Found 1121 chains in Genus chains table. Displaying 651 - 700. Applied filters: Proteins

Search results query: WD40

Total Genus Sequence Length pdb Title
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