review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | William Margolin | |
Kimberly K Busiek | |||
P2860 | cites work | Large-scale filament formation inhibits the activity of CTP synthetase | Q21128768 |
3D-SIM super resolution microscopy reveals a bead-like arrangement for FtsZ and the division machinery: implications for triggering cytokinesis | Q21145732 | ||
Coupled, circumferential motions of the cell wall synthesis machinery and MreB filaments in B. subtilis | Q24629706 | ||
The metabolic enzyme CTP synthase forms cytoskeletal filaments | Q24630587 | ||
New insights into mechanisms of resistance to microtubule inhibitors | Q24633853 | ||
Condensation of FtsZ filaments can drive bacterial cell division | Q24646706 | ||
Reconstitution of contractile FtsZ rings in liposomes | Q24650388 | ||
Bacterial actins and their diversity | Q27001005 | ||
Crystal structure of the cell division protein FtsA from Thermotoga maritima | Q27627489 | ||
Prokaryotic origin of the actin cytoskeleton | Q27634702 | ||
Plasmid protein TubR uses a distinct mode of HTH-DNA binding and recruits the prokaryotic tubulin homolog TubZ to effect DNA partition | Q27662143 | ||
FtsA forms actin-like protofilaments | Q27678310 | ||
SlmA forms a higher-order structure on DNA that inhibits cytokinetic Z-ring formation over the nucleoid | Q27678566 | ||
Tubulin homolog TubZ in a phage-encoded partition system | Q27678760 | ||
FtsZ Protofilaments Use a Hinge-Opening Mechanism for Constrictive Force Generation | Q27679200 | ||
Structural and genetic analyses reveal the protein SepF as a new membrane anchor for the Z ring | Q27680581 | ||
A Phage Tubulin Assembles Dynamic Filaments by an Atypical Mechanism to Center Viral DNA within the Host Cell | Q27681321 | ||
The Structure and Assembly Mechanism of a Novel Three-Stranded Tubulin Filament that Centers Phage DNA | Q27682231 | ||
Bacterial actin MreB forms antiparallel double filaments | Q27683843 | ||
Crystal structure of the bacterial cell-division protein FtsZ | Q27748785 | ||
FtsZ ring structure associated with division in Escherichia coli | Q28245159 | ||
A new FtsZ-interacting protein, YlmF, complements the activity of FtsA during progression of cell division in Bacillus subtilis | Q28488907 | ||
SepF, a novel FtsZ-interacting protein required for a late step in cell division | Q28488960 | ||
Large ring polymers align FtsZ polymers for normal septum formation | Q28489014 | ||
Rational design of berberine-based FtsZ inhibitors with broad-spectrum antibacterial activity | Q28538766 | ||
Bacterial motility complexes require the actin-like protein, MreB and the Ras homologue, MglA | Q28748834 | ||
The cell shape proteins MreB and MreC control cell morphogenesis by positioning cell wall synthetic complexes | Q29138517 | ||
Cell cycle-dependent transcriptional and proteolytic regulation of FtsZ in Caulobacter | Q29346645 | ||
Control of cell shape in bacteria: helical, actin-like filaments in Bacillus subtilis | Q29615777 | ||
Chlamydia trachomatis protein CT009 is a structural and functional homolog to the key morphogenesis component RodZ and interacts with division septal plane localized MreB | Q30368519 | ||
Single molecules of the bacterial actin MreB undergo directed treadmilling motion in Caulobacter crescentus | Q30477816 | ||
The structure of FtsZ filaments in vivo suggests a force-generating role in cell division | Q30480675 | ||
FtsZ in bacterial cytokinesis: cytoskeleton and force generator all in one. | Q30497729 | ||
Myxobacteria gliding motility requires cytoskeleton rotation powered by proton motive force | Q30498174 | ||
The helical MreB cytoskeleton in Escherichia coli MC1000/pLE7 is an artifact of the N-Terminal yellow fluorescent protein tag | Q30528331 | ||
The bacterial cytoskeleton: more than twisted filaments | Q30537603 | ||
Flagella stator homologs function as motors for myxobacterial gliding motility by moving in helical trajectories | Q30539054 | ||
MamK, a bacterial actin, forms dynamic filaments in vivo that are regulated by the acidic proteins MamJ and LimJ | Q36517891 | ||
An altered FtsA can compensate for the loss of essential cell division protein FtsN in Escherichia coli | Q36584033 | ||
FtsZ exhibits rapid movement and oscillation waves in helix-like patterns in Escherichia coli | Q36590750 | ||
The ftsA* gain-of-function allele of Escherichia coli and its effects on the stability and dynamics of the Z ring | Q36590761 | ||
Evidence for functional overlap among multiple bacterial cell division proteins: compensating for the loss of FtsK. | Q36592350 | ||
The bacterial actin MamK: in vitro assembly behavior and filament architecture | Q36596302 | ||
Dimerization or oligomerization of the actin-like FtsA protein enhances the integrity of the cytokinetic Z ring. | Q36608557 | ||
Colocalization of cell division proteins FtsZ and FtsA to cytoskeletal structures in living Escherichia coli cells by using green fluorescent protein | Q36686645 | ||
Diversification and specialization of the bacterial cytoskeleton | Q36687804 | ||
Determination of bacterial rod shape by a novel cytoskeletal membrane protein. | Q37008352 | ||
Force generation by a dynamic Z-ring in Escherichia coli cell division | Q37068245 | ||
RodZ, a component of the bacterial core morphogenic apparatus | Q37079064 | ||
Cell-division inhibitors: new insights for future antibiotics | Q37103616 | ||
Organization of FtsZ filaments in the bacterial division ring measured from polarized fluorescence microscopy | Q37299731 | ||
Gene product 0.4 increases bacteriophage T7 competitiveness by inhibiting host cell division. | Q37353210 | ||
Targeting cell division: small-molecule inhibitors of FtsZ GTPase perturb cytokinetic ring assembly and induce bacterial lethality | Q37416206 | ||
Z-ring-independent interaction between a subdomain of FtsA and late septation proteins as revealed by a polar recruitment assay | Q37596089 | ||
Sculpting the bacterial cell | Q37631271 | ||
Rod-like bacterial shape is maintained by feedback between cell curvature and cytoskeletal localization | Q37659819 | ||
Bacteria that glide with helical tracks. | Q37661606 | ||
MreB of Streptomyces coelicolor is not essential for vegetative growth but is required for the integrity of aerial hyphae and spores. | Q50731367 | ||
Multiple effects of benzamide antibiotics on FtsZ function. | Q53271602 | ||
Examination of the interaction between FtsZ and MinCN in E. coli suggests how MinC disrupts Z rings. | Q53344017 | ||
Lateral FtsZ association and the assembly of the cytokinetic Z ring in bacteria. | Q53364709 | ||
A new assembly pathway for the cytokinetic Z ring from a dynamic helical structure in vegetatively growing cells of Bacillus subtilis. | Q53554148 | ||
MipZ, a spatial regulator coordinating chromosome segregation with cell division in Caulobacter. | Q53611653 | ||
YeeU enhances the bundling of cytoskeletal polymers of MreB and FtsZ, antagonizing the CbtA (YeeV) toxicity in Escherichia coli. | Q54338270 | ||
Identification of a region of FtsA required for interaction with FtsZ. | Q54441393 | ||
Cell cycle-dependent abundance, stability and localization of FtsA and FtsQ in Caulobacter crescentus. | Q54498534 | ||
A point mutation converts Escherichia coli FtsZ septation GTPase to an ATPase. | Q54627299 | ||
Overproduction of FtsZ induces minicell formation in E. coli. | Q54792582 | ||
Partial functional redundancy of MreB isoforms, MreB, Mbl and MreBH, in cell morphogenesis ofBacillus subtilis | Q57990535 | ||
Actin Homolog MreBH Governs Cell Morphogenesis by Localization of the Cell Wall Hydrolase LytE | Q57990544 | ||
The essential bacterial cell-division protein FtsZ is a GTPase | Q59097751 | ||
Cell cycle and positional constraints on FtsZ localization and the initiation of cell division in Caulobacter crescentus | Q73622605 | ||
Asymmetric cell division in B. subtilis involves a spiral-like intermediate of the cytokinetic protein FtsZ | Q74083515 | ||
The bacterial cytoskeleton | Q80615984 | ||
Cell division in a minimal bacterium in the absence of ftsZ | Q84798169 | ||
Assembly of Bacillus subtilis FtsA: effects of pH, ionic strength and nucleotides on FtsA assembly | Q87410355 | ||
Direct interaction of FtsZ and MreB is required for septum synthesis and cell division in Escherichia coli | Q30541334 | ||
Three-dimensional super-resolution imaging of the midplane protein FtsZ in live Caulobacter crescentus cells using astigmatism. | Q30541524 | ||
Motion of variable-length MreB filaments at the bacterial cell membrane influences cell morphology. | Q30541938 | ||
Discovery of chlamydial peptidoglycan reveals bacteria with murein sacculi but without FtsZ | Q30558338 | ||
In vivo organization of the FtsZ-ring by ZapA and ZapB revealed by quantitative super-resolution microscopy | Q30565381 | ||
Accessory factors promote AlfA-dependent plasmid segregation by regulating filament nucleation, disassembly, and bundling | Q30572010 | ||
Effects of polymerization and nucleotide identity on the conformational dynamics of the bacterial actin homolog MreB. | Q30573803 | ||
A new metabolic cell-wall labelling method reveals peptidoglycan in Chlamydia trachomatis. | Q30576851 | ||
Asymmetric constriction of dividing Escherichia coli cells induced by expression of a fusion between two min proteins | Q30577589 | ||
The bacterial cell division proteins FtsA and FtsZ self-organize into dynamic cytoskeletal patterns | Q30577961 | ||
DNA segregation by the bacterial actin AlfA during Bacillus subtilis growth and development | Q31081811 | ||
Polymerization of Ftsz, a bacterial homolog of tubulin. is assembly cooperative? | Q31816073 | ||
Control of cell morphogenesis in bacteria: two distinct ways to make a rod-shaped cell | Q33187415 | ||
Life without a wall or division machine in Bacillus subtilis | Q33408535 | ||
Quantifying absolute protein synthesis rates reveals principles underlying allocation of cellular resources | Q33551343 | ||
Premature targeting of a cell division protein to midcell allows dissection of divisome assembly in Escherichia coli. | Q33594428 | ||
The dynamic nature of the bacterial cytoskeleton | Q33608181 | ||
Bacterial cell division protein FtsZ assembles into protofilament sheets and minirings, structural homologs of tubulin polymers | Q33634552 | ||
Evolution of diverse cell division and vesicle formation systems in Archaea | Q33684783 | ||
In vivo structure of the E. coli FtsZ-ring revealed by photoactivated localization microscopy (PALM) | Q33698067 | ||
FtsZ-independent septal recruitment and function of cell wall remodelling enzymes in chlamydial pathogens | Q33851666 | ||
Structure of bacterial tubulin BtubA/B: evidence for horizontal gene transfer | Q33879004 | ||
Genetic and functional analyses of the conserved C-terminal core domain of Escherichia coli FtsZ | Q33993310 | ||
The bacterial cytoskeleton. | Q34024555 | ||
Unique and overlapping roles for ZipA and FtsA in septal ring assembly in Escherichia coli | Q34085847 | ||
Filament structure, organization, and dynamics in MreB sheets | Q34103533 | ||
Pushing and pulling in prokaryotic DNA segregation | Q34120912 | ||
Imaging-based identification of a critical regulator of FtsZ protofilament curvature in Caulobacter. | Q34155531 | ||
A gain-of-function mutation in ftsA bypasses the requirement for the essential cell division gene zipA in Escherichia coli | Q34183360 | ||
Processive movement of MreB-associated cell wall biosynthetic complexes in bacteria. | Q34189431 | ||
FtsA mutants impaired for self-interaction bypass ZipA suggesting a model in which FtsA's self-interaction competes with its ability to recruit downstream division proteins | Q34235469 | ||
Failsafe mechanisms couple division and DNA replication in bacteria | Q34243485 | ||
The early divisome protein FtsA interacts directly through its 1c subdomain with the cytoplasmic domain of the late divisome protein FtsN. | Q34253906 | ||
Disassembly of the divisome in Escherichia coli: evidence that FtsZ dissociates before compartmentalization | Q37732584 | ||
Chlamydia co-opts the rod shape-determining proteins MreB and Pbp2 for cell division | Q37848764 | ||
Bacterial cytokinesis: From Z ring to divisome | Q38034197 | ||
L-form bacteria, cell walls and the origins of life | Q38072853 | ||
FtsZ ring stability: of bundles, tubules, crosslinks, and curves | Q38086221 | ||
FtsZ in chloroplast division: structure, function and evolution | Q38109759 | ||
The bacterial Min system | Q38120862 | ||
Bacterial cell division as a target for new antibiotics. | Q38128027 | ||
Cytoskeletal proteins participate in conserved viral strategies across kingdoms of life | Q38140359 | ||
Do the divisome and elongasome share a common evolutionary past? | Q38149457 | ||
Form and function of the bacterial cytokinetic ring | Q38188142 | ||
ZipA-induced bundling of FtsZ polymers mediated by an interaction between C-terminal domains | Q39500686 | ||
Role of the carboxy terminus of Escherichia coli FtsA in self-interaction and cell division | Q39501291 | ||
Inside-out Z rings--constriction with and without GTP hydrolysis | Q39575738 | ||
Dysfunctional MreB inhibits chromosome segregation in Escherichia coli. | Q39927847 | ||
Guanine nucleotide-dependent assembly of FtsZ into filaments | Q39931802 | ||
C-shaped cells caused by expression of an ftsA mutation in Escherichia coli | Q39935790 | ||
Mutant isolation and molecular cloning of mre genes, which determine cell shape, sensitivity to mecillinam, and amount of penicillin-binding proteins in Escherichia coli | Q39962792 | ||
Assembly dynamics of FtsZ rings in Bacillus subtilis and Escherichia coli and effects of FtsZ-regulating proteins | Q40000728 | ||
FtsZ ring formation in fts mutants | Q40024436 | ||
Localization of MreB in Rhodobacter sphaeroides under conditions causing changes in cell shape and membrane structure | Q40730548 | ||
Correlation between the structure and biochemical activities of FtsA, an essential cell division protein of the actin family | Q40793545 | ||
FtsZ-spirals and -arcs determine the shape of the invaginating septa in some mutants of Escherichia coli | Q40924830 | ||
Septins promote F-actin ring formation by crosslinking actin filaments into curved bundles | Q41791625 | ||
Peptide inhibitor of cytokinesis during sporulation in Bacillus subtilis | Q41886278 | ||
The C-terminal linker of Escherichia coli FtsZ functions as an intrinsically disordered peptide | Q41913709 | ||
Superresolution imaging of dynamic MreB filaments in B. subtilis--a multiple-motor-driven transport? | Q41966366 | ||
E93R substitution of Escherichia coli FtsZ induces bundling of protofilaments, reduces GTPase activity, and impairs bacterial cytokinesis. | Q41967455 | ||
SepF increases the assembly and bundling of FtsZ polymers and stabilizes FtsZ protofilaments by binding along its length | Q42034994 | ||
RodZ (YfgA) is required for proper assembly of the MreB actin cytoskeleton and cell shape in E. coli. | Q42105686 | ||
A role for FtsA in SPOR-independent localization of the essential Escherichia coli cell division protein FtsN. | Q42115316 | ||
Conditional lethality, division defects, membrane involution, and endocytosis in mre and mrd shape mutants of Escherichia coli. | Q42133021 | ||
ClpXP and ClpAP proteolytic activity on divisome substrates is differentially regulated following the Caulobacter asymmetric cell division | Q42170763 | ||
Bacterial division proteins FtsZ and ZipA induce vesicle shrinkage and cell membrane invagination. | Q42611094 | ||
The GTPase activity of Escherichia coli FtsZ determines the magnitude of the FtsZ polymer bundling by ZapA in vitro. | Q42642634 | ||
Self-enhanced accumulation of FtsN at Division Sites and Roles for Other Proteins with a SPOR domain (DamX, DedD, and RlpA) in Escherichia coli cell constriction | Q42688968 | ||
Manipulating each MreB of Bdellovibrio bacteriovorus gives diverse morphological and predatory phenotypes | Q42917947 | ||
Role of the FtsA C terminus as a switch for polymerization and membrane association | Q43050685 | ||
Positioning of chemosensory proteins and FtsZ through the Rhodobacter sphaeroides cell cycle | Q43778233 | ||
Three-dimensional structure of the Z-ring as a random network of FtsZ filaments. | Q44022826 | ||
Novel S-benzylisothiourea compound that induces spherical cells in Escherichia coli probably by acting on a rod-shape-determining protein(s) other than penicillin-binding protein 2. | Q44322297 | ||
Tetramerization of ZapA is required for FtsZ bundling. | Q44443644 | ||
MreB actin-mediated segregation of a specific region of a bacterial chromosome | Q45262711 | ||
Positioning cell wall synthetic complexes by the bacterial morphogenetic proteins MreB and MreD. | Q46234681 | ||
Diverse eukaryotes have retained mitochondrial homologues of the bacterial division protein FtsZ. | Q47603690 | ||
Plumbagin inhibits cytokinesis in Bacillus subtilis by inhibiting FtsZ assembly--a mechanistic study of its antibacterial activity | Q48032989 | ||
Actin homolog MreB and RNA polymerase interact and are both required for chromosome segregation in Escherichia coli | Q34324082 | ||
The crystal structure of ZapA and its modulation of FtsZ polymerisation | Q34337999 | ||
Role of two essential domains of Escherichia coli FtsA in localization and progression of the division ring | Q34351133 | ||
Liposome division by a simple bacterial division machinery | Q34351599 | ||
Cell division in cocci: localization and properties of the Streptococcus pneumoniae FtsA protein | Q34386288 | ||
Bacillus subtilis SepF binds to the C-terminus of FtsZ. | Q34389510 | ||
SlmA, a nucleoid-associated, FtsZ binding protein required for blocking septal ring assembly over Chromosomes in E. coli. | Q34421472 | ||
3D-SIM super-resolution of FtsZ and its membrane tethers in Escherichia coli cells | Q34423804 | ||
A thermosensitive defect in the ATP binding pocket of FtsA can be suppressed by allosteric changes in the dimer interface | Q34438104 | ||
Reconstitution of self-organizing protein gradients as spatial cues in cell-free systems | Q34441186 | ||
YeeV is an Escherichia coli toxin that inhibits cell division by targeting the cytoskeleton proteins, FtsZ and MreB | Q34494824 | ||
MreB, the cell shape-determining bacterial actin homologue, co-ordinates cell wall morphogenesis in Caulobacter crescentus | Q34545818 | ||
Treadmilling of a prokaryotic tubulin-like protein, TubZ, required for plasmid stability in Bacillus thuringiensis | Q34629413 | ||
Adenine nucleotide-dependent regulation of assembly of bacterial tubulin-like FtsZ by a hypermorph of bacterial actin-like FtsA. | Q34964917 | ||
An intrinsically disordered linker plays a critical role in bacterial cell division | Q35117405 | ||
The Kil peptide of bacteriophage λ blocks Escherichia coli cytokinesis via ZipA-dependent inhibition of FtsZ assembly | Q35126034 | ||
Location of dual sites in E. coli FtsZ important for degradation by ClpXP; one at the C-terminus and one in the disordered linker | Q35145217 | ||
Direct membrane binding by bacterial actin MreB. | Q35185171 | ||
SlmA antagonism of FtsZ assembly employs a two-pronged mechanism like MinCD. | Q35215971 | ||
The bacterial actin MreB rotates, and rotation depends on cell-wall assembly. | Q35229232 | ||
Structure and function of a spectrin-like regulator of bacterial cytokinesis | Q35429618 | ||
An ATP-binding cassette transporter-like complex governs cell-wall hydrolysis at the bacterial cytokinetic ring. | Q35546844 | ||
FtsA is localized to the septum in an FtsZ-dependent manner | Q35617997 | ||
Helical insertion of peptidoglycan produces chiral ordering of the bacterial cell wall. | Q35845001 | ||
Duplication and segregation of the actin (MreB) cytoskeleton during the prokaryotic cell cycle | Q36140646 | ||
ftsZ is an essential cell division gene in Escherichia coli | Q36146680 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell growth | Q189159 |
P304 | page(s) | R243-54 | |
P577 | publication date | 2015-03-01 | |
P1433 | published in | Current Biology | Q1144851 |
P1476 | title | Bacterial actin and tubulin homologs in cell growth and division | |
P478 | volume | 25 |
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