Spla/ryanodine receptor domain and socs box containing 3

SPRY domain
Identifiers
Symbol	SPRY
Pfam	PF00622
InterPro	IPR003877
Available protein structures: Pfam structures PDB RCSB PDB; PDBe; PDBj PDBsum structure summary

VALUE_ERROR (nil)
Identifiers
Aliases
External IDs	GeneCards: [1]
Orthologs
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a
Wikidata
View/Edit Human

SplA/ryanodine receptor domain and SOCS box containing 3 is a protein that in humans is encoded by the SPSB3 gene.

External links

• Eukaryotic Linear Motif resource motif class LIG_SPRY_1

Further reading

• Nishiya, T.; Matsumoto, K.; Maekawa, S.; Kajita, E.; Horinouchi, T.; Fujimuro, M.; Ogasawara, K.; Uehara, T.; Miwa, S. (2011). "Regulation of Inducible Nitric-oxide Synthase by the SPRY Domain- and SOCS Box-containing Proteins". Journal of Biological Chemistry. 286 (11): 9009–9019. doi:10.1074/jbc.M110.190678. PMC 3058989. PMID 21199876.
• Kile, B. T.; Schulman, B. A.; Alexander, W. S.; Nicola, N. A.; Martin, H. M.; Hilton, D. J. (2002). "The SOCS box: A tale of destruction and degradation". Trends in Biochemical Sciences. 27 (5): 235–241. doi:10.1016/S0968-0004(02)02085-6. PMID 12076535.
• Wang, D.; Li, Z.; Messing, E. M.; Wu, G. (2005). "The SPRY Domain-containing SOCS Box Protein 1 (SSB-1) Interacts with MET and Enhances the Hepatocyte Growth Factor-induced Erk-Elk-1-Serum Response Element Pathway". Journal of Biological Chemistry. 280 (16): 16393–16401. doi:10.1074/jbc.M413897200. PMID 15713673.
• Naukkarinen, J.; Surakka, I.; Pietiläinen, K. H.; Rissanen, A.; Salomaa, V.; Ripatti, S.; Yki-Järvinen, H.; Van Duijn, C. M.; Wichmann, H. -E.; Kaprio, J.; Taskinen, M. R.; Peltonen, L.; Engage, C. (2010). Gibson, Greg, ed. "Use of Genome-Wide Expression Data to Mine the "Gray Zone" of GWA Studies Leads to Novel Candidate Obesity Genes". PLoS Genetics. 6 (6): e1000976. doi:10.1371/journal.pgen.1000976. PMC 2880558. PMID 20532202.
• Daniels, R. J.; Peden, J. F.; Lloyd, C.; Horsley, S. W.; Clark, K.; Tufarelli, C.; Kearney, L.; Buckle, V. J.; Doggett, N. A.; Flint, J.; Higgs, D. R. (2001). "Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16". Human Molecular Genetics. 10 (4): 339–352. doi:10.1093/hmg/10.4.339. PMID 11157797.