1. Gene
  2. CAMK2A - calcium/calmodulin dependent protein kinase II alpha Gene

CAMK2A - calcium/calmodulin dependent protein kinase II alpha Gene

Homo sapiens

Also known as CAMKA; MRD53; MRT63; CaMKIIalpha; CaMKIINalpha

Gene ID: 815 | Gene type: protein coding

About CAMK2A

Cytogenetic location: 5q32 Genomic coordinates (GRCh38): 5:150,219,491-150,290,130 (from NCBI)

This gene has 23 transcripts (splice variants), 167 orthologues, 22 paralogues and is associated with 4 phenotypes. Restricted expression toward brain (RPKM 112.2).

Summary

The product of this gene belongs to the serine/threonine protein kinases family, and to the CA(2+)/calmodulin-dependent protein kinases subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. This calcium calmodulin-dependent protein kinase is composed of four different chains: alpha, beta, gamma, and delta. The alpha chain encoded by this gene is required for hippocampal long-term potentiation (LTP) and spatial learning. In addition to its calcium-calmodulin (CaM)-dependent activity, this protein can undergo autophosphorylation, resulting in CaM-independent activity. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2018]

CAMK2A Products(5)

mRNA Protein Name
NM_015981.4 NP_057065.2 calcium/calmodulin-dependent protein kinase type II subunit alpha isoform 1
NM_001369025.2 NP_001355954.1 calcium/calmodulin-dependent protein kinase type II subunit alpha isoform 3
NM_171825.3 NP_741960.1 calcium/calmodulin-dependent protein kinase type II subunit alpha isoform 2
NM_001363990.1 NP_001350919.1 calcium/calmodulin-dependent protein kinase type II subunit alpha isoform 2
NM_001363989.1 NP_001350918.1 calcium/calmodulin-dependent protein kinase type II subunit alpha isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables calcium/calmodulin-dependent protein kinase activity IDA
IDA: Inferred from direct assay
11972023 GOA
enables calmodulin binding IPI
IPI: Inferred from physical interaction
20668654 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
20668654 GOA
enables kinase activity IDA
IDA: Inferred from direct assay
17052756 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17052756 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
20668654 GOA
enables protein serine/threonine kinase activity IDA
IDA: Inferred from direct assay
28130356 GOA
Biological Process GO Annotation Evidence Reference Source
involved in angiotensin-activated signaling pathway IDA
IDA: Inferred from direct assay
20584908 GOA
involved in cellular response to interferon-beta IDA
IDA: Inferred from direct assay
35568036 GOA
involved in cellular response to type II interferon IDA
IDA: Inferred from direct assay
11972023 GOA
involved in dendritic spine development IMP
IMP: Inferred from mutant phenotype
28130356 GOA
involved in peptidyl-threonine autophosphorylation IMP
IMP: Inferred from mutant phenotype
28130356 GOA
involved in positive regulation of NF-kappaB transcription factor activity IMP
IMP: Inferred from mutant phenotype
17052756 GOA
involved in positive regulation of receptor signaling pathway via JAK-STAT IDA
IDA: Inferred from direct assay
11972023 GOA
involved in protein phosphorylation IDA
IDA: Inferred from direct assay
17052756 GOA
involved in regulation of neuron migration IMP
IMP: Inferred from mutant phenotype
29100089 GOA
Cellular Component GO Annotation Evidence Reference Source
part of calcium- and calmodulin-dependent protein kinase complex IDA
IDA: Inferred from direct assay
20668654 GOA
located in dendritic spine IDA
IDA: Inferred from direct assay
28130356 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CAMK2A Protein Structure

Pkinase

Pkinase: Protein kinase domain (13 - 271)

CaMKII_AD

CaMKII_AD: Calcium/calmodulin dependent protein kinase II association domain (346 - 473)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 478 a.a.
Protein Preferred Names Protein Names

calcium/calmodulin-dependent protein kinase type II subunit alpha

CaM kinase II alpha subunit

CaM-kinase II alpha chain

CaMK-II alpha subunit

caM kinase II subunit alpha

caMK-II subunit alpha

calcium/calmodulin-dependent protein kinase (CaM kinase) II alpha

calcium/calmodulin-dependent protein kinase II alpha-B subunit

calcium/calmodulin-dependent protein kinase type II alpha chain

CAMK2A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
CAMK2A Q9UQM7 CAMK2B Homo sapiens Q13554
Anti Bait CoIP
17353931
Intra
CAMK2A Q9UQM7 CAMK2B Homo sapiens Q13554
Pull Down
32707033
Intra
CAMK2A Q9UQM7 CAMK2B Homo sapiens Q13554
Anti Tag CoIP
33961781
Intra
CAMK2A Q9UQM7 CAMK2B Homo sapiens Q13554
TAP
27173435
Intra
CAMK2A Q9UQM7 TCAF1 Homo sapiens Q9Y4C2-2
Validated Y2H
32296183
Intra
CAMK2A Q9UQM7 CAMK2D Homo sapiens Q13557
Anti Tag CoIP
31980649
Intra
CAMK2A Q9UQM7 CAMK2D Homo sapiens Q13557
Pull Down
32707033
Intra
CAMK2A Q9UQM7 CAMK2G Homo sapiens Q13555
Anti Tag CoIP
31980649
Intra
CAMK2A Q9UQM7 CAMK2G Homo sapiens Q13555
Anti Tag CoIP
25852190
Intra
CAMK2A Q9UQM7 CAMK2D Homo sapiens Q13557
Anti Tag CoIP
33961781
Intra
CAMK2A Q9UQM7 CAMK2D Homo sapiens Q13557
Anti Bait CoIP
17353931
Intra
CAMK2A Q9UQM7 CAMK2D Homo sapiens Q13557
Solution Sedimentation
20668654
Intra
CAMK2A Q9UQM7 CAMK2G Homo sapiens Q13555
Anti Tag CoIP
33961781
Intra
CAMK2A Q9UQM7 CAMK2D Homo sapiens Q13557
Anti Tag CoIP
25852190
Intra
CAMK2A Q9UQM7 CAMK2G Homo sapiens Q13555
Pull Down
32707033
Intra
CAMK2A Q9UQM7 APBB2 Homo sapiens Q92870-2
Validated Y2H
32814053
Intra
CAMK2A Q9UQM7 APBB2 Homo sapiens Q92870-2
Y2H Array
32814053
Intra
CAMK2A Q9UQM7 APBB2 Homo sapiens Q92870-2
Y2H Pooling
32814053
Intra
CAMK2A Q9UQM7 GRIN2B Homo sapiens Q13224
Pull Down
19453375
Intra
CAMK2A Q9UQM7 GRIN2B Homo sapiens Q13224
Competition Binding
19453375
Intra
CAMK2A Q9UQM7 CDC37 Homo sapiens Q16543
Anti Tag CoIP
31980649
Intra
CAMK2A Q9UQM7 HSP90AA1 Homo sapiens P07900
Anti Tag CoIP
31980649
Intra
CAMK2A Q9UQM7 HSP90AB1 Homo sapiens P08238
Anti Tag CoIP
31980649
Intra
CAMK2A Q9UQM7 HSP90AB1 Homo sapiens P08238
Lumier
22939624
Intra
CAMK2A Q9UQM7 YWHAE Homo sapiens P62258
Crosslink
36931259
Intra
CAMK2A Q9UQM7 TAB2 Homo sapiens Q9NYJ8
Anti Tag CoIP
33961781
Intra
CAMK2A Q9UQM7 MRPL11 Homo sapiens Q9Y3B7
Validated Y2H
32296183
Intra
CAMK2A Q9UQM7 PNP Homo sapiens P00491
Y2H Pooling
32814053
Intra
CAMK2A Q9UQM7 PNP Homo sapiens P00491
Validated Y2H
32814053
Intra
CAMK2A Q9UQM7 PNP Homo sapiens P00491
Y2H Array
32814053
Intra
CAMK2A Q9UQM7 PECAM1 Homo sapiens P16284
Validated Y2H
32814053
Intra
CAMK2A Q9UQM7 PECAM1 Homo sapiens P16284
Y2H Array
32814053
Intra
CAMK2A Q9UQM7 PECAM1 Homo sapiens P16284
Y2H Pooling
32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CAMK2A Proteins

Cat. No. Product Name Accession Purity
HY-P76761 CaMKII alpha/CAMK2A Protein, Human (sf9, GST) Q9UQM7-1 (M1-H478) ≥95%

Related Diseases

Diseases Alias
Rett Syndrome

Atypical Rett Syndrome

RTT

Rts

Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

Rett Syndrome, Atypical

Rett Syndrome, Preserved Speech Variant

Rett'S Disorder

Rett Syndrome Variant

Rett Disorder

Cerebroatrophic Hyperammonemia

Rett Like Syndrome

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

Rett'S Syndrome

Atypical Rtt

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

Rett Syndrome Preserved Speech Variant

Rett Syndrome Zappella Variant

Rett Syndrome, Zappella Variant

Fragile X Syndrome

FXS

Martin-Bell Syndrome

Fraxa Syndrome

Marker X Syndrome

X-Linked Mental Retardation And Macroorchidism

Fragile X Mental Retardation Syndrome

Fra Syndrome

Mental Retardation, X-Linked, Associated With Marxq28

Frax Syndrome

Symptomatic Form Of Fragile X Syndrome In Female Carriers

Fragile-X Syndrome

Fraxe Syndrome

Schizophrenia 12

Sczd12

Schizophrenia Susceptibility Locus, Chromosome 1p-Related

Intellectual Developmental Disorder, Autosomal Recessive 63

MRT63

Mental Retardation, Autosomal Recessive 63

Intellectual Developmental Disorder, Autosomal Dominant 53

MRD53

Mental Retardation, Autosomal Dominant 53

Autosomal Dominant Intellectual Developmental Disorder 53

Autosomal Dominant Mental Retardation 53

Mental Retardation, Autosomal Dominant, Type 53

Schizophrenia

SCZD

Schizophrenia With Or Without An Affective Disorder

Schizophrenia 12

Schizophrenia, Susceptibility To

Schizophrenia-1

Dementia Praecox

Schizophrenia 1

Autosomal Dominant Non-Syndromic Intellectual Disability
Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris CAMK2A VGNC VGNC:38680
Macaca mulatta CAMK2A VGNC VGNC:70523
Bos taurus CAMK2A VGNC VGNC:26721
Rattus norvegicus CAMK2A RGD RGD:2261
Felis catus CAMK2A VGNC VGNC:60331
Mus musculus CAMK2A MGD MGI:88256
Others CAMK2A NCBI