Activation-induced (cytidine) deaminase
AICDA |
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Available structures |
PDB |
Ortholog search: PDBe RCSB
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List of PDB id codes |
5JJ4
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Identifiers |
Aliases |
AICDA, AID, ARP2, CDA2, HEL-S-284, HIGM2, activation-induced cytidine deaminase, activation induced cytidine deaminase |
External IDs |
MGI: 1342279 HomoloGene: 7623 GeneCards: AICDA |
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Gene location (Mouse) |
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Chr. |
Chromosome 6 (mouse) |
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Band |
6|6 F1 |
Start |
122,553,801 bp |
End |
122,564,180 bp |
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Orthologs |
Species |
Human |
Mouse |
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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RefSeq (protein) |
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Location (UCSC) |
Chr 12: 8.6 – 8.61 Mb |
Chr 12: 122.55 – 122.56 Mb |
PubMed search |
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5JJ4
57379
11628
ENSG00000111732
ENSMUSG00000040627
Q9GZX7
Q9WVE0
NM_020661
NM_001330343
NM_009645
NP_001317272
NP_065712
NP_033775
Activation-induced cytidine deaminase, also known as AICDA and AID, is a 24 kDa enzyme which in humans is encoded by the AICDA gene. It creates mutations in DNA by deamination of cytosine base, which turns it into uracil (which is recognized as a thymine). In other words, it changes a C:G base pair into a U:G mismatch. The cell's DNA replication machinery recognizes the U as a T, and hence C:G is converted to a T:A base pair. During germinal center development of B lymphocytes, AID also generates other types of mutations, such as C:G to A:T. The mechanism by which these other mutations are created is not well understood.
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