+ |
PKN1 | up-regulates
phosphorylation
|
PGM1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-128722 |
Thr467 |
SANDKVYtVEKADNF |
Homo sapiens |
Leukemia Cell |
pmid |
sentence |
15378030 |
Pak1-mediated phosphorylation of pgm selectively on threonine 466 significantly increased pgm enzymatic activity |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PAK1 | up-regulates
phosphorylation
|
PGM1 |
0.349 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-127135 |
Thr467 |
SANDKVYtVEKADNF |
Homo sapiens |
Leukemia Cell |
pmid |
sentence |
15378030 |
The signaling kinase p21-activated kinase 1 (pak1) binds to, phosphorylates and enhances the enzymatic activity of phosphoglucomutase 1 (pgm), |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PGM1 | up-regulates quantity
chemical modification
|
alpha-D-glucose 1-phosphate(2-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267929 |
|
|
Homo sapiens |
|
pmid |
sentence |
32898648 |
Human PGM1 deficiency is an inborn error of metabolism (OMIM: 614921), affecting cellular glucose homeostasis, the storage of glucose as glycogen, and the N-glycosylation of proteins. Like other PGM enzymes, the human protein catalyzes the Mg2+-dependent interconversion of glucose 1-phosphate (G1P) and glucose 6-phosphate (G6P). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Glycogenesis, Glycogenolysis |
+ |
PGM1 | up-regulates quantity
chemical modification
|
alpha-D-glucose 6-phosphate(2-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267930 |
|
|
Homo sapiens |
|
pmid |
sentence |
32898648 |
Human PGM1 deficiency is an inborn error of metabolism (OMIM: 614921), affecting cellular glucose homeostasis, the storage of glucose as glycogen, and the N-glycosylation of proteins. Like other PGM enzymes, the human protein catalyzes the Mg2+-dependent interconversion of glucose 1-phosphate (G1P) and glucose 6-phosphate (G6P). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Glycogenesis, Glycogenolysis |
+ |
PGM1 | down-regulates quantity
chemical modification
|
alpha-D-glucose 1-phosphate(2-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267931 |
|
|
Homo sapiens |
|
pmid |
sentence |
32898648 |
Human PGM1 deficiency is an inborn error of metabolism (OMIM: 614921), affecting cellular glucose homeostasis, the storage of glucose as glycogen, and the N-glycosylation of proteins. Like other PGM enzymes, the human protein catalyzes the Mg2+-dependent interconversion of glucose 1-phosphate (G1P) and glucose 6-phosphate (G6P). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Glycogenesis, Glycogenolysis |
+ |
PGM1 | down-regulates quantity
chemical modification
|
alpha-D-glucose 6-phosphate(2-) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267932 |
|
|
Homo sapiens |
|
pmid |
sentence |
32898648 |
Human PGM1 deficiency is an inborn error of metabolism (OMIM: 614921), affecting cellular glucose homeostasis, the storage of glucose as glycogen, and the N-glycosylation of proteins. Like other PGM enzymes, the human protein catalyzes the Mg2+-dependent interconversion of glucose 1-phosphate (G1P) and glucose 6-phosphate (G6P). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Glycogenesis, Glycogenolysis |