Faculty

Institution

Unit

Venue

James B Ames

Professor

University of California, Davis

Affiliations

College of Letters and Science

Chemistry

James B Ames is currently serving as a Chemistry Professor at University of California, Davis.

Honors

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Experiences

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Education

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James B Ames

University of California, Davis

Professor

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molecular biology structural biology biochemistry protein science neuroscience protein structure nuclear magnetic resonance biophysics biological chemistry enzymes chemical shift assignments membrane biology signal transduction gene expression structural molecular biology molecular physiology biomolecular structure molecular neurobiology protein nmr retina cell signaling cyanobacteria molecular regulation protein chemistry yeast receptor (biochemistry) neurochemistry redox biology avian biology protein function biological inorganic chemistry calmodulin bound plant science molecular science pheromone biochemistry structural basis insect molecular biology plo biology medicinal research biochemical sciences retinal guanylyl cyclase nmr structure insect biochemistry insect science plant physiology microbial physiology enzyme catalysis biomolecular interactions gene regulation photobiology guanylyl cyclase fission yeast protein biosynthesis transcription regulation protein x-ray crystallography tropical insect science cell interactions sensing mechanisms photoreceptor cells chromophore structure calcium-binding proteins yeast frequenin pheromone-binding protein protein dimerization structural characterization target recognition zebrafish photoreceptors bacteriology experimental biophysics biophysical modeling charge transport protein genetics ocular disease visual impairments biocatalysis light-driven proton pump cellular physiology bioenergetics neurophysiology neurotransmission biophysical chemistry

Notable Scholarly Works

Notable Federal Grants

Collaborators

Chemical Shift Assignments of the α-Actinin C-Terminal Ef-Hand Domain Bound to a Cytosolic C0 Domain of Glun1 (Residues 841–865) From the Nmda Receptor. Biomolecular NMR Assignments (2024)

Aritra BejJohannes W. HellJames B. Ames

nmda receptorchemical shift assignmentsprotein nmrmolecular biologybiomolecular structurenuclear magnetic resonance

Nmr Structure of Retinal Guanylate Cyclase Activating Protein 5 (Gcap5) With R22A Mutation That Abolishes Dimerization and Enhances Cyclase Activation. Biochemistry (2024)

Diana L. CudiaEffibe O. AhoulouAritra BejAnnika N. JanssenAlexander ScholtenKarl-W. KochJames B. Ames

retinal guanylate cyclasegeneticsmolecular biologystructural biologynuclear magnetic resonancenmr structurebiochemistry

Chemical Shift Assignments of Calmodulin Bound to a Cytosolic Domain of Glun2A (Residues 1004–1024) From the Nmda Receptor. Biomolecular NMR Assignments (2023)

Aritra BejJames B. Ames

molecular regulationprotein nmrreceptor (biochemistry)molecular neurobiologycell biologynmda receptormolecular cell biologystructural biologyprotein sciencemembrane proteinsnuclear magnetic resonancemolecular physiologycytosolic domainreceptorsgene expressioncalmodulin boundchemical shift assignmentsneurochemistrymolecular biologystructural molecular biologymedicinal researchneuroscience

Chemical Shift Assignments of Calmodulin Bound to the Glun1 C0 Domain (Residues 841–865) of the Nmda Receptor. Biomolecular NMR Assignments (2023)

Aritra BejJames B. Ames

neurologyreceptorscalmodulin boundnmda receptorchemical shift assignmentsmolecular neurosciencemolecular neurobiologyneuropharmacologyneurochemistryprotein nmrreceptor (biochemistry)molecular biologystructural biologynuclear magnetic resonanceprotein scienceneuroscience

Chemical Shift Assignments of Retinal Guanylyl Cyclase Activating Protein 5 (Gcap5) With a Mutation (R22A) That Abolishes Dimerization and Enhances Cyclase Activation. Biomolecular NMR Assignments (2023)

Diana CudiaEffibe O. AhoulouJames B. Ames

ophthalmologyretinachemical shift assignmentsmutagenesismolecular regulationprotein engineeringprotein nmrenzymesretinal guanylyl cyclasemolecular biologynuclear magnetic resonancesignal transductionprotein sciencemutagenesis (molecular biology technique)molecular physiologybiochemistry

Data From Optimization of Rgd-Containing Cyclic Peptides Against αVβ3 Integrin. (2023)

Yan WangWenwu XiaoYonghong ZhangLeah MezaHarry TsengYoshikazu TakadaJames B. AmesKit S. Lam

receptorspharmacologyrgd-containing cyclic peptidesbiological engineering

Supplementary Tables S1-S7; Supplementary Figures S1-S2; and Supplementary Materials Methods From Optimization of Rgd-Containing Cyclic Peptides Against αVβ3 Integrin. (2023)

Yan WangWenwu XiaoYonghong ZhangLeah MezaHarry TsengYoshikazu TakadaJames B. AmesKit S. Lam

receptorspharmacologysupplementary tablesbiomolecular engineeringrgd-containing cyclic peptidesprotein science

Calmodulin Promotes a Ca 2+ ‐Dependent Conformational Change in the C‐Terminal Regulatory Domain of Ca V 1.2. FEBS Letters (2022)

Deepak Kumar YadavDavid E. AndersonJohannes W. HellJames B. Ames

gene regulationgene expressionc-terminal regulatory domaincell signalingredox biologymolecular regulationconformational studiesmolecular biologysignal transductioncell regulationbiochemistry

Chemical Shift Assignments of Calmodulin Bound to a C-Terminal Site (Residues 1120–1147) in the β-Subunit of a Retinal Cyclic Nucleotide-Gated Channel (Cngb1). Biomolecular NMR Assignments (2022)

Aritra BejJames B. Ames

molecular neurobiologycell biologyretinasource apportionmentbiomolecular structurestructural biologyprotein sciencemembrane biologyc-terminal sitemammalian biologymembrane proteinscellular neurobiologycellular biochemistrybiophysicsgene expressioncalmodulin boundchemical shift assignmentsmolecular biologystructural molecular biologysecretory pathwaysignal transduction

Chemical Shift Assignments of Calmodulin Bound to the β-Subunit of a Retinal Cyclic Nucleotide-Gated Channel (Cngb1). Biomolecular NMR Assignments (2022)

Aritra BejJames B. Ames

molecular regulationbiological chemistrymolecular neurobiologycell biologyretinamolecular cell biologystructural biologyprotein sciencemembrane biologymolecular neurosciencenuclear magnetic resonancecellular neurobiologygene expressioncalmodulin boundchemical shift assignmentsneurochemistrymolecular biologystructural molecular biologyneuroscience

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James B Ames

Professor

University of California, Davis

Affiliations

College of Letters and Science

Chemistry

James B Ames is currently serving as a Chemistry Professor at University of California, Davis.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

James B Ames

University of California, Davis

Professor

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Chemical Shift Assignments of the α-Actinin C-Terminal Ef-Hand Domain Bound to a Cytosolic C0 Domain of Glun1 (Residues 841–865) From the Nmda Receptor. Biomolecular NMR Assignments (2024)

Aritra BejJohannes W. HellJames B. Ames

nmda receptorchemical shift assignmentsprotein nmrmolecular biologybiomolecular structurenuclear magnetic resonance

Nmr Structure of Retinal Guanylate Cyclase Activating Protein 5 (Gcap5) With R22A Mutation That Abolishes Dimerization and Enhances Cyclase Activation. Biochemistry (2024)

Diana L. CudiaEffibe O. AhoulouAritra BejAnnika N. JanssenAlexander ScholtenKarl-W. KochJames B. Ames

retinal guanylate cyclasegeneticsmolecular biologystructural biologynuclear magnetic resonancenmr structurebiochemistry

Chemical Shift Assignments of Calmodulin Bound to a Cytosolic Domain of Glun2A (Residues 1004–1024) From the Nmda Receptor. Biomolecular NMR Assignments (2023)

Aritra BejJames B. Ames

Chemical Shift Assignments of Calmodulin Bound to the Glun1 C0 Domain (Residues 841–865) of the Nmda Receptor. Biomolecular NMR Assignments (2023)

Aritra BejJames B. Ames

Diana CudiaEffibe O. AhoulouJames B. Ames

Data From Optimization of Rgd-Containing Cyclic Peptides Against αVβ3 Integrin. (2023)

Yan WangWenwu XiaoYonghong ZhangLeah MezaHarry TsengYoshikazu TakadaJames B. AmesKit S. Lam

receptorspharmacologyrgd-containing cyclic peptidesbiological engineering

Supplementary Tables S1-S7; Supplementary Figures S1-S2; and Supplementary Materials Methods From Optimization of Rgd-Containing Cyclic Peptides Against αVβ3 Integrin. (2023)

Yan WangWenwu XiaoYonghong ZhangLeah MezaHarry TsengYoshikazu TakadaJames B. AmesKit S. Lam

receptorspharmacologysupplementary tablesbiomolecular engineeringrgd-containing cyclic peptidesprotein science

Calmodulin Promotes a Ca 2+ ‐Dependent Conformational Change in the C‐Terminal Regulatory Domain of Ca V 1.2. FEBS Letters (2022)

Deepak Kumar YadavDavid E. AndersonJohannes W. HellJames B. Ames

gene regulationgene expressionc-terminal regulatory domaincell signalingredox biologymolecular regulationconformational studiesmolecular biologysignal transductioncell regulationbiochemistry

Aritra BejJames B. Ames

Chemical Shift Assignments of Calmodulin Bound to the β-Subunit of a Retinal Cyclic Nucleotide-Gated Channel (Cngb1). Biomolecular NMR Assignments (2022)

Aritra BejJames B. Ames

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5
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10 / page

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Michael A. Marletta

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University of California, Berkeley

biochemistry

enzymes

Heidi E. Hamm, Ph.D.

Institution

Vanderbilt University

neuroscience

photoreceptor cell

Hassane S. Mchaourab

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synthetic biology

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Walter Chazin

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molecular biology

proteomics

Wayne Hubbell

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Francis Castellino

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pharmacology

biochemistry

Steven Clarke

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Julian Whitelegge

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molecular informatics

proteomic technologies

Jack Kaplan

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molecular biology

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