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An anomalous abundance of tryptophan residues in ceramide synthases based on analysis of all membrane proteins in the Swiss-Prot database.

• Authors : Mestre B; Departments of Biomolecular Sciences and Weizmann Institute of Science, Rehovot 7610001, Israel.; Zelnik ID

• Source: The Journal of biological chemistry [J Biol Chem] 2024 Dec 07, pp. 108053. Date of Electronic Publication: 2024 Dec 07.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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A Donald F. Hunt Story (John's Version).

• Authors : Yates JR 3rd; Departments of Molecular Medicine and Neurobiology, The Scripps Research Institute, LaJolla, California, USA. Electronic address: .

Subjects: Proteomics*/Proteomics*/Proteomics*/methods ; Tandem Mass Spectrometry*; History, 20th Century

• Source: Molecular & cellular proteomics : MCP [Mol Cell Proteomics] 2024 Dec; Vol. 23 (12), pp. 100869. Date of Electronic Publication: 2024 Oct 24.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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Redox regulation of proteostasis.

• Authors : Duong LD; Department of Microbiology & Molecular Genetics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, Texas, USA.; West JD

• Source: The Journal of biological chemistry [J Biol Chem] 2024 Nov 08; Vol. 300 (12), pp. 107977. Date of Electronic Publication: 2024 Nov 08.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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Type I interferon signaling and peroxisomal dysfunction contribute to enhanced inflammatory cytokine production in IRGM1-deficient macrophages.

• Authors : Fee BE; Department of Medicine, Division of Geriatrics, and Center for the Study of Aging and Human Development; Duke University Medical Center, Durham, North Carolina, USA.

Subjects: Interferon Type I*/Interferon Type I*/Interferon Type I*/metabolism ; Macrophages*/Macrophages*/Macrophages*/metabolism ; Signal Transduction*

• Source: The Journal of biological chemistry [J Biol Chem] 2024 Nov; Vol. 300 (11), pp. 107883. Date of Electronic Publication: 2024 Oct 11.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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Experimental variables determine the outcome of RAS-RAS interactions.

• Authors : Zhou Z; Departments of Biochemistry and Radiation Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.; Nguyen TL

Subjects: ras Proteins*/ras Proteins*/ras Proteins*/metabolism ; ras Proteins*/ras Proteins*/ras Proteins*/genetics; Humans

• Source: The Journal of biological chemistry [J Biol Chem] 2024 Nov; Vol. 300 (11), pp. 107859. Date of Electronic Publication: 2024 Oct 05.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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Defining unique structural features in the MAFA and MAFB transcription factors that control Insulin gene activity.

• Authors : Cha J; Department of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, Tennessee, USA; Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

• Source: The Journal of biological chemistry [J Biol Chem] 2024 Oct 28; Vol. 300 (12), pp. 107938. Date of Electronic Publication: 2024 Oct 28.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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Distinct chemical structures inhibit the CEMIP hyaluronidase and promote oligodendrocyte progenitor cell maturation.

• Authors : Peters A; Division of Neuroscience, Oregon National Primate Research Center, Beaverton, Oregon, USA; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, Oregon, USA.

• Source: The Journal of biological chemistry [J Biol Chem] 2024 Oct 24; Vol. 300 (12), pp. 107916. Date of Electronic Publication: 2024 Oct 24.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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Development of a high throughput cytochrome P450 ligand-binding assay.

• Authors : Frydendall EK; Department of Pharmacology, University of Michigan, Ann Arbor, Michigan, USA.; Scott EE

Subjects: Cytochrome P-450 Enzyme System*/Cytochrome P-450 Enzyme System*/Cytochrome P-450 Enzyme System*/metabolism ; Cytochrome P-450 Enzyme System*/Cytochrome P-450 Enzyme System*/Cytochrome P-450 Enzyme System*/chemistry ; High-Throughput Screening Assays*/High-Throughput Screening Assays*/High-Throughput Screening Assays*/methods

• Source: The Journal of biological chemistry [J Biol Chem] 2024 Oct; Vol. 300 (10), pp. 107799. Date of Electronic Publication: 2024 Sep 19.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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Differential utilization of vitamin B 12 -dependent and independent pathways for propionate metabolism across human cells.

• Authors : Gouda H; Departments of Biological Chemistry, University of Michigan, Ann Arbor, Michigan, USA.; Ji Y

Subjects: Propionates*/Propionates*/Propionates*/metabolism ; Propionates*/Propionates*/Propionates*/pharmacology ; Vitamin B 12*/Vitamin B 12*/Vitamin B 12*/metabolism

• Source: The Journal of biological chemistry [J Biol Chem] 2024 Sep; Vol. 300 (9), pp. 107662. Date of Electronic Publication: 2024 Aug 14.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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Molecular basis and functional consequences of the interaction between the base excision repair DNA glycosylase NEIL1 and RPA.

• Authors : Le Meur RA; Departments of Biochemistry and Chemistry, Center for Structural Biology, Vanderbilt University, Nashville, Tennessee, USA.; Pecen TJ

Subjects: Replication Protein A*/Replication Protein A*/Replication Protein A*/metabolism ; Replication Protein A*/Replication Protein A*/Replication Protein A*/genetics ; Replication Protein A*/Replication Protein A*/Replication Protein A*/chemistry

• Source: The Journal of biological chemistry [J Biol Chem] 2024 Sep; Vol. 300 (9), pp. 107579. Date of Electronic Publication: 2024 Jul 25.Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID:

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