「ACTIN」の共起表現一覧(1語右で並び替え)
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| In plants, actibind binds | actin, a major component of the cytoskeleton, interf |
| Actin alpha 2, the human aortic smooth muscle actin | |
| Actin alpha 1 which is expressed in skeletal muscle | |
| Actin, alpha skeletal muscle is a protein that in hu | |
| Actin, alpha cardiac muscle 1 is a protein that in h | |
| mains of the MAPs and yeast coronin binds both | actin and microtubule and serve as bridge between th |
| g (1) cytoskeletal components as microtubules, | actin, and actin-binding proteins α-spectrin and dre |
| The complex folds various proteins, including | actin and tubulin. |
| Fascia adherens are anchoring sites for | actin, and connects to the closest sarcomere. |
| nin, initiating cross-bridge formation between | actin and myosin. |
| e proteins responsible for muscle contraction, | actin and myosin begin the process of forming the cl |
| e cell membrane of some cells that are rich in | actin and extend into the extracellular matrix (ECM) |
| n is a component of thin filaments (along with | actin and tropomyosin), and is the protein to which |
| The | actin and myosin filaments continue to slide past ea |
| ought to be active in the interactions between | actin and the extracellular matrix. |
| second type are larger (>0.7 μm), contain both | actin and microtubules and can carry components of t |
| less than 0.7 micrometres in diameter, contain | actin and carry portions of plasma membrane between |
| dges" that generate the sliding forces between | actin and myosin filaments, which cause the contract |
| cloned cDNAs coding for cytoskeleton proteins, | actin and alpha keratins. |
| Alpha-actin-2 also known as | actin, aortic smooth muscle or alpha smooth muscle a |
| cell shape and motility through lamellipodial | actin assembly and protrusion. |
| They are used to regulate | actin assembly. |
| Cortactin (from “cortical | actin binding protein”) is a monomeric protein locat |
| Bistramide A is a cytoskeleton, | actin binding protein, originally found in the marin |
| Arp 2/3, an | actin binding proteins complex, binds to the side of |
| HMMS-1 has an | Actin binding site and ATP binding site (myosin ATPa |
| Actin binding LIM protein 1, also known as ABLIM1, i | |
| Myosins are | actin binding molecular motors that use the enzymati |
| hows that these basic residues are involved in | actin binding. |
| in, which provides a nucleation site for a new | actin branch to form from the “mother” filament. |
| Cortactin-assisted Arp2/3-nucleated | actin branches are most prominent in the actin corte |
| This stimulates | actin branching and increases cell motility (Small, |
| ults in the shortening, or contraction, of the | actin bundle (but not the filament). |
| the extracellular matrix to the intracellular | actin cables, is thought to provide structural integ |
| Dystrophin binds to intracellular | actin cables. |
| Each | actin can bind to four others. |
| CTN3/p22/p24;(2)the Arp1 rod: Arp1/centractin, | actin, CapZ; and (3) the pointed end complex: Actr10 |
| ia formation is initiated with the assembly of | actin core structures, followed by the accumulation |
| Macroketone targets an | actin cytoskeletal protein known as fascin that is c |
| G proteins G12 and G13 regulate | actin cytoskeletal remodeling in cells. |
| vailable active Cdc42 and consequently disrupt | actin cytoskeletal structures, causing syndromic cut |
| intra-cellular membranes and organelles to the | actin cytoskeleton via interactions mediated by thei |
| n family and thereby helps to link them to the | actin cytoskeleton and to regulate their surface exp |
| P-selectin attaches to the | actin cytoskeleton through anchor proteins that are |
| It is capable of linking integrins to the | actin cytoskeleton either directly or indirectly by |
| tes Cofilin, which effectively reorganizes the | Actin cytoskeleton of the cell. |
| dylinositol signaling system and regulation of | actin cytoskeleton. |
| ylinositol signaling system, and regulation of | actin cytoskeleton. |
| he activities of the secretory pathway and the | actin cytoskeleton. |
| Actin depolymerizing factors are a family of microfi | |
| Cartoon representation of a cofilin ( | actin depolymerizing factor, ADF). |
| Increasing the rate constant, k, for | actin dissociation from the pointed ends was found t |
| Skeletal alpha | actin expression is induced by stimuli and condition |
| he protein encoded by this gene belongs to the | actin family which is composed of three main groups |
| intermediates results in the polymerization of | actin fibers by Ena/Vasp homology proteins. |
| n TnC, tropomyosin rolls out of the way of the | actin filament active sites, so that myosin (a molec |
| tion of 13 subunit repeat based on Ken Holmes' | actin filament model |
| th a resilience absent from the microtubule or | actin filament networks, when under mechanical stres |
| Furrow appears because a ring of | actin filament forms just inside the plasma membrane |
| rins produces a complex which is linked to the | actin filament network, and which seems to be of pri |
| e other end "walks" toward the plus end of the | actin filament. |
| Actin filaments | |
| They contain | actin filaments cross-linked into bundles by actin-b |
| Actin filaments are stabilized by actin binding prot | |
| ex and cofilin work together to reorganize the | actin filaments in the cytoskeleton. |
| It is usually associated with polarized | actin filaments in membrane ruffles, filopodia, ster |
| s gene could mediate such interactions between | actin filaments and cytoplasmic targets. |
| In the budding yeast Saccharomyces cerevisiae, | actin filaments are the major structural component o |
| Cytoplasmic streaming occurs along | Actin filaments in the cytoskeleton of the cell. |
| r activates condensation and polymerization of | actin filaments under the bacterial cell to form a p |
| HMM is used to determine the polarity of | actin filaments by decorating them with HMM then vie |
| Myosin moves the ring of | actin filaments on the side of the plasma membrane, |
| α-Actinin is necessary for the attachment of | actin filaments to the Z-lines in skeletal muscle ce |
| codes a cytoskeletal LIM protein that binds to | actin filaments via a domain that is homologous to e |
| -moesin-radixin group promoting the binding of | actin filaments to the filopodia membrane. |
| toward their filament's plus end, sliding the | actin filaments closer to each other. |
| Tensin is a multi-domain protein that binds to | actin filaments and functions as a focal-adhesion mo |
| ine kinases resulting in the polymerization of | actin filaments, which, when cross-linked, make up t |
| . In their unphosphorylated form, they bind to | actin filaments, causing them to crosslink, and sequ |
| or ADP-Pi are probably involved in binding to | actin filaments. |
| intercalated disk of cardiac muscle anchoring | actin filaments. |
| ies, where it helps to anchor the myofibrillar | actin filaments. |
| odies, where they help anchor the myofibrillar | actin filaments. |
| er of the melanosomes from the microtubules to | actin filaments. |
| Both actins and ARPs have an | actin fold, which is an ATP-binding cleft, as a comm |
| roteins, and the common structure is termed an | actin fold. |
| inometer, the first of many uses of the prefix | actin for scientific instruments, effects, and proce |
| r of secretory defect in yeast Golgi and yeast | actin function belongs to this family. |
| Actin, gamma 1, encoded by this gene, is a cytoplasm | |
| Actin, gamma 1, also known as ACTG1, is a gene. | |
| y transcription factor that activates skeletal | actin gene expression is Serum Response Factor ("SRF |
| MreB and | actin have a weak primary structure match, but are v |
| Thus, polymerization and branching of | actin is promoted in areas of the cell where cortact |
| In vertebrates, three main groups of | actin isoforms, alpha, beta and gamma have been iden |
| Skeletal | actin itself, when expressed, causes expression of s |
| junctions in lamellipodia, and help create the | actin meshwork. |
| Spectrin proteins and | actin microfilaments are attached to transmembrane p |
| brane in cells where the spectrin proteins and | actin microfilaments form a mesh-like structure much |
| spectrin proteins along with lesser amounts of | actin microfilaments. |
| tal dynamics (cell motility, molecular motors, | actin, microtubules, intermediate filaments) |
| Profilin is an | actin monomer binding protein that has been implicat |
| It binds | actin monomers with very high (sub-nanomolar) affini |
| e barbed ends of the microfilaments (localized | actin monomers in an ATP-bound form) face the "seeki |
| into two categories based on their substrates: | Actin motors such as myosin move along microfilament |
| In contrast to | actin, MSP lacks an ATP-binding site. |
| trusion from fibroblast cells characterized by | actin networks. |
| Also, as opposed to | actin or tubulin, intermediate filaments do not cont |
| ich are then delivered to the membrane via the | actin or microtubule networks. |
| inding/translocation protein (B), and prevents | actin polymerisation through ADP-ribosylation of mon |
| e PKG 1α promoter is inhibited by RhoA-induced | actin polymerisation, possibly via G-actin regulatio |
| It interacts with c-Abl and WAVE2 which is | actin polymerization regulator. |
| of the cytochalasin group, is an inhibitor of | actin polymerization in blood platelets. |
| complex has been implicated in the control of | actin polymerization in cells and has been conserved |
| ne-coat protein interactions, and to influence | actin polymerization. |
| The phosphorylation of c-Abl promotes | actin polymerization. |
| molecular scaffolding protein and functions in | actin recruitment. |
| Prk1p ( | actin regulating kinase) |
| TRIO is involved in coordinating | actin remodeling, which is necessary for cell migrat |
| hit and was followed by number one hit "She's | Actin' Single (I'm Drinkin' Doubles)." |
| - to late- 1970s, his biggest hit being "She's | Actin' Single (I'm Drinkin' Doubles)," which topped |
| Astral microtubules develop in the | actin skeleton and interact with the cell cortex to |
| of other proteins to the promoter of skeletal | actin, such as andogen receptor, and thereby contrib |
| ype junctions, where it is involved in binding | actin to the membrane. |
| These antibodies can be directed against | actin, troponin, and tropomyosin. |
| s cytoskeletal filaments like microtubules and | actin, which move under the influence of molecular m |
| r molecule that is often found in polymerizing | actin with Arp2/3 is cortactin, which appears to lin |
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