Fibroblast growth factor receptor
From Proteopedia
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== Function == | == Function == | ||
| - | '''Fibroblast growth factor receptors''' (FGFR) are receptors which bind fibroblast growth factors (FGF). Each FGFR can activate several FGFs. Five FGFRs have been identified so far. FGFRs differ in their ligand specificity and tissue distribution. The binding of FGF to FGFR starts a cascade of signaling which influences mitogenesis and differentiation<ref>PMID:8713482</ref>. | + | '''Fibroblast growth factor receptors''' (FGFR) are receptors which bind [[fibroblast growth factors]] (FGF). Each FGFR can activate several FGFs. Five FGFRs have been identified so far. FGFRs differ in their ligand specificity and tissue distribution. The binding of FGF to FGFR starts a cascade of signaling which influences mitogenesis and differentiation<ref>PMID:8713482</ref>. See also [[Receptor tyrosine kinases]] and [[Kinase-linked, enzyme-linked and related receptors]]. |
| + | *'''FGFR2''' is essential for limb induction<ref>PMID:9435295</ref>. | ||
| + | *'''FGFR3''' is involved in skeletal dysplasia<ref>PMID:22045636</ref>. | ||
== Disease == | == Disease == | ||
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</StructureSection> | </StructureSection> | ||
| - | ==3D structures of fibroblast growth factor receptor== | ||
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| - | Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}} | ||
| - | {{#tree:id=OrganizedByTopic|openlevels=0| | ||
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| - | *FGFR1 | ||
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| - | *''FGFR1 tyrosine kinase domain residues 458-765'' | ||
| - | |||
| - | **[[4uwy]], [[6mzq]] – hFGFR1 TKD - human<br /> | ||
| - | **[[1fgk]], [[3kxx]], [[3ky2]], [[4rwi]], [[5flf]] – hFGFR1 TKD (mutant) - human <br /> | ||
| - | **[[4wun]], [[5am6]], [[5ew8]], [[5o49]], [[5o4a], [[6mzw]], [[6c1o]] – hFGFR1 TKD + inhibitor <br /> | ||
| - | **[[1agw]], [[1fgi]], [[2fgi]], [[3c4f]], [[3js2]], [[3rhx]], [[4f63]], [[4f64]], [[4f65]], [[3tt0]], [[4nk9]], [[4nka]], [[4nks]], [[5b7v]], [[5am7]], [[4rwj]], [[4rwk]], [[4rwl]], [[4uwb]], [[4uwc]], [[4zsa]], [[5uq0]], [[5vnd]], [[5ur1]], [[6p68]], [[6p69]], [[6c18]], [[6c19]], [[6c1b]], [[6c1c]], [[5z0s]] – hFGFR1 TKD (mutant) + inhibitor <br /> | ||
| - | **[[5zv2]] – hFGFR1 TKD (mutant) + anti-cancer drug<br /> | ||
| - | **[[3krj]] – hFGFR1 TKD residues 538-678, 753-922 (mutant) + inhibitor <br /> | ||
| - | **[[1xr0]] – hFGFR1 residues 409-430 + FGFR signaling adaptor N terminal - NMR<br /> | ||
| - | **[[3gqi]] – hFGFR1 TKD (mutant) with PTR + ACP <br /> | ||
| - | **[[3gql]] – hFGFR1 TKD (mutant) + substrate <br /> | ||
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| - | *''FGFR1 ligand-binding domain D1 residues 35-208'' | ||
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| - | **[[2cr3]] – hFGFR1 LBD D1 - NMR<br /> | ||
| - | **[[2ckn]] – FGFR1 LBD D1 – mouse - NMR<br /> | ||
| - | |||
| - | *''FGFR1 D1 complex with FGF'' | ||
| - | |||
| - | **[[5w59]] – hFGFR1 LBD D1 + FGF9<br /> | ||
| - | |||
| - | *''FGFR1 D2,D3 residues 142-365 complex with FGF'' | ||
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| - | **[[3ojv]] – hFGFR1 LBD D2,D3 (mutant) + hFGF1 - human <br /> | ||
| - | **[[1cvs]] – hFGFR1 LBD D2,D3 (mutant) + hFGF2 (mutant) <br /> | ||
| - | **[[1evt]] – hFGFR1 LBD D2,D3 + hFGF1 <br /> | ||
| - | **[[1fq9]] – hFGFR1 (mutant) LBD D2,D3 + hFGF2 (mutant) + HS<br /> | ||
| - | **[[5w21]] – hFGFR1 LBD D2,D3 + hFGF23 + klotho <br /> | ||
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| - | *FGFR2 | ||
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| - | *''FGFR2 tyrosine kinase domain'' | ||
| - | |||
| - | **[[1gjo]], [[1oec]], [[2psq]] – hFGFR2 TKD <br /> | ||
| - | **[[2pvy]], [[2pwl]], [[2py3]], [[2pz5]], [[2pzp]], [[2pzr]], [[2q0b]], [[4j95]], [[4j96]], [[4j97]], [[4j98]], [[4j99]], [[5ugx]], [[5uhn]], [[5ui0]] – hFGFR2 TKD (mutant) + ACP<br /> | ||
| - | **[[5ugl]] – hFGFR2 TKD (mutant) + ANP<br /> | ||
| - | **[[3b2t]] – hFGFR2 TKD (mutant) + adenosine derivative<br /> | ||
| - | **[[2pvf]] – hFGFR2 TKD with PTR + ACP + substrate peptide<br /> | ||
| - | **[[3cly]] – hFGFR2 TKD (mutant) with PTR + ACP <br /> | ||
| - | **[[5eg3]] – hFGFR2 TKD (mutant) with PTR + ACP + phospholipase C γ<br /> | ||
| - | **[[3ri1]] – hFGFR2 TKD + inhibitor<br /> | ||
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| - | *''FGFR2 ligand-binding domain'' | ||
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| - | **[[3dar]], [[3caf]], [[3euu]] – hFGFR2 LBD D2 <br /> | ||
| - | **[[1wvz]] – hFGFR2 LBD D2 - NMR<br /> | ||
| - | **[[4wv1]] – hFGFR2 LBD D2 + antibody<br /> | ||
| - | **[[4hwu]] – hFGFR2 LBD D1 <br /> | ||
| - | |||
| - | *''FGFR2 complex with FGF'' | ||
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| - | **[[1e0o]] – hFGFR2 (mutant) LBD D2,D3 + hFGF1 (mutant) + HS<br /> | ||
| - | **[[3oj2]], [[3ojm]] – hFGFR2 (mutant) LBD D2,D3 + hFGF1 <br /> | ||
| - | **[[1djs]] – hFGFR2 LBD D2,D3 (mutant) + hFGF1 <br /> | ||
| - | **[[1ev2]], [[1ii4]], [[1iil]] – hFGFR2 LBD D2,D3 + hFGF2 (mutant) <br /> | ||
| - | **[[4j23]] – hFGFR2 LBD D2,D3 (mutant) + hFGF2 (mutant) + inhibitor <br /> | ||
| - | **[[3cu1]] – hFGFR2 LBD D2 + hFGF1 <br /> | ||
| - | **[[2fdb]] – hFGFR2 LBD D2,D3 + hFGF8b <br /> | ||
| - | **[[1nun]] – hFGFR2 LBD D2,D3 + hFGF10 <br /> | ||
| - | |||
| - | *FGFR3 | ||
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| - | **[[3grw]] – hFGFR3 LBD D2,D3 + antibody<br /> | ||
| - | **[[2lzl]] – hFGFR3 residues 357-399 – NMR<br /> | ||
| - | **[[4k33]] – hFGFR3 kinase domain (mutant)<br /> | ||
| - | |||
| - | *''FGFR3 complex with FGF'' | ||
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| - | **[[1ry7]] – hFGFR3 LBD + hFGF1<br /> | ||
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| - | *FGFR4 | ||
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| - | *''FGFR4 tyrosine kinase domain'' | ||
| - | |||
| - | **[[4tye]], [[4tyg]], [[4tyi]], [[4tyj]] – hFGFR4 TKD <br /> | ||
| - | **[[4qqj]], [[4qqt]] – hFGFR4 TKD (mutant) <br /> | ||
| - | **[[5jkg]], [[5nwz]], [[5nud]] – hFGFR4 TKD + inhibitor<br /> | ||
| - | **[[6jpj]], [[5xff]], [[5xfj]] – hFGFR4 TKD (mutant) + inhibitor<br /> | ||
| - | **[[4qrc]], [[4r6v]], [[4qqc]], [[4qq5]], [[4uxq]], [[4xcu]] – hFGFR4 TKD (mutant) + irreversible inhibitor<br /> | ||
| - | }} | ||
== References == | == References == | ||
<references/> | <references/> | ||
[[Category:Topic Page]] | [[Category:Topic Page]] | ||
Current revision
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References
- ↑ Coutts JC, Gallagher JT. Receptors for fibroblast growth factors. Immunol Cell Biol. 1995 Dec;73(6):584-9. PMID:8713482 doi:http://dx.doi.org/10.1038/icb.1995.92
- ↑ Xu X, Weinstein M, Li C, Naski M, Cohen RI, Ornitz DM, Leder P, Deng C. Fibroblast growth factor receptor 2 (FGFR2)-mediated reciprocal regulation loop between FGF8 and FGF10 is essential for limb induction. Development. 1998 Feb;125(4):753-65. PMID:9435295 doi:10.1242/dev.125.4.753
- ↑ Foldynova-Trantirkova S, Wilcox WR, Krejci P. Sixteen years and counting: the current understanding of fibroblast growth factor receptor 3 (FGFR3) signaling in skeletal dysplasias. Hum Mutat. 2012 Jan;33(1):29-41. PMID:22045636 doi:10.1002/humu.21636
- ↑ Wilkin DJ, Szabo JK, Cameron R, Henderson S, Bellus GA, Mack ML, Kaitila I, Loughlin J, Munnich A, Sykes B, Bonaventure J, Francomano CA. Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome. Am J Hum Genet. 1998 Sep;63(3):711-6. PMID:9718331 doi:http://dx.doi.org/10.1086/302000
- ↑ Intini D, Baldini L, Fabris S, Lombardi L, Ciceri G, Maiolo AT, Neri A. Analysis of FGFR3 gene mutations in multiple myeloma patients with t(4;14). Br J Haematol. 2001 Aug;114(2):362-4. PMID:11529856
- ↑ Meyers GA, Orlow SJ, Munro IR, Przylepa KA, Jabs EW. Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans. Nat Genet. 1995 Dec;11(4):462-4. PMID:7493034 doi:http://dx.doi.org/10.1038/ng1295-462
