| 10ev |
OX1-Matured in complex with GluN1-GluN2B, full refinement |
1 |
1 |
ELECTRON MICROSCOPY |
| 10ex |
SK5A-Matured apo state in complex with GluN1-GluN2B, full refinement |
1 |
1 |
ELECTRON MICROSCOPY |
| 10ey |
SK5B-Matured in complex with GluN1-GluN2B, full refinement |
1 |
1 |
ELECTRON MICROSCOPY |
| 10ez |
SK3D-Germline in complex with GluN1-GluN2B, full refinement |
1 |
1 |
ELECTRON MICROSCOPY |
| 10fd |
SK5G-Matured in complex with GluN1-GluN2B, full refinement |
1 |
1 |
ELECTRON MICROSCOPY |
| 10fe |
OX1-Germline in complex with GluN1-GluN2B, full refinement |
1 |
1 |
ELECTRON MICROSCOPY |
| 10ff |
SK5A-Matured glycine/glutamate in complex with GluN1-GluN2B, full refinement |
1 |
1 |
ELECTRON MICROSCOPY |
| 10fl |
SK5G-Germline |
1 |
1 |
ELECTRON MICROSCOPY |
| 10fm |
CryoEM structure of Aldehyde dehydrogenase from Francisella tularensis subsp. tularensis at 3.03A resolution |
1 |
1 |
ELECTRON MICROSCOPY |
| 10fn |
SK5A-Germline in complex with GluN1-GluN2B, full refinement |
1 |
1 |
ELECTRON MICROSCOPY |
| 10fo |
SK5B-Germline in complex with GluN1-GluN2B, full refinement |
1 |
1 |
ELECTRON MICROSCOPY |
| 10ft |
Cryo-EM structure of receptor tyrosine kinase ROS1 in complex with NELL2 |
1 |
1 |
ELECTRON MICROSCOPY |
| 10fy |
[112SE] Two turn tensegrity triangle with 1,1 and 2 bp sticky ends |
1 |
1 |
X-RAY DIFFRACTION |
| 10fz |
30S ribosomal subunit from E. coli missing the gene encoding for the 16S rRNA 2'-O-methyltransferase RsmI |
1 |
1 |
ELECTRON MICROSCOPY |
| 10gh |
Cryo-EM structure of Receptor Tyrosine Kinase ROS1 in complex with Fab-RX5 |
1 |
1 |
ELECTRON MICROSCOPY |
| 10gs |
HUMAN GLUTATHIONE S-TRANSFERASE P1-1, COMPLEX WITH TER117 |
1 |
1 |
X-RAY DIFFRACTION |
| 10gw |
Crystal structure of tetrameric 6-phosphogluconate dehydrogenase from Gluconobacter oxydans in complex with 6-phosphogluconate |
1 |
1 |
X-RAY DIFFRACTION |
| 10hc |
[17,17,7-7N_332] Isosceles tensegrity triangle with 17, 17 and 7 bp between junctions and 3, 3, and 2 turns of DNA per edge |
1 |
1 |
X-RAY DIFFRACTION |
| 10hd |
[17,17,7-17N_332] Isosceles tensegrity triangle with 17, 17 and 7 bp between junctions and 3, 3, and 2 turns of DNA per edge |
1 |
1 |
X-RAY DIFFRACTION |
| 10he |
[3T-17,17,7-17N] Isosceles tensegrity triangle with 17, 17 and 7 base pairs between junctions and three turn edges |
1 |
1 |
X-RAY DIFFRACTION |
| 10hf |
[17,17,7-7N_3T] Isosceles tensegrity triangle with 17, 17 and 7 base pairs between junctions, three turn edges |
1 |
1 |
X-RAY DIFFRACTION |
| 10hs |
[17,17,7-7N_234] Isosceles tensegrity triangle with 17, 17 and 7 base pairs between junctions and two, three, and four turn edges |
1 |
1 |
X-RAY DIFFRACTION |
| 10ht |
[17,17,7-17N_234] Isosceles tensegrity triangle with 17, 17 and 7 base pairs between junctions and two, three, and four turn edges |
1 |
1 |
X-RAY DIFFRACTION |
| 10hy |
Structure of CHK1 10-pt. mutant complex with macrocyclic LRRK2 inhibitor compound 1 ((11R)-8-chloro-3,11-dimethyl-2-(oxan-4-yl)-2,4,10,11,12,13-hexahydro-9,5-(azeno)pyrazolo[3,4-b][1,4,6,10]oxatriazacyclotridecine) |
1 |
1 |
X-RAY DIFFRACTION |
| 10hz |
Structure of CHK1 10-pt. mutant complex with macrocyclic LRRK2 inhibitor compound 7 ((10aS,13aS)-3-cyclobutyl-1-methyl-8-(trifluoromethyl)-3,4,10a,11,13a,14-hexahydro-10H,13H-9,5-(azeno)furo[3,4-k]pyrazolo[4,3-b][1,4,6,10]oxatriazacyclotridecine) |
1 |
1 |
X-RAY DIFFRACTION |
| 10ia |
Structure of CHK1 10-pt. mutant complex with macrocyclic LRRK2 inhibitor compound 12 ((10aS,13aS)-3-cyclopropyl-1-methyl-8-(trifluoromethyl)-3,4,10a,11,13a,14-hexahydro-10H,13H-9,5-(azeno)furo[3,4-k]pyrazolo[4,3-b][1,4,6,10]oxatriazacyclotridecine) |
1 |
1 |
X-RAY DIFFRACTION |
| 10ic |
Rhesus rotavirus (consensus structure at 4.7 Angstrom resolution from cryo-ET) |
1 |
5 |
ELECTRON MICROSCOPY |
| 10id |
Membrane-bound, reversed VP5* trimer (rotavirus spike protein) |
1 |
1 |
ELECTRON MICROSCOPY |
| 10ij |
S305I Frontotemporal Lobar Degeneration (FTLD) type I tau filament |
1 |
1 |
ELECTRON MICROSCOPY |
| 10ik |
S305I Frontotemporal Lobar Degeneration (FTLD) type II tau filament |
1 |
1 |
ELECTRON MICROSCOPY |
| 10jt |
CRYSTAL STRUCTURE OF KIRSTEN RAT SARCOMA G12C COMPLEXED WITH GMPPNP AND COVALENTLY BOUND TO 1-[(2R,3R)-3-{[(7P)-7-(8-ethynyl-7-fluoronaphthalen-1-yl)-8-fluoro-2-{ [(2R,4R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl]methoxy}pyrido[4,3-d] pyrimidin-4-yl](methyl)amino}-2-methylpyrrolidin-1-yl]-3-(pyrazin-2-yl)propan-1-one |
2 |
2 |
X-RAY DIFFRACTION |
| 10ju |
Crystal Structure of serine/threonine-protein kinase (AEK1) T376D, S395D Mutant from Trypanosoma brucei (AMP-PNP) |
1 |
1 |
X-RAY DIFFRACTION |
| 10jx |
Crystal structure of heme binding PAS domain from one component transcription factor, FG214 |
1 |
1 |
X-RAY DIFFRACTION |
| 10jy |
Crystal structure of heme binding PAS domain from one component transcription factor, FG214 reduced with dithionite |
1 |
1 |
X-RAY DIFFRACTION |
| 10ke |
Crystal structure of Capsular polysaccharide biosynthesis protein from Bordetella pertussis in complex with NAD and uridine-diphosphate-n-acetylgalactosamine (cocrystallization) |
2 |
2 |
X-RAY DIFFRACTION |
| 10kr |
Cryo-EM structure of tau filament |
1 |
1 |
ELECTRON MICROSCOPY |
| 10kt |
Crystal structure of A2A adenosine receptor A2AR-bRIL in complex with Compound50 |
1 |
1 |
X-RAY DIFFRACTION |
| 10ky |
X-ray structure of the Bacteroides fragilis Nramp/MntH divalent transition metal transporter WT in an inward-open, state |
2 |
2 |
X-RAY DIFFRACTION |
| 10kz |
N-Alkyl & N-Aryl Aminopyrazole Spirocarbamates: A Two-Pronged Lead Optimization Strategy to Identify Orally Bioavailable Plasma Kallikrein Inhibitors |
1 |
1 |
X-RAY DIFFRACTION |
| 10le |
X-ray structure of the Bacteroides fragilis Nramp/MntH divalent transition metal transporter WT in an inward-open, manganese-bound state |
2 |
2 |
X-RAY DIFFRACTION |
| 10lg |
Crystal structure of Streptococcus thermophilus SHP pheromone receptor Rgg3 in complex with Rgg3bp13 |
1 |
1 |
X-RAY DIFFRACTION |
| 10li |
D-Ornithine/D-lysine decarboxylase complexed with putrescine and agmatine |
1 |
1 |
X-RAY DIFFRACTION |
| 10lr |
N-Alkyl & N-Aryl Aminopyrazole Spirocarbamates: A Two-Pronged Lead Optimization Strategy to Identify Orally Bioavailable PlasmaKallikrein Inhibitors complex with Compound 4 ((3'R)-1'-(5-amino-1-benzyl-1H-pyrazole-4-carbonyl)-6-chloro-5-fluorospiro[[3,1]benzoxazine-4,3'-piperidin]-2(1H)-one) |
1 |
1 |
X-RAY DIFFRACTION |
| 10lw |
Final Adduct of Human Ornithine Aminotransferase Inactivated by (1R,4S)-4-Amino-3-(trifluoromethyl)cyclopent-2-ene-1-carboxylic Acid |
2 |
2 |
X-RAY DIFFRACTION |
| 10lx |
High Stable Quinonoid Intermediate of Human Ornithine Aminotransferase Complexed with (1R,4S)-4-Amino-3-(trifluoromethyl)cyclopent-2-ene-1-carboxylic Acid |
2 |
2 |
X-RAY DIFFRACTION |
| 10ma |
Closed Eco-ePEC: Cryo-EM structure of Eco RNAP his-elemental paused elongation complex with a closed active site (closed TL, SI3 and RH-FL) |
1 |
1 |
ELECTRON MICROSCOPY |
| 10mb |
Open1 Eco-ePEC: Cryo-EM structure of Eco RNAP his-elemental paused elongation complex with an open active site (open TL, SI3 and RH-FL) |
1 |
1 |
ELECTRON MICROSCOPY |
| 10mc |
Open2 Eco-ePEC: Cryo-EM structure of Eco RNAP his-elemental paused elongation complex with an open active site (open TL, SI3 and RH-FL) |
1 |
1 |
ELECTRON MICROSCOPY |
| 10md |
Open3 Eco-ePEC: Cryo-EM structure of Eco RNAP his-elemental paused elongation complex with an open active site (open TL, SI3 and RH-FL) |
1 |
1 |
ELECTRON MICROSCOPY |
| 10mh |
TERNARY STRUCTURE OF HHAI METHYLTRANSFERASE WITH ADOHCY AND HEMIMETHYLATED DNA CONTAINING 5,6-DIHYDRO-5-AZACYTOSINE AT THE TARGET |
1 |
1 |
X-RAY DIFFRACTION |