+ |
SLC2A1 | form complex
binding
|
Ankyrin complex |
0.306 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266017 |
|
|
Homo sapiens |
Erythrocyte |
pmid |
sentence |
22465511 |
The ankyrin associated complex brings together proteins of both the band 3 tetrameric complex (band 3, glycophorin A (GPA), protein 4.2, carbonic anhydrase II) and the Rh complex (RhAG, RhCE, RhD, CD47, ICAM-4, glycophorin B (GPB)) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TP53 | down-regulates quantity by repression
transcriptional regulation
|
SLC2A1 |
0.585 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267464 |
|
|
Homo sapiens |
|
pmid |
sentence |
27692180 |
P53 regulates basal expression of AIF and SCO2 and facilitates oxidative phosphorylation. The expression of GLUT1, GLUT4, and HK2 is negatively regulated by p53, whereas TIGAR expression is induced by p53. The net result of p53-mediated regulation of these glycolytic enzymes is the suppression of glycolysis. In addition, p53 directly binds and inhibits G6PD activity and downregulates the pentose phosphate pathway. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Glycolysis and Gluconeogenesis |
+ |
MYC | up-regulates quantity
transcriptional regulation
|
SLC2A1 |
0.442 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259987 |
|
|
Rattus norvegicus |
|
pmid |
sentence |
10823814 |
C-Myc directly transactivates genes encoding GLUT1, phosphofructokinase, and enolase and increases glucose uptake in Rat1 fibroblasts. Nuclear run-on studies confirmed that the GLUT1 transcriptional rate is elevated by c-Myc. Our findings suggest that overexpression of the c-Myc oncoprotein deregulates glycolysis through the activation of several components of the glucose metabolic pathway. |
|
Publications: |
1 |
Organism: |
Rattus Norvegicus |
+ |
YAP1 | up-regulates quantity by expression
transcriptional regulation
|
SLC2A1 |
0.263 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276584 |
|
|
|
|
pmid |
sentence |
30348863 |
Transcriptomic and metabolomic analyses reveal that Yap regulates expression of glucose transporter glut1, causing decreased glucose uptake and use for nucleotide biosynthesis in yap-/- mutants, and impaired glucose tolerance in adults. |
|
Publications: |
1 |
+ |
SLC2A1 | up-regulates quantity
relocalization
|
glucose |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267460 |
|
|
Homo sapiens |
|
pmid |
sentence |
23506862 |
GLUT1 plays a critical role in cerebral glucose uptake as the major GLUT isoform expressed in brain endothelial cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SP1 | up-regulates quantity by expression
transcriptional regulation
|
SLC2A1 |
0.367 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-241485 |
|
|
Mus musculus |
|
pmid |
sentence |
9148896 |
These data suggest a regulatory model in which MyoD activation during myogenesis causes the down-regulation of Sp1, which contributes to the repression of GLUT1 gene transcription and, therefore, leads to the reduction in GLUT1 expression and glucose transport. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
AKT1 | up-regulates quantity by expression
transcriptional regulation
|
SLC2A1 |
0.565 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252579 |
|
|
Homo sapiens |
|
pmid |
sentence |
8940145 |
The constitutively active akt also increased the synthesis of the ubiquitously expressed glucose transporter 1. The increased glucose influx in the 3t3-l1 adipocytes directed lipid but not glycogen synthesis |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SLC2A1 | up-regulates quantity
relocalization
|
α-D-glucose |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267458 |
|
|
Homo sapiens |
|
pmid |
sentence |
23506862 |
GLUT1 plays a critical role in cerebral glucose uptake as the major GLUT isoform expressed in brain endothelial cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Glycolysis and Gluconeogenesis |
+ |
AKT | up-regulates quantity by expression
transcriptional regulation
|
SLC2A1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-45064 |
|
|
Homo sapiens |
|
pmid |
sentence |
8940145 |
The constitutively active akt also increased the synthesis of the ubiquitously expressed glucose transporter 1. The increased glucose influx in the 3t3-l1 adipocytes directed lipid but not glycogen synthesis |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Glycolysis and Gluconeogenesis |
+ |
SLC2A1 | form complex
binding
|
4.1 complex |
0.37 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266038 |
|
|
Homo sapiens |
Erythrocyte |
pmid |
sentence |
33187473 |
The cytoskeleton plays a key role in maintaining the morphology and function of erythrocyte membranes. Many proteins, such as ankyrin, spectrin alpha- and beta-chains, proteins 4.1, or 4.1R and actin, cover the inner surface of the erythrocyte membrane to form two protein complexes, the ankyrin and protein 4.1 complex| the latter consists of Band 3 dimers binding Adducins alpha and beta, Glycophorin C, GLUT1 and Stomatin [15, 16] |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIF-1 complex | up-regulates quantity
transcriptional regulation
|
SLC2A1 |
0.422 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267478 |
|
|
Rattus norvegicus |
|
pmid |
sentence |
11120745 |
Collectively these results indicate that H-Ras up-regulates the glut1 promoter, at least in part, by increasing HIF-1alpha protein levels leading to transactivation of promoter through the HIF-1 binding site. |
|
Publications: |
1 |
Organism: |
Rattus Norvegicus |
Pathways: | Glycolysis and Gluconeogenesis |
+ |
HIF-1 complex | up-regulates quantity by expression
transcriptional regulation
|
SLC2A1 |
0.422 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267450 |
|
|
Homo sapiens |
|
pmid |
sentence |
27692180 |
HIF-1 promotes glycolysis by transcriptionally upregulating GLUT1, GLUT3, HK1, and HK2. HIF-1 also suppresses oxidative phosphorylation by the upregulation of gene expression of BNIP3, BNIP3L, LDHA, and PDK1. In addition, HIF-1 can inhibit apoptosis by suppressing the expression of BID. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Glycolysis and Gluconeogenesis |
+ |
STOM | down-regulates activity
binding
|
SLC2A1 |
0.543 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261278 |
|
|
Homo sapiens |
|
pmid |
sentence |
10562431 |
Similar to the results obtained in the RBC, Glut1 and stomatin immunoprecipitated with each other in lysates of Clone 9 cells. The above results suggest that stomatin is closely associated with Glut1 in the plasma membrane and that overexpression of stomatin results in a depression in the basal rate of glucose transport. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |