 |
1B7X |
STRUCTURE OF HUMAN ALPHA-THROMBIN Y225I MUTANT BOUND TO D-PHE-PRO-ARG-CHLOROMETHYLKETONE |
A |
B |
|
|
 |
1DIT |
COMPLEX OF A DIVALENT INHIBITOR WITH THROMBIN |
L |
H |
|
|
 |
1DPJ |
THE STRUCTURE OF PROTEINASE A COMPLEXED WITH IA3 PEPTIDE INHIBITOR |
B |
A |
Acid proteases |
|
 |
1EKB |
THE SERINE PROTEASE DOMAIN OF ENTEROPEPTIDASE BOUND TO INHIBITOR VAL-ASP-ASP-ASP-ASP-LYS-CHLOROMETHANE |
A |
B |
Trypsin-like serine proteases |
|
 |
1F2S |
CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN BOVINE BETA-TRYPSIN AND MCTI-A, A TRYPSIN INHIBITOR OF SQUASH FAMILY AT 1.8 A RESOLUTION |
I |
E |
Trypsin-like serine proteases |
|
 |
1G0V |
THE STRUCTURE OF PROTEINASE A COMPLEXED WITH A IA3 MUTANT, MVV |
B |
A |
Acid proteases |
|
 |
1G9I |
CRYSTAL STRUCTURE OF BETA-TRYSIN COMPLEX IN CYCLOHEXANE |
I |
E |
Trypsin-like serine proteases |
|
 |
1GG6 |
CRYSTAL STUCTURE OF GAMMA CHYMOTRYPSIN WITH N-ACETYL-PHENYLALANINE TRIFLUOROMETHYL KETONE BOUND AT THE ACTIVE SITE |
A |
CB |
|
|
 |
1GGD |
CRYSTAL STUCTURE OF GAMMA CHYMOTRYPSIN WITH N-ACETYL-LEUCIL-PHENYLALANINE ALDEHYDE BOUND AT THE ACTIVE SITE |
A |
CB |
|
|
 |
1MT7 |
Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral therapy |
P |
A |
Acid proteases |
|
 |
1MT8 |
Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral therapy |
P |
A |
Acid proteases |
|
 |
1QUR |
HUMAN ALPHA-THROMBIN IN COMPLEX WITH BIVALENT, BENZAMIDINE-BASED SYNTHETIC INHIBITOR |
I |
H |
|
|
 |
1SBW |
CRYSTAL STRUCTURE OF MUNG BEAN INHIBITOR LYSINE ACTIVE FRAGMENT COMPLEX WITH BOVINE BETA-TRYPSIN AT 1.8A RESOLUTION |
I |
A |
Trypsin-like serine proteases |
|
 |
1TMT |
CHANGES IN INTERACTIONS IN COMPLEXES OF HIRUDIN DERIVATIVES AND HUMAN ALPHA-THROMBIN DUE TO DIFFERENT CRYSTAL FORMS |
J |
H |
|
|
 |
2A2X |
Orally Active Thrombin Inhibitors in Complex with Thrombin Inh12 |
L |
H |
|
|
 |
2ANK |
orally active thrombin inhibitors in complex with thrombin and an exosite decapeptide |
L |
H |
|
|
 |
2BTC |
BOVINE TRYPSIN IN COMPLEX WITH SQUASH SEED INHIBITOR (CUCURBITA PEPO TRYPSIN INHIBITOR II) |
I |
E |
Trypsin-like serine proteases |
|
 |
2F91 |
1.2A resolution structure of a crayfish trypsin complexed with a peptide inhibitor, SGTI |
B |
A |
Trypsin-like serine proteases |
|
 |
2FEQ |
orally active thrombin inhibitors |
L |
H |
|
|
 |
2FES |
Orally active thrombin inhibitors |
L |
H |
|
|
 |
2STA |
ANIONIC SALMON TRYPSIN IN COMPLEX WITH SQUASH SEED INHIBITOR (CUCURBITA MAXIMA TRYPSIN INHIBITOR I) |
I |
E |
Trypsin-like serine proteases |
|
 |
2STB |
ANIONIC SALMON TRYPSIN IN COMPLEX WITH SQUASH SEED INHIBITOR (CUCURBITA PEPO TRYPSIN INHIBITOR II) |
I |
E |
Trypsin-like serine proteases |
|
 |
2ZFQ |
Exploring thrombin S3 pocket |
L |
H |
|
|
 |
2ZFR |
Exploring thrombin S3 pocket |
L |
H |
|
|
 |
2ZG0 |
Exploring thrombin S3 pocket |
L |
H |
|
|
 |
2ZHE |
Exploring thrombin S3 pocket |
L |
H |
|
|
 |
2ZHF |
Exploring thrombin S3 pocket |
L |
H |
|
|
 |
2ZHW |
Exploring thrombin S3 pocket |
L |
H |
|
|
 |
3BG4 |
The crystal structure of guamerin in complex with chymotrypsin and the development of an elastase-specific inhibitor |
A |
CB |
|
|
 |
3BIU |
Human thrombin-in complex with UB-THR10 |
L |
H |
|
|
 |
3BIV |
Human thrombin-in complex with UB-THR11 |
L |
H |
|
|
 |
3FP7 |
Anionic trypsin variant S195A in complex with bovine pancreatic trypsin inhibitor (BPTI) cleaved at the scissile bond (LYS15-ALA16) determined to the 1.46 A resolution limit |
I |
JE |
|
|