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P23771 of Proteins GATA-type domain repeats
Uniprot ID:P23771
Protein name: Trans-acting T-cell-specific transcription factor GATA-3
Gene : GATA3
Protein Family:
Squence Length : 443
Sequnce
>P23771 444 MEVTADQPRWVSHHHPAVLNGQHPDTHHPGLSHSYMDAAQYPLPEEVDVLFNIDGQGNHVPPYYGNSVRATVQRYPPTHHGSQVCRPPLLHGSLPWLDGGKALGSHHTASPWNLSPFSKTSIHHGSPGPLSVYPPASSSSLSGGHASPHLFTFPPTPPKDVSPDPSLSTPGSAGSARQDEKECLKYQVPLPDSMKLESSHSRGSMTALGGASSSTHHPITTYPPYVPEYSSGLFPPSSLLGGSPTGFGCKSRPKARSSTGRECVNCGATSTPLWRRDGTGHYLCNACGLYHKMNGQNRPLIKPKRRLSAARRAGTSCANCQTTTTTLWRRNANGDPVCNACGLYYKLHNINRPLTMKKEGIQTRNRKMSSKSKKCKKVHDSLEDFPKNSSFNPAALSRHMSSLSHISPFSHSSHMLTTPTPMHPPSSLSFGPHHPSSMVTAMG
GATA-type domains repeats
ZN_FING 263 287 GATA-type 1 ZN_FING 317 341 GATA-type 2
Domin repeated regions
263 - 287 CVNCGATSTPLWRRDGTGHYLCNAC 317 - 341 CANCQTTTTTLWRRNANGDPVCNAC
Function
Transcriptional activator which binds to the enhancer of the T-cell receptor alpha and delta genes. Binds to the consensus sequence 5'-AGATAG-3'. Required for the T-helper 2 (Th2) differentiation process following immune and inflammatory responses
Motifs
MOTIF 344 353 YxKxHxxxRP
Disease
"DISEASE: Hypoparathyroidism, sensorineural deafness, and renal disease (HDR) [MIM:146255]: A disease characterized by steroid-resistant nephrosis with progressive renal failure, hypoparathyroidism, sensorineural deafness, and renal dysplasia Note=The disease is caused by mutations affecting the gene represented in this entry"