Filamin
From Proteopedia
Revision as of 09:38, 2 March 2016 by Michal Harel (talk | contribs)
Function
For more details on filamin C see Group:MUZIC:FilaminC. DiseaseMutations in FLNA cause frontometaphyseal dysplasia, intestinal pseudo-obstruction, Melnick-Needles syndrome, otopalatodigital syndrome and periventricular heterotopia. Mutations in FLNAB cause boomerang dysplasia[4].
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3D structures of filamin
Updated on 02-March-2016
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- Filamin A
- 3isw – hFLNA repeat 21+CFTR peptide – human
- 3rgh - hFLNA repeat 10
- 2wfn, 3hop, 3hor – hFLNA ABD
- 3hoc – hFLNA ABD (mutant)
- 4m9p - hFLNA domains 3-5
- 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
- 3isw – hFLNA repeat 21+CFTR peptide – human
- Filamin B
- Filamin C
- Other Filamins
References
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