Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

STRAP

From Wikipedia, the free encyclopedia

STRAP
Identifiers
AliasesSTRAP, MAWD, PT-WD, UNRIP, serine/threonine kinase receptor associated protein
External IDsOMIM: 605986; MGI: 1329037; GeneCards: STRAP
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_007178

NM_011499

RefSeq (protein)

NP_009109

NP_035629

Location (UCSC)Chr 12: 15.88 – 15.9 MbChr 6: 137.71 – 137.73 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
The figure illustrates the inhibitory effect of NM23-H1 on Smad3 nuclear translocation in the TGF-β signaling pathway. Panels A and B show NM23-H1's impact on the association of activated TGF-β receptor with Smad7 and STRAP, respectively. Panels C and D demonstrate NM23-H1's modulation of Smad3 localization in Hep3B cells. Panel E extends this analysis with NM23-H1(C145S). Quantitative analysis, using densitometry, shows the relative Smad3 expression levels compared to controls. These experiments collectively highlight NM23-H1's role in regulating Smad3 and its association with TGF-β signaling components. The data are representative of multiple independent experiments.[5]

Serine-threonine kinase receptor-associated protein is an protein that in humans is encoded by the STRAP gene.[6]

Structure

[edit]

STRAP is a 38.5 kDa, 350-amino acid protein belonging to the WD40 repeat protein family. It contains seven WD40 repeats that fold into a seven-bladed β-propeller structure that spans almost the entire length of the protein.[7] The N-terminal WD40 repeats binds to TGF-β receptor I, whereas the C-terminal region is phosphorylated by TGF-β receptor II.[8]

Function

[edit]

STRAP is a WD40-repeat protein that binds both the type I and type II TGF-β receptors. Its primary function is to recruit and stabilize the inhibitory Smad, SMAD7, at the activated TGF-β receptor complex.[9]

By stabilizing this STRAP/SMAD7/TGF-β receptor complex, STRAP sterically blocks SMAD2 and SMAD3 from binding to the activated type I TGF-β receptor, preventing its phosphorylation and thus blunting TGF-β mediated up-regulation of gene expression.[9][10][11]

Apoptosis

[edit]

STRAP binds directly to ASK1 through ASK1's C-terminal domain and the fourth and sixth WD40 repeats of STRAP.[12] This binding allows STRAP to be phosphorylated by ASK1, and the resulting complex reduces ASK1's downstream signaling to the JNK and p38 stress-response pathways.[13] It does so by helping to stabilize ASK1's association with its own inhibitory proteins, thioredoxin and 14-3-3. It also reduces ASK1's ability to form a complex with its downstream target MKK3.[13] Through this mechanism, STRAP protects cells from H2O2-induced, ASK1-driven apoptosis, favoring cell survival. STRAP has also been described as a positive regulator of PDK1 signaling.[13][14]

Clinical significance

[edit]

STRAP is a component of the survival motor neuron (SMN) complex, binding to it through an interaction with GEMIN7.[15] Loss of the complex's core protein, SMN, causes spinal muscular atrophy, a childhood disorder characterized by motor neuron degeneration.[16]

STRAP also inhibits TGF-β receptor signaling by stabilizing the inhibitory protein SMAD7, which in turn limits activation of SMAD2 and SMAD3.[17][18] This pathway is frequently dysregulated in cancer and elevated STRAP expression has been reported in several tumor types, including colorectal and lung carcinoma, where it promotes proliferation and reduces apoptosis.[19]

Interactions

[edit]

STRAP has been shown to interact with:

References

[edit]
  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000023734 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000030224 Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Seong HA, Jung H, Ha H (April 2007). "NM23-H1 tumor suppressor physically interacts with serine-threonine kinase receptor-associated protein, a transforming growth factor-beta (TGF-beta) receptor-interacting protein, and negatively regulates TGF-beta signaling". The Journal of Biological Chemistry. 282 (16): 12075–12096. doi:10.1074/jbc.m609832200. PMID 17314099.
  6. "Entrez Gene: STRAP serine/threonine kinase receptor associated protein".
  7. Karfa S, Saurav S, Feng B, Li S, Law BK, Datta PK (June 2025). "The Role of Serine-Threonine Kinase Receptor-Associated Protein (STRAP) Signaling in Cancer". Cells. 14 (12). doi:10.3390/cells14120854. PMC 12190354. PMID 40558481.
  8. Vukmirovic M, Manojlovic Z, Stefanovic B (October 2013). "Serine-threonine kinase receptor-associated protein (STRAP) regulates translation of type I collagen mRNAs". Molecular and Cellular Biology. 33 (19): 3893–3906. doi:10.1128/MCB.00195-13. PMC 3811873. PMID 23918805.
  9. 1 2 3 4 5 6 7 8 Datta PK, Moses HL (May 2000). "STRAP and Smad7 synergize in the inhibition of transforming growth factor beta signaling". Molecular and Cellular Biology. 20 (9): 3157–3167. doi:10.1128/MCB.20.9.3157-3167.2000. PMC 85610. PMID 10757800.
  10. Halder SK, Anumanthan G, Maddula R, Mann J, Chytil A, Gonzalez AL, et al. (June 2006). "Oncogenic function of a novel WD-domain protein, STRAP, in human carcinogenesis". Cancer Research. 66 (12): 6156–6166. doi:10.1158/0008-5472.CAN-05-3261. PMID 16778189.
  11. Xu P, Liu J, Derynck R (July 2012). "Post-translational regulation of TGF-β receptor and Smad signaling". FEBS Letters. 586 (14): 1871–1884. doi:10.1016/j.febslet.2012.05.010. PMC 4240271. PMID 22617150.
  12. Jung H, Seong HA, Manoharan R, Ha H (January 2010). "Serine-threonine kinase receptor-associated protein inhibits apoptosis signal-regulating kinase 1 function through direct interaction". The Journal of Biological Chemistry. 285 (1): 54–70. doi:10.1074/jbc.M109.045229. PMC 2804202. PMID 19880523.
  13. 1 2 3 Manoharan R, Seong HA, Ha H (April 2018). "Dual Roles of Serine-Threonine Kinase Receptor-Associated Protein (STRAP) in Redox-Sensitive Signaling Pathways Related to Cancer Development". Oxidative Medicine and Cellular Longevity. 2018 5241524. doi:10.1155/2018/5241524. PMC 5933018. PMID 29849900.
  14. Karfa S, Saurav S, Feng B, Li S, Law BK, Datta PK (June 2025). "The Role of Serine-Threonine Kinase Receptor-Associated Protein (STRAP) Signaling in Cancer". Cells. 14 (12): 854. doi:10.3390/cells14120854. PMC 12190354. PMID 40558481.
  15. Otter S, Grimmler M, Neuenkirchen N, Chari A, Sickmann A, Fischer U (2007). "A comprehensive interaction map of the human survival of motor neuron (SMN) complex". The Journal of Biological Chemistry. 282 (8): 5825–5833. doi:10.1074/jbc.M608528200. hdl:21.11116/0000-0007-E7EE-9. PMID 17178713.
  16. Chaytow H, Huang YT, Gillingwater TH, Faller KM (2018). "The role of survival motor neuron protein (SMN) in protein homeostasis". Cellular and Molecular Life Sciences. 75 (21): 3877–3894. doi:10.1007/s00018-018-2849-1. PMC 6182345. PMID 29872871.
  17. Datta PK, Moses HL (2000). "STRAP and Smad7 synergize in the inhibition of transforming growth factor beta signaling". Molecular and Cellular Biology. 20 (9): 3157–3167. doi:10.1128/MCB.20.9.3157-3167.2000. PMC 85610. PMID 10757800.
  18. Xu P, Liu J, Derynck R (2012). "Post-translational regulation of TGF-β receptor and Smad signaling". FEBS Letters. 586 (14): 1871–1884. doi:10.1016/j.febslet.2012.05.010. PMC 4240271. PMID 22617150.
  19. Karfa S, Saurav S, Feng B, Li S, Law BK, Datta PK (2025). "The Role of Serine-Threonine Kinase Receptor-Associated Protein (STRAP) Signaling in Cancer". Cells. 14 (12): 854. doi:10.3390/cells14120854. PMC 12190354. PMID 40558481.
  20. 1 2 Datta PK, Chytil A, Gorska AE, Moses HL (December 1998). "Identification of STRAP, a novel WD domain protein in transforming growth factor-beta signaling". The Journal of Biological Chemistry. 273 (52): 34671–34674. doi:10.1074/jbc.273.52.34671. PMID 9856985.

Further reading

[edit]