|
10
|
53
|
2vwmK |
Aminopyrrolidine factor xa inhibitor |
|
43
|
175
|
2w1tA |
Crystal structure of b. subtilis spovt |
|
9
|
51
|
2vwoL |
Aminopyrrolidine factor xa inhibitor |
|
12
|
53
|
2vvcK |
Aminopyrrolidine factor xa inhibitor |
|
7
|
48
|
2w2pE |
Pcsk9-deltac d374a mutant bound to wt egf-a of ldlr |
|
8
|
47
|
2w2qE |
Pcsk9-deltac d374h mutant bound to wt egf-a of ldlr |
|
10
|
51
|
2vwnL |
Aminopyrrolidine factor xa inhibitor |
|
50
|
205
|
2vrsA |
Structure of avian reovirus sigmac117-326, c2 crystal form |
|
12
|
54
|
2vvvL |
Aminopyrrolidine-related triazole factor xa inhibitor |
|
11
|
97
|
2vweA |
Crystal structure of vascular endothelial growth factor-b in complex with a neutralizing antibody fab fragment |
|
9
|
50
|
2vwlL |
Aminopyrrolidine factor xa inhibitor |
|
39
|
173
|
2w1tB |
Crystal structure of b. subtilis spovt |
|
12
|
51
|
2w3iB |
Crystal structure of fxa in complex with 4,4-disubstituted pyrrolidine-1,2-dicarboxamide inhibitor 2 |
|
8
|
49
|
2w2nE |
Wt pcsk9-deltac bound to egf-a h306y mutant of ldlr |
|
50
|
311
|
2vyuA |
Crystal structure of choline binding protein f from streptococcus pneumoniae in the presence of a peptidoglycan analogue (tetrasaccharide-pentapeptide) |
|
12
|
54
|
2vvuL |
Aminopyrrolidine factor xa inhibitor |
|
8
|
65
|
2vlwA |
Crystal structure of the muscarinic toxin mt7 diiodotyr51 derivative. |
|
8
|
95
|
2vxsA |
Structure of il-17a in complex with a potent, fully human neutralising antibody |
|
18
|
97
|
2vpfA |
Vascular endothelial growth factor refined to 1.93 angstroms resolution |
|
12
|
52
|
2vh0B |
Structure and property based design of factor xa inhibitors:biaryl pyrrolidin-2-ones incorporating basic heterocyclic motifs |
|
84
|
320
|
2viuA |
Influenza virus hemagglutinin |
|
15
|
55
|
2vghA |
Heparin-binding domain from vascular endothelial growth factor, nmr, minimized average structure |
|
12
|
52
|
2uwlB |
Selective and dual action orally active inhibitors of thrombin and factor xa |
|
78
|
267
|
2vitC |
Influenza virus hemagglutinin, mutant with thr 155 replaced by ile, complexed with a neutralizing antibody |
|
12
|
54
|
2vh6B |
Structure and property based design of factor xa inhibitors: pyrrolidin-2-ones with biaryl p4 motifs |
|
37
|
187
|
2uwnA |
Crystal structure of human complement factor h, scr domains 6-8 (h402 risk variant), in complex with ligand. |
|
74
|
267
|
2virC |
Influenza virus hemagglutinin complexed with a neutralizing antibody |
|
34
|
187
|
2v8eA |
Crystal structure of human complement factor h, scr domains 6-8 (h402 risk variant), in complex with ligand. |
|
149
|
489
|
2uwxA |
Active site restructuring regulates ligand recognition in class a penicillin-binding proteins |
|
21
|
120
|
2vj3A |
Human notch-1 egfs 11-13 |
|
12
|
52
|
2uwpB |
Factor xa inhibitor complex |
|
80
|
267
|
2visC |
Influenza virus hemagglutinin, (escape) mutant with thr 131 replaced by ile, complexed with a neutralizing antibody |
|
62
|
311
|
2v05A |
Crystal structure of choline binding protein f from streptococcus pneumoniae. crystal form ii. |
|
17
|
101
|
2v5eB |
The structure of the gdnf:coreceptor complex: insights into ret signalling and heparin binding. |
|
9
|
73
|
2rtsA |
Chitin binding domain1 |
|
22
|
79
|
2uwrA |
High resolution structure of human cd59 |
|
6
|
54
|
2ro3A |
Rdc-refined solution structure of the n-terminal dna recognition domain of the bacillus subtilis transition-state regulator abh |
|
17
|
89
|
2rkzA |
Crystal structure of the second and third fibronectin f1 modules in complex with a fragment of staphylococcus aureus fnbpa-1 |
|
56
|
311
|
2v04A |
Crystal structure of choline binding protein f from streptococcus pneumoniae |
|
5
|
55
|
2ro5A |
Rdc-refined solution structure of the n-terminal dna recognition domain of the bacillus subtilis transition-state regulator spovt |
|
62
|
342
|
2rftA |
Crystal structure of influenza b virus hemagglutinin in complex with lsta receptor analog |
|
112
|
613
|
2v5oA |
Structure of human igf2r domains 11-14 |
|
20
|
78
|
2ux2A |
High resolution structure of human cd59 |
|
12
|
52
|
2uwoB |
Selective and dual action orally active inhibitors of thrombin and factor xa |
|
22
|
123
|
2rlqA |
Nmr structure of ccp modules 2-3 of complement factor h |
|
18
|
90
|
2rkyA |
Crystal structure of the fourth and fifth fibronectin f1 modules in complex with a fragment of staphylococcus aureus fnbpa-1 |
|
13
|
50
|
2tgfA |
The solution structure of human transforming growth factor alpha |
|
5
|
53
|
2ro4A |
Rdc-refined solution structure of the n-terminal dna recognition domain of the bacillus subtilis transition-state regulator abrb |
|
14
|
89
|
2rl0A |
Crystal structure of the fourth and fifth fibronectin f1 modules in complex with a fragment of staphylococcus aureus fnbpa-5 |
|
12
|
51
|
2ra0L |
X-ray structure of fxa in complex with 7-fluoroindazole |
