Homo sapiens Protein: ANK2
Summary
InnateDB Protein IDBP-477600.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ANK2
Protein Name ankyrin 2, neuronal
Synonyms ANK-2; brank-2; LQT4;
Species Homo sapiens
Ensembl Protein ENSP00000421067
InnateDB Gene IDBG-34685 (ANK2)
Protein Structure
UniProt Annotation
Function In skeletal muscle, required for proper localization of DMD and DCTN4 and for the formation and/or stability of a special subset of microtubules associated with costameres and neuromuscular junctions (By similarity). Attaches integral membrane proteins to cytoskeletal elements. Also binds to cytoskeletal proteins. Required for coordinate assembly of Na/Ca exchanger, Na/K ATPase and InsP3 receptor at sarcoplasmic reticulum sites in cardiomyocytes. Required for the coordinated expression of the Na/K ATPase, Na/Ca exchanger and beta-2-spectrin (SPTBN1) in the inner segment of rod photoreceptors. Required for expression and targeting of SPTBN1 in neonatal cardiomyocytes and for the regulation of neonatal cardiomyocyte contraction rate. {ECO:0000250, ECO:0000269PubMed:12571597}.
Subcellular Localization Cytoplasm, cytoskeleton {ECO:0000269PubMed:19007774}. Membrane {ECO:0000269PubMed:19007774}. Cytoplasm, myofibril, sarcomere, M line {ECO:0000250}. Apical cell membrane {ECO:0000250}. Cell membrane {ECO:0000269PubMed:19007774}. Cell junction, synapse, postsynaptic cell membrane {ECO:0000250}. Note=Expressed at the apical membrane of airway lung epithelial cells (By similarity). Localized to the plasma membrane of the inner segments of photoreceptors in retina. Colocalizes with SPTBN1 in a distict intracellular compartment of neonatal cardiomyocytes (By similarity). In skeletal muscle, localizes to neuromuscular junctions (By similarity). {ECO:0000250}.
Disease Associations Long QT syndrome 4 (LQT4) [MIM:600919]: A heart disorder characterized by a prolonged QT interval on the ECG and polymorphic ventricular arrhythmias. They cause syncope and sudden death in response to exercise or emotional stress, and can present with a sentinel event of sudden cardiac death in infancy. Long QT syndrome type 4 shows many atypical features compared to classical long QT syndromes, including pronounced sinus bradycardia, polyphasic T waves and atrial fibrillation. Cardiac repolarization defects may be not as severe as in classical LQT syndromes and prolonged QT interval on EKG is not a consistent feature. {ECO:0000269PubMed:12571597, ECO:0000269PubMed:15178757}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Present in plasma membrane of neurons as well as glial cells throughout the brain. Expressed in fetal brain and in temporal cortex of adult brain. Also expressed in the inner segments of rod photoreceptors in retina. {ECO:0000269PubMed:1830053, ECO:0000269PubMed:1833308, ECO:0000269PubMed:19007774}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 14 experimentally validated interaction(s) in this database.
Experimentally validated
Total 14 [view]
Protein-Protein 14 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0019899 enzyme binding
GO:0019901 protein kinase binding
GO:0030507 spectrin binding
GO:0030674 protein binding, bridging
GO:0044325 ion channel binding
GO:0051117 ATPase binding
Biological Process
GO:0002027 regulation of heart rate
GO:0003283 atrial septum development
GO:0006874 cellular calcium ion homeostasis
GO:0007165 signal transduction
GO:0007411 axon guidance
GO:0010628 positive regulation of gene expression
GO:0010881 regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion
GO:0010882 regulation of cardiac muscle contraction by calcium ion signaling
GO:0031647 regulation of protein stability
GO:0033292 T-tubule organization
GO:0033365 protein localization to organelle
GO:0034394 protein localization to cell surface
GO:0034613 cellular protein localization
GO:0036309 protein localization to M-band
GO:0036371 protein localization to T-tubule
GO:0043268 positive regulation of potassium ion transport
GO:0050821 protein stabilization
GO:0051279 regulation of release of sequestered calcium ion into cytosol
GO:0051924 regulation of calcium ion transport
GO:0051928 positive regulation of calcium ion transport
GO:0055117 regulation of cardiac muscle contraction
GO:0060307 regulation of ventricular cardiac muscle cell membrane repolarization
GO:0070296 sarcoplasmic reticulum calcium ion transport
GO:0070972 protein localization to endoplasmic reticulum
GO:0072659 protein localization to plasma membrane
GO:0086004 regulation of cardiac muscle cell contraction
GO:0086005 ventricular cardiac muscle cell action potential
GO:0086014 atrial cardiac muscle cell action potential
GO:0086015 SA node cell action potential
GO:0086046 membrane depolarization involved in regulation of SA node cell action potential
GO:0086066 atrial cardiac muscle cell to AV node cell communication
GO:0086070 SA node cell to atrial cardiac muscle cell communication
GO:0086091 regulation of heart rate by cardiac conduction
GO:1901018 positive regulation of potassium ion transmembrane transporter activity
GO:1901019 regulation of calcium ion transmembrane transporter activity
GO:1901021 positive regulation of calcium ion transmembrane transporter activity
GO:2001259 positive regulation of cation channel activity
Cellular Component
GO:0005622 intracellular
GO:0005829 cytosol
GO:0005856 cytoskeleton
GO:0005886 plasma membrane
GO:0014704 intercalated disc
GO:0016323 basolateral plasma membrane
GO:0016324 apical plasma membrane
GO:0030018 Z disc
GO:0030315 T-tubule
GO:0031430 M band
GO:0031672 A band
GO:0042383 sarcolemma
GO:0043034 costamere
GO:0045211 postsynaptic membrane
Protein Structure and Domains
PDB ID
InterPro IPR000488 Death domain
IPR000906 ZU5 domain
IPR002110 Ankyrin repeat
IPR011029 Death-like domain
IPR020683 Ankyrin repeat-containing domain
PFAM PF00531
PF00791
PF00023
PF13606
PF11929
PF12796
PRINTS PR01415
PIRSF
SMART SM00005
SM00218
SM00248
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q01484
PhosphoSite PhosphoSite-Q01484
TrEMBL D6RHC5
UniProt Splice Variant
Entrez Gene 287
UniGene Hs.620813
RefSeq NP_001120965
HUGO HGNC:493
OMIM 106410
CCDS CCDS54796
HPRD 00110
IMGT
EMBL AC004057 AC017007 AC093617 AC093879 AC093900 AC108042 BC125235 BC125236 BX537758 M37123 X56957 X56958 Z26634
GenPept AAA62828 AAI25236 AAI25237 CAA40278 CAA40279 CAB42644 CAD97827