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Repository for lectin-assisted multimodality data
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MIRAGE
calcium/calmodulin dependent protein kinase II beta
Summary
- Gene Symbol
-
- CAMK2B
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Actin-binding
- Alternative splicing
- Calmodulin-binding
- Cytoskeleton
- Developmental protein
- Differentiation
- Intellectual disability
- Kinase
- Membrane
- Neurogenesis
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Sarcoplasmic reticulum
- Serine/threonine-protein kinase
- Synapse
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein phosphorylation | ||
| signal transduction | ||
| nervous system development | ||
| positive regulation of neuron projection development | ||
| regulation of skeletal muscle adaptation |
GO Hierarchy
biological process
biological regulation [inference]
regulation of biological process [inference]
positive regulation of biological process [inference]
regulation of developmental process [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleoplasm | ||
| cytoplasm | ||
| centrosome | ||
| cytosol | ||
| calcium- and calmodulin-dependent protein kinase complex |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| actin binding | ||
| calmodulin-dependent protein kinase activity | ||
| calmodulin-dependent protein kinase activity | ||
| protein binding | ||
| calmodulin binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Kinase
- Functional Category
-
- E: Amino acid transport and metabolism
- K: Transcription
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| ATP binding |
| calmodulin binding |
| kinase activity |
| nucleotide binding |
| phosphorylation |
| InterPro |
|---|
| Protein kinase domain |
| Protein kinase, ATP binding site |
| Protein kinase-like domain superfamily |
| Serine/threonine-protein kinase, active site |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080230 | autosomal dominant intellectual developmental disorder 54 |
