scholarly article | Q13442814 |
P50 | author | Olga Mayans | Q30158947 |
Alexandra Holinski | Q64700427 | ||
Patrick Babinger | Q64700467 | ||
P2093 | author name string | Cian Stutz | |
Daniel Schneider | |||
Wolfgang Kaiser | |||
P2860 | cites work | Structural analysis of two enzymes catalysing reverse metabolic reactions implies common ancestry | Q24536893 |
PHENIX: a comprehensive Python-based system for macromolecular structure solution | Q24654617 | ||
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 | ||
The crystal structure of anthranilate phosphoribosyltransferase from the enterobacterium Pectobacterium carotovorum | Q27639379 | ||
Structural conservation of RecF and Rad50: implications for DNA recognition and RecF function | Q27643663 | ||
Activation of anthranilate phosphoribosyltransferase from Sulfolobus solfataricus by removal of magnesium inhibition and acceleration of product release | Q27655077 | ||
The substrate capture mechanism of Mycobacterium tuberculosis anthranilate phosphoribosyltransferase provides a mode for inhibition | Q27683860 | ||
Structural and theoretical studies suggest domain movement produces an active conformation of thymidine phosphorylase | Q27765011 | ||
The crystal structure of pyrimidine nucleoside phosphorylase in a closed conformation | Q27766042 | ||
SOLVE and RESOLVE: automated structure solution and density modification | Q27860481 | ||
WebLogo: A Sequence Logo Generator | Q27860646 | ||
Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega | Q27860809 | ||
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products | Q27860842 | ||
Automated macromolecular model building for X-ray crystallography using ARP/wARP version 7 | Q27860936 | ||
T-Coffee: A novel method for fast and accurate multiple sequence alignment | Q27860999 | ||
Features and development of Coot | Q27861079 | ||
Structural analyses reveal two distinct families of nucleoside phosphorylases | Q28366428 | ||
The crystal structure of TrpD, a metabolic enzyme essential for lung colonization by Mycobacterium tuberculosis, in complex with its substrate phosphoribosylpyrophosphate | Q28486620 | ||
Automatic processing of rotation diffraction data from crystals of initially unknown symmetry and cell constants | Q29546524 | ||
An efficient recombination system for chromosome engineering in Escherichia coli | Q29615038 | ||
MEGA: a biologist-centric software for evolutionary analysis of DNA and protein sequences | Q29617490 | ||
The evolution of gene duplications: classifying and distinguishing between models | Q29619358 | ||
Stabilization of a metabolic enzyme by library selection in Thermus thermophilus | Q30401353 | ||
Connected gene neighborhoods in prokaryotic genomes | Q31051729 | ||
Glyceraldehyde-3-phosphate dehydrogenase: a universal internal control for Western blots in prokaryotic and eukaryotic cells | Q34156708 | ||
Identification of two DNA helicases UvrD and DinG as suppressors for lethality caused by mutant cspA mRNAs | Q34351824 | ||
Stoichiometry and affinity for thymine DNA glycosylase binding to specific and nonspecific DNA | Q34723697 | ||
Stimulation of Escherichia coli DNA damage inducible DNA helicase DinG by the single-stranded DNA binding protein SSB. | Q36354576 | ||
LuxArray, a high-density, genomewide transcription analysis of Escherichia coli using bioluminescent reporter strains | Q39504901 | ||
Two WXXF-based motifs in NECAPs define the specificity of accessory protein binding to AP-1 and AP-2. | Q40197173 | ||
Staphylococcus aureus DinG, a helicase that has evolved into a nuclease | Q40794077 | ||
Characterization of the DNA damage-inducible helicase DinG from Escherichia coli. | Q42441246 | ||
The helicases DinG, Rep and UvrD cooperate to promote replication across transcription units in vivo | Q42600355 | ||
Differential modes of DNA binding by mismatch uracil DNA glycosylase from Escherichia coli: implications for abasic lesion processing and enzyme communication in the base excision repair pathway | Q42714261 | ||
E. coli genome manipulation by P1 transduction | Q46760894 | ||
Role of each residue in catalysis in the active site of pyrimidine nucleoside phosphorylase from Bacillus subtilis: a hybrid QM/MM study | Q46937162 | ||
A rationally designed monomeric variant of anthranilate phosphoribosyltransferase from Sulfolobus solfataricus is as active as the dimeric wild-type enzyme but less thermostable. | Q54428578 | ||
The DinG protein from Escherichia coli is a structure-specific helicase. | Q54443591 | ||
Fluorescence and NMR investigations on the ligand binding properties of adenylate kinases. | Q54710050 | ||
Structural and Mutational Analysis of Substrate Complexation by Anthranilate Phosphoribosyltransferase fromSulfolobus solfataricus | Q57091000 | ||
Analysis of RNA hydrolyzates by liquid chromatography-mass spectrometry | Q67684207 | ||
Two-stage polymerase chain reaction protocol allowing introduction of multiple mutations, deletions, and insertions, using QuikChange site-directed mutagenesis | Q77426888 | ||
P433 | issue | 32 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
cell biology | Q7141 | ||
P304 | page(s) | 19527-19539 | |
P577 | publication date | 2015-06-10 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | YbiB from Escherichia coli, the Defining Member of the Novel TrpD2 Family of Prokaryotic DNA-binding Proteins | |
P478 | volume | 290 |