of 13 members of the human equilibrative glucose transport protein family. Three isoforms of the human protein are produced by alternative splicing due to three different first exons that code for three different N-termini of 7, 14 and 10 amino acids. Exon 1-c encodes a dileucine motif that may influence its subcellular localization. Note: This description may include information from UniProtKB.
Protein type: Membrane protein, multi-pass; Membrane protein, integral; Transporter, SLC family; Transporter
Cellular Component: integral to membrane; plasma membrane
Molecular Function: substrate-specific transmembrane transporter activity
Biological Process: carbohydrate transport; transmembrane transport
Reference #:  Q9BYW1 (UniProtKB)
Alt. Names/Synonyms: facilitative glucose transporter GLUT11; glucose transporter protein 10; glucose transporter protein 11; Glucose transporter type 10; Glucose transporter type 11; glucose transporter-like protein XI; GLUT-10; GLUT-11; GLUT10; GLUT11; GTR11; MGC118830; MGC118833; SLC2A11; SLC2A11-a; SLC2A11-c; solute carrier family 2 (facilitated glucose transporter), member 11; Solute carrier family 2, facilitated glucose transporter member 11
Gene Symbols: SLC2A11
Molecular weight: 53,703 Da
Basal Isoelectric point: 8.57  Predict pI for various phosphorylation states
CST Pathways:  Warburg Effect
Select Structure to View Below

GLUT11

Protein Structure Not Found.


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Modification Sites and Domains Show Modification Legend
Click here to view phosphorylation modifications only

Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

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 T16-p QGRILLLtICAAGIG
0 1 Y74-p WSLIVSLyPLGGLFG
0 1 K117-ub ILFGFSRkAGSFEMI
0 1 T484-p PRRAQGPtWRSLEVI
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