Listing of New BMRB NMR-STAR files
Entries released in the last month, starting from most recent release to least recent one.
The latest entries may not be immediately available here
or through the BMRB database search. They can be found in "entry lists" under "FTP access".
| Entry ID | Release Date | Title |
|---|---|---|
| 54037 | 2026-10-27 | Conformational dynamics at the pre-miR-377 Dicer site governs selective small-molecule recognition |
| 52906 | 2026-10-26 | Chemical shift assignments for SET-9/26 PHD domain in isolation |
| 54060 | 2026-10-22 | The disordered region 1 of Mdm2 weakens p53-binding in both its unmodified and hyperphospho-forms |
| 54045 | 2026-10-22 | Deamidation and isomerization to elusive isoaspartate in a computationally designed miniprotein |
| 54046 | 2026-10-22 | Deamidation and isomerization to elusive isoaspartate in a computationally designed miniprotein |
| 53778 | 2026-10-21 | Distinct Ca2+-binding thermodynamics reveal a paralogue-specific structural response in the calmodulin-like domain of alpha-actinin-4 |
| 35045 | 2026-10-21 | Solution structure of a peptide-conjugated aggregation-induced-emission (AIE) fluorophore bound to a protein |
| 53779 | 2026-10-21 | Distinct Ca2+-binding thermodynamics reveal a paralogue-specific structural response in the calmodulin-like domain of alpha-actinin-4 |
| 54019 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54023 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 53206 | 2026-10-20 | NMR crystallography reveals active-site protonation states of Toho-1 b-lactamase in complex with avibactam |
| 54022 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 53207 | 2026-10-20 | NMR crystallography reveals active-site protonation states of Toho-1 b-lactamase in complex with avibactam |
| 54024 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54021 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 53885 | 2026-10-20 | Allosteric Inhibition of NDM-1 by Thanatin Preserves the Di-Zinc Center While Restricting Dynamics |
| 54020 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54016 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54017 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 54018 | 2026-10-20 | Tubulin C-terminal tails are pH sensors that regulate microtubule function |
| 53839 | 2026-10-17 | Multisite Threonine Phosphorylation in the SPT5 C-Terminal Region 1 Enables Sequence-Dependent Regulation without Global Structural Remodeling |
| 53838 | 2026-10-17 | Multisite Threonine Phosphorylation in the SPT5 C-Terminal Region 1 Enables Sequence-Dependent Regulation without Global Structural Remodeling |
| 53820 | 2026-10-17 | 1H, 13C, and 15N backbone and side-chain resonance assignments of the Nostoc sp. H-NOX C139A variant in complex with the soluble Guanylyl Cyclase inhibitor Zinc Protoporphyrin IX |
| 54027 | 2026-10-17 | The core interaction network of transcription elongation factors is broadly maintained across diverse bacteria |
| 54026 | 2026-10-17 | The core interaction network of transcription elongation factors is broadly maintained across diverse bacteria |
| 54052 | 2026-10-16 | Backbone and side-chain 1H, 13C, and 15N resonance assignments of the human Sin3A PAH2 domain (residues 295-395) |
| 53884 | 2026-10-13 | Transmembrane domains of TLR1 and TLR2 tend to specific heterotypic interaction |
| 53858 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53859 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53860 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53861 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53862 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53863 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53864 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53865 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53866 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 53867 | 2026-10-13 | Modulating Nucleosomal H3 Tail Dynamics with Lysine and Serine Modifications |
| 52907 | 2026-10-11 | Chemical shift assignments of SET-9/26 PHD finger in the peptide (H3K4me3)-bound state |
| 31299 | 2026-10-11 | New insights into chemokine N-terminus dynamics by a high-resolution solution NMR ensemble of CCL11 |
| 53243 | 2026-10-05 | The DUF2439 domain of ZGRF1 is a RAD51 interactor and facilitator |
| 52054 | 2026-10-01 | Gatekeeping of peroxisomal import by an allosteric modulation of receptor/cargo interactions |
| 52048 | 2026-10-01 | Gatekeeping of peroxisomal import by an allosteric modulation of receptor/cargo interactions |
| 35088 | 2026-10-01 | Cu(II)-bound alpha-synuclein monomer complex - local structure of N-terminal binding site |
| 35087 | 2026-10-01 | Cu(II)-bound alpha-synuclein monomer complex - local structure of N-terminal binding site |
| 35086 | 2026-10-01 | Cu(II)-bound alpha-synuclein monomer complex - local structure of N-terminal binding site |
| 54000 | 2026-10-01 | Ensemble-Based Segmental Helical Organization in an Aib-Rich Lipidated Peptide: Biomacromolecular Insights from High-Field NMR |
| 31298 | 2026-10-01 | NMR structure and free-energy simulations for rational design of myotonic dystrophy RNA inhibitors |
| 31297 | 2026-10-01 | NMR structure and free-energy simulations for rational design of myotonic dystrophy RNA inhibitors |
| 52055 | 2026-10-01 | Gatekeeping of peroxisomal import by an allosteric modulation of receptor/cargo interactions |