|
47
|
326
|
7kg4A |
Recombinant beta-2-glycoprotein i antibody recognition loop mutant |
|
124
|
382
|
7pmuA |
Crystal structure of native iripin-8 |
|
64
|
254
|
7phxH |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - acid-stable sulfotyrosine analogue |
|
6
|
29
|
7phxL |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - acid-stable sulfotyrosine analogue |
|
1
|
32
|
7phxI |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - acid-stable sulfotyrosine analogue |
|
69
|
205
|
7a6oA |
Crystal structure of the complex of the recombinant von willebrand factor aim-a1 domain and vhh81 at 2.1 angstrom resolution |
|
29
|
128
|
7a6oB |
Crystal structure of the complex of the recombinant von willebrand factor aim-a1 domain and vhh81 at 2.1 angstrom resolution |
|
51
|
326
|
7jikA |
Human recombinant beta-2-glycoprotein 1 |
|
54
|
326
|
6xsdA |
Patient-derived b2gpi |
|
52
|
326
|
6xstA |
Recombinant beta-2-glycoprotein i with putative membrane insertion loop |
|
69
|
198
|
7f49A |
Von willebrand factor (vwf) a1 domain with bt-100 aptamer rna |
|
9
|
52
|
7ahuD |
Anti-fx fab of mim8 in complex with human fxa |
|
38
|
222
|
7ahuB |
Anti-fx fab of mim8 in complex with human fxa |
|
56
|
235
|
7ahvH |
Anti-fixa fab of mim8 in complex with human fixa |
|
47
|
223
|
7ahvA |
Anti-fixa fab of mim8 in complex with human fixa |
|
43
|
216
|
7ahuA |
Anti-fx fab of mim8 in complex with human fxa |
|
58
|
234
|
7ahuC |
Anti-fx fab of mim8 in complex with human fxa |
|
49
|
214
|
7ahvB |
Anti-fixa fab of mim8 in complex with human fixa |
|
12
|
54
|
7ahvL |
Anti-fixa fab of mim8 in complex with human fixa |
|
58
|
258
|
6x0sA |
Structure of human plasma factor xiia in complex with (2s)-4-(5-chloro-1,3-benzoxazol-2-yl)-1-(n,3-dicyclohexyl-d-alanyl)-n-[(thiophen-2-yl)methyl]piperazine-2-carboxamide (compound 7) |
|
57
|
258
|
6x0tA |
Structure of human plasma factor xiia in complex with (2s)-1-(n,3-dicyclohexyl-d-alanyl)-4-[(4r,5s)-4-methyl-5-phenyl-4,5-dihydro-1,3-oxazol-2-yl]-n-[(thiophen-2-yl)methyl]piperazine-2-carboxamide (compound 8h) |
|
178
|
2196
|
7kvfB |
Cryo-em structure of human factor v at 3.6 angstrom resolution |
|
46
|
651
|
7kxyB |
Cryo-em structure of human factor va at 4.4 angstrom resolution |
|
26
|
128
|
7nmuCCC |
Crystal structure of human platelet glycoprotein vi in complex with an inhibitory nanobody. |
|
69
|
205
|
7a6oAAA |
Crystal structure of the complex of the recombinant von willebrand factor aim-a1 domain and vhh81 at 2.1 angstrom resolution |
|
178
|
2196
|
7kveB |
Cryo-em structure of human factor v at 3.3 angstrom resolution |
|
14
|
182
|
7nmuAAA |
Crystal structure of human platelet glycoprotein vi in complex with an inhibitory nanobody. |
|
29
|
128
|
7a6oBBB |
Crystal structure of the complex of the recombinant von willebrand factor aim-a1 domain and vhh81 at 2.1 angstrom resolution |
|
291
|
1717
|
7kwoA |
Rfviiifc-vwf-xten (bivv001) |
|
90
|
478
|
7kwoV |
Rfviiifc-vwf-xten (bivv001) |
|
46
|
654
|
7kxyA |
Cryo-em structure of human factor va at 4.4 angstrom resolution |
|
48
|
243
|
6l63A |
Human coagulation factor xiia (fxiia) bound with the macrocyclic peptide f3 containing two (1s,2s)-2-achc residues |
|
0
|
17
|
6l63B |
Human coagulation factor xiia (fxiia) bound with the macrocyclic peptide f3 containing two (1s,2s)-2-achc residues |
|
7
|
47
|
6lsqA |
Crystal structure of echistatin, an rgd-containing short disintegrin |
|
1
|
31
|
6tkhI |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - orthorhombic form at 7kev |
|
9
|
31
|
6tkjL |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - tetragonal form at 7kev |
|
8
|
36
|
6tkhL |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - orthorhombic form at 7kev |
|
63
|
258
|
6tklH |
Non-cleavable tsetse thrombin inhibitor in complex with human alpha-thrombin |
|
66
|
258
|
6tkhH |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - orthorhombic form at 7kev |
|
1
|
31
|
6tklI |
Non-cleavable tsetse thrombin inhibitor in complex with human alpha-thrombin |
|
7
|
36
|
6tklL |
Non-cleavable tsetse thrombin inhibitor in complex with human alpha-thrombin |
|
61
|
257
|
6tkjH |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - tetragonal form at 7kev |
|
9
|
30
|
6tkiL |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - tetragonal form at 12.7kev |
|
1
|
31
|
6tkgI |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - orthorhombic form at 12kev |
|
67
|
259
|
6tkgH |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - orthorhombic form at 12kev |
|
8
|
36
|
6tkgL |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - orthorhombic form at 12kev |
|
62
|
259
|
6tkiH |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - tetragonal form at 12.7kev |
|
2
|
27
|
6zuuL |
Crystal structure of thrombin in complex with compound30 |
|
57
|
257
|
6zuuH |
Crystal structure of thrombin in complex with compound30 |
|
2
|
27
|
6zuhL |
Crystal structure of thrombin in complex with compound17 |
