EG:171D11.3 , CPD, slv
Please see the JBrowse view of Dmel\svr 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 5.50
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.55
6-7, 3.9, 3.3, 2.5, 1.5 (compiled cDNA)
1119 (aa); 126.5 (kD predicted)
There are 3 carboxypeptidase-like domains (PubMed:12393882, PubMed:20386952). Only the first two domains seem to have catalytic activity (PubMed:12393882, PubMed:16556608, PubMed:20386952). However, in svr proteins there are two alternative carboxypeptidase-like 1 domains (CP-1), a catalytically inactive 1A form (in isoforms 3, 4 and 6) and an active 1B form (in isoforms 1, 5, and 7) (PubMed:12393882). All 3 carboxypeptidase-like domains (active CP-1, CP-2 and CP-3) appear to necessary for maintaining full viability (PubMed:20386952). The active CP-1 and CP-2 domains display redundant functions in terms of processing peptides involved in viability, and in behaviors like cold and ethanol sensitivity, as well as long-term memory (PubMed:20386952). However, the active CP-1 domain appears to preferentially remove C-terminal Arg residues while CP-2 preferentially removes C-terminal Lys residues (PubMed:20386952). The active CP-1 is sufficient for survival (PubMed:16556608). The CP-3 domain appears to be important for development from embryo to adult (PubMed:20386952).
The C-terminus in isoforms 4, 5 and 6 may be required for the retrograde transport of these proteins from the cell membrane to the trans-Golgi network.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\svr 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).
svr transcripts are detected in Northern blots of embryonic RNA.
JBrowse - Visual display of RNA-Seq signals
View Dmel\svr in JBrowse1-0
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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.
S2 cells treated with dsRNA generated against this gene show reduced phagocytosis of Candida albicans compared to untreated cells.
svr has been cloned and sequenced.
Source for merge of: svr CG18503
Source for merge of: svr CpepE
Source for merge of svr CpepE was sequence comparison ( date:000117 ).
may be allelic to pld: pallid
Source for identity of: svr CG4122