|
28
|
75
|
4cocA |
Hiv-1 capsid c-terminal domain mutant (y169l) |
|
63
|
178
|
4by5A |
Crystal structure of drosophila frq2 |
|
109
|
362
|
4c0aA |
Arf1(delta1-17)in complex with brag2 sec7-ph domain |
|
98
|
308
|
4cliA |
Structure of the human anaplastic lymphoma kinase in complex with pf- 06463922 ((10r)-7-amino-12-fluoro-2,10,16-trimethyl-15-oxo-10,15,16, 17-tetrahydro-2h-8,4-(metheno)pyrazolo(4,3-h)(2,5,11) benzoxadiazacyclotetradecine-3-carbonitrile). |
|
82
|
298
|
4bzdA |
Structure of cdk2 in complex with a benzimidazopyrimidine |
|
95
|
314
|
4ckiA |
Crystal structure of oncogenic ret tyrosine kinase m918t bound to adenosine |
|
19
|
69
|
4bxuA |
Structure of pex14 in complex with pex5 lvxef motif |
|
108
|
337
|
4c38A |
Pka-s6k1 chimera with compound 21e (cct239066) bound |
|
135
|
458
|
4ccmA |
60s ribosomal protein l8 histidine hydroxylase (no66) in complex with mn(ii), n-oxalylglycine (nog) and 60s ribosomal protein l8 (rpl8 g220c) peptide fragment (complex-1) |
|
83
|
273
|
4bznA |
Crystal structure of pim1 in complex with a pyrrolo(1,2-a)pyrazinone inhibitor |
|
103
|
308
|
4cc6A |
Fragment-based discovery of 6 azaindazoles as inhibitors of bacterial dna ligase |
|
155
|
449
|
4cohA |
Crystal structure of trypanosoma cruzi cyp51 bound to the sulfonamide derivative of the 4-aminopyridyl-based inhibitor |
|
83
|
261
|
4c3fA |
Structure of lck in complex with a compound discovered by virtual fragment linking |
|
70
|
307
|
4c59A |
Structure of gak kinase in complex with nanobody (nbgak_4) |
|
54
|
215
|
4cgyB |
Crystal structure of the human topoisomerase iii alpha-rmi1 complex |
|
85
|
284
|
4cizA |
Crystal structure of the complex of the cellular retinal binding protein with 9-cis-retinal |
|
137
|
408
|
4c9nA |
Structure of camphor and hydroxycamphor bound d259n mutant of cyp101d1 |
|
92
|
262
|
4cfuD |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
83
|
267
|
4ch3A |
Structure of pyrrolysyl-trna synthetase in complex with adenylated butyryl lysine |
|
124
|
413
|
4bwxA |
Structure of neurospora crassa pan3 pseudokinase mutant |
|
76
|
218
|
4c4sA |
Structure of beta-phosphoglucomutase in complex with an alpha- fluorophosphonate analogue of beta-glucose-1-phosphate and magnesium trifluoride |
|
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 |
|
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 |
|
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. |
|
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. |
|
208
|
645
|
4b74A |
Discovery of an allosteric mechanism for the regulation of hcv ns3 protein function |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
82
|
303
|
4bdcA |
Fragment-based screening identifies a new area for inhibitor binding to checkpoint kinase 2 (chk2) |
