about
The Myosin Chaperone UNC-45 Is Organized in Tandem Modules to Support Myofilament Formation in C. elegansMyosin Va's adaptor protein melanophilin enforces track selection on the microtubule and actin networks in vitro.The DNA binding CXC domain of MSL2 is required for faithful targeting the Dosage Compensation Complex to the X chromosomeRegulation of a heterodimeric kinesin-2 through an unprocessive motor domain that is turned processive by its partner.Rapid purification of recombinant histonesISWI remodelling of physiological chromatin fibres acetylated at lysine 16 of histone H4.DNA topoisomerase II selects DNA cleavage sites based on reactivity rather than binding affinity.Coupling between ATP binding and DNA cleavage by DNA topoisomerase II: A unifying kinetic and structural mechanism.Nucleosome sliding mechanisms: new twists in a looped history.No need for a power stroke in ISWI-mediated nucleosome slidingNucleosome spacing generated by ISWI and CHD1 remodelers is constant regardless of nucleosome density.Interdomain communication in DNA topoisomerase II. DNA binding and enzyme activation.Crossfinder-assisted mapping of protein crosslinks formed by site-specifically incorporated crosslinkers.Concerted regulation of ISWI by an autoinhibitory domain and the H4 N-terminal tail.Probing the conformation of the ISWI ATPase domain with genetically encoded photoreactive crosslinkers and mass spectrometry.The ATPase domain of ISWI is an autonomous nucleosome remodeling machine.A Poly-ADP-Ribose Trigger Releases the Auto-Inhibition of a Chromatin Remodeling Oncogene.Kinesin-2 motors adapt their stepping behavior for processive transport on axonemes and microtubules.Structural Architecture of the Nucleosome Remodeler ISWI Determined from Cross-Linking, Mass Spectrometry, SAXS, and Modeling.
P50
Q27675937-F1C4C05A-44FF-408B-B897-F96078F6F3EAQ33810384-C7A2C20A-3CDA-48A9-BDAF-9AB1E749593CQ33889307-F9E83996-2816-4D1F-86D9-788AD737C7DFQ33935150-A1002D73-F316-4DD2-AE73-99BBD4864342Q33999978-E2E564D8-68EC-47F5-BD19-839237748807Q35091749-11BB4CEB-66FB-4DA4-A375-49B8957AFCF1Q35893882-16FDC3B1-CC2F-4937-A282-6F7F72989260Q36719248-FC7C4CE5-0D41-4CFE-ABBF-F155FB294F8BQ38134612-AF1A93B5-A3ED-403E-AE08-E7612A4705DBQ38677064-980254EA-D15D-430A-881D-88414395416CQ39301715-F1BC1E75-3C7F-433C-ACDD-6E53114D8850Q40314755-24A8700C-5990-45C5-B6AF-7681689F6845Q41194954-0A8239CD-2937-433D-8249-E254696669F7Q42321964-62BF2A93-E170-405D-9826-9113384C029DQ42552419-8B6408AB-B55C-4D57-8D7F-E3310BB97336Q44496055-0CC42537-28D7-4566-BA8C-E927E3BDE8BFQ47315162-35DF5C21-0E46-4CF8-9043-DF87CF0E6787Q47831568-177599BC-4C56-4043-AF51-11104FAD5502Q50108994-56219520-6699-480D-961C-4099E6011831
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Felix Mueller-Planitz
@ast
Felix Mueller-Planitz
@en
Felix Mueller-Planitz
@es
Felix Mueller-Planitz
@nl
Felix Mueller-Planitz
@sl
type
label
Felix Mueller-Planitz
@ast
Felix Mueller-Planitz
@en
Felix Mueller-Planitz
@es
Felix Mueller-Planitz
@nl
Felix Mueller-Planitz
@sl
prefLabel
Felix Mueller-Planitz
@ast
Felix Mueller-Planitz
@en
Felix Mueller-Planitz
@es
Felix Mueller-Planitz
@nl
Felix Mueller-Planitz
@sl
P1053
P-8461-2014
P106
P21
P31
P3829
P496
0000-0001-8273-6473