Hauptseite > Publikationsdatenbank > Molecular basis of the CYFIP2 and NCKAP1 autism-linked variants in the WAVE regulatory complex > print |
001 | 1037752 | ||
005 | 20250203103245.0 | ||
024 | 7 | _ | |a 10.26434/chemrxiv-2024-x3sn8 |2 doi |
024 | 7 | _ | |a 10.34734/FZJ-2025-00912 |2 datacite_doi |
037 | _ | _ | |a FZJ-2025-00912 |
041 | _ | _ | |a English |
100 | 1 | _ | |a Xie, Song |0 P:(DE-Juel1)201922 |b 0 |
245 | _ | _ | |a Molecular basis of the CYFIP2 and NCKAP1 autism-linked variants in the WAVE regulatory complex |
260 | _ | _ | |c 2024 |
336 | 7 | _ | |a Preprint |b preprint |m preprint |0 PUB:(DE-HGF)25 |s 1738068095_32537 |2 PUB:(DE-HGF) |
336 | 7 | _ | |a WORKING_PAPER |2 ORCID |
336 | 7 | _ | |a Electronic Article |0 28 |2 EndNote |
336 | 7 | _ | |a preprint |2 DRIVER |
336 | 7 | _ | |a ARTICLE |2 BibTeX |
336 | 7 | _ | |a Output Types/Working Paper |2 DataCite |
520 | _ | _ | |a The WAVE regulatory pentameric complex regulates actin remodeling. Two components of it (CYFIP2 and NCKAP1) are encoded by genes whose genetic mutations increase the risk for Autism Spectrum Disorder (ASD) and related neurodevelopmental disorders. Here, we use a newly developed computational protocol and hotspot analysis to uncover the functional impact of these mutations at the interface of the correct isoforms of the two proteins into the complex. The mutations turn out to be located on the surfaces involving the largest number of hotspots of the complex. Most of them decrease the affinity of the proteins for the rest of the complex, but some have the opposite effect. The results are fully consistent with the available experimental data. The observed changes in the WAVE regulatory complex stability might impact on complex activation and ultimately play a role in the aberrant pathway of the complex, leading to the cell derangement associated with the disease. |
536 | _ | _ | |a 5252 - Brain Dysfunction and Plasticity (POF4-525) |0 G:(DE-HGF)POF4-5252 |c POF4-525 |f POF IV |x 0 |
588 | _ | _ | |a Dataset connected to CrossRef |
700 | 1 | _ | |a Zuo, Ke |0 P:(DE-Juel1)192214 |b 1 |e Corresponding author |u fzj |
700 | 1 | _ | |a De Rubeis, Silvia |0 P:(DE-HGF)0 |b 2 |
700 | 1 | _ | |a Ruggerone, Paolo |0 P:(DE-HGF)0 |b 3 |e Corresponding author |
700 | 1 | _ | |a Carloni, Paolo |0 P:(DE-Juel1)145614 |b 4 |e Corresponding author |u fzj |
773 | _ | _ | |a 10.26434/chemrxiv-2024-x3sn8 |
856 | 4 | _ | |y OpenAccess |u https://juser.fz-juelich.de/record/1037752/files/molecular-basis-of-the-cyfip2-and-nckap1-autism-linked-variants-in-the-wave-regulatory-complex.pdf |
856 | 4 | _ | |y Restricted |u https://juser.fz-juelich.de/record/1037752/files/the-supplementary-materials.pdf |
909 | C | O | |o oai:juser.fz-juelich.de:1037752 |p openaire |p open_access |p VDB |p driver |p dnbdelivery |
910 | 1 | _ | |a Forschungszentrum Jülich |0 I:(DE-588b)5008462-8 |k FZJ |b 0 |6 P:(DE-Juel1)201922 |
910 | 1 | _ | |a Forschungszentrum Jülich |0 I:(DE-588b)5008462-8 |k FZJ |b 1 |6 P:(DE-Juel1)192214 |
910 | 1 | _ | |a Forschungszentrum Jülich |0 I:(DE-588b)5008462-8 |k FZJ |b 4 |6 P:(DE-Juel1)145614 |
913 | 1 | _ | |a DE-HGF |b Key Technologies |l Natural, Artificial and Cognitive Information Processing |1 G:(DE-HGF)POF4-520 |0 G:(DE-HGF)POF4-525 |3 G:(DE-HGF)POF4 |2 G:(DE-HGF)POF4-500 |4 G:(DE-HGF)POF |v Decoding Brain Organization and Dysfunction |9 G:(DE-HGF)POF4-5252 |x 0 |
914 | 1 | _ | |y 2024 |
915 | _ | _ | |a OpenAccess |0 StatID:(DE-HGF)0510 |2 StatID |
920 | _ | _ | |l yes |
920 | 1 | _ | |0 I:(DE-Juel1)INM-9-20140121 |k INM-9 |l Computational Biomedicine |x 0 |
920 | 1 | _ | |0 I:(DE-Juel1)IAS-5-20120330 |k IAS-5 |l Computational Biomedicine |x 1 |
980 | _ | _ | |a preprint |
980 | _ | _ | |a VDB |
980 | _ | _ | |a UNRESTRICTED |
980 | _ | _ | |a I:(DE-Juel1)INM-9-20140121 |
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