Adk2, Dak2, l(2)k04201, l(2)k16120, Adk2-60B
Please see the JBrowse view of Dmel\Ak2 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.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.52
There is only one protein coding transcript and one polypeptide associated with this gene
Monomer.
Consists of three domains, a large central CORE domain and two small peripheral domains, NMPbind and LID, which undergo movements during catalysis. The LID domain closes over the site of phosphoryl transfer upon ATP binding. Assembling and dissambling the active center during each catalytic cycle provides an effective means to prevent ATP hydrolysis.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Ak2 using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
Comment: maternally deposited
Comment: reported as muscle system primordium
Comment: reported as muscle system primordium
JBrowse - Visual display of RNA-Seq signals
View Dmel\Ak2 in JBrowse2-106
2-109.9
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 JBrowse 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: Adk2 BcDNA:SD09634
Source for merge of: Adk2-60B Adk2-44B Adk2
Source for merge of: Adk2 Adk2-44B
Sequence and complementation results indicate that P{lacW}k16120 maps to 60B and not 44B. Since localization of this insertion to 44B was the only evidence for an Adk2 gene in 44B, the Adk2-44B gene (FBgn0021824) should be eliminated and the information on P{lacW}k16120 should be merged into the entry for Adk2.
The 'Adk2-44B' gene was originally mapped to 44B based on in situs against the k16120 insertion, but presumably this was an error as the flanking sequence of the k16120 insertion localizes it to the 'Adk2' gene in 60B.
Source for identity of: anon-Dak2 CG3140
Source for identity of: Ak2 Adk2
FlyBase curator comment: Renamed from Adk2 to Ak2 because (i) 'Ak' is the standard abbreviation for 'adenylate kinase' (this enzyme), whereas 'Adk' is the standard abbreviation for 'adenosine kinase'; (ii) an 'ak' (rather than 'adk') prefix has been used in all papers that focus on the Drosophila gene/protein, including the first to characterize it (this one - FBrf0127253); (iii) we are already using the 'ak' prefix for the 'Ak6' gene.