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9.A.48.1.1
The Unconventional Protein Secretion System, UPSS (Giuliani et al., 2011).  IT secretes FGF1 (an annexin; TC#1.A.31) and Epimorphin (syntaxin 2; 8.A.91) (Hirai et al. 2007). GRASP55 regulates this unconventional secretion and aggregation of mutant huntingtin (Ahat et al. 2022). Golgi reassembly stacking proteins (GRASPs) regulate Golgi-independent unconventional secretion of certain cytosolic and transmembrane protein cargoes.  Ahat et al. 2022 surveyed several neurodegenerative disease-related proteins, including mutant huntingtin (Htt-Q74), superoxide dismutase 1 (SOD1), tau, and TAR DNA-binding protein 43 (TDP-43), for unconventional secretion; Htt-Q74 was most robustly secreted in a GRASP55-dependent manner. Unconventional secretion of Htt is GRASP55 and autophagy dependent and is enhanced under stress conditions such as starvation and ER stress. GRASP55 facilitates Htt secretion by tethering autophagosomes to lysosomes to promote autophagosome maturation and subsequent lysosome secretion and by stabilizing p23/TMED10, a channel for translocation of cytoplasmic proteins into the lumen of the ER-Golgi intermediate compartment. Novel cytosolic cargoes secreted by the same unconventional pathway, include transgelin (TAGLN), multifunctional protein ADE2 (PAICS), and peroxiredoxin-1 (PRDX1) (Ahat et al. 2022). Golgi reassembly-stacking protein 2, (GRS2; GRASP55; Golgi phosphoprotein 6, GOLPH6) regulates this unconventional protein secretion (Ahat et al. 2022).  

Accession Number:P97352
Protein Name:S100a13 aka Protein S100-A13
Length:98
Molecular Weight:11158.00
Species:Mus musculus (Mouse) [10090]
Location1 / Topology2 / Orientation3: Cytoplasm1
Substrate protein polypeptide chain

Cross database links:

RefSeq: NP_033139.1   
Entrez Gene ID: 20196   
Pfam: PF01023   
KEGG: mmu:20196   

Gene Ontology

GO:0005829 C:cytosol
GO:0005615 C:extracellular space
GO:0005509 F:calcium ion binding
GO:0005507 F:copper ion binding
GO:0008289 F:lipid binding
GO:0050703 P:interleukin-1 alpha secretion

References (8)

[1] “Characterization of the human and mouse cDNAs coding for S100A13, a new member of the S100 protein family.”  Wicki R.et.al.   8878558
[2] “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).”  The MGC Project Teamet.al.   15489334
[3] “The intracellular translocation of the components of the fibroblast growth factor 1 release complex precedes their assembly prior to export.”  Prudovsky I.et.al.   12135982
[4] “S100A13 mediates the copper-dependent stress-induced release of IL-1alpha from both human U937 and murine NIH 3T3 cells.”  Mandinova A.et.al.   12746488
[5] “S100A13-lipid interactions-role in the non-classical release of the acidic fibroblast growth factor.”  Kathir K.M.et.al.   17991455
[6] “Solid tumor proteome and phosphoproteome analysis by high resolution mass spectrometry.”  Zanivan S.et.al.   19367708
[7] “Copper induces the assembly of a multiprotein aggregate implicated in the release of fibroblast growth factor 1 in response to stress.”  Landriscina M.et.al.   11432880
[8] “Protein folding does not prevent the nonclassical export of FGF1 and S100A13.”  Graziani I.et.al.   19233122
Structure:
2CXJ     

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FASTA formatted sequence
1:	MAAETLTELE AAIETVVSTF FTFAGREGRK GSLNINEFKE LATQQLPHLL KDVGSLDEKM 
61:	KTLDVNQDSE LRFSEYWRLI GELAKEVRKE KALGIRKK