|
79
|
299
|
7ug1A |
Cdk2 liganded with para chloro ans |
|
76
|
296
|
8curA |
Crystal structure of cdk2 in complex with cyclin a inhibitor 6-[(e)-2-(4-chlorophenyl)ethenyl]-2-{[(2r)-3-(4-hydroxyphenyl)-1-methoxy-1-oxopropan-2-yl]carbamoyl}quinoline-4-carboxylic acid |
|
80
|
294
|
8b54A |
Cdk2/cyclin a2 in complex with pyrazolo[4,3-d]pyrimidine inhibitor lgr6768 |
|
80
|
298
|
8h6tA |
Complex structure of cdk2/cyclin e1 and a potent, selective small molecule inhibitor |
|
85
|
298
|
8h6pA |
Complex structure of cdk2/cyclin e1 and a potent, selective macrocyclic inhibitor |
|
87
|
298
|
7zpcA |
Cdk2 in complex 9k-dos |
|
80
|
297
|
7uxiA |
Structure of cdk2 in complex with fp19711, a helicon polypeptide |
|
63
|
286
|
7uxkA |
Structure of cdk2 in complex with fp24322, a helicon polypeptide |
|
83
|
297
|
7mkxA |
Crystal structure analysis of human cdk2 and ccna2 complex |
|
51
|
299
|
8gxqHI |
Pic-mediator in complex with +1 nucleosome (t40n) in mh-binding state |
|
50
|
299
|
8gxsHI |
Pic-mediator in complex with +1 nucleosome (t40n) in h-binding state |
|
70
|
294
|
7sj3A |
Structure of cdk4-cyclin d3 bound to abemaciclib |
|
78
|
303
|
7ukzA |
Cdk11 in complex with small molecule inhibitor ots964 |
|
82
|
298
|
7sa0A |
Crystal structure of cdk2 liganded with compound ef4195 |
|
79
|
296
|
7s9xA |
Crystal structure of cdk2 liganded with compound wn378 |
|
81
|
297
|
7s7aA |
Crystal structure of cdk2 liganded with compound ef3019 |
|
82
|
298
|
7s84A |
Crystal structure of cdk2 liganded with compound tw8972 |
|
81
|
296
|
7s85A |
Crystal structure of cdk2 liganded with compound wn316 |
|
84
|
296
|
7s4tA |
Crystal structure of cdk2 liganded with compound ef2252 |
|
77
|
296
|
7rxoA |
Crystal structure of cdk2 liganded with compound wn333 |
|
87
|
299
|
7rwfA |
Crystal structure of cdk2 in complex with tw8672 |
|
73
|
296
|
7rweA |
Crystal structure of cdk2 liganded with compound gphr787 |
|
81
|
298
|
7ra5A |
Cdk2 in complex with compound 4 |
|
84
|
320
|
7nwkA |
Crystal structure of cdk9-cyclin t1 bound by compound 6 |
|
54
|
290
|
7nj0B |
Cryoem structure of the human separase-cdk1-cyclin b1-cks1 complex |
|
80
|
293
|
7b7sA |
Cdk2/cyclin a2 in complex with 3h-pyrazolo[4,3-f]quinoline-based derivative hsd1368 |
|
82
|
320
|
6w9eA |
Crystal structure of human cdk9/cyclint1 in complex with mc180295 |
|
79
|
298
|
7m2fA |
Cdk2 with compound 14 inhibitor with carboxylate |
|
83
|
297
|
7kjsA |
Crystal structure of cdk2/cyclin e in complex with pf-06873600 |
|
84
|
294
|
7nvqA |
Aerosol-soaked human cdk2 crystals with staurosporine |
|
57
|
299
|
7enc8 |
Tfiid-based pic-mediator holo-complex in fully-assembled state (hpic-med) |
|
51
|
299
|
7ena8 |
Tfiid-based pic-mediator holo-complex in pre-assembled state (pre-hpic-med) |
|
82
|
326
|
7nxkA |
Crystal structure of human cdk12/cyclin k in complex with the inhibitor bsj-01-175 |
|
81
|
329
|
7nxjA |
Crystal structure of human cdk13/cyclin k in complex with the inhibitor thz531 |
|
42
|
298
|
7egc8 |
P53-bound tfiid-based holo pic on hdm2 promoter |
|
45
|
298
|
7egb8 |
Tfiid-based holo pic on scp promoter |
|
102
|
365
|
6y0aA |
Crystal structure of cdk8-cycc in complex with bi00690300 |
|
88
|
324
|
6z45A |
Cdk9-cyclin-t1 complex bound by compound 24 |
|
98
|
361
|
6tpaA |
Cdk8/cyclinc in complex with drug etp-50775 |
|
79
|
267
|
6sg4A |
Structure of cdk2/cyclin a m246q, s247en |
|
58
|
442
|
7kpvA |
Structure of kinase and central lobes of yeast ckm |
|
58
|
442
|
7kpxA |
Structure of the yeast ckm |
|
87
|
303
|
6yl6A |
Cdk2(f80c) |
|
85
|
303
|
6yl1A |
Cdk2(f80c) with covalent adduct tk37 at f80c |
|
85
|
303
|
6ylkA |
Cdk2(f80c) with covalent adduct tk22 at f80c |
|
90
|
333
|
6td3B |
Structure of ddb1 bound to cr8-engaged cdk12-cyclink |
|
86
|
290
|
6rijA |
Cdk2/cyclin a2 in complex with open-ring 5-nitrosopyrimidine inhibitor lc436 |
|
79
|
298
|
6inlA |
Crystal structure of cdk2 in complex with inhibitor cvt-313 |
|
83
|
323
|
5l1zA |
Tar complex with hiv-1 tat-aff4-p-tefb |
|
82
|
297
|
6gueC |
Cdk2/cyclina in complex with azd5438 |
