Q13362

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession 2A5G_HUMAN; Q13362;
Entrez ID 5527
GenBank Protein ID NM_001161725.1; NM_001161726.1; NM_002719.3; NM_178586.2; NM_178587.2; XM_005267827.1; XM_011536920.1;
GenBank Nucleotide ID NP_001155197.1; NP_001155198.1; NP_002710.2; NP_848701.1; NP_848702.1; XP_005267884.1; XP_011535222.1;
Protein Name Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform (PP2A B subunit isoform B'-gamma) (PP2A B subunit isoform B56-gamma) (PP2A B subunit isoform PR61-gamma) (PP2A B subunit isoform R5-gamma) (Renal carcinoma antigen NY-REN-29)
Gene Name PPP2R5C; KIAA0044
Organism Homo sapiens
NCBI Taxa ID 9606
Functional DescriptionThe 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. The PP2A-PPP2R5C holoenzyme may specifically dephosphorylate and activate TP53 and play a role in DNA damage-induced inhibition of cell proliferation. PP2A-PPP2R5C may also regulate the ERK signaling pathway through ERK dephosphorylation.
Sequence
(Fasta)
MLTCNKAGSR MVVDAANSNG PFQPVVLLHI RDVPPADQEK LFIQKLRQCC VLFDFVSDPL 60
SDLKWKEVKR AALSEMVEYI THNRNVITEP IYPEVVHMFA VNMFRTLPPS SNPTGAEFDP 120
EEDEPTLEAA WPHLQLVYEF FLRFLESPDF QPNIAKKYID QKFVLQLLEL FDSEDPRERD 180
FLKTTLHRIY GKFLGLRAYI RKQINNIFYR FIYETEHHNG IAELLEILGS IINGFALPLK 240
EEHKIFLLKV LLPLHKVKSL SVYHPQLAYC VVQFLEKDST LTEPVVMALL KYWPKTHSPK 300
EVMFLNELEE ILDVIEPSEF VKIMEPLFRQ LAKCVSSPHF QVAERALYYW NNEYIMSLIS 360
DNAAKILPIM FPSLYRNSKT HWNKTIHGLI YNALKLFMEM NQKLFDDCTQ QFKAEKLKEK 420
LKMKEREEAW VKIENLAKAN PQYTVYSQAS TMSIPVAMET DGPLFEDVQM LRKTVKDEAH 480
QAQKDPKKDR PLARRKSELP QDPHTKKALE AHCRADELAS QDGR 525

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1MethylationAlzheimer's diseaseP23943618; 3779734
[Reference]: We propose that alterations in the membrane localization of PP2A and Tau following down-regulation of LCMT1 may lead to PP2A and Tau dysfunction in AD.

※ Disease Cross-ref Annotation

DatabaseAnnotation
CTD (Curated)
(count: 3)
MESH:D043171 ; Chromosomal Instability
MESH:D015451 ; Leukemia, Lymphocytic, Chronic, B-Cell
MESH:D048629 ; Micronuclei, Chromosome-Defective
GWASdb
(count: 15)
(view all)
rs11625483; Coronary heart disease; coronary artery disease
rs1746598; Salmonella-induced pyroptosis; Null
rs8016207; Urinary metabolites; kidney disease
rs1678002; Salmonella-induced pyroptosis; Null
rs8015021; Response to cytadine analogues (cytosine arabinoside); cancer
rs1746595; Multiple complex diseases; Null

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 13)
(view all)
209       KQINNIFYRFIYETE     dbPAF
298       KYWPKTHSPKEVMFL     dbPAF
336       RQLAKCVSSPHFQVA     dbPAF
348       QVAERALYYWNNEYI     dbPAF
349       VAERALYYWNNEYIM     dbPAF
354       LYYWNNEYIMSLISD     dbPAF
Acetylation
(count: 3)
156       DFQPNIAKKYIDQKF     PLMD
413       DDCTQQFKAEKLKEK     PLMD
45        QEKLFIQKLRQCCVL     PLMD
Ubiquitination
(count: 11)
(view all)
156       DFQPNIAKKYIDQKF     PLMD
157       FQPNIAKKYIDQKFV     PLMD
183       PRERDFLKTTLHRIY     PLMD
258       LLPLHKVKSLSVYHP     PLMD
291       PVVMALLKYWPKTHS     PLMD
333       PLFRQLAKCVSSPHF     PLMD
Malonylation
(count: 2)
156       DFQPNIAKKYIDQKF     PLMD
413       DDCTQQFKAEKLKEK     PLMD

※ Protein-Protein Interaction

NetworkInteraction
ABSource