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Extensive Targeting of Chemical Space at the Prime Side of Ketoamide Inhibitors of Rhomboid Proteases by Branched Substituents Empowers Their Selectivity and Potency

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Chemical Blockage of the Mitochondrial Rhomboid Protease PARL by Novel Ketoamide Inhibitors Reveals Its Role in PINK1/Parkin-Dependent Mitophagy
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Bicyclic and tricyclic ergoline partial structures. Rigid 3-(2-aminoethyl)pyrroles and 3- and 4-(2-aminoethyl)pyrazoles as dopamine agonists
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QM/MM Calculations Reveal the Different Nature of the Interaction of Two Carborane-Based Sulfamide Inhibitors of Human Carbonic Anhydrase II
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Functions of Rhomboid Family Protease RHBDL2 and Thrombomodulin in Wound Healing
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PARL mediates Smac proteolytic maturation in mitochondria to promote apoptosis
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Rhomboid domain containing 1 promotes colorectal cancer growth through activation of the EGFR signalling pathway
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Synthesis of a HyCoSuL peptide substrate library to dissect protease substrate specificity
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Improved R-factors for diffraction data analysis in macromolecular crystallography
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SQM2.20: Semiempirical quantum-mechanical scoring function yields DFT-quality protein–ligand binding affinity predictions in minutes
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Mitochondria regulate intracellular coenzyme Q transport and ferroptotic resistance via STARD7
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Quantitative proteomics screen identifies a substrate repertoire of rhomboid protease RHBDL2 in human cells and implicates it in epithelial homeostasis
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Rhomboid intramembrane protease RHBDL4 triggers ER-export and non-canonical secretion of membrane-anchored TGFα
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Rhomboid protease AarA mediates quorum-sensing in Providencia stuartii by activating TatA of the twin-arginine translocase
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Tuning Escherichia coli for membrane protein overexpression
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PARL deficiency in mouse causes Complex III defects, coenzyme Q depletion, and Leigh-like syndrome
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Structural Basis for Inhibition of Cathepsin B Drug Target from the Human Blood Fluke, Schistosoma mansoni
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Rhomboid Protease PARL Mediates the Mitochondrial Membrane Potential Loss-induced Cleavage of PGAM5
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Sensitive Versatile Fluorogenic Transmembrane Peptide Substrates for Rhomboid Intramembrane Proteases
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Intramembrane protease PARL defines a negative regulator of PINK1- and PARK2/Parkin-dependent mitophagy
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Functional alteration of PARL contributes to mitochondrial dysregulation in Parkinson's disease
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Interleukin‐11 (IL‐11) receptor cleavage by the rhomboid protease RHBDL2 induces IL‐11 trans‐signaling
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Scaling and assessment of data quality
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electronic Ligand Builder and Optimisation Workbench (eLBOW): A tool for ligand coordinate and restraint generation
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XDS
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Data processing and analysis with the autoPROC toolbox
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Refinement of Macromolecular Structures by the Maximum-Likelihood Method
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The mitochondrial intramembrane protease PARL cleaves human Pink1 to regulate Pink1 trafficking
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Loss‐of‐function analyses defines vital and redundant functions of the P lasmodium rhomboid protease family
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Linking Crystallographic Model and Data Quality
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Functional Analysis of Rhomboid Proteases during Toxoplasma Invasion
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RHBDL2 Is a Critical Membrane Protease for Anoikis Resistance in Human Malignant Epithelial Cells
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Two Plasmodium Rhomboid Proteases Preferentially Cleave Different Adhesins Implicated in All Invasive Stages of Malaria
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Crystallization in Lipidic Cubic Phases: A Case Study with Bacteriorhodopsin
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Substrate binding and specificity of rhomboid intramembrane protease revealed by substrate–peptide complex structures
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PARL partitions the lipid transfer protein STARD7 between the cytosol and mitochondria
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Rhomboid intramembrane protease YqgP licenses bacterial membrane protein quality control as adaptor of FtsH AAA protease
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Rhomboid-Like-2 Intramembrane Protease Mediates Metalloprotease-Independent Regulation of Cadherins
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