InnateDB Protein
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IDBP-241648.6
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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PPP2R2B
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Protein Name
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protein phosphatase 2, regulatory subunit B, beta
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Synonyms
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B55BETA; PP2AB55BETA; PP2ABBETA; PP2APR55B; PP2APR55BETA; PR2AB55BETA; PR2ABBETA; PR2APR55BETA; PR52B; PR55-BETA; PR55BETA; SCA12;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000377931
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InnateDB Gene
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IDBG-52116 (PPP2R2B)
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Protein Structure
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Function |
The B regulatory subunit might modulate substrate selectivity and catalytic activity, and also might direct the localization of the catalytic enzyme to a particular subcellular compartment. Within the PP2A holoenzyme complex, isoform 2 is required to promote proapoptotic activity (By similarity). Isoform 2 regulates neuronal survival through the mitochondrial fission and fusion balance (By similarity). {ECO:0000250}.
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Subcellular Localization |
Isoform 1: Cytoplasm {ECO:0000250}. Cytoplasm, cytoskeleton {ECO:0000250}. Membrane {ECO:0000250}.Isoform 2: Cytoplasm {ECO:0000250}. Mitochondrion {ECO:0000250}. Mitochondrion outer membrane {ECO:0000250}. Note=Under basal conditions, localizes to both cytosolic and mitochondrial compartments. Relocalizes from the cytosolic to the mitochondrial compartment during apoptosis. Its targeting to the outer mitochondrial membrane (OMM) involves an association with import receptors of the TOM complex and is required to promote proapoptotic activity (By similarity). {ECO:0000250}.
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Disease Associations |
Spinocerebellar ataxia 12 (SCA12) [MIM:604326]: Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA12 is an autosomal dominant cerebellar ataxia (ADCA). {ECO:0000269PubMed:10581021}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
Brain.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 53 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
53
[view]
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Protein-Protein |
51
[view]
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Protein-DNA |
2
[view]
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
Accession |
GO Term |
GO:0005515
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protein binding
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GO:0008601
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protein phosphatase type 2A regulator activity
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR000009
Protein phosphatase 2A, regulatory subunit PR55
IPR001680
WD40 repeat
IPR017986
WD40-repeat-containing domain
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PFAM |
PF00400
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PRINTS |
PR00600
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PIRSF |
PIRSF037309
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SMART |
SM00320
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TIGRFAMs |
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Modification |
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SwissProt |
Q00005
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PhosphoSite |
PhosphoSite-Q00005
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TrEMBL |
Q9NS07
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UniProt Splice Variant |
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Entrez Gene |
5521
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UniGene |
Hs.739387
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RefSeq |
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HUGO |
HGNC:9305
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OMIM |
604325
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CCDS |
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HPRD |
05059
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IMGT |
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EMBL |
AC008728
AC009186
AC010251
AC011357
AC011386
AC091919
AC091924
AF152102
AK056192
AK289717
AK294659
AK295347
BC031790
BI490027
BI669304
CH471062
M64930
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GenPept |
AAA36493
AAF74024
AAH31790
BAF82406
BAG51642
BAH11838
BAH12040
EAW61829
EAW61831
EAW61832
EAW61833
EAW61834
EAW61835
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