WERAM Information
Tag | Content | ||||||||||||
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WERAM ID | WERAM-Hos-0208 | ||||||||||||
Ensembl Protein ID | ENSP00000478672.1 | ||||||||||||
Uniprot Accession | P55895; RAG2_HUMAN; A8K9E9; Q8TBL4 | ||||||||||||
Genbank Protein ID | NP_000527.2; NP_001230714.1; NP_001230715.1 | ||||||||||||
Protein Name | V(D)J recombination-activating protein 2 | ||||||||||||
Genbank Nucleotide ID | NM_000536.3; NM_001243785.1; NM_001243786.1 | ||||||||||||
Gene Name | RAG2 | ||||||||||||
Ensembl Information |
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Details |
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Status | Reviewed | ||||||||||||
Classification |
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Organism | Homo sapiens | ||||||||||||
NCBI Taxa ID | 9606 | ||||||||||||
Functional Description (View) |
Core 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 phosphodiester bond on the opposite strand in a direct transesterification reaction, thereby creating 4 DNA ends: 2 hairpin coding ends and 2 blunt, 5'-phosphorylated ends. The chromatin structure plays an essential role in the V(D)J recombination reactions and the presence of histone H3 trimethylated at 'Lys-4' (H3K4me3) stimulates both the nicking and haipinning steps. The RAG complex also plays a role in pre-B cell allelic exclusion, a process leading to expression of a single immunoglobulin heavy chain allele to enforce clonality and monospecific recognition by the B-cell antigen receptor (BCR) expressed on individual B-lymphocytes. The introduction of DNA breaks by the RAG complex on one immunoglobulin allele induces ATM-dependent repositioning of the other allele to pericentromeric heterochromatin, preventing accessibility to the RAG complex and recombination of the second allele. In the RAG complex, RAG2 is not the catalytic component but is required for all known catalytic activities mediated by RAG1. It probably acts as a sensor of chromatin state that recruits the RAG complex to H3K4me3 (By similarity). | ||||||||||||
Domain Profile | Me_Reader PHD PHD.txt 2 tiClvCgkddeg.......eke.....mvqCdeCd.dwfHlkCvklp...lsslpeg.kswyCpsCke 52 |
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Protein 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 527 |
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Nucleotide Sequence (Fasta) | ATTAGATCAG TGTTCATAAG AACATCTGTA GGCACACATA CACACTCTCT TTACAGTCAG 60 CCTTCTGCTT GCCACAGTCA TAGTGGGCAG TCAGTGAATC TTCCCCAAGT GCTGACAATT 120 AATACCTGGT TTAGCGGCAA AGATTCAGAG AGGCGTGAGC AGCCCCTCTG GCCTTCAGAA 180 TGAAGATGAA AAGAAGATGT GTTTAGGAAC CTTCTCTGCT TCCCTAAAAG AACCCTAAAA 240 ACAGGAGTAA AAACAGTGAA GAAAACAAAG GACCTTCAAA GTGCACTCGT TAAAACCTAA 300 TAACTGTATT TCTATTACTA AATGTAGAAG TGGTAAACAT CTTTAACAGG CAATGTCTCC 360 CCTGCACTCT AGGGATTCAA AGATCCATCT TTCGGTTCTG TAAGACAGTC ACGGCTTTTG 420 TAACCTCGGT GCCCCCTTCA ACCTCCCGCC CCAAGCACCT CCAGGGTCGT CAGGGGTGTA 480 GTTTTGAGTC GCGCTCCTAA GCATCCAGAC AGGCAGGACA CCGTAACGAC ATCTCTGCCG 540 GGAGTCCCTT CAGACTGCGG TCTCCAGACA AAAATCTACG TACCATCAGA AACTATGTCT 600 CTGCAGATGG TAACAGTCAG TAATAACATA GCCTTAATTC AGCCAGGCTT CTCACTGATG 660 AATTTTGATG GACAAGTTTT CTTCTTTGGA CAAAAAGGCT GGCCCAAAAG ATCCTGCCCC 720 ACTGGAGTTT TCCATCTGGA TGTAAAGCAT AACCATGTCA AACTGAAGCC TACAATTTTC 780 TCTAAGGATT CCTGCTACCT CCCTCCTCTT CGCTACCCAG CCACTTGCAC ATTCAAAGGC 840 AGCTTGGAGT CTGAAAAGCA TCAATACATC ATCCATGGAG GGAAAACACC AAACAATGAG 900 GTTTCAGATA AGATTTATGT CATGTCTATT GTTTGCAAGA ACAACAAAAA GGTTACTTTT 960 CGCTGCACAG AGAAAGACTT GGTAGGAGAT GTTCCTGAAG CCAGATATGG TCATTCCATT 1020 AATGTGGTGT ACAGCCGAGG GAAAAGTATG GGTGTTCTCT TTGGAGGACG CTCATACATG 1080 CCTTCTACCC ACAGAACCAC AGAAAAATGG AATAGTGTAG CTGACTGCCT GCCCTGTGTT 1140 TTCCTGGTGG ATTTTGAATT TGGGTGTGCT ACATCATACA TTCTTCCAGA ACTTCAGGAT 1200 GGGCTATCTT TTCATGTCTC TATTGCCAAA AATGACACCA TCTATATTTT AGGAGGACAT 1260 TCACTTGCCA ATAATATCCG GCCTGCCAAC CTGTACAGAA TAAGGGTTGA TCTTCCCCTG 1320 GGTAGCCCAG CTGTGAATTG CACAGTCTTG CCAGGAGGAA TCTCTGTCTC CAGTGCAATC 1380 CTGACTCAAA CTAACAATGA TGAATTTGTT ATTGTTGGTG GCTATCAGCT TGAAAATCAA 1440 AAAAGAATGA TCTGCAACAT CATCTCTTTA GAGGACAACA AGATAGAAAT TCGTGAGATG 1500 GAGACCCCAG ATTGGACCCC AGACATTAAG CACAGCAAGA TATGGTTTGG AAGCAACATG 1560 GGAAATGGAA CTGTTTTTCT TGGCATACCA GGAGACAATA AACAAGTTGT TTCAGAAGGA 1620 TTCTATTTCT ATATGTTGAA ATGTGCTGAA GATGATACTA ATGAAGAGCA GACAACATTC 1680 ACAAACAGTC AAACATCAAC AGAAGATCCA GGGGATTCCA CTCCCTTTGA AGACTCTGAA 1740 GAATTTTGTT TCAGTGCAGA AGCAAATAGT TTTGATGGTG ATGATGAATT TGACACCTAT 1800 AATGAAGATG ATGAAGAAGA TGAGTCTGAG ACAGGCTACT GGATTACATG CTGCCCTACT 1860 TGTGATGTGG ATATCAACAC TTGGGTACCA TTCTATTCAA CTGAGCTCAA CAAACCCGCC 1920 ATGATCTACT GCTCTCATGG GGATGGGCAC TGGGTCCATG CTCAGTGCAT GGATCTGGCA 1980 GAACGCACAC TCATCCATCT GTCAGCAGGA AGCAACAAGT ATTACTGCAA TGAGCATGTG 2040 GAGATAGCAA GAGCTCTACA CACTCCCCAA AGAGTCCTAC CCTTAAAAAA GCCTCCAATG 2100 AAATCCCTCC GTAAAAAAGG TTCTGGAAAA ATCTTGACTC CTGCCAAGAA ATCCTTTCTT 2160 AGAAGGTTGT TTGATTAGTT TTGCAAAAGC CTTTCAGATT CAGGTGTATG GAATTTTTGA 2220 ATCTATTTTT AAAATCATAA CATTGATTTT AAAAATACAT TTTTGTTTAT TTAAAATGCC 2280 TATGTTTTCT TTTAGTTACA TGAATTAAGG GCCAGAAAAA AGTGTTTATA ATGCAATGAT 2340 AAATAAAGTC ATTCTAGACC CTATACATTT TGAAAATATT TTACCCAAAT ACTCAATTTA 2400 CTAATTTATT CTTCACTGAG GATTTCTGAT CTGATTTTTT ATTCAACAAA CCTTAAACAC 2460 CCAGAAGCAG TAATAATCAT CGAGGTATGT TTATATTTAT TATATAAGTC TTGGTAACAA 2520 ATAACCTATA AAGTGTTTAT GACAAATTTA GCCAATAAAG AAATTAACAC CCAAAAGAAT 2580 TAAATTGATT ATTTTGTGCA ACATAACAAT TCGGCAGTTG GCCAAAACTT AAAAGCAAGA 2640 TCTACTACAT CCCACATTAG TGTTCTTTAT ATACCTTCAA GCAACCCTTT GGATTATGCC 2700 CATGAACAAG TTAGTTTCTC ATAGCTTTAC AGATGTAGAT ATAAATATAA ATATATGTAT 2760 ACATATAGAT AGATAATGTT CTCCACTGAC ACAAAAGAAG AAATAAATAA TCTACATC 2819 |
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Sequence Source | Ensembl | ||||||||||||
Keyword | KW-0156--Chromatin regulator |
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Interpro | IPR011043--Gal_Oxase/kelch_b-propeller |
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PROSITE | |||||||||||||
Pfam | PF03089--RAG2 |
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Gene Ontology | GO:0005654--C:nucleoplasm |
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Orthology | |||||||||||||
Created Date | 25-Jun-2016 |