Fibroblast growth factor receptor 3D receptor
3D structures of fibroblast growth factor receptor3D structures of fibroblast growth factor receptor
Updated on 05-March-2023
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- FGFR1
- FGFR1 tyrosine kinase domain (TKD) residues 458-765
- 4uwy – hFGFR1 TKD - human
- 1fgk, 3kxx, 3ky2, 4rwi, 5flf – hFGFR1 TKD (mutant) - human
- 4wun, 5am6, 5ew8, 5o49, 5o4a, 6mzw, 6c1o, 6mzq, 6mzw – hFGFR1 TKD + inhibitor
- 1agw, 1fgi, 2fgi, 3c4f, 3js2, 3rhx, 4f63, 4f64, 4f65, 3tt0, 4nk9, 4nka, 4nks, 5b7v, 5am7, 4rwj, 4rwk, 4rwl, 4uwb, 4uwc, 4zsa, 5uq0, 5vnd, 5ur1, 6c18, 6c19, 6c1b, 6c1c, 5z0s, 6agx, 6itj, 6nvl, 6p68, 6p69, 7ozb, 7ozd, 7ozf, 7ozy, 7wcw – hFGFR1 TKD (mutant) + inhibitor
- 5zv2, 7wcl – hFGFR1 TKD (mutant) + anti-cancer drug
- 3krj – hFGFR1 TKD residues 538-678, 753-922 (mutant) + inhibitor
- 1xr0 – hFGFR1 residues 409-430 + FGFR signaling adaptor N terminal - NMR
- 3gqi – hFGFR1 TKD (mutant) with PTR + ACP
- 3gql – hFGFR1 TKD (mutant) + substrate
- 4uwy – hFGFR1 TKD - human
- FGFR1 ligand-binding domain (LBD) D1 residues 35-208
- FGFR1 LBD D1 complex with FGF
- 5w59 – hFGFR1 LBD D1 + FGF9
- 5w59 – hFGFR1 LBD D1 + FGF9
- FGFR1 LBD D2,D3 residues 142-365 complex with FGF
- FGFR2
- FGFR2 tyrosine kinase domain 413-821
- 1gjo, 1oec, 2psq – hFGFR2 TKD
- 2pvy, 2pwl, 2py3, 2pz5, 2pzp, 2pzr, 2q0b, 4j95, 4j96, 4j97, 4j98, 4j99, 5ugx, 5uhn, 5ui0 – hFGFR2 TKD (mutant) + ACP
- 5ugl – hFGFR2 TKD (mutant) + ANP
- 3b2t – hFGFR2 TKD (mutant) + adenosine derivative
- 2pvf – hFGFR2 TKD with PTR + ACP + substrate peptide
- 3cly, 6v6q – hFGFR2 TKD (mutant) with PTR + ACP
- 5eg3 – hFGFR2 TKD (mutant) with PTR + ACP + phospholipase C γ
- 3ri1, 6lvk, 6lvl, 8e1x – hFGFR2 TKD + inhibitor
- 7kia, 7kie – hFGFR2 TKD (mutant) + inhibitor
- 1gjo, 1oec, 2psq – hFGFR2 TKD
- FGFR2 ligand-binding domain
- FGFR2 complex with FGF
- 1e0o – hFGFR2 (mutant) LBD D2,D3 + hFGF1 (mutant) + HS
- 3oj2, 3ojm – hFGFR2 (mutant) LBD D2,D3 + hFGF1
- 1djs – hFGFR2 LBD D2,D3 (mutant) + hFGF1
- 1ev2, 1ii4, 1iil – hFGFR2 LBD D2,D3 + hFGF2 (mutant)
- 4j23 – hFGFR2 LBD D2,D3 (mutant) + hFGF2 (mutant) + inhibitor
- 3cu1 – hFGFR2 LBD D2 + hFGF1
- 2fdb – hFGFR2 LBD D2,D3 + hFGF8b
- 1nun – hFGFR2 LBD D2,D3 + hFGF10
- 1e0o – hFGFR2 (mutant) LBD D2,D3 + hFGF1 (mutant) + HS
- FGFR3
- FGFR3 complex with FGF
- 1ry7 – hFGFR3 LBD + hFGF1
- 1ry7 – hFGFR3 LBD + hFGF1
- FGFR4
- FGFR4 tyrosine kinase domain
- 4tye, 4tyg, 4tyi, 4tyj – hFGFR4 TKD
- 4qqj, 4qqt – hFGFR4 TKD (mutant)
- 5jkg, 5nwz, 5nud, [6nvg]], 6nvh, 6nvi, 6nvj, 6nvk, 6v9c, 7dtz, 7f3m, 7v29, 7vjl, 7wct, 7ybo, 7yc1, 7yc3 – hFGFR4 TKD + inhibitor
- 6yi8 – hFGFR4 TKD + drug
- 6jpj, 5xff, 5xfj, 6iuo, 6iup, 6jpe, 6jpj, 7wcx, 7ybp, 7ybx – hFGFR4 TKD (mutant) + inhibitor
- 4qrc, 4r6v, 4qqc, 4qq5, 4uxq, 4xcu – hFGFR4 TKD (mutant) + irreversible inhibitor
- 4tye, 4tyg, 4tyi, 4tyj – hFGFR4 TKD
- FGFR4 LBD