dNmnat
NAD salvage pathway - catalyzing the last step of NAD synthesis - stress response protein - required for thermotolerance and mitigation of oxidative stress-induced shortened lifespan - protects against axonal degeneration through chaperone activity - protects against neurodegeneration through a proteasome-mediated pathway - required for maintaining active zone structural integrity by interacting Bruchpilot - regulated post-transcriptionally by Highwire function
Please see the JBrowse view of Dmel\Nmnat 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 5.48
Gene model reviewed during 6.19
None of the polypeptides share 100% sequence identity.
The N-terminal region, which includes the putative catalytic motif, is not required for chaperone activity.
The C-terminal region, which includes a putative ATP binding motif, is required for efficient chaperone activity.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Nmnat 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
JBrowse - Visual display of RNA-Seq signals
View Dmel\Nmnat in JBrowse3-86
3-85.1
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.
Nmnat is cell-autonomously required for maintaining type-specific dendritic coverage of dendritic arborization (da) sensory neurons.
Loss of Nmnat affects the axons of all classes of da neurons demonstrating its function in maintaining axonal integrity is not restricted to distinct neuronal subtypes.
Source for identity of: Nmnat CG13645