Dfur1, Dfurin1, dKLIP-1, Furin, l(3)rL205
Please see the JBrowse view of Dmel\Fur1 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 5.43
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Gene model reviewed during 5.48
7.6, 6.5, 4.5, 4.0 (northern blot)
8.4, 6.8, 4.5, 4.0 (northern blot)
6.5, 4.5, 4.0 (northern blot)
1101, 892 (aa)
1101 (aa); 140 (kD observed); 131 (kD predicted)
899 (aa)
The 1101aa Fur1 protein is identical over most of its length to the other Fur1 isoforms but has two cysteine-rich regions near the carboxyl end of the protein (called CRR by authors). Its activity as a proprotein processing enzyme was demonstrated in gene transfer experiments, where it is capable of processing the precursor of the βA-chain of activin-A and the precursor of von Willebrand factor to the mature forms.
The 1269aa Fur1 protein is identical over most of its length to the other Fur1 isoforms but has a unique domain of 377aa inserted near the carboxyl end (called domain X by authors). Its activity as a proprotein processing enzyme was demonstrated in gene transfer experiments, where it is capable of processing the precursor of the βA-chain of activin-A and the precursor of von Willebrand factor to the mature forms.
The 892aa Fur1 protein is identical over most of its length to the other Fur1 isoforms but lacks the inserted domains present near the carboxyl end in the other two isoforms. Its activity as a proprotein processing enzyme was demonstrated in gene transfer experiments, where it is capable of processing the precursor of the βA-chain of activin-A and the precursor of von Willebrand factor to the mature forms.
One of several protein products generated by alternative splicing.
The 899aa Fur1 protein species was predicted from a composite cDNA sequence from two cDNA clones.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Fur1 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).
Co-localisation of Fur1 and ScerGAL4dimm-929 is observed in a subset of Fur1-positive neurons of the central nervous system.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Fur1 in JBrowse3-87
3-86.0
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.
The Fur1 gene encodes structurally different subtilisin-like proprotein processing enzymes with distinct physiological functions.
Cloning, tissue and developmental expression, and endoproteolytic activity of Fur1 is studied.
Isolated from a genomic library using a human furin cDNA as a probe, under reduced stringency conditions.
Fur1 has been cloned and sequenced.
Source for merge of: Fur1 l(3)rL205
Source for merge of: Fur1 CG10772