scholarly article | Q13442814 |
P50 | author | Vinay Kumar Nandicoori | Q57060364 |
P2093 | author name string | Archana Singh | |
Yogesh Chawla | |||
Divya Arora | |||
Basanti Malakar | |||
P2860 | cites work | Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence | Q22122411 |
A new antibiotic kills pathogens without detectable resistance | Q24091299 | ||
The Membrane Steps of Bacterial Cell Wall Synthesis as Antibiotic Targets | Q26738402 | ||
The enduring hypoxic response of Mycobacterium tuberculosis | Q27302134 | ||
Phosphorylation of the Peptidoglycan Synthase PonA1 Governs the Rate of Polar Elongation in Mycobacteria | Q27318744 | ||
PknB-mediated phosphorylation of a novel substrate, N-acetylglucosamine-1-phosphate uridyltransferase, modulates its acetyltransferase activity | Q27653322 | ||
Unusual Conformation of the SxN Motif in the Crystal Structure of Penicillin-Binding Protein A from Mycobacterium tuberculosis | Q27660125 | ||
A Phosphorylated Pseudokinase Complex Controls Cell Wall Synthesis in Mycobacteria | Q27676873 | ||
Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes | Q27860838 | ||
An in vitro model for sequential study of shiftdown of Mycobacterium tuberculosis through two stages of nonreplicating persistence | Q28378895 | ||
NADH dehydrogenase defects confer isoniazid resistance and conditional lethality in Mycobacterium smegmatis | Q28379488 | ||
Role of the extracytoplasmic-function sigma factor sigma(H) in Mycobacterium tuberculosis global gene expression | Q28486621 | ||
The Mycobacterium tuberculosis ECF sigma factor sigmaE: role in global gene expression and survival in macrophages | Q28486647 | ||
Ability of PknA, a mycobacterial eukaryotic-type serine/threonine kinase, to transphosphorylate MurD, a ligase involved in the process of peptidoglycan biosynthesis | Q28486801 | ||
The role of RelMtb-mediated adaptation to stationary phase in long-term persistence of Mycobacterium tuberculosis in mice | Q28486838 | ||
The Mycobacterium tuberculosis serine/threonine kinases PknA and PknB: substrate identification and regulation of cell shape | Q28487135 | ||
Characterization of CrgA, a new partner of the Mycobacterium tuberculosis peptidoglycan polymerization complexes | Q28487435 | ||
Retracted: Novel Role of Phosphorylation-Dependent Interaction between FtsZ and FipA in Mycobacterial Cell Division | Q28487635 | ||
Tuberculous granulomas are hypoxic in guinea pigs, rabbits, and nonhuman primates | Q29618010 | ||
The spectrum of latent tuberculosis: rethinking the biology and intervention strategies | Q29619404 | ||
A philosophy of anti-infectives as a guide in the search for new drugs for tuberculosis. | Q30371769 | ||
Protein kinase B (PknB) of Mycobacterium tuberculosis is essential for growth of the pathogen in vitro as well as for survival within the host | Q33619370 | ||
Specificity of the transport of lipid II by FtsW in Escherichia coli | Q33652106 | ||
From the regulation of peptidoglycan synthesis to bacterial growth and morphology. | Q33694168 | ||
Specialized transduction designed for precise high-throughput unmarked deletions in Mycobacterium tuberculosis. | Q33724924 | ||
Nitrile-inducible gene expression in mycobacteria. | Q33754978 | ||
Regulation of polar peptidoglycan biosynthesis by Wag31 phosphorylation in mycobacteria | Q33781664 | ||
Phosphorylation of Mycobacterium tuberculosis Ser/Thr phosphatase by PknA and PknB | Q33851543 | ||
Comprehensive Essentiality Analysis of the Mycobacterium tuberculosis Genome via Saturating Transposon Mutagenesis | Q34047835 | ||
Granuloma formation by synthetic bacterial cell wall fragment: muramyl dipeptide | Q34077109 | ||
The Stringent Response Is Required for Full Virulence ofMycobacterium tuberculosisin Guinea Pigs | Q34172559 | ||
Bacterial cell wall. MurJ is the flippase of lipid-linked precursors for peptidoglycan biogenesis. | Q34175962 | ||
Annotation of the M. tuberculosis hypothetical orfeome: adding functional information to more than half of the uncharacterized proteins | Q34224850 | ||
Moenomycin family antibiotics: chemical synthesis, biosynthesis, and biological activity | Q34329962 | ||
Phosphorylation of enoyl-acyl carrier protein reductase InhA impacts mycobacterial growth and survival | Q34333844 | ||
ftsW is an essential cell‐division gene in Escherichia coli | Q34432128 | ||
Nucleotide sequence of the rodA gene, responsible for the rod shape of Escherichia coli: rodA and the pbpA gene, encoding penicillin-binding protein 2, constitute the rodA operon | Q34497084 | ||
Peptidoglycan synthesis in the absence of class A penicillin-binding proteins in Bacillus subtilis | Q34514614 | ||
Depletion of antibiotic targets has widely varying effects on growth | Q34651942 | ||
Carbon flux rerouting during Mycobacterium tuberculosis growth arrest | Q34768891 | ||
Lipid II: a central component in bacterial cell wall synthesis and a target for antibiotics | Q34879830 | ||
Bacillus subtilis homologs of MviN (MurJ), the putative Escherichia coli lipid II flippase, are not essential for growth | Q34996462 | ||
A solid phase extraction-based platform for rapid phosphoproteomic analysis | Q35165042 | ||
Comparative Ser/Thr/Tyr phosphoproteomics between two mycobacterial species: the fast growing Mycobacterium smegmatis and the slow growing Mycobacterium bovis BCG. | Q35315738 | ||
Protein kinase A (PknA) of Mycobacterium tuberculosis is independently activated and is critical for growth in vitro and survival of the pathogen in the host | Q35351818 | ||
MurJ and a novel lipid II flippase are required for cell wall biogenesis in Bacillus subtilis. | Q35644600 | ||
Depletion of M. tuberculosis GlmU from Infected Murine Lungs Effects the Clearance of the Pathogen | Q35816288 | ||
Tuberculosis - metabolism and respiration in the absence of growth | Q35988766 | ||
The O-Antigen Flippase Wzk Can Substitute for MurJ in Peptidoglycan Synthesis in Helicobacter pylori and Escherichia coli | Q36106787 | ||
Structural similarity among Escherichia coli FtsW and RodA proteins and Bacillus subtilis SpoVE protein, which function in cell division, cell elongation, and spore formation, respectively | Q36184478 | ||
RodA as the missing glycosyltransferase in Bacillus subtilis and antibiotic discovery for the peptidoglycan polymerase pathway | Q36248543 | ||
Lipid II as a target for antibiotics | Q36419233 | ||
Targeting the formation of the cell wall core of M. tuberculosis | Q36561313 | ||
Staying in Shape: the Impact of Cell Shape on Bacterial Survival in Diverse Environments | Q36631405 | ||
Development of a new generation of vectors for gene expression, gene replacement, and protein-protein interaction studies in mycobacteria | Q36667361 | ||
Comparative Proteomic Analyses of Avirulent, Virulent, and Clinical Strains of Mycobacterium tuberculosis Identify Strain-specific Patterns | Q37065764 | ||
A cytoplasmic peptidoglycan amidase homologue controls mycobacterial cell wall synthesis | Q37098870 | ||
Hypoxia: a window into Mycobacterium tuberculosis latency | Q37456945 | ||
Acid resistance in Mycobacterium tuberculosis | Q37494077 | ||
SEDS proteins are a widespread family of bacterial cell wall polymerases | Q37510553 | ||
Chapter 2: Biogenesis of the cell wall and other glycoconjugates of Mycobacterium tuberculosis | Q37591593 | ||
Mycobacterial outer membrane is a lipid bilayer and the inner membrane is unusually rich in diacyl phosphatidylinositol dimannosides | Q37687576 | ||
Division and cell envelope regulation by Ser/Thr phosphorylation: Mycobacterium shows the way. | Q37757175 | ||
How sisters grow apart: mycobacterial growth and division | Q38226730 | ||
Epigenetic Phosphorylation Control of Mycobacterium tuberculosis Infection and Persistence. | Q39172602 | ||
Resazurin microtiter assay plate testing of Mycobacterium tuberculosis susceptibilities to second-line drugs: rapid, simple, and inexpensive method | Q39218310 | ||
Serine/Threonine Protein Phosphatase PstP of Mycobacterium tuberculosis Is Necessary for Accurate Cell Division and Survival of Pathogen | Q39272388 | ||
Determinants of Bacterial Morphology: From Fundamentals to Possibilities for Antimicrobial Targeting | Q39455734 | ||
BOCILLIN FL, a sensitive and commercially available reagent for detection of penicillin-binding proteins | Q39470055 | ||
Mycobacterial stationary phase induced by low oxygen tension: cell wall thickening and localization of the 16-kilodalton alpha-crystallin homolog. | Q39564571 | ||
Identification of the rodA gene product of Escherichia coli | Q39976586 | ||
Cell shape and division in Escherichia coli: experiments with shape and division mutants | Q39981015 | ||
Protein Kinase G confers survival advantage to Mycobacterium tuberculosis during latency like conditions. | Q40087605 | ||
Interaction sites of DivIVA and RodA from Corynebacterium glutamicum | Q41361049 | ||
A role for the class A penicillin-binding protein PonA2 in the survival of Mycobacterium smegmatis under conditions of nonreplication | Q41787109 | ||
Validation of FRET Assay for the Screening of Growth Inhibitors of Escherichia coli Reveals Elongasome Assembly Dynamics | Q42015222 | ||
Interplay between Penicillin-binding proteins and SEDS proteins promotes bacterial cell wall synthesis | Q42154160 | ||
Cell-wall alterations as an attribute of Mycobacterium tuberculosis in latent infection | Q44639570 | ||
Lipid II overproduction allows direct assay of transpeptidase inhibition by β-lactams | Q44699614 | ||
Resistance of Gram-positive bacteria to nisin is not determined by lipid II levels | Q45080511 | ||
The lipid II flippase RodA determines morphology and growth in Corynebacterium glutamicum | Q46844312 | ||
Characterization of the tuberculous granuloma in murine and human lungs: cellular composition and relative tissue oxygen tension | Q46915063 | ||
Control of cell shape and elongation by the rodA gene in Bacillus subtilis | Q47986877 | ||
In vitro synthesis of cross-linked murein and its attachment to sacculi by PBP1A from Escherichia coli | Q48086083 | ||
Conditional lethality of cell shape mutations of Salmonella typhimurium: rodA and mre mutants are lethal on solid but not in liquid medium | Q50127836 | ||
Oxygen status of lung granulomas in Mycobacterium tuberculosis-infected mice. | Q51128421 | ||
Insights into the function of FhaA, a cell division-associated protein in mycobacteria. | Q51237575 | ||
Identification of pneumococcal proteins that are functionally linked to penicillin-binding protein 2b (PBP2b). | Q51449936 | ||
Interaction between FtsW and penicillin-binding protein 3 (PBP3) directs PBP3 to mid-cell, controls cell septation and mediates the formation of a trimeric complex involving FtsZ, FtsW and PBP3 in mycobacteria. | Q53560180 | ||
Use of the cell wall precursor lipid II by a pore-forming peptide antibiotic. | Q54068526 | ||
The integral membrane FtsW protein and peptidoglycan synthase PBP3 form a subcomplex in Escherichia coli. | Q54379250 | ||
Recombineering in Mycobacterium tuberculosis. | Q54449978 | ||
Expression of the green fluorescent protein (GFP) in mycobacterium avium as a tool to study the interaction between Mycobacteria and host cells. | Q54568331 | ||
Binding of bacitracin to cells and protoplasts of Micrococcus lysodeikticus | Q68680518 | ||
Evidence for complex interactions of stress-associated regulons in an mprAB deletion mutant of Mycobacterium tuberculosis | Q80019159 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | Mycobacterium tuberculosis | Q130971 |
P577 | publication date | 2018-03-12 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | The transpeptidase PbpA and non-canonical transglycosylase RodA of Mycobacterium tuberculosis play important roles in regulating bacterial cell lengths. |
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