349 results on '"Giglione, Carmela"'
Search Results
52. Impact of the N-terminal amino acid on targeted protein degradation
53. Differential actions of p60c-Src and Lck kinases on the Ras regulators p120-GAP and GDP/GTP exchange factor CDC25Mm
54. Peptide deformylase as a target for new generation, broad spectrum antimicrobial agents: MicroReview
55. Targeted profiling of A. thaliana sub-proteomes illuminates new co- and post-translationally N-terminal Myristoylated proteins
56. NatB-Mediated N-Terminal Acetylation Affects Growth and Biotic Stress Responses
57. The Scope, Functions, and Dynamics of Posttranslational Protein Modifications
58. The C-terminal residue of phage Vp16 PDF, the smallest peptide deformylase, acts as an offset element locking the active conformation
59. Additional file 4: of EnCOUNTer: a parsing tool to uncover the mature N-terminus of organelle-targeted proteins in complex samples
60. Additional file 5: Figure S1. of EnCOUNTer: a parsing tool to uncover the mature N-terminus of organelle-targeted proteins in complex samples
61. Additional file 6: Figure S2. of EnCOUNTer: a parsing tool to uncover the mature N-terminus of organelle-targeted proteins in complex samples
62. Additional file 3: of EnCOUNTer: a parsing tool to uncover the mature N-terminus of organelle-targeted proteins in complex samples
63. Additional file 7: Figure S3. of EnCOUNTer: a parsing tool to uncover the mature N-terminus of organelle-targeted proteins in complex samples
64. The Arabidopsis Nα‐acetyltransferase NAA60 locates to the plasma membrane and is vital for the high salt stress response.
65. NAA50 Is an Enzymatically Active Nα-Acetyltransferase That Is Crucial for Development and Regulation of Stress Responses.
66. NatB-Mediated N-Terminal Acetylation Affects Growth and Biotic Stress Responses.
67. N-myristoyltransferases inhibitory activity of ellagitannins from Terminalia bentzoë (L.) L. f. subsp. bentzoë
68. Structural and genomic decoding of human and plant myristoylomes reveals a definitive recognition pattern
69. EnCOUNTer: a parsing tool to uncover the mature N-terminus of organelle-targeted proteins in complex samples
70. Correction: Corrigendum: A unique peptide deformylase platform to rationally design and challenge novel active compounds
71. MetAP1 and MetAP2 drive cell selectivity for a potent anti-cancer agent in synergy, by controlling glutathione redox state
72. Influence of various endogenous and artefact modifications on large-scale proteomics analysis
73. N-terminal modifications contribute to flowering time and immune response regulations
74. Downregulation of N-terminal acetylation triggers ABA-mediated drought responses in Arabidopsis
75. Proteome‐wide analysis of the amino terminal status of Escherichia coli proteins at the steady‐state and upon deformylation inhibition
76. N-terminal protein modifications: Bringing back into play the ribosome
77. Molecular identification and functional characterization of the first Nα‐acetyltransferase in plastids by global acetylome profiling
78. Ion mobility coupled to native mass spectrometry as a relevant tool to investigate extremely small ligand-induced conformational changes
79. A viral peptide deformylase‐ribosome complex reveals mechanism of host gene expression control (558.2)
80. Protein N‐terminal N‐myristoylation at the proteome scale (587.1)
81. Understanding the highly efficient catalysis of prokaryotic peptide deformylases by shedding light on the determinants specifying the low activity of the human counterpart
82. Roles of N-Terminal Fatty Acid Acylations in Membrane Compartment Partitioning:Arabidopsis h-Type Thioredoxins as a Case Study
83. High-throughput profiling ofN-myristoylation substrate specificity across species including pathogens
84. High yield production of myristoylated Arf6 small GTPase by recombinant N-myristoyl transferase
85. Comparative Large Scale Characterization of Plant versus Mammal Proteins Reveals Similar and Idiosyncratic N-α-Acetylation Features
86. Trapping Conformational States Along Ligand-Binding Dynamics of Peptide Deformylase: The Impact of Induced Fit on Enzyme Catalysis
87. Synthesis and evaluation of 1-(1H-indol-3-yl)ethanamine derivatives as new antibacterial agents
88. Dynamics of post‐translational modifications and protein stability in the stroma of Chlamydomonas reinhardtii chloroplasts
89. Comparative metagenomics of microbial traits within oceanic viral communities
90. New Antibiotic Molecules: Bypassing the Membrane Barrier of Gram Negative Bacteria Increases the Activity of Peptide Deformylase Inhibitors
91. Mutations in Three Distinct Loci Cause Resistance to Peptide Deformylase Inhibitors in Bacillus subtilis
92. Cover Picture: Structure-Activity Relationship Analysis of the Peptide Deformylase Inhibitor 5-Bromo-1H-indole-3-acetohydroxamic Acid (ChemMedChem 2/2009)
93. Structure–Activity Relationship Analysis of the Peptide Deformylase Inhibitor 5‐Bromo‐1H‐indole‐3‐acetohydroxamic Acid
94. Extent of N-terminal modifications in cytosolic proteins from eukaryotes
95. Expanded impact of protein N-myristoylation in plants
96. Tools for analyzing and predicting N‐terminal protein modifications
97. Alternative and effective proteomic analysis inArabidopsis
98. Discovery and Refinement of a New Structural Class of Potent Peptide Deformylase Inhibitors
99. The Proteomics of N-terminal Methionine Cleavage
100. The Crystal Structure of Mitochondrial (Type 1A) Peptide Deformylase Provides Clear Guidelines for the Design of Inhibitors Specific for the Bacterial Forms
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.