Attacin, Att, Att-A, att A
Please see the JBrowse view of Dmel\AttA for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Gene model reviewed during 5.40
Gene model reviewed during 5.50
There is only one protein coding transcript and one polypeptide associated with this gene
224 (aa)
Small AttA-derived peptides identified by nano LC-MS/MS: pQVLGGSLTSNPAGGADA, pQVLGGSLTSNPAGGADAR.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\AttA using the Feature Mapper tool.
Reporter constructs were used to show that expression of AttA is bacterially induced.
GBrowse - Visual display of RNA-Seq signals
View Dmel\AttA in GBrowse 22-72
2-76.4
Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete
Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see GBrowse for alignment of the cDNAs and ESTs to the gene model.
For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.
Source for merge of: AttA BcDNA:LP05763
Source for merge of: AttA anon-WO0140519.5
Source for merge of AttA anon-WO0140519.5 was sequence comparison ( date:051113 ).
Identified as a gene with significant level of mRNA cycling as assessed by expression analysis using high density oligonucleotide arrays with probe generated from adult heads harvested over six time points over the course of a day. Shows alteration in expression in a Clk mutant background.
Ecol\lacZDpt.PR adults are pricked with a sterile needle dipped in culture pellets of various living microorganisms (distinct bacterial strains, fungal spores or hyphae). Pricking results in a low but clearly detectable expression of all antimicrobial genes and these genes are induced above the background level by specific classes of microorganism.
Genes encoding antibacterial peptides are regulated in a manner distinct from that of Drs, encoding the antifungal peptide.
Differential display can be applied to a whole organism to identify induced immune genes, the technique has been used to isolate and characterise AttA.