about
Kinesin-5: cross-bridging mechanism to targeted clinical therapyInsights into antiparallel microtubule crosslinking by PRC1, a conserved nonmotor microtubule binding proteinMechanistic analysis of the mitotic kinesin Eg5.A nonmotor microtubule binding site in kinesin-5 is required for filament crosslinking and slidingThe bipolar assembly domain of the mitotic motor kinesin-5Kinesin-12, a mitotic microtubule-associated motor protein, impacts axonal growth, navigation, and branching.Pathway of ATP hydrolysis by monomeric kinesin Eg5Microtubule cross-linking triggers the directional motility of kinesin-5The bipolar kinesin, KLP61F, cross-links microtubules within interpolar microtubule bundles of Drosophila embryonic mitotic spindlesKinesin-5 regulates the growth of the axon by acting as a brake on its microtubule array.Identification and phylogenetic analysis of Dictyostelium discoideum kinesin proteins.Regulatory mechanisms that control mitotic kinesinsThe Msd1-Wdr8-Pkl1 complex anchors microtubule minus ends to fission yeast spindle pole bodies.Kinesin-12 motors cooperate to suppress microtubule catastrophes and drive the formation of parallel microtubule bundles.Crystal structure of the mitotic spindle kinesin Eg5 reveals a novel conformation of the neck-linkerStructural basis for the assembly of the mitotic motor Kinesin-5 into bipolar tetramersSaccharomyces cerevisiae genes required in the absence of the CIN8-encoded spindle motor act in functionally diverse mitotic pathways.The molecular function of Ase1p: evidence for a MAP-dependent midzone-specific spindle matrix. Microtubule-associated proteinsMinus-end-directed Kinesin-14 motors align antiparallel microtubules to control metaphase spindle lengthMotile properties of the bi-directional kinesin-5 Cin8 are affected by phosphorylation in its motor domain.Directional switching of the kinesin Cin8 through motor coupling.Chromosome congression by Kinesin-5 motor-mediated disassembly of longer kinetochore microtubules.Anaphase BPhosphorylation by p34cdc2 protein kinase regulates binding of the kinesin-related motor HsEg5 to the dynactin subunit p150A novel plant kinesin-related protein specifically associates with the phragmoplast organellesThe tetrameric kinesin Kif25 suppresses pre-mitotic centrosome separation to establish proper spindle orientation.Family-specific Kinesin Structures Reveal Neck-linker Length Based on Initiation of the Coiled-coil.A structural model for monastrol inhibition of dimeric kinesin Eg5.Functional coordination of three mitotic motors in Drosophila embryos.Dynamic partitioning of mitotic kinesin-5 cross-linkers between microtubule-bound and freely diffusing states.Single-headed mode of kinesin-5.Kinesin-5-dependent poleward flux and spindle length control in Drosophila embryo mitosisKLP-18, a Klp2 kinesin, is required for assembly of acentrosomal meiotic spindles in Caenorhabditis elegans.Midzone organization restricts interpolar microtubule plus-end dynamics during spindle elongationKinesin-5 acts as a brake in anaphase spindle elongation.Dynamic reorganization of Eg5 in the mammalian spindle throughout mitosis requires dynein and TPX2.Nuclear envelope-associated dynein drives prophase centrosome separation and enables Eg5-independent bipolar spindle formation.Unsupervised automated high throughput phenotyping of RNAi time-lapse moviesEndogenous localizome identifies 43 mitotic kinesins in a plant cellThe microtubule cross-linker Feo controls the midzone stability, motor composition, and elongation of the anaphase B spindle in Drosophila embryos.
P2860
Q21710690-0785FB34-974D-424A-B348-1860E83F78B3Q24294562-C5E71CDB-77A8-4E8F-B111-3DF45F207BBAQ24540197-17274B83-8491-42A3-9066-ADD8F537D48CQ24608232-F331722E-B95B-4CE1-A28F-72E4DAC3546EQ24628680-BC45D5A8-E1E1-4FCF-8266-A7151BA276DCQ24632164-DEFA7A49-FA85-4D8E-9074-17E6D1C412D9Q24644762-7E2EDDB0-AD1E-4C7A-9708-EA1157C384B4Q24647999-5D78CE33-EC9A-41FF-A254-31F143A9E709Q24670581-3CA2FE58-2B65-4EA4-9B40-DBE640461C04Q24682691-D390ED06-C587-443A-A2D7-928851B0DE79Q24801614-BF9C7F15-DE13-4997-BAD7-99CC93892B7CQ27027646-FA1427AC-5881-4EE9-93BF-13430B1309BEQ27310316-4A37D875-1E82-4DF6-8E74-935DFBB3F0C2Q27318472-BBB12AAB-9F05-41E9-AFE5-E75364035E34Q27631520-A6D3AC8E-8C92-4777-89EA-3BFA2E5C3E1EQ27683140-A36D49AB-6D5E-47E7-84C0-24715C4DCB31Q27931564-CE8BBC36-1147-496C-8428-57515E94D8EDQ27932270-5507B9E8-44B2-41EA-A68A-6ED49DFCBEBBQ27935370-95AF333D-A55C-4541-A125-07A090862496Q27935489-25C0B007-D247-463F-AAFC-B8E91EA28F8BQ27936177-33E1169D-E6BF-4362-AC98-AD6C8E135898Q27938562-6076B723-4347-4ECC-A1CD-722558252B04Q28078705-70130C1B-3CD1-4BB0-9507-7E6550013B8FQ28244586-91A25BE6-CFDF-4949-A759-265ABF18563DQ28363613-4FE1C902-341F-4E72-913B-E63EF9690DBFQ29871491-B2E25DD2-3A17-4F2D-8E69-45F884710FD1Q30391011-81305478-D55B-45DA-ADCF-0944E372B85FQ30477323-028EEC36-32FA-45D8-A929-167529999E3DQ30477413-A1D751BE-7D5C-4F2C-9EBF-2B536648B057Q30482990-180A8FFE-86F6-413A-A2C2-16E9B4AA9723Q30483041-D2655EE9-6474-477D-96C7-AA2768185F9BQ30486464-B3BB4436-4860-46D3-91C7-B4562D492732Q30486975-C3ECA0A1-B6F0-4C02-9E48-5C79EE3D7544Q30487204-244FEDD6-BF14-4777-884F-03B19768B4BEQ30491649-C77B1687-8D6F-46E2-BB41-63A3028C8CF5Q30512383-D9DBCE09-CFA2-4030-9C18-B8057A2FE9C7Q30528108-F372ABFC-45E5-4C20-B010-EBECBA57DEABQ30558691-4C89FED3-FC67-4752-B816-6F067DBD52DFQ30574583-770B16FC-2BD8-4AA5-9514-44896E2DFAD7Q30638664-3E07CE75-95B5-4761-9B57-CF97606F6F75
P2860
description
1996 nî lūn-bûn
@nan
1996 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
A bipolar kinesin
@ast
A bipolar kinesin
@en
A bipolar kinesin
@nl
type
label
A bipolar kinesin
@ast
A bipolar kinesin
@en
A bipolar kinesin
@nl
prefLabel
A bipolar kinesin
@ast
A bipolar kinesin
@en
A bipolar kinesin
@nl
P2093
P2860
P3181
P356
P1433
P1476
A bipolar kinesin
@en
P2093
A S Kashina
J M Scholey
K P Wedaman
R J Baskin
W M Saxton
P2860
P2888
P3181
P356
10.1038/379270A0
P407
P577
1996-01-18T00:00:00Z
P5875
P6179
1004145399