|
52
|
160
|
5bxoA |
Human tankyrase-2 in complex with macrocyclised extended peptide cp4n2m3 |
|
50
|
163
|
5bxuA |
Human tankyrase-2 in complex with macrocyclised extended peptide cp4n4m5 |
|
280
|
715
|
5bnwA |
The active site of o-glcnac transferase imposes constraints on substrate sequence |
|
218
|
653
|
5bv1A |
Crystal structure of a vps33-vps16 complex from chaetomium thermophilum |
|
90
|
231
|
5cl3A |
Alkylpurine dna glycosylase alkd bound to dna containing a 3-methyladenine analog (100% substrate at 4 hours) |
|
339
|
888
|
4zx6A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 10s |
|
342
|
889
|
4zx4A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 10o |
|
161
|
429
|
5b56A |
Crystal structure of hiv-1 vpr c-terminal domain and dibb-m-importin-alpha2 complex |
|
224
|
608
|
5aenA |
Structure of human leukotriene a4 hydrolase in complex with inhibitor dimethyl(2- (4-phenoxyphenoxy)ethyl)amine |
|
42
|
105
|
5b3sE |
Bovine heart cytochrome c oxidase in the carbon monoxide-bound mixed-valence state at 1.68 angstrom resolution (50 k) |
|
336
|
889
|
4zw5A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 9f |
|
234
|
635
|
5aijA |
P. aeruginosa sdsa hexagonal polymorph |
|
333
|
889
|
4zw3A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 9b |
|
88
|
231
|
5cl4A |
Alkylpurine dna glycosylase alkd bound to dna containing a 3-methyladenine analog or dna containing an abasic site and a free nucleobase (71% substrate/29% product at 24 hours) |
|
337
|
889
|
4zx3A |
X-ray crystal structure of pfa-m1 in complex with hydroxamic acid-based inhibitor 10b |
|
88
|
231
|
5cl5A |
Alkylpurine dna glycosylase alkd bound to dna containing a 3-methyladenine analog or dna containing an abasic site and a free nucleobase (51% substrate/49% product at 48 hours) |
|
89
|
332
|
5bt1A |
Histone chaperone hif1 playing with histone h2a-h2b dimer |
|
152
|
397
|
5bz1A |
Crystal structure of the rna-binding domain of yeast puf5p bound to mfa2 rna |
|
147
|
396
|
5bzuA |
Crystal structure of the rna-binding domain of yeast puf5p bound to aat2 rna |
|
54
|
156
|
5aaoA |
Crystal structure of fluorogen-activating designed ankyrin repeat protein (darpin) dimer in complex with malachite green |
|
336
|
889
|
4zqtA |
Crystal structure of pfa-m1 with virtual ligand inhibitor |
|
219
|
635
|
5a23A |
Sdsa sulfatase triclinic form |
|
314
|
902
|
4homA |
Crystal structure of porcine aminopeptidase-n complexed with substance p |
|
259
|
867
|
4z7iA |
Crystal structure of insulin regulated aminopeptidase in complex with ligand |
|
324
|
866
|
4xndA |
Crystal structure of e. coli aminopeptidase n in complex with l-beta homotryptophan |
|
242
|
946
|
4hleA |
Compound 21 (1-alkyl-substituted 1,2,4-triazoles) |
|
55
|
156
|
4zfhA |
Crystal structure of artificial ankyrin repeat protein_ank(gag)1d4 mutant -y56a |
|
31
|
104
|
4zhbA |
N-terminal structure of ankyrin repeat-containing protein lega11 from legionella pneumophila |
|
166
|
421
|
4zduA |
Crystal structure of importin-alpha bound to a non-classical nuclear localization signal of the influenza a virus nucleoprotein |
|
48
|
155
|
4z68A |
Hybrid structural analysis of the arp2/3 regulator arpin identifies its acidic tail as a primary binding epitope |
|
264
|
947
|
4hvbA |
Catalytic unit of pi3kg in complex with pi3k/mtor dual inhibitor pf-04979064 |
|
281
|
905
|
4f5cA |
Crystal structure of the spike receptor binding domain of a porcine respiratory coronavirus in complex with the pig aminopeptidase n ectodomain |
|
279
|
951
|
4ezlA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
253
|
950
|
4fadA |
Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor |
|
273
|
951
|
4ezjA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
267
|
949
|
4fa6A |
Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor |
|
265
|
945
|
4f1sA |
Crystal structure of human pi3k-gamma in complex with a pyridyl-triazine-sulfonamide inhibitor |
|
304
|
864
|
4pvbA |
Crystal structure of aminopeptidase n in complex with the phosphonic acid analogue of leucine (d-(s)-leup) |
|
275
|
949
|
4ezkA |
Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf |
|
187
|
498
|
4f53A |
Crystal structure of a susd homolog (bacova_04803) from bacteroides ovatus atcc 8483 at 2.25 a resolution |
|
143
|
456
|
4q69A |
Crystal structure of a susd homolog (bt2259) from bacteroides thetaiotaomicron vpi-5482 at 2.50 a resolution |
|
76
|
291
|
4f1pA |
Crystal structure of mutant s554d for arfgap and ank repeat domain of acap1 |
|
106
|
275
|
4f3vA |
Crystal structure of n-terminal domain of ecca1 atpase from esx-1 secretion system of mycobacterium tuberculosis |
|
197
|
498
|
4f7aA |
Crystal structure of a susd homolog (bvu_2203) from bacteroides vulgatus atcc 8482 at 1.85 a resolution |
|
82
|
229
|
4qmjA |
The xmap215 family drives microtubule polymerization using a structurally diverse tog array |
|
196
|
504
|
4ev9A |
Crystal structure of mouse catenin beta-59 in 4.0m urea |
|
178
|
427
|
4htvA |
Mouse importin alpha: bfdv cap nls peptide complex |
|
196
|
504
|
4ev8A |
Crystal structure of mouse catenin beta-59 in 2.4m urea. |
|
196
|
503
|
4evaA |
Crystal structure of mouse catenin beta-59 in 5.6m urea |
|
295
|
908
|
4e36A |
Crystal structure of the human endoplasmic reticulum aminopeptidase 2 variant n392k |
