| scholarly article | Q13442814 |
| P356 | DOI | 10.3390/LIFE6010002 |
| P8608 | Fatcat ID | release_ux7fplxuebeidniuvqhzklsy3i |
| P932 | PMC publication ID | 4810233 |
| P698 | PubMed publication ID | 26729173 |
| P5875 | ResearchGate publication ID | 289489557 |
| P50 | author | Angela W Fung | Q83282044 |
| P2093 | author name string | Richard P Fahlman | |
| Roshani Payoe | |||
| P2860 | cites work | The leucyl/phenylalanyl-tRNA-protein transferase. Overexpression and characterization of substrate recognition, domain structure, and secondary structure | Q72017076 |
| Twelve species of the nucleoid-associated protein from Escherichia coli. Sequence recognition specificity and DNA binding affinity | Q73157405 | ||
| Applying Arginylation for Bottom-Up Proteomics | Q85926490 | ||
| Unexpectedly fast transfer of positron-emittable artificial substrate into N-terminus of peptide/protein mediated by wild-type L/F-tRNA-protein transferase | Q87221780 | ||
| The RelA/SpoT homolog (RSH) superfamily: distribution and functional evolution of ppGpp synthetases and hydrolases across the tree of life | Q21135259 | ||
| Synthesis of Guanosine Tetra- and Pentaphosphate Requires the Presence of a Codon-Specific, Uncharged Transfer Ribonucleic Acid in the Acceptor Site of Ribosomes | Q24564295 | ||
| The N-end rule pathway | Q24598290 | ||
| Compilation of tRNA sequences and sequences of tRNA genes | Q24793116 | ||
| Conditional Tek promoter-driven deletion of arginyltransferase in the germ line causes defects in gametogenesis and early embryonic lethality in mice | Q27335779 | ||
| X-ray crystal structure of Staphylococcus aureus FemA | Q27639499 | ||
| Crystal structures of Weissella viridescens FemX and its complex with UDP-MurNAc-pentapeptide: insights into FemABX family substrates recognition | Q27643131 | ||
| In vivo half-life of a protein is a function of its amino-terminal residue | Q28287702 | ||
| Thermodynamic characterization of ppGpp binding to EF-G or IF2 and of initiator tRNA binding to free IF2 in the presence of GDP, GTP, or ppGpp | Q28290627 | ||
| Structures of two bacterial resistance factors mediating tRNA-dependent aminoacylation of phosphatidylglycerol with lysine or alanine | Q28493059 | ||
| N-terminal protein modification using simple aminoacyl transferase substrates | Q30406776 | ||
| High-throughput mass spectrometric discovery of protein post-translational modifications. | Q30640679 | ||
| Quantification of the post-translational addition of amino acids to proteins by MALDI-TOF mass spectrometry. | Q30857554 | ||
| ClpS is the recognition component for Escherichia coli substrates of the N-end rule degradation pathway. | Q50598911 | ||
| Co-variation of tRNA abundance and codon usage in Escherichia coli at different growth rates. | Q52888301 | ||
| Phosphorylation of elongation factor Tu prevents ternary complex formation. | Q54008053 | ||
| Probing the leucyl/phenylalanyl tRNA protein transferase active site with tRNA substrate analogues. | Q54295194 | ||
| Selective charging of tRNA isoacceptors explains patterns of codon usage. | Q54523461 | ||
| Transfer of methionyl residues by leucyl, phenylalanyl-tRNA-protein transferase | Q67489442 | ||
| Utilization of isoaccepting leucyl-tRNA in the soluble incorporation system and protein synthesizing systems from E.coli | Q69355923 | ||
| The elongation factor Tu . guanosine tetraphosphate complex | Q70166995 | ||
| Methylation in vivo of elongation factor EF-Tu at lysine-56 decreases the rate of tRNA-dependent GTP hydrolysis | Q70312207 | ||
| ppGpp inhibition of elongation factors Tu, G and Ts during polypeptide synthesis | Q70404037 | ||
| Aminoacyl-tRNA recognition by the leucyl/phenylalanyl-tRNA-protein transferase | Q71514688 | ||
| Just-in-time transcription program in metabolic pathways | Q33202257 | ||
| A novel form of neurotensin post-translationally modified by arginylation | Q33221326 | ||
| Arginyltransferase ATE1 catalyzes midchain arginylation of proteins at side chain carboxylates in vivo | Q33566696 | ||
| tRNAs as regulators of biological processes | Q33737299 | ||
| DNA protection by stress-induced biocrystallization | Q33867772 | ||
| An alternative mechanism for the catalysis of peptide bond formation by L/F transferase: substrate binding and orientation. | Q33885217 | ||
| Fusidic acid-resistant EF-G perturbs the accumulation of ppGpp | Q33912678 | ||
| Polyamines: mysterious modulators of cellular functions | Q33920552 | ||
| The determination of tRNALeu recognition nucleotides for Escherichia coli L/F transferase | Q33929029 | ||
| RGS4 and RGS5 are in vivo substrates of the N-end rule pathway | Q34085136 | ||
| Differential arginylation of actin isoforms is regulated by coding sequence-dependent degradation | Q34139712 | ||
| Selective charging of tRNA isoacceptors induced by amino-acid starvation | Q34166656 | ||
| Peptide Acceptors in the Leucine, Phenylalanine Transfer Reaction | Q34213812 | ||
| A soluble enzyme from Escherichia coli which catalyzes the transfer of leucine and phenylalanine from tRNA to acceptor proteins | Q34221693 | ||
| Structural basis for transcription regulation by alarmone ppGpp. | Q34316432 | ||
| Universality and structure of the N-end rule | Q34430814 | ||
| Polyamines protect Escherichia coli cells from the toxic effect of oxygen | Q34804453 | ||
| The N-end rule in bacteria. | Q34993240 | ||
| Differential utilization of leucyl-tRNAs by Escherichia coli | Q35017893 | ||
| Alanyl-phosphatidylglycerol synthase: mechanism of substrate recognition during tRNA-dependent lipid modification in Pseudomonas aeruginosa | Q35034095 | ||
| The nucleotide-binding site of bacterial translation initiation factor 2 (IF2) as a metabolic sensor | Q35080376 | ||
| tRNA-dependent peptide bond formation by the transferase PacB in biosynthesis of the pacidamycin group of pentapeptidyl nucleoside antibiotics | Q35134064 | ||
| Single-molecule investigations of the stringent response machinery in living bacterial cells | Q35149470 | ||
| Protein synthesis during cellular quiescence is inhibited by phosphorylation of a translational elongation factor | Q35796219 | ||
| Amino-terminal arginylation targets endoplasmic reticulum chaperone BiP for autophagy through p62 binding | Q35812368 | ||
| Arginylation regulates purine nucleotide biosynthesis by enhancing the activity of phosphoribosyl pyrophosphate synthase | Q35856331 | ||
| Arginylated calreticulin at plasma membrane increases susceptibility of cells to apoptosis | Q36052477 | ||
| The N-end rule pathway counteracts cell death by destroying proapoptotic protein fragments | Q36079454 | ||
| The N-end rule in Escherichia coli: cloning and analysis of the leucyl, phenylalanyl-tRNA-protein transferase gene aat | Q36103007 | ||
| Recent functional insights into the role of (p)ppGpp in bacterial physiology | Q36319374 | ||
| A genetic locus for the regulation of ribonucleic acid synthesis | Q36442193 | ||
| RNA-dependent lipid remodeling by bacterial multiple peptide resistance factors | Q36534465 | ||
| Investigations of valanimycin biosynthesis: elucidation of the role of seryl-tRNA. | Q36638728 | ||
| Killing of macrophages by anthrax lethal toxin: involvement of the N-end rule pathway | Q36817991 | ||
| Polyamines in bacteria: pleiotropic effects yet specific mechanisms | Q36983999 | ||
| The Francisella tularensis migR, trmE, and cphA genes contribute to F. tularensis pathogenicity island gene regulation and intracellular growth by modulation of the stress alarmone ppGpp | Q37036014 | ||
| The N-degradome of Escherichia coli: limited proteolysis in vivo generates a large pool of proteins bearing N-degrons | Q37213857 | ||
| Modification of PATase by L/F-transferase generates a ClpS-dependent N-end rule substrate in Escherichia coli | Q37234965 | ||
| Magic spot: (p) ppGpp | Q37458434 | ||
| The plant N-end rule pathway: structure and functions | Q37772351 | ||
| Posttranslational arginylation as a global biological regulator | Q37904336 | ||
| The molecular basis for the post-translational addition of amino acids by L/F transferase in the N-end rule pathway | Q38360410 | ||
| tRNA--the golden standard in molecular biology | Q38628517 | ||
| Calreticulin-dimerization induced by post-translational arginylation is critical for stress granules scaffolding | Q39169417 | ||
| Dependence of RelA-mediated (p)ppGpp formation on tRNA identity | Q39575407 | ||
| Regulation of bacterial ppGpp and pppGpp | Q39955411 | ||
| tRNAs as primer of reverse transcriptases | Q40402097 | ||
| Elevated guanosine 5'-diphosphate 3'-diphosphate level inhibits bacterial growth and interferes with FtsZ assembly. | Q40451713 | ||
| An essential role of N-terminal arginylation in cardiovascular development | Q40720569 | ||
| Growth rate dependence of transfer RNA abundance in Escherichia coli | Q41237752 | ||
| RelA-dependent (p)ppGpp production controls exoenzyme synthesis in Erwinia carotovora subsp. atroseptica | Q41762424 | ||
| The ribosome triggers the stringent response by RelA via a highly distorted tRNA | Q41809118 | ||
| Positive allosteric feedback regulation of the stringent response enzyme RelA by its product | Q41850367 | ||
| Enzymatic generation of peptides flanked by basic amino acids to obtain MS/MS spectra with 2× sequence coverage | Q42034532 | ||
| Calreticulin and Arginylated Calreticulin Have Different Susceptibilities to Proteasomal Degradation | Q42126098 | ||
| Kinetic analysis of the leucyl/phenylalanyl-tRNA-protein transferase with acceptor peptides possessing different N-terminal penultimate residues | Q42544067 | ||
| The C-terminal proteolytic fragment of the breast cancer susceptibility type 1 protein (BRCA1) is degraded by the N-end rule pathway | Q42605172 | ||
| The NEXT-A (N-terminal EXtension with Transferase and ARS) reaction | Q43277412 | ||
| Charging levels of four tRNA species in Escherichia coli Rel(+) and Rel(-) strains during amino acid starvation: a simple model for the effect of ppGpp on translational accuracy. | Q43556218 | ||
| Two Compounds implicated in the Function of the RC Gene of Escherichia coli | Q43606324 | ||
| Dissection of the mechanism for the stringent factor RelA. | Q44206960 | ||
| Proteomic discovery of cellular substrates of the ClpXP protease reveals five classes of ClpX-recognition signals | Q44384522 | ||
| Degradation of DIAP1 by the N-end rule pathway is essential for regulating apoptosis. | Q44401479 | ||
| Dynamic control of Dps protein levels by ClpXP and ClpAP proteases in Escherichia coli | Q44570308 | ||
| The degradation signal in a short-lived protein | Q45180905 | ||
| On the role of an unusual tRNAGly isoacceptor in Staphylococcus aureus. | Q45755014 | ||
| Global dynamics of the Escherichia coli proteome and phosphoproteome during growth in minimal medium | Q45886058 | ||
| CpgA, EF-Tu and the stressosome protein YezB are substrates of the Ser/Thr kinase/phosphatase couple, PrkC/PrpC, in Bacillus subtilis | Q46107284 | ||
| Promoter-specific control of E. coli RNA polymerase by ppGpp and a general transcription factor | Q46145648 | ||
| The N-end rule pathway as a nitric oxide sensor controlling the levels of multiple regulators | Q46742633 | ||
| Regulation of the Drosophila ubiquitin ligase DIAP1 is mediated via several distinct ubiquitin system pathways | Q47072230 | ||
| Chemoenzymatic transfer of fluorescent non-natural amino acids to the N terminus of a protein/peptide | Q47920963 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 2 | |
| P577 | publication date | 2015-12-31 | |
| P1433 | published in | Life | Q17064586 |
| P1476 | title | Perspectives and Insights into the Competition for Aminoacyl-tRNAs between the Translational Machinery and for tRNA Dependent Non-Ribosomal Peptide Bond Formation | |
| P478 | volume | 6 |
| Q39224176 | Self-Referential Encoding on Modules of Anticodon Pairs-Roots of the Biological Flow System | cites work | P2860 |
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