about
A highly coordinated cell wall degradation machine governs spore morphogenesis in Bacillus subtilis.Recycling of the anhydro-N-acetylmuramic acid derived from cell wall murein involves a two-step conversion to N-acetylglucosamine-phosphate.MurQ Etherase is required by Escherichia coli in order to metabolize anhydro-N-acetylmuramic acid obtained either from the environment or from its own cell wall.Beta-lactam antibiotics induce a lethal malfunctioning of the bacterial cell wall synthesis machinery.Lipoprotein cofactors located in the outer membrane activate bacterial cell wall polymerases.An ATP-binding cassette transporter-like complex governs cell-wall hydrolysis at the bacterial cytokinetic ring.More than just lysins: peptidoglycan hydrolases tailor the cell wallAn anhydro-N-acetylmuramyl-L-alanine amidase with broad specificity tethered to the outer membrane of Escherichia coliGrowth of Escherichia coli: significance of peptidoglycan degradation during elongation and septationCofactor bypass variants reveal a conformational control mechanism governing cell wall polymerase activity.How bacteria consume their own exoskeletons (turnover and recycling of cell wall peptidoglycan)SEDS proteins are a widespread family of bacterial cell wall polymerases.The N-acetyl-D-glucosamine kinase of Escherichia coli and its role in murein recyclingPeptidoglycan Recycling.LytM-domain factors are required for daughter cell separation and rapid ampicillin-induced lysis in Escherichia coli.Molecular characterization and verification of azido-3,8-dideoxy-d-manno-oct-2-ulosonic acid incorporation into bacterial lipopolysaccharide.Optimization of novel monobactams with activity against carbapenem-resistant Enterobacteriaceae - Identification of LYS228.A temperature-sensitive replicon enables efficient gene inactivation in Pseudomonas aeruginosa.A pathway-directed screen for inhibitors of the bacterial cell elongation machineryTargeted lipopolysaccharide biosynthetic intermediate analysis with normal-phase liquid chromatography mass spectrometryTwo Distinct Mechanisms of Inhibition of LpxA Acyltransferase Essential for Lipopolysaccharide BiosynthesisMode of Action of the Monobactam LYS228 and Mechanisms Decreasing In Vitro Susceptibility in Escherichia coli and Klebsiella pneumoniaeAcylated-acyl carrier protein stabilizes the Pseudomonas aeruginosa WaaP lipopolysaccharide heptose kinaseStructural and Biological Basis of Small Molecule Inhibition of Escherichia coli LpxD Acyltransferase Essential for Lipopolysaccharide Biosynthesis
P50
Q33531617-48114566-3F6C-46E7-80FA-76BF93EB1980Q33788488-B559A1B6-0D53-4424-A07C-03025D59D989Q34353827-56AB23C2-FC5D-44E0-A0CA-B0230970DB11Q34645039-253A10A2-4019-4082-B3D0-89D9EC470DE6Q34894908-E0C9781F-2F44-4E6F-9D5F-267CED1E9DBCQ35546844-650D3FFB-7780-4871-916C-5EDD422CAFDDQ35945716-75B43481-57D7-483C-A355-FDA6F2BBB874Q35949220-B7300184-D8E0-4ECB-9715-6357216BD6B4Q36672951-8D8C7E27-A0FF-4219-A7E2-54AC65A4387AQ36866217-BD27A68E-5616-4CB4-A659-B015FC7A2356Q37183911-D5CB3C0A-3BF9-4FAD-A56B-7825DC2E9A8CQ37510553-972942E7-3406-48FF-B596-009EBA4004C8Q37583323-E76DF85A-B1FF-4952-B9AD-BE9DDF42E15FQ40458965-47C39978-6C87-4D2F-8F31-B3FC89FAA6A2Q41815173-501CFF3E-0534-45DA-AFE7-F712ADADBE40Q46406220-373AC86F-443F-41C6-8C44-92CA3F35DF9AQ50034439-0C87E4DA-80BB-4CE5-B350-AD075B4F8436Q50133138-BE05D329-EAFF-4F8B-97B0-06D2B8D6F408Q57461268-1F38A305-BC08-4FFC-BC03-112D64D0C4C4Q64234568-0346E5B2-3D58-462D-ACF8-694FBCD5DEB2Q89740176-0D078E9D-0A54-4309-80C9-CE28527220BDQ90645407-DDE37872-D94C-479D-8679-DE4946AD0B42Q91598196-9CADD519-4BE9-4189-832E-02325A20D0ECQ92555051-8F3FD61A-2787-4959-A5DD-941251932CB7
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Tsuyoshi Uehara
@ast
Tsuyoshi Uehara
@en
Tsuyoshi Uehara
@es
Tsuyoshi Uehara
@nl
type
label
Tsuyoshi Uehara
@ast
Tsuyoshi Uehara
@en
Tsuyoshi Uehara
@es
Tsuyoshi Uehara
@nl
prefLabel
Tsuyoshi Uehara
@ast
Tsuyoshi Uehara
@en
Tsuyoshi Uehara
@es
Tsuyoshi Uehara
@nl
P106
P31
P496
0000-0001-6994-4286