125
|
417
|
5mzhA |
Crystal structure of oda16 from chlamydomonas reinhardtii |
96
|
359
|
5nafA |
Co-crystal structure of an mecp2 peptide with tblr1 wd40 domain |
78
|
336
|
5mwjA |
Structure enabled discovery of a stapled peptide inhibitor to target the oncogenic transcriptional repressor tle1 |
166
|
879
|
5n1aA |
Crystal structure of utp4 from chaetomium thermophilum |
156
|
786
|
5m2nA |
Crystal structure of elongator subunit elp2 |
75
|
326
|
5m89A |
Spliceosome component |
128
|
552
|
5m5gA |
Crystal structure of the chaetomium thermophilum polycomb repressive complex 2 (prc2) |
123
|
548
|
5l8wB |
Structure of usp12-ub-prg/uaf1 |
88
|
365
|
5ls6B |
Structure of human polycomb repressive complex 2 (prc2) with inhibitor |
103
|
300
|
5m23A |
Modulation of mll1 methyltransferase activity |
98
|
427
|
5lcwR |
Cryo-em structure of the anaphase-promoting complex/cyclosome, in complex with the mitotic checkpoint complex (apc/c-mcc) at 4.2 angstrom resolution |
88
|
374
|
5lcwQ |
Cryo-em structure of the anaphase-promoting complex/cyclosome, in complex with the mitotic checkpoint complex (apc/c-mcc) at 4.2 angstrom resolution |
97
|
300
|
5m25A |
Modulation of mll1 methyltransferase activity |
93
|
326
|
5kwnA |
The wd domain ofarabidopsis thaliana e3 ubiquitin ligase cop1 in complex with peptide from hy5 |
116
|
552
|
5kklA |
Structure of ctprc2 in complex with h3k27me3 and h3k27m |
128
|
552
|
5kjhA |
Crystal structure of an active polycomb repressive complex 2 in the stimulated state |
101
|
359
|
5k0mA |
Targeting the prc2 complex through a novel protein-protein interaction inhibitor of eed |
124
|
662
|
5k1bB |
Crystal structure of the uaf1/usp12 complex in f222 space group |
110
|
339
|
5kdoB |
Heterotrimeric complex of the 4 alanine insertion variant of the gi alpha1 subunit and the gbeta1-ggamma1 |
123
|
552
|
5kjiA |
Crystal structure of an active polycomb repressive complex 2 in the basal state |
86
|
553
|
5k19A |
Crystal structure of wd repeat-containing protein 20 |
158
|
662
|
5k1aB |
Crystal structure of the uaf1-usp12 complex in c2 space group |
74
|
341
|
5igqA |
Wd40 domain of human e3 ubiquitin ligase cop1 (rfwd2) bound to peptide from trib1 |
96
|
358
|
5ij8E |
Structure of the primary oncogenic mutant y641n hs/acprc2 in complex with a pyridone inhibitor |
98
|
360
|
5ij7E |
Structure of hs/acprc2 in complex with a pyridone inhibitor |
146
|
704
|
5i2tA |
Domain characterization of the wd protein pwp2 and their relevance in ribosome biogenesis |
90
|
365
|
5hynB |
Structure of human polycomb repressive complex 2 (prc2) with oncogenic histone h3k27m peptide |
103
|
375
|
5h13A |
Eed in complex with prc2 allosteric inhibitor eed396 |
97
|
363
|
5gsaA |
Eed in complex with an allosteric prc2 inhibitor |
149
|
640
|
4ci8A |
Crystal structure of the tandem atypical beta-propeller domain of eml1 |
70
|
336
|
6gdgB |
Cryo-em structure of the adenosine a2a receptor bound to a minigs heterotrimer |
68
|
338
|
6g79B |
Coupling specificity of heterotrimeric go to the serotonin 5-ht1b receptor |
91
|
402
|
6g16A |
Structure of the human rbbp4:mta1(464-546) complex showing loop exchange |
83
|
357
|
6f9nB |
Crystal structure of the human cpsf160-wdr33 complex |
9
|
36
|
6f1zo |
Roadblock-1 region of the dynein tail/dynactin/bicdr1 complex |
32
|
417
|
6f3ag |
Cryo-em structure of a single dynein tail domain bound to dynactin and bicd2n |
49
|
358
|
6f1uh |
N terminal region of dynein tail domains in complex with dynactin filament and bicdr-1 |
23
|
417
|
6f38g |
Cryo-em structure of two dynein tail domains bound to dynactin and hook3 |
33
|
417
|
6f1tg |
Cryo-em structure of two dynein tail domains bound to dynactin and bicdr1 |
73
|
444
|
6eojD |
Polya polymerase module of the cleavage and polyadenylation factor (cpf) from saccharomyces cerevisiae |
48
|
300
|
6emkB |
Cryo-em structure of saccharomyces cerevisiae target of rapamycin complex 2 |
73
|
336
|
6e3yB |
Cryo-em structure of the active, gs-protein complexed, human cgrp receptor |
80
|
330
|
6e29A |
Crystal structure of myceliophteria_thermophila cps50 (swd1) beta-propeller domain |
73
|
338
|
6d9hB |
Cryo-em structure of the human adenosine a1 receptor-gi2-protein complex bound to its endogenous agonist |
103
|
305
|
6d9xA |
Discovery of potent 2-aryl-6,7-dihydro-5hpyrrolo[ 1,2-a]imidazoles as wdr5 win-site inhibitors using fragment-based methods and structure-based design |
101
|
305
|
6dasA |
Discovery of potent 2-aryl-6,7-dihydro-5hpyrrolo[ 1,2-a]imidazoles as wdr5 win-site inhibitors using fragment-based methods and structure-based design |
106
|
302
|
6darA |
Discovery of potent 2-aryl-6,7-dihydro-5hpyrrolo[ 1,2-a]imidazoles as wdr5 win-site inhibitors using fragment-based methods and structure-based design |
59
|
336
|
6ddfB |
Mu opioid receptor-gi protein complex |
106
|
304
|
6dakA |
Discovery of potent 2-aryl-6,7-dihydro-5hpyrrolo[ 1,2-a]imidazoles as wdr5 win-site inhibitors using fragment-based methods and structure-based design |
65
|
336
|
6ddeB |
Mu opioid receptor-gi protein complex |