s36, dec2, fs(1)C2, dec-2
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 5.45
There is only one protein coding transcript and one polypeptide associated with this gene
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Cp36 using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Cp36 in GBrowse 2
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 identity of: Cp36 CG1478
In a sample of 79 genes with multiple introns, 33 showed significant heterogeneity in G+C content among introns of the same gene and significant positive correspondence between the intron and the third codon position G+C content within genes. These results are consistent with selection adding against preferred codons at the start of genes.
P element constructs carrying Ecol\lacZ and Ecol\CAT reporter genes demonstrate that if the 5' untranslated and coding regions of Cp36 are deleted then normal ovarian expression is maintained but tissue specificity is relaxed.
Ecol\lacZ reporter gene constructs carrying deletions of the Cp36 regulatory area have defined an 84bp proximal regulatory region (PRR) between nucleotides -132 and -49 from the 5' end of Cp36 and a distal regulatory region (DRR) between nucleotides -1213 to -422.
Transcription termination sites of Cp36 and Cp38 have been mapped using EM analysis. Results demonstrate that Cp36 and Cp38 terminate more closely to the poly(A) addition sites and in a shorter region than many other polyadenylation genes examined to date.
Approximately 1,000 daltons cleaved from primary translation product to yield mature protein.