Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform
| GO Term | Evidence Code | Reference |
|---|---|---|
| chromosome segregation | ||
| female meiotic nuclear division |
|
|
| negative regulation of hippo signaling | ||
| intracellular signal transduction | ||
| regulation of growth |
| GO Term | Evidence Code | Reference |
|---|---|---|
| protein phosphatase type 2A complex | ||
| protein phosphatase type 2A complex | ||
| protein phosphatase type 2A complex | ||
| protein phosphatase type 2A complex | ||
| chromosome, centromeric region |
| GO Term | Evidence Code | Reference |
|---|---|---|
| protein serine/threonine phosphatase activity |
|
|
| protein phosphatase regulator activity | ||
| protein phosphatase regulator activity | ||
| protein heterodimerization activity | ||
| protein antigen binding |
| Pathway Name | Organism |
|---|---|
| APC truncation mutants have impaired AXIN binding | Homo sapiens |
| AURKA Activation by TPX2 | Homo sapiens |
| AXIN missense mutants destabilize the destruction complex | Homo sapiens |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | Homo sapiens |
| Anchoring of the basal body to the plasma membrane | Homo sapiens |
| Beta-catenin phosphorylation cascade | Homo sapiens |
| CD28 co-stimulation | Homo sapiens |
| CTNNB1 S33 mutants aren't phosphorylated | Homo sapiens |
| CTNNB1 S37 mutants aren't phosphorylated | Homo sapiens |
| CTNNB1 S45 mutants aren't phosphorylated | Homo sapiens |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070066 | autosomal dominant intellectual developmental disorder 36 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026