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 |
|---|---|---|
| 53411 | 2026-01-20 | Helical conformational tendencies in RIPK1 reveal early structural organization that may precede amyloid assembly |
| 53401 | 2026-01-20 | Unravelling conformation tendencies in RIPK1 prior amyloid formation |
| 31266 | 2026-01-18 | Peptide Macrocycle MC4H-MeAMeH |
| 31265 | 2026-01-18 | Peptide Macrocycle MC4H |
| 31233 | 2026-01-18 | Ground state of Src kinase domain |
| 31234 | 2026-01-18 | Intermediate state of Src kinase domain |
| 31187 | 2026-01-18 | Solution NMR structure of the RiPP proteusin DprE2 |
| 34957 | 2026-01-18 | Cyclized peptide inhibitors of the small G protein Cdc42 mimic binding of effector proteins |
| 34958 | 2026-01-18 | Cyclized peptide inhibitors of the small G protein Cdc42 mimic binding of effector proteins |
| 34959 | 2026-01-18 | Synthetic heme-peroxidases: new insights into MC6*a structure |
| 34975 | 2026-01-18 | CS-ROSETTA Structure of the Z Domain of the IgG-Binding Staphylococcal Protein A |
| 53380 | 2026-01-15 | The essential co-chaperone Sgt1 regulates client dwell time in the Hsp90 chaperone cycle |
| 52910 | 2026-01-15 | NMR 1H, 13C, and 15N resonance assignments of the oncogenic Q61R variant of human NRAS in the active, GTP-bound conformation |
| 52953 | 2026-01-15 | Beyond DNA binding: single C2H2 zinc fingers with adjacent beta-strands mediate dimerization in Drosophila transcription factors |
| 27933 | 2026-01-13 | Assigned 1H, 13C, and 15N chemical shifts for Loop A of the Hairpin Ribozyme |
| 53100 | 2026-01-12 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53458 | 2026-01-12 | Histone H3 tail charge patterns govern nucleosome condensate formation and dynamics |
| 53110 | 2026-01-12 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53111 | 2026-01-12 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53057 | 2026-01-12 | Histone H3 tail charge patterns govern nucleosome condensate formation and dynamics |
| 53058 | 2026-01-12 | Histone H3 tail charge patterns govern nucleosome condensate formation and dynamics |
| 53059 | 2026-01-12 | Histone H3 tail charge patterns govern nucleosome condensate formation and dynamics |
| 36493 | 2026-01-08 | Insight into the C-terminal SH3 domain mediated binding of Drosophila Drk to Sos and Dos. |
| 53096 | 2026-01-07 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53104 | 2026-01-07 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53106 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53109 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53112 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53113 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53114 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53115 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53116 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53117 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53118 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53119 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53103 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53105 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53108 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53097 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53098 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53099 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53101 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 53102 | 2026-01-06 | Oligomerization enables the selective targeting of an intrinsically disordered region by a small molecule |
| 52970 | 2026-01-05 | Bora Bridges Aurora-A Activation and Substrate Recognition of PLK1 |
| 52443 | 2026-01-05 | Convergent evolution of intrinsically disordered regions in vertebrate galectins for liquid-liquid phase separation |
| 53417 | 2026-01-05 | Solution NMR Assignment of the MCM6 NTD1 Domain Reveals No Detectable Binding to BLM MBD-N and MBD-D Regions |
| 31278 | 2025-12-30 | Backbone engineering in the hydrophobic core of villin headpiece |
| 31178 | 2025-12-30 | NMR structure of the Tetrahymena Slr1 La Motif |
| 31261 | 2025-12-30 | Structure of the disulfide-rich modules of a striking tandem repeat protein, avian cysteine-rich eggshell membrane protein |
| 31270 | 2025-12-30 | Backbone engineering in the hydrophobic core of villin headpiece |
| 31271 | 2025-12-30 | Backbone engineering in the hydrophobic core of villin headpiece |
| 31272 | 2025-12-30 | Backbone engineering in the hydrophobic core of villin headpiece |
| 31273 | 2025-12-30 | Backbone engineering in the hydrophobic core of villin headpiece |
| 31274 | 2025-12-30 | Backbone engineering in the hydrophobic core of villin headpiece |
| 31275 | 2025-12-30 | Backbone engineering in the hydrophobic core of villin headpiece |
| 31276 | 2025-12-30 | Backbone engineering in the hydrophobic core of villin headpiece |
| 31277 | 2025-12-30 | Backbone engineering in the hydrophobic core of villin headpiece |
| 53492 | 2025-12-30 | Backbone 1H and 15N chemical shift assignments of His-tagged M1-linked di-ubiquitin |
| 53493 | 2025-12-30 | 1H and 15N chemical shift assignments of K11-linked di-ubiquitin |
| 52757 | 2025-12-29 | Phosphatase SHP2 pathogenic mutations enhance activity by altering conformational sampling |
| 52759 | 2025-12-29 | Phosphatase SHP2 pathogenic mutations enhance activity by altering conformational sampling |
| 52758 | 2025-12-29 | Phosphatase SHP2 pathogenic mutations enhance activity by altering conformational sampling |
| 52760 | 2025-12-29 | Phosphatase SHP2 pathogenic mutations enhance activity by altering conformational sampling |
| 53439 | 2025-12-26 | STI1 domain dynamically engages transient helices in disordered regions to drive self-association and phase separation of yeast ubiquilin Dsk2 |
| 53085 | 2025-12-26 | Acidic bicelles are a suitable membrane mimic for structural studies of the Lassa virus fusion domain |
| 53084 | 2025-12-26 | Acidic bicelles are a suitable membrane mimic for structural studies of the Lassa virus fusion domain |