| scholarly article | Q13442814 |
| P50 | author | Lewis E. Kay | Q29046014 |
| John L. Rubinstein | Q43276745 | ||
| Aaron Schimmer | Q56378117 | ||
| P2093 | author name string | Xiaoming Li | |
| Remco Sprangers | |||
| Xinliang Mao | |||
| P433 | issue | 26 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 6727-6734 | |
| P577 | publication date | 2008-06-10 | |
| P1433 | published in | Biochemistry | Q764876 |
| P1476 | title | TROSY-based NMR evidence for a novel class of 20S proteasome inhibitors | |
| P478 | volume | 47 |
| Q92284614 | Aromatic 19F-13C TROSY: a background-free approach to probe biomolecular structure, function, and dynamics |
| Q55401911 | Cationic porphyrins are tunable gatekeepers of the 20S proteasome. |
| Q26825417 | DangER: protein ovERload. Targeting protein degradation to treat myeloma |
| Q27660397 | Dynamic regulation of archaeal proteasome gate opening as studied by TROSY NMR |
| Q35063122 | Dynamics of the degradation of ubiquitinated proteins by proteasomes and autophagy: association with sequestosome 1/p62. |
| Q33588424 | Effect of noncompetitive proteasome inhibition on bortezomib resistance |
| Q89865089 | Exploring long-range cooperativity in the 20S proteasome core particle from Thermoplasma acidophilum using methyl-TROSY-based NMR |
| Q39602920 | Fundamental reaction pathway and free energy profile for inhibition of proteasome by Epoxomicin |
| Q37365069 | Fundamental reaction pathway for peptide metabolism by proteasome: insights from first-principles quantum mechanical/molecular mechanical free energy calculations |
| Q38177328 | Harnessing proteasome dynamics and allostery in drug design. |
| Q90729473 | Improving yields of deuterated, methyl labeled protein by growing in H2O |
| Q37351110 | Inhibition of the human proteasome by imidazoline scaffolds |
| Q39287034 | Intermediate filament transcription in astrocytes is repressed by proteasome inhibition. |
| Q35843506 | Interplay between Structure and Charge as a Key to Allosteric Modulation of Human 20S Proteasome by the Basic Fragment of HIV-1 Tat Protein |
| Q88962136 | Methyl group reorientation under ligand binding probed by pseudocontact shifts |
| Q26781075 | Methyl groups as NMR probes for biomolecular interactions |
| Q37604187 | Methyl groups as probes of supra-molecular structure, dynamics and function |
| Q39278628 | Molecular mechanisms of acquired proteasome inhibitor resistance |
| Q34490414 | N-terminal domain of human Hsp90 triggers binding to the cochaperone p23. |
| Q46064467 | NMR spectroscopy of soluble protein complexes at one mega-dalton and beyond |
| Q36691554 | Noncompetitive modulation of the proteasome by imidazoline scaffolds overcomes bortezomib resistance and delays MM tumor growth in vivo |
| Q37878771 | Novel proteasome inhibitors to overcome bortezomib resistance |
| Q34062354 | Nuclear magnetic resonance captures the elusive. |
| Q30428673 | PARAssign--paramagnetic NMR assignments of protein nuclei on the basis of pseudocontact shifts |
| Q36483667 | Proteasome allostery as a population shift between interchanging conformers |
| Q42058162 | Selective editing of Val and Leu methyl groups in high molecular weight protein NMR. |
| Q38081952 | Structural biology of the proteasome |
| Q35998619 | Substituted quinolines as noncovalent proteasome inhibitors. |
| Q34769338 | Synthesis and proteasome inhibition of lithocholic acid derivatives |
| Q38246060 | The future of proteasome inhibitors in relapsed/refractory multiple myeloma. |
| Q36721779 | The role of allostery in the ubiquitin-proteasome system |
Search more.