lxd
Please see the JBrowse view of Dmel\Mocs1 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 5.45
Low-frequency RNA-Seq exon junction(s) not annotated.
Two enzyme activities are encoded by Mocs1. MOCS1B orthologous activity is encoded by the final exon and is produced as a bifunctional protein from transcripts using the downstream splice acceptor site for the final intron, which bypasses the stop codon. All transcripts encode the MOCS1A orthologous activity. (FBrf0131302)
Gene model reviewed during 5.46
None of the polypeptides share 100% sequence identity.
Isoform Mocs1a and isoform Mocs1b probably form a heterooligomer.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Mocs1 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).
JBrowse - Visual display of RNA-Seq signals
View Dmel\Mocs1 in JBrowse3-34
3-28.4
3-34.5
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.
Expression is enriched in embryonic gonads.
The Mocs1 locus produces a bicistronic transcript containing separate, adjacent open reading frames ("Mocs1A" and "Mocs1B" proteins) and also produces a splice form that fuses these ORFs to produce a single, fused "Mocs1A-B" protein.
Adenine resistant lines were generated with diminished xanthine dehydrogenase activity.
Aldehyde oxidase deficient mutants of lxd have appreciable levels of aldehyde oxidase cross-reacting material in both larval haemolymph and adult extracts.
Rocket immunoelectrophoresis was used to estimate xanthine dehydrogenase cross-reacting material (XDH-CRM). Results show high levels of XDH-CRM in mutant lxd flies, this suggests that the primary effects of the mutant gene is on the function of XDH protein rather than its accumulation.
Mutations of lxd exhibit the reduced levels of sulfite oxidase activity compared to wild-type flies. Reduced levels of xanthine dehydrogenase, aldehyde oxidase and alcohol dehydrogenase are also present.
Source for merge of: Mocs1 lxd
"lxd" probably corresponds to "Mocs1". Mutations in "lxd" have only 10% of the normal molybdenum cofactor activity (FBrf0043787) and "Mocs1" is predicted to encode a protein with a high degree of similarity to molybdenum-binding proteins.
Source for identity of Mocs1 CG7858 was sequence comparison ( date:000509 ).
All alleles noncomplementing.
Source for identity of: Mocs1 CG7858