Identification |
HMDB Protein ID
| CDBP01150 |
Secondary Accession Numbers
| Not Available |
Name
| Sodium/potassium-transporting ATPase subunit beta-2 |
Description
| Not Available |
Synonyms
|
- Sodium/potassium-dependent ATPase subunit beta-2
|
Gene Name
| ATP1B2 |
Protein Type
| Enzyme |
Biological Properties |
General Function
| Involved in sodium:potassium-exchanging ATPase activity |
Specific Function
| This is the non-catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of Na(+) and K(+) ions across the plasma membrane. The exact function of the beta-2 subunit is not known |
GO Classification
|
Component |
membrane |
cell part |
Function |
potassium ion transmembrane transporter activity |
potassium-transporting atpase activity |
sodium:potassium-exchanging atpase activity |
transmembrane transporter activity |
substrate-specific transmembrane transporter activity |
ion transmembrane transporter activity |
cation transmembrane transporter activity |
inorganic cation transmembrane transporter activity |
monovalent inorganic cation transmembrane transporter activity |
transporter activity |
Process |
cellular nitrogen compound metabolic process |
nucleobase, nucleoside, nucleotide and nucleic acid metabolic process |
nucleobase, nucleoside and nucleotide metabolic process |
nucleoside phosphate metabolic process |
nucleotide metabolic process |
sodium ion transport |
establishment of localization |
transport |
monovalent inorganic cation transport |
potassium ion transport |
purine nucleotide metabolic process |
ion transport |
purine nucleotide biosynthetic process |
atp biosynthetic process |
purine nucleoside triphosphate biosynthetic process |
cation transport |
purine ribonucleoside triphosphate biosynthetic process |
metabolic process |
nitrogen compound metabolic process |
|
Cellular Location
|
- Membrane
- Single-pass type II membrane protein
|
Pathways
|
Name | SMPDB/Pathwhiz | KEGG | Kidney Function | | Not Available | Glucose Transporter Defect (SGLT2) | | Not Available | Hartnup Disorder | | Not Available | Iminoglycinuria | | Not Available | Lysinuric Protein Intolerance | | Not Available |
|
Gene Properties |
Chromosome Location
| Chromosome:1 |
Locus
| 17p13.1 |
SNPs
| ATP1B2 |
Gene Sequence
|
>873 bp
ATGGTCATCCAGAAAGAGAAGAAGAGCTGCGGGCAGGTGGTTGAGGAGTGGAAGGAGTTC
GTGTGGAACCCGAGGACGCACCAGTTTATGGGCCGCACCGGGACCAGCTGGGCCTTTATC
CTCCTCTTCTACCTCGTTTTTTATGGGTTCCCCACCGCCATGTTCACCCTCACCATGTGG
GTGATGCTGCAGACTGTCTCCGACCATACCCCCAAGTACCAGGACCGACTGGCCACACCG
GGCTTGATGATTCGCCCCAAGACTGAGAACCTTGATGTCATTGTCAATGTCAGTGACACT
GAAAGCTGGGACCAGCATGTTCAGAAGCTCAACAAGTTCTTGGAGCCTTACAACGACTCT
ATGCAAGCCCAAAAGAATGATGTCTGCCGCCCTGGGCGCTATTACGAACAGCCAGATAAT
GGAGTCCTCAACTACCCCAAACTGGCCTGCCAATTCAACCGGACCCAGCTGGGCAACTGC
TCCGGCATTGGGGACTCCACCCACTATGGTTACAGCACTGGGCAGCCCTGTGTCTTCATC
AAGATGAACCGGGTCATCAACTTCTATGCAGGAGCAAACCAGAGCATGAATGTTACCTGT
GCTGGGAAGCGAGATGAAGATGCTGAGAATCTCGGCAACTTCGTCATGTTCCCCGCCAAC
GGCAACATCGACCTCATGTACTTCCCCTACTATGGCAAAAAGTTCCACGTGAACTACACA
CAGCCCCTGGTGGCTGTGAAGTTCCTGAATGTGACCCCCAACGTGGAGGTGAATGTAGAA
TGTCGCATCAACGCCGCCAACATCGCCACAGACGATGAGCGAGACAAGTTCGCCGGCCGC
GTGGCCTTCAAACTCCGCATCAACAAAACCTGA
|
Protein Properties |
Number of Residues
| 290 |
Molecular Weight
| 33366.9 |
Theoretical pI
| 8.44 |
Pfam Domain Function
|
|
Signals
|
|
Transmembrane Regions
|
|
Protein Sequence
|
>Sodium/potassium-transporting ATPase subunit beta-2
MVIQKEKKSCGQVVEEWKEFVWNPRTHQFMGRTGTSWAFILLFYLVFYGFLTAMFTLTMW
VMLQTVSDHTPKYQDRLATPGLMIRPKTENLDVIVNVSDTESWDQHVQKLNKFLEPYNDS
IQAQKNDVCRPGRYYEQPDNGVLNYPKRACQFNRTQLGNCSGIGDSTHYGYSTGQPCVFI
KMNRVINFYAGANQSMNVTCAGKRDEDAENLGNFVMFPANGNIDLMYFPYYGKKFHVNYT
QPLVAVKFLNVTPNVEVNVECRINAANIATDDERDKFAGRVAFKLRINKT
|
External Links |
GenBank ID Protein
| 179245 |
UniProtKB/Swiss-Prot ID
| P14415 |
UniProtKB/Swiss-Prot Entry Name
| AT1B2_HUMAN |
PDB IDs
|
Not Available |
GenBank Gene ID
| M81181 |
GeneCard ID
| ATP1B2 |
GenAtlas ID
| ATP1B2 |
HGNC ID
| HGNC:805 |
References |
General References
| Not Available |