NSTL国家科技图书文献中心

1. NMR chemical shift assignment of the IMLV methyl groups of a didomain of the Tomaymycin non-ribosomal peptide synthetase NSTL国家科技图书文献中心

John P. Kirkpatrick | Megha N. Karanth ... - 《Biomolecular NMR assignments》 - 2025,19(1) - 153～164 - 共12页

摘要：. Here, we report the near-complete assignment* of the* | foundation for future NMR* studies of the complex dynamic* | Non-ribosomal peptide synthetases (NRPSs) are | macromolecular enzymatic complexes responsible for the | biosynthesis of an array of microbial natural products, many

关键词： Tomaymycin | Non-ribosomal peptide synthetases | Methyl assignment | Condensation domain

2. Backbone resonance assignment of the catalytic and ATP-binding domain of CpxA from Escherichia coli NSTL国家科技图书文献中心

Jing Deng | Guofang Zeng ... - 《Biomolecular NMR assignments》 - 2025,19(1) - 59～62 - 共4页

摘要： chemical shift assignments of CpxA~(CA) by heteronuclear | CpxA is an extensively studied histidine | kinase implicated in cellular stress responses. The | highly conserved CA domain of CpxA (CpxA~(CA)) is an | essential domain for the hydrolysis of ATP and the binding

关键词： Chemical shift assignment | NMR | CpxA~(CA) | Secondary structure | HSQC

3. NMR resonance assignment of a ligand-binding domain of ephrin receptor A2 NSTL国家科技图书文献中心

Konstantin S. Mineev | Santosh L. Gande ... - 《Biomolecular NMR assignments》 - 2025,19(1) - 23～28 - 共6页

摘要： complete ~1H, ~(15)N and ~(13)C NMR chemical shift | assignment of EphA2 ligand binding domain that provides the | basis for NMR-assisted drug design. | Ephrin receptors regulate intercellular | communication and are thus involved in tumor development

关键词： Ephrin receptor | EphA2 | Ephrin | NMR assignment | Ligand binding domain | Extracellular domain

4. ~1H, ~(15)N, ~(13)C backbone resonance assignment of human Alkbh7 NSTL国家科技图书文献中心

Baboucarr Faal | Jeffrey A. Purslow ... - 《Biomolecular NMR assignments》 - 2025,19(1) - 65～69 - 共5页

摘要： ~1H, ~(15)N, ~(13)C chemical* shift assignment of the* | . This paper focuses on the NMR* backbone resonance* | assignment of Alkbh7, a fundamental step in understanding | at 25 °C by heteronuclear multidimensional NMR | end of Alkbh7 are not NMR* visible, suggesting that*

关键词： Alkb homologue 7 | Backbone resonance assignment | AlkB dioxygenases | AlkB demethylases | Transverse relaxation optimized spectroscopy

5. ~1H, ~(13)C and ~(15)N chemical shift assignments of Rubella virus macro domain in the free and in the ADPr bound state NSTL国家科技图书文献中心

Danai Moschidi | Nikolaos K. Fourkiot...... - 《Biomolecular NMR assignments》 - 2025,19(1) - 117～125 - 共9页

摘要： chemical shift-based secondary structure element | screening of fragments or chemical libraries using NMR | study, we present the almost complete NMR* backbone and* | side-chain resonance assignment* of RuV MD in both* | free and ADPr bound forms, along with the NMR

关键词： Rubella virus (RuV) | Macro domain (MD) | ADP-ribosylation | Solution NMR spectroscopy

6. Photovoltaic performance of 4-Cyano-3-fluorobenzaldehyde: spectroscopic (FT-IR, 1 H and 13 C-NMR, FT-Raman, and UV-vis.) and DFT studies NSTL国家科技图书文献中心

Bahceli, Semiha | Sarikaya, Ebru Karak...... - 《Research on Chemical Intermediates》 - 2025,51(5) - 2645～2667 - 共23页

摘要： DMSO solvent) chemical* shift standards, and the UV* | obtained by analyzing the chemical* structure of the* | , conformational evaluation, the full vibrational assignment* and* | ) analyses, the H-1 and C-13 NMR* (both in gas phase and in* | The FT-Raman and FT-IR wavelengths of 4-Cyano

关键词： FT-IR | FT-Raman | NMR UV-vis spectroscopies | DFT 4-Cyano-3-fluorobenzaldehyde | Photovoltaic performance

7. NMR characterisation of the antibiotic resistance-mediating 32mer RNA from the 23S ribosomal RNA NSTL国家科技图书文献中心

Christina Muhs | Lena Kemper ... - 《Biomolecular NMR assignments》 - 2025,19(1) - 133～145 - 共13页

摘要： and ~(15)N NMR* resonance assignment for the part of* | antimicrobial resistance. Furthermore, we compare the chemical | shift signature of the unmethylated to the | The increasing prevalence of antibiotic | resistance represents a significant public health concern

关键词： m6A | DMA | Erythromycin methyl transferase | Antibiotic resistance | Solution NMR-spectroscopy | 23S ribosomal RNA

8. Solution NMR chemical shift assignment of apo and molybdate-bound ModA at two pHs NSTL国家科技图书文献中心

Nguyen, Hiep L. D. | Crowhurst, Karin A. - 《Biomolecular NMR assignments》 - 2024,18(1) - 93～98 - 共6页

摘要： chemical shift perturbations are observed, not only in | , we might expect the large chemical* shift changes to* | design. Backbone 1H, 13C and 15N chemical* shifts of apo* | ModA is a soluble periplasmic molybdate | -binding protein found in most gram-negative bacteria. It

关键词： ModA | Molybdate | Molybdenum | NMR | Chemical shift assignment

9. 1 H, 13 C and 15 N backbone and side-chain resonance assignments of the human oncogenic protein NCYM NSTL国家科技图书文献中心

Mouhand, Assia | Nakatani, Kazuma ... - 《Biomolecular NMR assignments》 - 2024,18(1) - 65～70 - 共6页

摘要： structure prediction using Secondary Chemical* Shifts and* | NCYM is a cis-antisense gene of MYCN oncogene | and encodes an oncogenic protein that stabilizes | MYCN via inhibition of GSK3b. High NCYM expression | levels are associated with poor clinical outcomes in

关键词： NCYM | Oncogene | NMR chemical shift assignment | Secondary structure prediction | CHEMICAL-SHIFTS | MYCN | NEUROBLASTOMA | COMPLEX

10. Backbone 1 H, 13 C and 15 N resonance assignment of the ubiquitin specific protease 7 catalytic domain (residues 208-554) in complex with a small molecule ligand NSTL国家科技图书文献中心

Pandya, Maya J. | Augustyniak, Wojciec...... - 《Biomolecular NMR assignments》 - 2024,18(1) - 33～44 - 共12页

摘要： determine chemical* shift perturbations on ligand binding* | assignment of Ubiquitin Specific Protease 7 catalytic | The backbone H-1, C-13 and N-15 resonance | domain (residues 208-554) was performed in its complex | with a small molecule ligand and in its apo form as a

关键词： USP7 | NMR resonance assignment | Amide hydrogen exchange | Chemical shift perturbation | Ligand binding | STRUCTURE-GUIDED DEVELOPMENT | MULTIDIMENSIONAL NMR | ACTIVE-SITE | RESOLUTION | REVEALS...

摘要：. Here, we report the near-complete assignment of the | foundation for future NMR studies of the complex dynamic | Non-ribosomal peptide synthetases (NRPSs) are | macromolecular enzymatic complexes responsible for the | biosynthesis of an array of microbial natural products, many

关键词： Tomaymycin | Non-ribosomal peptide synthetases | Methyl assignment | Condensation domain

摘要： chemical shift assignments of CpxA~(CA) by heteronuclear | CpxA is an extensively studied histidine | kinase implicated in cellular stress responses. The | highly conserved CA domain of CpxA (CpxA~(CA)) is an | essential domain for the hydrolysis of ATP and the binding

关键词： Chemical shift assignment | NMR | CpxA~(CA) | Secondary structure | HSQC

摘要： complete ~1H, ~(15)N and ~(13)C NMR chemical shift | assignment of EphA2 ligand binding domain that provides the | basis for NMR-assisted drug design. | Ephrin receptors regulate intercellular | communication and are thus involved in tumor development

关键词： Ephrin receptor | EphA2 | Ephrin | NMR assignment | Ligand binding domain | Extracellular domain

摘要： ~1H, ~(15)N, ~(13)C chemical shift assignment of the | . This paper focuses on the NMR backbone resonance | assignment of Alkbh7, a fundamental step in understanding | at 25 °C by heteronuclear multidimensional NMR | end of Alkbh7 are not NMR visible, suggesting that

关键词： Alkb homologue 7 | Backbone resonance assignment | AlkB dioxygenases | AlkB demethylases | Transverse relaxation optimized spectroscopy

摘要： chemical shift-based secondary structure element | screening of fragments or chemical libraries using NMR | study, we present the almost complete NMR backbone and | side-chain resonance assignment of RuV MD in both | free and ADPr bound forms, along with the NMR

关键词： Rubella virus (RuV) | Macro domain (MD) | ADP-ribosylation | Solution NMR spectroscopy

摘要： DMSO solvent) chemical shift standards, and the UV | obtained by analyzing the chemical structure of the | , conformational evaluation, the full vibrational assignment and | ) analyses, the H-1 and C-13 NMR (both in gas phase and in | The FT-Raman and FT-IR wavelengths of 4-Cyano

关键词： FT-IR | FT-Raman | NMR UV-vis spectroscopies | DFT 4-Cyano-3-fluorobenzaldehyde | Photovoltaic performance

摘要： and ~(15)N NMR resonance assignment for the part of | antimicrobial resistance. Furthermore, we compare the chemical | shift signature of the unmethylated to the | The increasing prevalence of antibiotic | resistance represents a significant public health concern

关键词： m6A | DMA | Erythromycin methyl transferase | Antibiotic resistance | Solution NMR-spectroscopy | 23S ribosomal RNA

摘要： chemical shift perturbations are observed, not only in | , we might expect the large chemical shift changes to | design. Backbone 1H, 13C and 15N chemical shifts of apo | ModA is a soluble periplasmic molybdate | -binding protein found in most gram-negative bacteria. It

关键词： ModA | Molybdate | Molybdenum | NMR | Chemical shift assignment

摘要： structure prediction using Secondary Chemical Shifts and | NCYM is a cis-antisense gene of MYCN oncogene | and encodes an oncogenic protein that stabilizes | MYCN via inhibition of GSK3b. High NCYM expression | levels are associated with poor clinical outcomes in

关键词： NCYM | Oncogene | NMR chemical shift assignment | Secondary structure prediction | CHEMICAL-SHIFTS | MYCN | NEUROBLASTOMA | COMPLEX

摘要： determine chemical shift perturbations on ligand binding | assignment of Ubiquitin Specific Protease 7 catalytic | The backbone H-1, C-13 and N-15 resonance | domain (residues 208-554) was performed in its complex | with a small molecule ligand and in its apo form as a

关键词： USP7 | NMR resonance assignment | Amide hydrogen exchange | Chemical shift perturbation | Ligand binding | STRUCTURE-GUIDED DEVELOPMENT | MULTIDIMENSIONAL NMR | ACTIVE-SITE | RESOLUTION | REVEALS...

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国家科技图书文献中心

摘要：. Here, we report the near-complete assignment* of the* | foundation for future NMR* studies of the complex dynamic* | Non-ribosomal peptide synthetases (NRPSs) are | macromolecular enzymatic complexes responsible for the | biosynthesis of an array of microbial natural products, many

摘要： ~1H, ~(15)N, ~(13)C chemical* shift assignment of the* | . This paper focuses on the NMR* backbone resonance* | assignment of Alkbh7, a fundamental step in understanding | at 25 °C by heteronuclear multidimensional NMR | end of Alkbh7 are not NMR* visible, suggesting that*

摘要： chemical shift-based secondary structure element | screening of fragments or chemical libraries using NMR | study, we present the almost complete NMR* backbone and* | side-chain resonance assignment* of RuV MD in both* | free and ADPr bound forms, along with the NMR

摘要： DMSO solvent) chemical* shift standards, and the UV* | obtained by analyzing the chemical* structure of the* | , conformational evaluation, the full vibrational assignment* and* | ) analyses, the H-1 and C-13 NMR* (both in gas phase and in* | The FT-Raman and FT-IR wavelengths of 4-Cyano

摘要： and ~(15)N NMR* resonance assignment for the part of* | antimicrobial resistance. Furthermore, we compare the chemical | shift signature of the unmethylated to the | The increasing prevalence of antibiotic | resistance represents a significant public health concern

摘要： chemical shift perturbations are observed, not only in | , we might expect the large chemical* shift changes to* | design. Backbone 1H, 13C and 15N chemical* shifts of apo* | ModA is a soluble periplasmic molybdate | -binding protein found in most gram-negative bacteria. It

摘要： structure prediction using Secondary Chemical* Shifts and* | NCYM is a cis-antisense gene of MYCN oncogene | and encodes an oncogenic protein that stabilizes | MYCN via inhibition of GSK3b. High NCYM expression | levels are associated with poor clinical outcomes in

摘要： determine chemical* shift perturbations on ligand binding* | assignment of Ubiquitin Specific Protease 7 catalytic | The backbone H-1, C-13 and N-15 resonance | domain (residues 208-554) was performed in its complex | with a small molecule ligand and in its apo form as a