P55895

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession RAG2_HUMAN; P55895;
Entrez ID 5897
GenBank Protein ID NM_000536.3; NM_001243785.1; NM_001243786.1;
GenBank Nucleotide ID NP_000527.2; NP_001230714.1; NP_001230715.1;
Protein Name V(D)J recombination-activating protein 2 (RAG-2)
Gene Name RAG2
Organism Homo sapiens
NCBI Taxa ID 9606
Functional DescriptionCore component of the RAG complex, a multiprotein complex that mediates the DNA cleavage phase during V(D)J recombination. V(D)J recombination assembles a diverse repertoire of immunoglobulin and T-cell receptor genes in developing B and T-lymphocytes through rearrangement of different V (variable), in some cases D (diversity), and J (joining) gene segments. DNA cleavage by the RAG complex occurs in 2 steps: a first nick is introduced in the top strand immediately upstream of the heptamer, generating a 3'-hydroxyl group that can attack the phos(view all)
Sequence
(Fasta)
MSLQMVTVSN NIALIQPGFS LMNFDGQVFF FGQKGWPKRS CPTGVFHLDV KHNHVKLKPT 60
IFSKDSCYLP PLRYPATCTF KGSLESEKHQ YIIHGGKTPN NEVSDKIYVM SIVCKNNKKV 120
TFRCTEKDLV GDVPEARYGH SINVVYSRGK SMGVLFGGRS YMPSTHRTTE KWNSVADCLP 180
CVFLVDFEFG CATSYILPEL QDGLSFHVSI AKNDTIYILG GHSLANNIRP ANLYRIRVDL 240
PLGSPAVNCT VLPGGISVSS AILTQTNNDE FVIVGGYQLE NQKRMICNII SLEDNKIEIR 300
EMETPDWTPD IKHSKIWFGS NMGNGTVFLG IPGDNKQVVS EGFYFYMLKC AEDDTNEEQT 360
TFTNSQTSTE DPGDSTPFED SEEFCFSAEA NSFDGDDEFD TYNEDDEEDE SETGYWITCC 420
PTCDVDINTW VPFYSTELNK PAMIYCSHGD GHWVHAQCMD LAERTLIHLS AGSNKYYCNE 480
HVEIARALHT PQRVLPLKKP PMKSLRKKGS GKILTPAKKS FLRRLFD 528

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1Threonine PhosphorylationB-cell lymphomaNT49021349429
[Reference]: On a p53-deficient background, the RAG-2(T490A) mutation induced lymphoid malignancies characterized by clonal chromosomal translocations involving antigen receptor genes.

※ Disease Cross-ref Annotation

DatabaseAnnotation
CTD (Curated)
(count: 7)
(view all)
MESH:D001169 ; Arthritis, Experimental
MESH:C567115 ; Combined Cellular And Humoral Immune Defects With Granulomas
MESH:D004802 ; Eosinophilia
MESH:D008679 ; Metaplasia
MESH:D065626 ; Non-alcoholic Fatty Liver Disease
MESH:C538564 ; Reticuloendotheliosis, familial, with eosinophilia

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 7)
(view all)
121       CKNNKKVTFRCTEKD     dbPAF
138       GDVPEARYGHSINVV     dbPAF
146       GHSINVVYSRGKSMG     dbPAF
291       RMICNIISLEDNKIE     dbPAF
346       VSEGFYFYMLKCAED     dbPAF
365       EQTTFTNSQTSTEDP     dbPAF