scholarly article | Q13442814 |
review article | Q7318358 |
P356 | DOI | 10.1007/S00709-012-0403-9 |
P8608 | Fatcat ID | release_q67naeu4w5cghlywad3ty6dxq4 |
P932 | PMC publication ID | 3459087 |
P698 | PubMed publication ID | 22526202 |
P5875 | ResearchGate publication ID | 224819223 |
P2093 | author name string | Roger Karlsson | |
Julie Grantham | |||
Ingrid Lassing | |||
P2860 | cites work | The essential role of profilin in the assembly of actin for microspike formation | Q22008023 |
WAVE, a novel WASP-family protein involved in actin reorganization induced by Rac | Q22008483 | ||
p140mDia, a mammalian homolog of Drosophila diaphanous, is a target protein for Rho small GTPase and is a ligand for profilin | Q24316148 | ||
Prefoldin, a chaperone that delivers unfolded proteins to cytosolic chaperonin | Q24336409 | ||
Elucidation of the subunit orientation in CCT (chaperonin containing TCP1) from the subunit composition of CCT micro-complexes. | Q24532436 | ||
A WASp-VASP complex regulates actin polymerization at the plasma membrane. | Q24535834 | ||
Motility determinants in WASP family proteins | Q24537166 | ||
Structure of eukaryotic prefoldin and of its complexes with unfolded actin and the cytosolic chaperonin CCT. | Q24539197 | ||
The proline-rich focal adhesion and microfilament protein VASP is a ligand for profilins | Q24568320 | ||
RIAM regulates the cytoskeletal distribution and activation of PLC-gamma1 in T cells | Q24604073 | ||
Profilin1 regulates PI(3,4)P2 and lamellipodin accumulation at the leading edge thus influencing motility of MDA-MB-231 cells | Q24628847 | ||
Hsp70 chaperones: cellular functions and molecular mechanism | Q24644472 | ||
RIAM activates integrins by linking talin to ras GTPase membrane-targeting sequences | Q24652493 | ||
The interaction of Arp2/3 complex with actin: nucleation, high affinity pointed end capping, and formation of branching networks of filaments | Q24653380 | ||
Cell motility through plasma membrane blebbing | Q24656957 | ||
Tropomyosin inhibits ADF/cofilin-dependent actin filament dynamics | Q24673007 | ||
Exchange of actin subunits at the leading edge of living fibroblasts: possible role of treadmilling | Q24680491 | ||
Arp2/3 complex and actin depolymerizing factor/cofilin in dendritic organization and treadmilling of actin filament array in lamellipodia | Q24682164 | ||
Prefoldin-nascent chain complexes in the folding of cytoskeletal proteins | Q24682236 | ||
Filopodia and adhesion in cancer cell motility | Q26823315 | ||
Stretching actin filaments within cells enhances their affinity for the myosin II motor domain | Q27316621 | ||
Prokaryotic origin of the actin cytoskeleton | Q27634702 | ||
Crystal structure of Arp2/3 complex | Q27636380 | ||
Crystal structure of the CCTgamma apical domain: implications for substrate binding to the eukaryotic cytosolic chaperonin | Q27639250 | ||
High-resolution structural analysis of mammalian profilin 2a complex formation with two physiological ligands: the formin homology 1 domain of mDia1 and the proline-rich domain of VASP | Q27649039 | ||
Structural and functional studies of the Ras-associating and pleckstrin-homology domains of Grb10 and Grb14 | Q27656836 | ||
Direct visualization of secondary structures of F-actin by electron cryomicroscopy | Q27664529 | ||
The crystal structure of yeast CCT reveals intrinsic asymmetry of eukaryotic cytosolic chaperonins | Q27670539 | ||
How a single residue in individual β-thymosin/WH2 domains controls their functions in actin assembly | Q27676361 | ||
Structural basis for profilin-mediated actin nucleotide exchange | Q27677495 | ||
Atomic structure of the actin:DNase I complex | Q27685392 | ||
The structure of crystalline profilin-beta-actin | Q27732069 | ||
The structure of an open state of beta-actin at 2.65 A resolution | Q27733933 | ||
Cellular motility driven by assembly and disassembly of actin filaments | Q27860676 | ||
GMF is a cofilin homolog that binds Arp2/3 complex to stimulate filament debranching and inhibit actin nucleation | Q27930057 | ||
Physiological effects of unassembled chaperonin Cct subunits in the yeast Saccharomyces cerevisiae. | Q27932168 | ||
Quantitative actin folding reactions using yeast CCT purified via an internal tag in the CCT3/gamma subunit. | Q27935184 | ||
Accelerated aging and failure to segregate damaged proteins in Sir2 mutants can be suppressed by overproducing the protein aggregation-remodeling factor Hsp104p | Q27936629 | ||
Compartmentation of protein folding in vivo: sequestration of non-native polypeptide by the chaperonin-GimC system | Q27937256 | ||
Defining the TRiC/CCT interactome links chaperonin function to stabilization of newly made proteins with complex topologies | Q27967631 | ||
Individual subunits of the eukaryotic cytosolic chaperonin mediate interactions with binding sites located on subdomains of beta-actin | Q28140760 | ||
The functional importance of multiple actin isoforms | Q28251664 | ||
Asymmetric inheritance of oxidatively damaged proteins during cytokinesis | Q34180285 | ||
Myosin-X provides a motor-based link between integrins and the cytoskeleton. | Q34322246 | ||
How profilin promotes actin filament assembly in the presence of thymosin beta 4. | Q34345724 | ||
VASP is a processive actin polymerase that requires monomeric actin for barbed end association | Q34412426 | ||
ATPase activity and conformational changes in the regulation of actin | Q34426697 | ||
Actin interacts with CCT via discrete binding sites: a binding transition-release model for CCT-mediated actin folding | Q34469279 | ||
The beta-thymosin/WH2 fold: multifunctionality and structure | Q34623970 | ||
The filamins: organizers of cell structure and function | Q34891266 | ||
Molecular architecture and function of matrix adhesions | Q35006506 | ||
Tropomyosin isoforms and reagents | Q35534685 | ||
Regulation of the Actin Cytoskeleton by PI(4,5)P2 and PI(3,4,5)P3 | Q35573994 | ||
Alpha-actinin revisited: a fresh look at an old player | Q35745364 | ||
A yeast TCP-1-like protein is required for actin function in vivo | Q35763868 | ||
Identification of the TRiC/CCT substrate binding sites uncovers the function of subunit diversity in eukaryotic chaperonins | Q35920579 | ||
Synapses: sites of cell recognition, adhesion, and functional specification. | Q36012269 | ||
Actin from Thyone sperm assembles on only one end of an actin filament: a behavior regulated by profilin | Q36207465 | ||
EGF-induced PIP2 hydrolysis releases and activates cofilin locally in carcinoma cells | Q36274523 | ||
Modulation of the interaction between G-actin and thymosin beta 4 by the ATP/ADP ratio: possible implication in the regulation of actin dynamics | Q36333123 | ||
Suppression of tumorigenicity in breast cancer cells by the microfilament protein profilin 1. | Q36368457 | ||
Specialisation of the tropomyosin composition of actin filaments provides new potential targets for chemotherapy. | Q36482991 | ||
The unique hetero-oligomeric nature of the subunits in the catalytic cooperativity of the yeast Cct chaperonin complex | Q36595095 | ||
Profilin-1 is a negative regulator of mammary carcinoma aggressiveness | Q36610582 | ||
Differential epitope tagging of actin in transformed Drosophila produces distinct effects on myofibril assembly and function of the indirect flight muscle | Q36836754 | ||
Tropomyosins as interpreters of the signalling environment to regulate the local cytoskeleton | Q36973961 | ||
The microfilament system and malignancy | Q37006988 | ||
Organizing the fluid membrane bilayer: diseases linked to spectrin and ankyrin | Q37033360 | ||
Role of tropomyosin in formin-mediated contractile ring assembly in fission yeast | Q37158388 | ||
Alpha-actinin structure and regulation | Q37167269 | ||
Development of free-energy-based models for chaperonin containing TCP-1 mediated folding of actin | Q37245567 | ||
Spire and Cordon-bleu: multifunctional regulators of actin dynamics | Q37262049 | ||
Review of the mechanism of processive actin filament elongation by formins | Q37491020 | ||
Mechanical modes of 'amoeboid' cell migration. | Q37518200 | ||
Similarity of the three-dimensional structures of actin and the ATPase fragment of a 70-kDa heat shock cognate protein | Q37529426 | ||
Structural insights into de novo actin polymerization | Q37680176 | ||
Quality control of cytoskeletal proteins and human disease | Q37684113 | ||
Control of actin filament treadmilling in cell motility | Q37700675 | ||
Multifunctionality of the beta-thymosin/WH2 module: G-actin sequestration, actin filament growth, nucleation, and severing | Q37763970 | ||
Multiple Conformations of F-actin | Q37773504 | ||
WASH, WHAMM and JMY: regulation of Arp2/3 complex and beyond | Q37796281 | ||
Actin structure and function. | Q37840146 | ||
Ezrin, Radixin and Moesin: key regulators of membrane-cortex interactions and signaling | Q37877027 | ||
Unraveling the enigma: progress towards understanding the coronin family of actin regulators. | Q37883703 | ||
Building distinct actin filament networks in a common cytoplasm | Q37904227 | ||
Actin-depolymerizing factor homology domain: a conserved fold performing diverse roles in cytoskeletal dynamics | Q37919427 | ||
Control of actin assembly by the WH2 domains and their multifunctional tandem repeats in Spire and Cordon-Bleu | Q37923549 | ||
Cease-fire at the leading edge: new perspectives on actin filament branching, debranching, and cross-linking. | Q37946325 | ||
Phosphatidylinositol 4, 5 bisphosphate and the actin cytoskeleton | Q37989034 | ||
Arp2/3 is critical for lamellipodia and response to extracellular matrix cues but is dispensable for chemotaxis | Q39386624 | ||
A molecular pathway for myosin II recruitment to stress fibers. | Q39566063 | ||
Rap1-GTP-interacting adaptor molecule (RIAM) protein controls invasion and growth of melanoma cells | Q39567425 | ||
An ezrin-rich, rigid uropod-like structure directs movement of amoeboid blebbing cells | Q39569182 | ||
Tropomyosin assembly intermediates in the control of microfilament system turnover. | Q39944767 | ||
Human spire interacts with the barbed end of the actin filament. | Q53268656 | ||
The polarisome is required for segregation and retrograde transport of protein aggregates. | Q53343132 | ||
Counting cytokinesis proteins globally and locally in fission yeast. | Q53653661 | ||
Differentially oriented populations of actin filaments generated in lamellipodia collaborate in pushing and pausing at the cell front | Q58009677 | ||
Actin polymerization and ATP hydrolysis | Q69433184 | ||
Cooperativity in F-actin: binding of gelsolin at the barbed end affects structure and dynamics of the whole filament | Q71262844 | ||
Acanthamoeba profilin interacts with G-actin to increase the rate of exchange of actin-bound adenosine 5'-triphosphate | Q71851561 | ||
Visualization of the peripheral weave of microfilaments in glia cells | Q71853581 | ||
A green fluorescent protein-actin fusion protein dominantly inhibits cytokinesis, cell spreading, and locomotion in Dictyostelium | Q73568214 | ||
Inhibition of the Arp2/3 complex-nucleated actin polymerization and branch formation by tropomyosin | Q74431841 | ||
Silencing profilin-1 inhibits endothelial cell proliferation, migration and cord morphogenesis | Q80250774 | ||
Structural modeling and molecular dynamics simulation of the actin filament | Q84071510 | ||
Equivalent mutations in the eight subunits of the chaperonin CCT produce dramatically different cellular and gene expression phenotypes | Q84519832 | ||
The beta-thymosin/WH2 domain; structural basis for the switch from inhibition to promotion of actin assembly | Q28263506 | ||
Lamellipodin, an Ena/VASP ligand, is implicated in the regulation of lamellipodial dynamics | Q28286512 | ||
RIAM, an Ena/VASP and Profilin ligand, interacts with Rap1-GTP and mediates Rap1-induced adhesion | Q28286523 | ||
Blebs lead the way: how to migrate without lamellipodia | Q28287258 | ||
The 'sequential allosteric ring' mechanism in the eukaryotic chaperonin-assisted folding of actin and tubulin | Q28345083 | ||
Mouse MIM, a tissue-specific regulator of cytoskeletal dynamics, interacts with ATP-actin monomers through its C-terminal WH2 domain | Q28507602 | ||
Latrunculin B or ATP depletion induces cofilin-dependent translocation of actin into nuclei of mast cells | Q28570802 | ||
c-Abl, Lamellipodin, and Ena/VASP proteins cooperate in dorsal ruffling of fibroblasts and axonal morphogenesis | Q28589079 | ||
Mammalian mitochondrial nitric oxide synthase: characterization of a novel candidate | Q28594293 | ||
Subunit 1 of the prefoldin chaperone complex is required for lymphocyte development and function | Q28594712 | ||
Thymosin beta 4 and Fx, an actin-sequestering peptide, are indistinguishable | Q28910376 | ||
Architecture and Assembly of a Divergent Member of the ParM Family of Bacterial Actin-like Proteins | Q28946356 | ||
An ATPase domain common to prokaryotic cell cycle proteins, sugar kinases, actin, and hsp70 heat shock proteins | Q29615894 | ||
Regulation of actin assembly associated with protrusion and adhesion in cell migration | Q29616028 | ||
A nucleator arms race: cellular control of actin assembly | Q29616146 | ||
The WASP-WAVE protein network: connecting the membrane to the cytoskeleton | Q29616493 | ||
Molecular mechanisms controlling actin filament dynamics in nonmuscle cells | Q29616514 | ||
The ARP2/3 complex: an actin nucleator comes of age | Q29617347 | ||
Proteins of the ADF/cofilin family: essential regulators of actin dynamics | Q29618546 | ||
Actin filaments as tension sensors | Q30422462 | ||
Structural polymorphism in F-actin | Q30432555 | ||
A crucial role for profilin-actin in the intracellular motility of Listeria monocytogenes | Q30476565 | ||
Arp2/3 complex interactions and actin network turnover in lamellipodia. | Q30481401 | ||
How tropomyosin regulates lamellipodial actin-based motility: a combined biochemical and reconstituted motility approach | Q30492836 | ||
The motor protein myosin-X transports VE-cadherin along filopodia to allow the formation of early endothelial cell-cell contacts. | Q30493646 | ||
Intracellular fluid flow in rapidly moving cells. | Q30494402 | ||
Molecular mechanism of Ena/VASP-mediated actin-filament elongation. | Q30498103 | ||
Control of actin dynamics by proteins made of beta-thymosin repeats: the actobindin family | Q30675520 | ||
Myosin X transports Mena/VASP to the tip of filopodia. | Q31065358 | ||
F- and G-actin concentrations in lamellipodia of moving cells | Q33416795 | ||
Electron tomography reveals unbranched networks of actin filaments in lamellipodia | Q33564094 | ||
Dicing with dogma: de-branching the lamellipodium | Q33690284 | ||
A central role for the WH2 domain of Srv2/CAP in recharging actin monomers to drive actin turnover in vitro and in vivo | Q33801875 | ||
Eukaryotic type II chaperonin CCT interacts with actin through specific subunits | Q33884171 | ||
A nucleotide state-sensing region on actin | Q34055903 | ||
Actin-based plasticity in dendritic spines | Q34071209 | ||
Human CAP1 is a key factor in the recycling of cofilin and actin for rapid actin turnover | Q34123515 | ||
Eukaryotic chaperonin containing T-complex polypeptide 1 interacts with filamentous actin and reduces the initial rate of actin polymerization in vitro | Q39956697 | ||
Actin polymerization and its regulation by proteins from nonmuscle cells | Q40128974 | ||
Polymerizing actin fibers position integrins primed to probe for adhesion sites | Q40170442 | ||
PREL1 provides a link from Ras signalling to the actin cytoskeleton via Ena/VASP proteins. | Q40265815 | ||
Substantial CCT activity is required for cell cycle progression and cytoskeletal organization in mammalian cells. | Q40269280 | ||
Tropomyosins are present in lamellipodia of motile cells | Q40307517 | ||
Eukaryotic chaperonin CCT stabilizes actin and tubulin folding intermediates in open quasi-native conformations | Q40388182 | ||
Rapid actin transport during cell protrusion. | Q40658177 | ||
The fimbrin and alpha-actinin footprint on actin | Q40673977 | ||
Effects of cross-linked profilin:beta/gamma-actin on the dynamics of the microfilament system in cultured cells | Q40890635 | ||
cdc12p, a protein required for cytokinesis in fission yeast, is a component of the cell division ring and interacts with profilin | Q40897448 | ||
The interaction network of the chaperonin CCT | Q40987014 | ||
Review: the Cct eukaryotic chaperonin subunits of Saccharomyces cerevisiae and other yeasts | Q41083231 | ||
Expression of chicken beta-actin in Saccharomyces cerevisiae | Q41267614 | ||
On the dynamics of the microfilament system in HeLa cells | Q41376681 | ||
Organization of actin in the leading edge of cultured cells: influence of osmium tetroxide and dehydration on the ultrastructure of actin meshworks | Q41438820 | ||
Incorporation and turnover of biotin-labeled actin microinjected into fibroblastic cells: an immunoelectron microscopic study | Q41588193 | ||
A novel form of motility in filopodia revealed by imaging myosin-X at the single-molecule level | Q41978648 | ||
Formins filter modified actin subunits during processive elongation | Q42156443 | ||
Interactions between the actin filament capping and severing protein gelsolin and the molecular chaperone CCT: evidence for nonclassical substrate interactions | Q42699747 | ||
Subunits of the chaperonin CCT interact with F-actin and influence cell shape and cytoskeletal assembly | Q42832230 | ||
Tropomyosin is a tetramer under physiological salt conditions | Q42958235 | ||
Crystal structure of an archaeal actin homolog | Q43019641 | ||
Visualizing branched actin filaments in lamellipodia by electron tomography | Q43233762 | ||
Tropomyosin regulates elongation by formin at the fast-growing end of the actin filament. | Q43244096 | ||
Formins direct Arp2/3-independent actin filament assembly to polarize cell growth in yeast | Q43820583 | ||
A cross-linked profilin-actin heterodimer interferes with elongation at the fast-growing end of F-actin | Q43886308 | ||
Mammalian cell-based optimization of the biarsenical-binding tetracysteine motif for improved fluorescence and affinity | Q43938954 | ||
New biarsenical ligands and tetracysteine motifs for protein labeling in vitro and in vivo: synthesis and biological applications | Q44001816 | ||
Actin-ATP hydrolysis is a major energy drain for neurons. | Q44270163 | ||
Sequential ATP-induced allosteric transitions of the cytoplasmic chaperonin containing TCP-1 revealed by EM analysis | Q45254396 | ||
A single amino acid residue is responsible for species-specific incompatibility between CCT and alpha-actin. | Q46138539 | ||
Head to tail polymerization of actin | Q46173625 | ||
Efficient production of native actin upon translation in a bacterial lysate supplemented with the eukaryotic chaperonin TRiC. | Q46733347 | ||
ATP-induced allostery in the eukaryotic chaperonin CCT is abolished by the mutation G345D in CCT4 that renders yeast temperature-sensitive for growth | Q46755963 | ||
Ciboulot regulates actin assembly during Drosophila brain metamorphosis | Q47070830 | ||
Origin and evolution of eukaryotic chaperonins: phylogenetic evidence for ancient duplications in CCT genes | Q47658456 | ||
The role of profilin in actin polymerization and nucleotide exchange. | Q47901071 | ||
Formation of actin-ADF/cofilin rods transiently retards decline of mitochondrial potential and ATP in stressed neurons | Q48515576 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P921 | main subject | actin | Q185269 |
cytoskeletal proteins | Q66563066 | ||
contractile proteins | Q69633297 | ||
macromolecular substance | Q75174158 | ||
P304 | page(s) | 1001-1015 | |
P577 | publication date | 2012-04-15 | |
2012-10-01 | |||
P1433 | published in | Protoplasma | Q15765986 |
P1476 | title | Controlling the cortical actin motor | |
P478 | volume | 249 |
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