Homo sapiens Protein: ATP2B2
Summary
InnateDB Protein IDBP-18193.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ATP2B2
Protein Name ATPase, Ca++ transporting, plasma membrane 2
Synonyms PMCA2; PMCA2a; PMCA2i;
Species Homo sapiens
Ensembl Protein ENSP00000353414
InnateDB Gene IDBG-18189 (ATP2B2)
Protein Structure
UniProt Annotation
Function This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium out of the cell.
Subcellular Localization Cell membrane; Multi-pass membrane protein.
Disease Associations
Tissue Specificity Mainly expressed in brain cortex. Found in low levels in skeletal muscle, heart muscle, stomach, liver, kidney and lung. Isoforms containing segment B are found in brain cortex and at low levels in other tissues. Isoforms containing segments X and W are found at low levels in all tissues. Isoforms containing segment A and segment Z are found at low levels in skeletal muscle and heart muscle.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 15 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 15 [view]
Protein-Protein 15 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0005388 calcium-transporting ATPase activity
GO:0005509 calcium ion binding
GO:0005515 protein binding
GO:0005516 calmodulin binding
GO:0005524 ATP binding
GO:0008022 protein C-terminus binding
GO:0019829 cation-transporting ATPase activity
GO:0030165 PDZ domain binding
GO:0030899 calcium-dependent ATPase activity
GO:0046872 metal ion binding
Biological Process
GO:0000902 cell morphogenesis
GO:0006200 ATP catabolic process
GO:0006810 transport
GO:0006812 cation transport
GO:0006816 calcium ion transport
GO:0006874 cellular calcium ion homeostasis
GO:0006996 organelle organization
GO:0007595 lactation
GO:0007596 blood coagulation
GO:0007605 sensory perception of sound
GO:0007626 locomotory behavior
GO:0008361 regulation of cell size
GO:0021549 cerebellum development
GO:0021692 cerebellar Purkinje cell layer morphogenesis
GO:0021702 cerebellar Purkinje cell differentiation
GO:0021707 cerebellar granule cell differentiation
GO:0030182 neuron differentiation
GO:0034220 ion transmembrane transport
GO:0040011 locomotion
GO:0042428 serotonin metabolic process
GO:0042472 inner ear morphogenesis
GO:0045299 otolith mineralization
GO:0046068 cGMP metabolic process
GO:0048167 regulation of synaptic plasticity
GO:0048839 inner ear development
GO:0050808 synapse organization
GO:0050885 neuromuscular process controlling balance
GO:0050910 detection of mechanical stimulus involved in sensory perception of sound
GO:0051480 cytosolic calcium ion homeostasis
GO:0051928 positive regulation of calcium ion transport
GO:0055085 transmembrane transport
GO:0060088 auditory receptor cell stereocilium organization
GO:0060113 inner ear receptor cell differentiation
GO:0070588 calcium ion transmembrane transport
GO:0090102 cochlea development
Cellular Component
GO:0005737 cytoplasm
GO:0005783 endoplasmic reticulum
GO:0005886 plasma membrane
GO:0005929 cilium
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016324 apical plasma membrane
GO:0043025 neuronal cell body
Protein Structure and Domains
PDB ID
InterPro IPR001757 Cation-transporting P-type ATPase
IPR004014 Cation-transporting P-type ATPase, N-terminal
IPR006068 Cation-transporting P-type ATPase, C-terminal
IPR006408 Calcium-transporting P-type ATPase, subfamily IIB
IPR008250 P-type ATPase, A domain
IPR022141 Calcium transporting P-type ATPase, C-terminal, plasma membrane
IPR023214 HAD-like domain
IPR023299 P-type ATPase, cytoplasmic domain N
PFAM PF00690
PF00689
PF00122
PF12424
PF00702
PF08282
PF13419
PRINTS PR00119
PR00120
PIRSF
SMART SM00831
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q01814
PhosphoSite PhosphoSite-Q01814
TrEMBL Q4J699
UniProt Splice Variant
Entrez Gene 491
UniGene Hs.268942
RefSeq NP_001001331
HUGO HGNC:815
OMIM 108733
CCDS CCDS33701
HPRD 00160
IMGT
EMBL AC018839 AC090841 AH000321 CH471055 L00620 L20977 M97260 S95738 U15688 X63575
GenPept AAA08378 AAA36456 AAA50877 AAA51893 AAA60985 AAZ04475 CAA45131 EAW64080 EAW64084