|
32
|
141
|
4b9kC |
Pvhl-elob-eloc complex_(2s,4r)-1-(3-amino-2-methylbenzoyl)-4-hydroxy-n-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide bound |
|
88
|
299
|
4bcoA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
102
|
312
|
4asdA |
Crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with sorafenib (bay 43-9006) |
|
112
|
337
|
4bm1A |
Crystal structure of manganese peroxidase 4 from pleurotus ostreatus - crystal form i |
|
168
|
515
|
4b7fA |
Structure of a liganded bacterial catalase |
|
82
|
271
|
4bieA |
Crystal structures of ask1-inhibitor complexes |
|
13
|
105
|
4aybF |
Rnap at 3.2ang |
|
46
|
129
|
4b1aA |
Crystal structure of lysozyme with keggin molecule |
|
256
|
945
|
4anwA |
Complexes of pi3kgamma with isoform selective inhibitors. |
|
99
|
255
|
4bcnD |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
145
|
393
|
4aw3A |
Structure of the mixed-function p450 mycg f286v mutant in complex with mycinamicin v in p1 space group |
|
82
|
279
|
4bi0A |
Scaffold focused virtual screening: prospective application to the discovery of ttk inhibitor |
|
197
|
645
|
4b71A |
Discovery of an allosteric mechanism for the regulation of hcv ns3 protein function |
|
79
|
283
|
4bb4A |
Ephb4 kinase domain inhibitor complex |
|
28
|
90
|
4bhxA |
Crystal structure of the scan domain from human paternally expressed gene 3 protein |
|
112
|
337
|
4bm2A |
Crystal structure of manganese peroxidase 4 from pleurotus ostreatus - crystal form ii |
|
260
|
952
|
3zqjA |
Mycobacterium tuberculosis uvra |
|
49
|
129
|
4bafA |
Hen egg-white lysozyme structure in complex with the europium tris- hydroxyethyltriazoledipicolinate complex at 1.51 a resolution. |
|
208
|
645
|
4b74A |
Discovery of an allosteric mechanism for the regulation of hcv ns3 protein function |
|
78
|
294
|
4bgqA |
Crystal structure of the human cdkl5 kinase domain |
|
115
|
347
|
4armB |
Structure of the inactive pesticin t201a mutant |
|
26
|
93
|
5e8iA |
Crystal structure of the dna binding domain of human transcription factor fli1 in complex with a 10-mer dna accggaagtg |
|
25
|
106
|
5d8kB |
Human hsf2 dna-binding domain bound to 2-site hse dna at 1.73 angstroms resolution |
|
50
|
129
|
4bapA |
Hen egg-white lysozyme structure in complex with the europium tris- hydroxyethylcholinetriazoledipicolinate complex at 1.21 a resolution. |
|
100
|
316
|
4bbmA |
Crystal structure of the human cdkl2 kinase domain with bound tcs 2312 |
|
77
|
207
|
4auxA |
Tet repressor class d in complex with 9-nitrotetracycline |
|
99
|
299
|
4b4lA |
Crystal structure of an ard dap-kinase 1 mutant |
|
91
|
257
|
4bckB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
17
|
116
|
4behB |
Solution structure of human ribosomal protein p1.p2 heterodimer |
|
113
|
369
|
4atbB |
Crystal structure of the nf90-nf45 dimerisation domain complex with ctp |
|
98
|
354
|
4b47A |
Bacterial translation initiation factor if2 (1-363), complex with gdp at ph6.5 |
|
74
|
265
|
4b8lA |
Aurora b kinase p353g mutant |
|
88
|
257
|
4bcqB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
82
|
303
|
4bdcA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
|
236
|
664
|
4b02A |
The c-terminal priming domain is strongly associated with the main body of bacteriophage phi6 rna-dependent rna polymerase |
|
206
|
952
|
4aofA |
Selective small molecule inhibitor discovered by chemoproteomic assay platform reveals regulation of th17 cell differentiation by pi3kgamma |
|
183
|
578
|
4bcaA |
Mammalian alkyldihydroxyacetonephosphate synthase: tyr578phe mutant |
|
212
|
916
|
4ajwA |
Discovery and optimization of new benzimidazole- and benzoxazole-pyrimidone selective pi3kbeta inhibitors for the treatment of phosphatase and tensin homologue (pten)-deficient cancers |
|
65
|
241
|
4bpaA |
Crystal structure of ampdh2 from pseudomonas aeruginosa in complex with nag-nam-nag-nam tetrasaccharide |
|
105
|
355
|
4b43A |
Bacterial translation initiation factor if2 (1-363), apo form, double mutant k86l h130a |
|
104
|
311
|
4asxA |
Crystal structure of activin receptor type-iia (acvr2a) kinase domain in complex with dihydro-bauerine c |
|
76
|
298
|
4bcqA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
43
|
110
|
4avdA |
C.lacteus nerve hb in complex with co |
|
51
|
163
|
4b4sA |
Crystal structure of a pro-survival bcl-2:bim bh3 complex |
|
208
|
645
|
4b75A |
Discovery of an allosteric mechanism for the regulation of hcv ns3 protein function |
|
80
|
322
|
4arkA |
Crystal structure of the catalytic domain of human map kinase kinase 1 (mek1) in complex with a small molecule inhibitor and adp |
|
15
|
114
|
4behA |
Solution structure of human ribosomal protein p1.p2 heterodimer |
|
82
|
279
|
4bi1A |
Scaffold focused virtual screening: prospective application to the discovery of ttk inhibitor |
|
102
|
363
|
4b3xA |
Bacterial translation initiation factor if2 (1-363), apo form |
|
96
|
291
|
4aqcA |
Triazolopyridine-based inhibitor of janus kinase 2 |
