|
313
|
879
|
4kxdA |
Crystal structure of human aminopeptidase a complexed with glutamate and calcium |
|
275
|
716
|
4n3bA |
Crystal structure of human o-glcnac transferase bound to a peptide from hcf-1 pro-repeat2(1-26)e10q and udp-5sglcnac |
|
56
|
136
|
4nacA |
Crystal structure of the n-terminal domain of p15rs |
|
124
|
325
|
4o27A |
Crystal structure of mst3-mo25 complex with wif motif |
|
283
|
716
|
4n39A |
Crystal structure of human o-glcnac transferase bound to a peptide from hcf-1 pro-repeat 2 (11-26) |
|
102
|
334
|
4nq0A |
Structural insights into yeast histone chaperone hif1: a scaffold protein recruiting protein complexes to core histones |
|
221
|
708
|
4o1oA |
Crystal structure of rnase l in complex with 2-5a |
|
222
|
608
|
4ms6A |
Human leukotriene a4 hydrolase in complex with pro-gly-pro analogue |
|
70
|
230
|
4o60A |
Structure of ankyrin repeat protein |
|
283
|
716
|
4n3aA |
Crystal structure of human o-glcnac transferase bound to a peptide from hcf-1 pro-repeat 2 (1-26)e10a |
|
335
|
889
|
4k5mA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
316
|
879
|
4kx9A |
Crystal structure of human aminopeptidase a complexed with arginine |
|
256
|
794
|
4n5cA |
Crystal structure of ypp1 |
|
334
|
889
|
4k5nA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
176
|
426
|
4mz6E |
Structure of importin-alpha: dutpase s11e nls mutant complex |
|
181
|
427
|
4mz5E |
Structure of importin-alpha: dutpase nls complex |
|
246
|
949
|
4kz0A |
Structure of pi3k gamma with imidazopyridine inhibitors |
|
308
|
1046
|
4l2yA |
Crystal structure of p110alpha complexed with nish2 of p85alpha and compound 9d |
|
311
|
879
|
4kxbA |
Crystal structure of human aminopeptidase a complexed with bestatin |
|
180
|
487
|
4mfuA |
Crystal structure of human ctnnbl1(residues 77~563) |
|
76
|
199
|
4m7cA |
Crystal structure of the trf2-binding motif of slx4 in complex with the trfh domain of trf2 |
|
334
|
889
|
4k5lA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
130
|
347
|
4lnbA |
Aspergillus fumigatus protein farnesyltransferase ternary complex with farnesyldiphosphate and ethylenediamine scaffold inhibitor 5 |
|
267
|
727
|
4kvoA |
The nata (naa10p/naa15p) amino-terminal acetyltrasferase complex bound to accoa |
|
316
|
879
|
4kxaA |
Crystal structure of human aminopeptidase a complexed with aspartate and calcium |
|
311
|
879
|
4kx8A |
Crystal structure of human aminopeptidase a complexed with amastatin |
|
133
|
347
|
4mbgA |
Crystal structure of aspergillus fumigatus protein farnesyltransferase binary complex with farnesyldiphosphate |
|
52
|
157
|
4m3oA |
Crystal structure of k.lactis rtr1 ntd |
|
50
|
153
|
4lszE |
Caspase-7 in complex with darpin d7.18 |
|
284
|
727
|
4kvmA |
The nata (naa10p/naa15p) amino-terminal acetyltransferase complex bound to a bisubstrate analog |
|
174
|
487
|
4mruA |
Crystal structure of a susd homolog (bt1281) from bacteroides thetaiotaomicron vpi-5482 at 1.90 a resolution |
|
314
|
879
|
4kx7A |
Crystal structure of human aminopeptidase a |
|
340
|
1060
|
4jpsA |
Co-crystal structures of the lipid kinase pi3k alpha with pan and isoform selective inhibitors |
|
299
|
908
|
4jbsA |
Crystal structure of the human endoplasmic reticulum aminopeptidase 2 in complex with phosphinic pseudotripeptide inhibitor. |
|
124
|
315
|
4lunU |
Structure of the n-terminal mif4g domain from s. cerevisiae upf2, a protein involved in the degradation of mrnas containing premature stop codons |
|
132
|
347
|
4lngA |
Aspergillus fumigatus protein farnesyltransferase complex with farnesyldiphosphate and tipifarnib |
|
182
|
489
|
4mfvA |
Crystal structure of human ctnnbl1(residues 33~563) |
|
309
|
879
|
4kxcA |
Crystal structure of human aminopeptidase a complexed with glutamate |
|
71
|
194
|
4me2A |
Crystal structure of tha8 protein from brachypodium distachyon |
|
330
|
889
|
4k5oA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
51
|
157
|
4lnuD |
Nucleotide-free kinesin motor domain in complex with tubulin and a darpin |
|
129
|
318
|
4lctA |
Crystal structure and versatile functional roles of the cop9 signalosome subunit 1 |
|
226
|
608
|
4mktA |
Human leukotriene a4 hydrolase in complex with pro-gly-pro analogue and 4-(4-benzylphenyl)thiazol-2-amine |
|
179
|
492
|
4mlpA |
Mammalian cryptochrome in complex with a small molecule competitor of its ubiquitin ligase |
|
240
|
949
|
4kzcA |
Structure of pi3k gamma with imidazopyridine inhibitors |
|
335
|
889
|
4k5pA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
86
|
211
|
4lrzA |
Crystal structure of the e.coli dhar(n)-dhal complex |
|
57
|
170
|
4k5cA |
From darpins to loopdarpins: novel loopdarpin design allows the selection of low picomolar binders in a single round of ribosome display |
|
52
|
163
|
4lg6A |
Crystal structure of ankra2-ccdc8 complex |
|
320
|
851
|
4jlqA |
Crystal structure of human karyopherin-beta2 bound to the py-nls of saccharomyces cerevisiae nab2 |
