| 1 | Light‐Activated Reactivity of Nitrones with Amino Acids and Proteins | 1.4 | 1 | Citations (PDF) |
| 2 | Light‐Activated Reactivity of Nitrones with Amino Acids and Proteins | 14.4 | 4 | Citations (PDF) |
| 3 | Enhancing the Small-Scale Screenable Biological Space beyond Known Chemogenomics Libraries with Gray Chemical Matter─Compounds with Novel Mechanisms from High-Throughput Screening Profiles | 3.7 | 5 | Citations (PDF) |
| 4 | Ophiobolin A Covalently Targets Mitochondrial Complex IV Leading to Metabolic Collapse in Cancer Cells | 3.7 | 8 | Citations (PDF) |
| 5 | Chemoproteomics-enabled discovery of a covalent molecular glue degrader targeting NF-κB | 6.2 | 95 | Citations (PDF) |
| 6 | Targeted Protein Degradation through E2 Recruitment | 3.7 | 52 | Citations (PDF) |
| 7 | Rational Chemical Design of Molecular Glue Degraders | 9.2 | 173 | Citations (PDF) |
| 8 | Activation of human STING by a molecular glue-like compound | 11.8 | 67 | Citations (PDF) |
| 9 | A strategy to assess the cellular activity of E3 ligase components against neo-substrates using electrophilic probes | 6.2 | 20 | Citations (PDF) |
| 10 | PHY34 inhibits autophagy through V-ATPase V0A2 subunit inhibition and CAS/CSE1L nuclear cargo trafficking in high grade serous ovarian cancer | 8.5 | 31 | Citations (PDF) |
| 11 | Discovery of a Covalent FEM1B Recruiter for Targeted Protein Degradation Applications | 15.0 | 201 | Citations (PDF) |
| 12 | Photo-Brook rearrangement of acyl silanes as a strategy for photoaffinity probe design | 7.1 | 32 | Citations (PDF) |
| 13 | Deubiquitinase-targeting chimeras for targeted protein stabilization | 11.8 | 311 | Citations (PDF) |
| 14 | Donor–Acceptor Pyridinium Salts for Photo-Induced Electron-Transfer-Driven Modification of Tryptophan in Peptides, Proteins, and Proteomes Using Visible Light | 15.0 | 72 | Citations (PDF) |
| 15 | An Activity-Based Oxaziridine Platform for Identifying and Developing Covalent Ligands for Functional Allosteric Methionine Sites: Redox-Dependent Inhibition of Cyclin-Dependent Kinase 4 | 15.0 | 35 | Citations (PDF) |
| 16 | Chemoproteomics-enabled discovery of covalent RNF114-based degraders that mimic natural product function | 6.2 | 174 | Citations (PDF) |
| 17 | Proteomics in the pharmaceutical and biotechnology industry: a look to the next decade | 2.0 | 51 | Citations (PDF) |
| 18 | Chemoproteomics Enabled Discovery of Selective Probes for NuA4 Factor BRD8 | 3.7 | 15 | Citations (PDF) |
| 19 | BET bromodomain inhibitors regulate keratinocyte plasticity | 11.8 | 12 | Citations (PDF) |
| 20 | Discovery of a Functional Covalent Ligand Targeting an Intrinsically Disordered Cysteine within MYC | 6.2 | 155 | Citations (PDF) |
| 21 | Bardoxolone conjugation enables targeted protein degradation of BRD4 | 3.4 | 133 | Citations (PDF) |
| 22 | A Nimbolide-Based Kinase Degrader Preferentially Degrades Oncogenic BCR-ABL | 3.7 | 109 | Citations (PDF) |
| 23 | Manumycin polyketides act as molecular glues between UBR7 and P53 | 11.8 | 120 | Citations (PDF) |
| 24 | A small-molecule inhibitor of C5 complement protein | 11.8 | 22 | Citations (PDF) |
| 25 | Harnessing the anti-cancer natural product nimbolide for targeted protein degradation | 11.8 | 408 | Citations (PDF) |
| 26 | Covalent Ligand Screening Uncovers a RNF4 E3 Ligase Recruiter for Targeted Protein Degradation Applications | 3.7 | 323 | Citations (PDF) |
| 27 | An Activity‐Based Probe Targeting Non‐Catalytic, Highly Conserved Amino Acid Residues within Bromodomains | 1.4 | 7 | Citations (PDF) |
| 28 | Previously Uncharacterized Vacuolar-type ATPase Binding Site Discovered from Structurally Similar Compounds with Distinct Mechanisms of Action | 3.7 | 15 | Citations (PDF) |
| 29 | Discovery of a ZIP7 inhibitor from a Notch pathway screen | 11.8 | 71 | Citations (PDF) |
| 30 | CPSF3-dependent pre-mRNA processing as a druggable node in AML and Ewing’s sarcoma | 11.8 | 85 | Citations (PDF) |
| 31 | Identification of a novel NAMPT inhibitor by CRISPR/Cas9 chemogenomic profiling in mammalian cells | 3.4 | 38 | Citations (PDF) |
| 32 | Direct Interaction of Chivosazole F with Actin Elicits Cell Responses Similar to Latrunculin A but Distinct from Chondramide | 3.7 | 10 | Citations (PDF) |
| 33 | Examining the influence of specificity ligands and ATP-competitive ligands on the overall effectiveness of bivalent kinase inhibitors | 1.6 | 7 | Citations (PDF) |
| 34 | Tankyrase Inhibitor Sensitizes Lung Cancer Cells to Endothelial Growth Factor Receptor (EGFR) Inhibition via Stabilizing Angiomotins and Inhibiting YAP Signaling | 2.2 | 77 | Citations (PDF) |
| 35 | Conversion of a Single Polypharmacological Agent into Selective Bivalent Inhibitors of Intracellular Kinase Activity | 3.7 | 27 | Citations (PDF) |
| 36 | Identifying compound efficacy targets in phenotypic drug discovery | 6.6 | 149 | Citations (PDF) |
| 37 | Nannocystin A: an Elongation Factor 1 Inhibitor from Myxobacteria with Differential Anti‐Cancer Properties | 14.4 | 103 | Citations (PDF) |
| 38 | Gift from Nature: Cyclomarin A Kills Mycobacteria and Malaria Parasites by Distinct Modes of Action | 2.6 | 51 | Citations (PDF) |
| 39 | Quantitative Lys-ϵ-Gly-Gly (diGly) Proteomics Coupled with Inducible RNAi Reveals Ubiquitin-mediated Proteolysis of DNA Damage-inducible Transcript 4 (DDIT4) by the E3 Ligase HUWE1 | 2.2 | 73 | Citations (PDF) |
| 40 | Selective VPS34 inhibitor blocks autophagy and uncovers a role for NCOA4 in ferritin degradation and iron homeostasis in vivo | 16.3 | 729 | Citations (PDF) |
| 41 | Target identification for a Hedgehog pathway inhibitor reveals the receptor GPR39 | 11.8 | 58 | Citations (PDF) |
| 42 | Structure of the DDB1–CRBN E3 ubiquitin ligase in complex with thalidomide | 37.9 | 1,070 | Citations (PDF) |
| 43 | Deubiquitinase FAM/USP9X Interacts with the E3 Ubiquitin Ligase SMURF1 Protein and Protects It from Ligase Activity-dependent Self-degradation | 2.2 | 114 | Citations (PDF) |
| 44 | Mass Spectrometry-Based Proteomics in Preclinical Drug Discovery | 4.7 | 178 | Citations (PDF) |
| 45 | Natural products reveal cancer cell dependence on oxysterol-binding proteins | 11.8 | 257 | Citations (PDF) |
| 46 | RNF146 is a poly(ADP-ribose)-directed E3 ligase that regulates axin degradation and Wnt signalling | 16.3 | 425 | Citations (PDF) |
| 47 | Bone Overgrowth-associated Mutations in the LRP4 Gene Impair Sclerostin Facilitator Function | 2.2 | 284 | Citations (PDF) |
| 48 | Class III Phosphatidylinositol 4-Kinase Alpha and Beta Are Novel Host Factor Regulators of Hepatitis C Virus Replication | 3.6 | 189 | Citations (PDF) |
| 49 | Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling | 37.9 | 1,989 | Citations (PDF) |
| 50 | Post-translational Tyrosine Nitration of Eosinophil Granule Toxins Mediated by Eosinophil Peroxidase | 2.2 | 44 | Citations (PDF) |
| 51 | Quantitative mass spectrometry in proteomics: a critical review | 3.4 | 1,531 | Citations (PDF) |
| 52 | Proteome survey reveals modularity of the yeast cell machinery | 37.9 | 2,430 | Citations (PDF) |
| 53 | Multiple synergizing factors contribute to the strength of the CD8+ T cell response against listeriolysin O | 3.1 | 7 | Citations (PDF) |
| 54 | Computational prediction of proteotypic peptides for quantitative proteomics | 29.8 | 681 | Citations (PDF) |
| 55 | Scoring proteomes with proteotypic peptide probes | 78.1 | 350 | Citations (PDF) |
| 56 | Bartonella Adhesin A Mediates a Proangiogenic Host Cell Response | 9.3 | 207 | Citations (PDF) |
| 57 | Arf1p Provides an Unexpected Link between COPI Vesicles and mRNA in Saccharomyces cerevisiae | 2.5 | 47 | Citations (PDF) |
| 58 | A physical and functional map of the human TNF-α/NF-κB signal transduction pathway | 16.3 | 1,031 | Citations (PDF) |
| 59 | A 14-3-3 protein of Chlamydomonas reinhardtii associated with the endoplasmic reticulum: nucleotide sequence of the cDNA and the corresponding gene and derived amino acid sequence | 3.4 | 11 | Citations (PDF) |
| 60 | Profiling Core Proteomes of Human Cell Lines by One-dimensional PAGE and Liquid Chromatography-Tandem Mass Spectrometry | 3.0 | 213 | Citations (PDF) |
| 61 | Biosynthese von Glycopeptid-Antibiotika vom Vancomycin-Typ: die Reihenfolge der Ringschlüsse | 1.4 | 36 | Citations (PDF) |
| 62 | The Biosynthesis of Vancomycin-Type Glycopeptide Antibiotics-The Order of the Cyclization Steps | 14.4 | 141 | Citations (PDF) |
| 63 | Dermcidin: a novel human antibiotic peptide secreted by sweat glands | 23.5 | 690 | Citations (PDF) |
| 64 | Combining computer algorithms with experimental approaches permits the rapid and accurate identification of T cell epitopes from defined antigens | 1.4 | 90 | Citations (PDF) |
| 65 | A Naturally Processed Rat Major Histocompatibility Complex Class I-associated Viral Peptide as Target Structure of Borna Disease Virus-specific CD8+ T Cells | 2.2 | 24 | Citations (PDF) |
| 66 | Identification of tumor-associated MHC class I ligands by a novel T cell-independent approach | 3.1 | 133 | Citations (PDF) |
| 67 | Two new proteases in the MHC class I processing pathway | 23.5 | 236 | Citations (PDF) |
| 68 | The HLA-A*6601 peptide motif: prediction by pocket structure and verification by peptide analysis | 2.8 | 15 | Citations (PDF) |
| 69 | Peptide motif of HLA-B*1510 | 2.8 | 6 | Citations (PDF) |
| 70 | Contribution of Proteasomal β-Subunits to the Cleavage of Peptide Substrates Analyzed with Yeast Mutants | 2.2 | 244 | Citations (PDF) |
| 71 | Discovery of EGT710, an Oral Nonpeptidomimetic Reversible Covalent SARS-CoV-2 Main Protease Inhibitor | 5.6 | 0 | Citations (PDF) |
