Filamin
From Proteopedia
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[[Image:3hop.png|left|200px|thumb|Crystal structure of Human Filamin A complex with phosphate, [[3hop]]]] | [[Image:3hop.png|left|200px|thumb|Crystal structure of Human Filamin A complex with phosphate, [[3hop]]]] | ||
| - | {{STRUCTURE_3hop| PDB=3hop | SIZE=300| SCENE=Filamin/Cv/1 |right|CAPTION=Human Filamin A, [[3hop]] }} | + | {{STRUCTURE_3hop| PDB=3hop | SIZE=300| SCENE=Filamin/Cv/1 |right|CAPTION=Human Filamin A complex with phosphate, [[3hop]] }} |
[[Filamin]] '''A (FLNA)''' has an actin-binding domain (ABD). It crosslinks actin filaments and participates in anchoring of membrane proteins. '''Filamin B (FLNB)''' is a human cytoplasmic protein which functions similarly to FLNA and guides proper skeletal development. '''Filamin C (FLNC)''' is functionally similar and contains 3 domains: the N-terminal ABD, the C-terminal dimerization domain (DD) and a membrane glycoprotein-binding domain. The images at the left and at the right correspond to one representative filamin structure, ''i.e.'' the crystal structure of human filamin A ([[3hop]]), it forms a <scene name='Filamin/Cv/2'>dimer</scene> <ref>PMID:19773341</ref>. Two phosphate ions are rendered as space filling objects. | [[Filamin]] '''A (FLNA)''' has an actin-binding domain (ABD). It crosslinks actin filaments and participates in anchoring of membrane proteins. '''Filamin B (FLNB)''' is a human cytoplasmic protein which functions similarly to FLNA and guides proper skeletal development. '''Filamin C (FLNC)''' is functionally similar and contains 3 domains: the N-terminal ABD, the C-terminal dimerization domain (DD) and a membrane glycoprotein-binding domain. The images at the left and at the right correspond to one representative filamin structure, ''i.e.'' the crystal structure of human filamin A ([[3hop]]), it forms a <scene name='Filamin/Cv/2'>dimer</scene> <ref>PMID:19773341</ref>. Two phosphate ions are rendered as space filling objects. | ||
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[[3isw]] – hFLNA repeat 21+CFTR peptide – human<br /> | [[3isw]] – hFLNA repeat 21+CFTR peptide – human<br /> | ||
| - | [[3rgh]] - hFLNA repeat 10 | + | [[3rgh]] - hFLNA repeat 10<br /> |
[[2wfn]], [[3hop]], [[3hor]] – hFLNA ABD<br /> | [[2wfn]], [[3hop]], [[3hor]] – hFLNA ABD<br /> | ||
[[3hoc]] – hFLNA ABD (mutant)<br /> | [[3hoc]] – hFLNA ABD (mutant)<br /> | ||
Revision as of 11:26, 13 November 2011
Template:STRUCTURE 3hop Filamin A (FLNA) has an actin-binding domain (ABD). It crosslinks actin filaments and participates in anchoring of membrane proteins. Filamin B (FLNB) is a human cytoplasmic protein which functions similarly to FLNA and guides proper skeletal development. Filamin C (FLNC) is functionally similar and contains 3 domains: the N-terminal ABD, the C-terminal dimerization domain (DD) and a membrane glycoprotein-binding domain. The images at the left and at the right correspond to one representative filamin structure, i.e. the crystal structure of human filamin A (3hop), it forms a [1]. Two phosphate ions are rendered as space filling objects.
Contents |
3D structures of filamin
Update November 2011
Filamin A
3isw – hFLNA repeat 21+CFTR peptide – human
3rgh - hFLNA repeat 10
2wfn, 3hop, 3hor – hFLNA ABD
3hoc – hFLNA ABD (mutant)
2aav - hFLNA domain 17 – NMR
2bp3 - hFLNA domain 17+GPIB peptide
2k7p – hFLNA domains 16-17
2k7q - hFLNA domains 18-19
2j3s - hFLNA domains 19-21
2w0p - hFLNA domain 21+migfilin peptide
2jf1, 2brq - hFLNA domain 21+integrin peptide
2k3t - hFLNA domain 23 – NMR
3cnk - hFLNA DD
Filamin B
2wa5, 3fer, 2eea - hFLNB ABD
2wa6, 2wa7 - hFLNB ABD (mutant)
2di9, 2dia, 2dib, 2dic, 2dj4, 2e9j, 2dmb, 2ee9, 2ee7, 2dmc, 2di8, 2dlg, 2e9i, 2ee6, 2eeb, 2eec, 2eed - hFLNB domains 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 20, 21, 22, 23, 24 – NMR
Filamin C
2k9u – hFLNC+migfilin peptide
2d7m, 2d7n, 2d7o, 2d7p - hFLNC domains 14, 16, 17, 22 - NMR
2nqc - hFLNC domain 21
2d7q - hFLNC domain 23 – NMR
1v05 - hFLNC DD
Other Filamins
1wlh, 1qfh – FLN rod domain – Dictyostelium discoideum
References
- ↑ Clark AR, Sawyer GM, Robertson SP, Sutherland-Smith AJ. Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders. Hum Mol Genet. 2009 Dec 15;18(24):4791-800. Epub 2009 Sep 22. PMID:19773341 doi:10.1093/hmg/ddp442
