Homo sapiens Protein: ATP13A4
Summary
InnateDB Protein IDBP-70002.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ATP13A4
Protein Name ATPase type 13A4
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000295548
InnateDB Gene IDBG-69998 (ATP13A4)
Protein Structure
UniProt Annotation
Function
Subcellular Localization Membrane {ECO:0000305}; Multi-pass membrane protein {ECO:0000305}.
Disease Associations Note=A chromosomal aberration involving ATP13A4 is found in 2 patients with specific language impairment (SLI) disorders. Paracentric inversion inv(3)(q25;q29). The inversion produces a disruption of the protein.
Tissue Specificity Expressed in heart, placenta, liver, skeletal muscles, and pancreas. Lower levels of expression are also detected in brain, lung and kidney. Weakly expressed in the adult brain. Expression in fetal brain is higher than in adult brain, with levels similar to several other fetal tissues including spleen and skeletal muscle. In adult brain expressed at low levels in all tissues examined, including the temporal lobe and putamen. {ECO:0000269PubMed:15925480}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0005524 ATP binding
GO:0016887 ATPase activity
GO:0019829 cation-transporting ATPase activity
GO:0046872 metal ion binding
Biological Process
GO:0006200 ATP catabolic process
GO:0006812 cation transport
Cellular Component
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR001757 Cation-transporting P-type ATPase
IPR004014 Cation-transporting P-type ATPase, N-terminal
IPR006544 Cation-transporting P-type ATPase, subfamily V
IPR008250 P-type ATPase, A domain
IPR023214 HAD-like domain
PFAM PF00690
PF12409
PF00122
PF00702
PF08282
PF13419
PRINTS PR00119
PR00120
PIRSF
SMART SM00831
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q4VNC1
PhosphoSite PhosphoSite-Q4VNC1
TrEMBL
UniProt Splice Variant
Entrez Gene 84239
UniGene Hs.674423
RefSeq
HUGO HGNC:25422
OMIM 609556
CCDS
HPRD 12502
IMGT
EMBL AC048351 AC092942 AC105057 AK095277 AL512736 AY358110 AY823162 BC101496
GenPept AAI01497 AAQ88477 AAX24102 BAC04520 CAC21667