Characterisation of the MID1/alpha4 multiprotein complex
Mutations in the MID1 gene cause Opitz BBB/G syndrome (OS), a congenital disorder characterised by malformations of the ventral midline, with hypertelorism and hypospadias being the two cardinal phenotypic manifestations. The RBCC protein MID1 has been shown to form macromolecular complexes, the components of which were, up to now, mainly unknown.
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LINE-1 silencing by retinoblastoma proteins is effected through the nucleosomal and remodeling deacetylase multiprotein complex [PDF]
Diego E. Montoya–Durango +5 more
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Elucidating Steps in Actin Polymerization and Nucleation using a Coarse-Grained Model of Multiprotein Complex Formation [PDF]
Brandon G. Horan +2 more
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Characterization of Multiprotein Complexes of the Borrelia burgdorferi Outer Membrane Vesicles
Xiuli Yang +7 more
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Structural Analysis of Siah1-Siah-interacting Protein Interactions and Insights into the Assembly of an E3 Ligase Multiprotein Complex [PDF]
Eugenio Santelli +10 more
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Scaffold Protein Connector Enhancer of Kinase Suppressor of Ras Isoform 3 (CNK3) Coordinates Assembly of a Multiprotein Epithelial Sodium Channel (ENaC)-regulatory Complex [PDF]
Rama Soundararajan +6 more
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Molecular basis for chromatin assembly and modification by multiprotein complexes. [PDF]
Ricketts MD +3 more
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The PCI domain: a common theme in three multiprotein complexes
Kay Hofmann, Philipp Bücher
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A Multiprotein Complex Regulates Interference-Sensitive Crossover Formation in Rice [PDF]
Jie Zhang +7 more
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