| Structure Region |
Pdb Id |
Title |
Resolution |
Technique |
|
1EZQ
| crystal structure of human coagulation factor xa complexed with rpr128515 |
2.2 |
x-ray |
|
1F0R
| crystal structure of human coagulation factor xa complexed with rpr208815 |
2.1 |
x-ray |
|
1F0S
| crystal structure of human coagulation factor xa complexed with rpr208707 |
2.1 |
x-ray |
|
1KSN
| crystal structure of human coagulation factor xa complexed with fxv673 |
2.1 |
x-ray |
|
1NFU
| crystal structure of human coagulation factor xa complexed with rpr132747 |
2.05 |
x-ray |
|
1NFW
| crystal structure of human coagulation factor xa complexed with rpr209685 |
2.1 |
x-ray |
|
1NFX
| crystal structure of human coagulation factor xa complexed with rpr208944 |
2.15 |
x-ray |
|
1NFY
| crystal structure of human coagulation factor xa complexed with rpr200095 |
2.1 |
x-ray |
|
1LPG
| crystal structure of fxa in complex with 79. |
2 |
x-ray |
|
1LPK
| crystal structure of fxa in complex with 125. |
2.2 |
x-ray |
|
1LPZ
| crystal structure of fxa in complex with 41. |
2.4 |
x-ray |
|
1LQD
| crystal structure of fxa in complex with 45. |
2.7 |
x-ray |
|
1P0S
| crystal structure of blood coagulation factor xa in complex with ecotin m84r |
2.8 |
x-ray |
|
2BOH
| crystal structure of factor xa in complex with compound "1" |
2.2 |
x-ray |
|
1C5M
| structural basis for selectivity of a small molecule, s1- binding, sub-micromolar inhibitor of urokinase type plasminogen activator |
1.95 |
x-ray |
|
2BQ6
| crystal structure of factor xa in complex with 21 |
3 |
x-ray |
|
2BQ7
| crystal structure of factor xa in complex with 43 |
2.2 |
x-ray |
|
2BQW
| crystal structure of factor xa in complex with compound 45 |
2.95 |
x-ray |
|
1FAX
| coagulation factor xa inhibitor complex |
3 |
x-ray |
|
1HCG
| |
2.2 |
|
|
2BOK
| factor xa - cation |
1.64 |
x-ray |
|
1XKA
| factor xa complexed with a synthetic inhibitor fx-2212a,(2s) -(3'-amidino-3-biphenylyl)-5-(4-pyridylamino)pentanoic acid |
2.3 |
x-ray |
|
1XKB
| factor xa complexed with a synthetic inhibitor fx-2212a,(2s) -(3'-amidino-3-biphenylyl)-5-(4-pyridylamino)pentanoic acid |
2.4 |
x-ray |
|
1G2L
| factor xa inhibitor complex |
1.9 |
x-ray |
|
1G2M
| factor xa inhibitor complex |
3.02 |
x-ray |
|
1IOE
| hunman coagulation factor xa complexd with m55532 |
2.9 |
x-ray |
|
1IQE
| human coagulation factor xa complexd with m55590 |
2.9 |
x-ray |
|
1IQF
| human coagulation factor xa complexd with m55165 |
3.2 |
x-ray |
|
1IQG
| hunman coagulation factor xa complexd with m55159 |
2.6 |
x-ray |
|
1IQH
| hunman coagulation factor xa complexd with m55143 |
3 |
x-ray |
|
1IQI
| hunman coagulation factor xa complexd with m55125 |
2.9 |
x-ray |
|
1IQJ
| hunman coagulation factor xa complexd with m55124 |
3 |
x-ray |
|
1IQK
| hunman coagulation factor xa complexd with m55113 |
3.2 |
x-ray |
|
1IQL
| hunman coagulation factor xa complexd with m54476 |
2.7 |
x-ray |
|
1IQM
| hunman coagulation factor xa complexd with m54471 |
2.6 |
x-ray |
|
1IQN
| human coagulation factor xa complexd with m55192 |
2.6 |
x-ray |
|
1FJS
| crystal structure of the inhibitor zk-807834 (ci-1031) complexed with factor xa |
1.92 |
x-ray |
|
1KYE
| factor xa in complex with (r)-2-(3-adamantan-1-yl-ureido)-3- (3-carbamimidoyl-phenyl)-n-phenethyl-propionamide |
2.22 |
x-ray |
|
1Z6E
| crystal structure of factor xa complexed to razaxaban |
1.8 |
x-ray |
|
2BMG
| crystal structure of factor xa in complex with 50 |
2.7 |
x-ray |
|
1MQ5
| crystal structure of 3-chloro-n-[4-chloro-2-[[(4- chlorophenyl)amino]carbonyl]phenyl]-4-[(4-methyl-1- piperazinyl)methyl]-2-thiophenecarboxamide complexed with human factor xa |
2.1 |
x-ray |
|
1MQ6
| crystal structure of 3-chloro-n-[4-chloro-2-[[(5-chloro-2- pyridinyl)amino]carbonyl]-6-methoxyphenyl]-4-[[(4,5- dihydro-2-oxazolyl)methylamino]methyl]-2- thiophenecarboxamide complexed with human factor xa |
2.1 |
x-ray |
|
1V3X
| factor xa in complex with the inhibitor 1-[6-methyl-4,5,6,7- tetrahydrothiazolo(5,4-c)pyridin-2-yl] carbonyl-2- carbamoyl-4-(6-chloronaphth-2-ylsulphonyl)piperazine |
2.2 |
x-ray |
|
1WU1
| factor xa in complex with the inhibitor 4-[(5-chloroindol-2- yl)sulfonyl]-2-(2-methylpropyl)-1-[[5-(pyridin-4-yl) pyrimidin-2-yl]carbonyl]piperazine |
2.3 |
x-ray |
|
1FXY
| coagulation factor xa-trypsin chimera inhibited with d-phe-pro-arg-chloromethylketone |
2.15 |
x-ray |