3rxv:A    (LYS87) to   (SER240)  CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH BENZAMIDE (F05 AND F03, COCKTAIL EXPERIMENT)  |   TRYPSIN-LIKE SERINE PROTEASES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1ntp:A    (LYS87) to   (VAL235)  USE OF THE NEUTRON DIFFRACTION H/D EXCHANGE TECHNIQUE TO DETERMINE THE CONFORMATIONAL DYNAMICS OF TRYPSIN  |   HYDROLASE (SERINE PROTEINASE) 
1azz:A    (ASP87) to   (GLN241)  FIDDLER CRAB COLLAGENASE COMPLEXED TO ECOTIN  |   COMPLEX (SERINE PROTEASE/INHIBITOR), SERINE PROTEASE, INHIBITOR, COMPLEX, PROTEASE-SUBSTRATE INTERACTIONS, COLLAGEN 
2bdg:A    (GLY79) to   (VAL242)  HUMAN KALLIKREIN 4 COMPLEX WITH NICKEL AND P-AMINOBENZAMIDINE  |   SERINE PROTEINASE, S1 SUBSITE, 70-80 LOOP, STRUCTURAL PROTEOMICS IN EUROPE, SPINE, STRUCTURAL GENOMICS, HYDROLASE 
2bdg:B    (GLY79) to   (ALA244)  HUMAN KALLIKREIN 4 COMPLEX WITH NICKEL AND P-AMINOBENZAMIDINE  |   SERINE PROTEINASE, S1 SUBSITE, 70-80 LOOP, STRUCTURAL PROTEOMICS IN EUROPE, SPINE, STRUCTURAL GENOMICS, HYDROLASE 
2bdi:G    (LEU87) to   (VAL242)  HUMAN KALLIKREIN 4 COMPLEX WITH COBALT AND P- AMINOBENZAMIDINE  |   SERINE PROTEINASE, S1 SUBSITE, 70-80 LOOP, STRUCTURAL PROTEOMICS IN EUROPE, SPINE, STRUCTURAL GENOMICS, HYDROLASE 
4x0l:C   (GLU234) to   (ASN406)  HUMAN HAPTOGLOBIN-HAEMOGLOBIN COMPLEX  |   HAPTOGLOBIN-HAEMOGLOBIN COMPLEX, OXYGEN TRANSPORT 
4x0w:U    (GLU86) to   (THR242)  THE CRYSTAL STRUCTURE OF MUPAIN-1-17 IN COMPLEX WITH MURINISED HUMAN UPA  |   SERINE PROTEASE, PEPTIDIC INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE INHIBITOR-HYDROLASE COMPLEX 
1o2j:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2k:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2l:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2s:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2u:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2w:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o31:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o33:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o35:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3a:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3c:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3f:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3e:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3g:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3m:A    (SER86) to   (ASN245)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3n:A    (SER86) to   (ASN245)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
3s9b:A    (ARG86) to   (GLY244)  RUSSELL'S VIPER VENOM SERINE PROTEINASE, RVV-V (OPEN-FORM)  |   SERINE PROTEINASE, DOUBLE SIX-STRANDED BETA-BARRELS, HYDROLASE, GLYCOSYLATION 
1btu:A    (GLN86) to   (ASN245)  PORCINE PANCREATIC ELASTASE COMPLEXED WITH (3S, 4R)-1- TOLUENESULPHONYL-3-ETHYL-AZETIDIN-2-ONE-4-CARBOXYLIC ACID  |   HYDROLASE, SERINE PROTEINASE, SERINE PROTEASE 
1btx:A    (SER86) to   (VAL235)  EPISELECTION: NOVEL KI ~NANOMOLAR INHIBITORS OF SERINE PROTEASES SELECTED BY BINDING OR CHEMISTRY ON AN ENZYME SURFACE  |   TRIPEPTIDEBORONATE ETHYL ESTER INHIBITED, SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1bty:A    (LYS87) to   (ASN245)  CRYSTAL STRUCTURE OF BETA-TRYPSIN IN COMPLEX WITH BENZAMIDINE  |   BENZAMIDINE INHIBITED, HYDROLASE (SERINE PROTEINASE), HYDROLASE 
1c5q:A    (SER86) to   (VAL235)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1- BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, HYDROLASE 
1c9t:A    (SER86) to   (ASN245)  COMPLEX OF BDELLASTASIN WITH BOVINE TRYPSIN  |   COMPLEX (HYDROLASE/INHIBITOR), HYDROLASE, INHIBITOR, ANTISTASIN, PLASMIN, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1c9t:D    (SER86) to   (SER244)  COMPLEX OF BDELLASTASIN WITH BOVINE TRYPSIN  |   COMPLEX (HYDROLASE/INHIBITOR), HYDROLASE, INHIBITOR, ANTISTASIN, PLASMIN, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1op2:A    (LYS86) to   (GLY244)  CRYSTAL STRUCTURE OF AAV-SP-II, A GLYCOSYLATED SNAKE VENOM SERINE PROTEINASE FROM AGKISTRODON ACUTUS  |   SNAKE VENOM, SERINE PROTEINASE, GLYCOPROTEIN, AGKISTRODON ACUTUS, HYDROLASE 
1op8:C    (LYS87) to   (ALA245)  CRYSTAL STRUCTURE OF HUMAN GRANZYME A  |   GRANZYME A, SERINE PROTEINASE, APOPTOSIS, HYDROLASE 
1oss:A    (THR86) to   (ALA235)  T190P STREPTOMYCES GRISEUS TRYPSIN IN COMPLEX WITH BENZAMIDINE  |   TRYPSIN, SERINE PROTEASE, MUTANT, HYDROLASE 
1p2i:A    (SER86) to   (ASN245)  STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON- COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN  |   TRYPSIN; CHYMOTRYPSIN; SERINE PROTEINASE; BOVINE PANCREATIC TRYPSIN INHIBITOR; PROTEIN-PROTEIN INTERACTION; NON-COGNATE BINDING; S1 POCKET; PRIMARY SPECIFICITY; CRYSTAL STRUCTURE, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1p2k:A    (SER86) to   (ASN245)  STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON- COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN  |   TRYPSIN; CHYMOTRYPSIN; SERINE PROTEINASE; BOVINE PANCREATIC TRYPSIN INHIBITOR; PROTEIN-PROTEIN INTERACTION; NON-COGNATE BINDING; S1 POCKET; PRIMARY SPECIFICITY; CRYSTAL STRUCTURE, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
2qxj:A    (ALA80) to   (ARG246)  CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 7 IN COMPLEX WITH SUC- ALA-ALA-PRO-PHE-CHLOROMETHYLKETONE AND COPPER  |   COPPER, HISTIDINE LIGANDS, CATALYTIC TRIAD HIS, ALTERNATIVE SPLICING, GLYCOPROTEIN, HYDROLASE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN 
2rdl:A    (GLU86) to   (ASN245)  HAMSTER CHYMASE 2  |   CHYMASE 2, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3tvj:B   (GLU515) to   (PHE686)  CATALYTIC FRAGMENT OF MASP-2 IN COMPLEX WITH ITS SPECIFIC INHIBITOR DEVELOPED BY DIRECTED EVOLUTION ON SGCI SCAFFOLD  |   IN VITRO EVOLUTION, SPECIFIC INHIBITOR, ALLOSTERY, HYDROLASE 
1fdp:B    (ARG87) to   (ALA243)  PROENZYME OF HUMAN COMPLEMENT FACTOR D, RECOMBINANT PROFACTOR D  |   SERINE PROTEASE, COMPLEMENT, FACTOR D, PROFACTOR D, ZYMOGEN, PROENZYME, HYDROLASE 
1fdp:C    (ARG87) to   (LEU242)  PROENZYME OF HUMAN COMPLEMENT FACTOR D, RECOMBINANT PROFACTOR D  |   SERINE PROTEASE, COMPLEMENT, FACTOR D, PROFACTOR D, ZYMOGEN, PROENZYME, HYDROLASE 
1fdp:D    (ARG87) to   (ALA243)  PROENZYME OF HUMAN COMPLEMENT FACTOR D, RECOMBINANT PROFACTOR D  |   SERINE PROTEASE, COMPLEMENT, FACTOR D, PROFACTOR D, ZYMOGEN, PROENZYME, HYDROLASE 
4k1e:A    (GLY79) to   (ALA244)  ATOMIC RESOLUTION CRYSTAL STRUCTURES OF KALLIKREIN-RELATED PEPTIDASE 4 COMPLEXED WITH A MODIFIED SFTI INHIBITOR FCQR  |   PROTEIN-PEPTIDE COMPLEX, BOWMAN-BIRK INHIBITOR, PROTEASE, PROTEASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4yta:A    (LYS87) to   (ASN245)  BOND LENGTH ANALYSIS OF ASP, GLU AND HIS RESIDUES IN TRYPSIN AT 1.2A RESOLUTION  |   SERINE PROTEASE, HYDROLASE 
4k8y:A    (GLY79) to   (ALA244)  ATOMIC RESOLUTION CRYSTAL STRUCTURES OF KALLIKREIN-RELATED PEPTIDASE 4 COMPLEXED WITH SUNFLOWER TRYPSIN INHIBITOR (SFTI-1)  |   BOWMAN-BIRK INHIBITOR, PROTEASE, PROTEASE INHIBITOR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
4kel:A    (GLY79) to   (ALA244)  ATOMIC RESOLUTION CRYSTAL STRUCTURE OF KALLIKREIN-RELATED PEPTIDASE 4 COMPLEXED WITH A MODIFIED SFTI INHIBITOR FCQR(N)  |   BOWMAN-BIRK INHIBITOR, PROTEASE, PROTEASE INHIBITOR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3unr:A    (LYS87) to   (ASN245)  BOND LENGTH ANALYSIS OF ASP, GLU AND HIS RESIDUES IN TRYPSIN AT 1.2A RESOLUTION  |   SERINE PROTEASE, HYDROLASE 
2fi3:E    (SER86) to   (ASN245)  CRYSTAL STRUCTURE OF A BPTI VARIANT (CYS14->SER, CYS38->SER) IN COMPLEX WITH TRYPSIN  |   PROTEASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2fi4:E    (SER86) to   (ASN245)  CRYSTAL STRUCTURE OF A BPTI VARIANT (CYS14->SER) IN COMPLEX WITH TRYPSIN  |   PROTEASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2fi5:E    (SER86) to   (ASN245)  CRYSTAL STRUCTURE OF A BPTI VARIANT (CYS38->SER) IN COMPLEX WITH TRYPSIN  |   PROTEASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2fmj:A    (THR86) to   (ALA235)  220-LOOP MUTANT OF STREPTOMYCES GRISEUS TRYPSIN  |   TRYPSIN, SERINE PROTEASE, HYDROLASE 
1gi2:A    (LYS87) to   (VAL235)  A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI- CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, HYDROLASE 
1gi6:A    (SER86) to   (VAL235)  A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI- CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, HYDROLASE 
2ftl:E    (SER86) to   (ASN245)  CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH BPTI AT 100K  |   PROTEASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3i77:A    (THR86) to   (LEU245)  35/99/170-LOOPS OF FXA IN SGT  |   BETA SHEETS, SERINE PROTEASE, HYDROLASE, DISULFIDE BOND, PROTEASE, ZYMOGEN 
4o3t:A   (GLN569) to   (ILE719)  ZYMOGEN HGF-BETA/MET WITH ZYMOGEN ACTIVATOR PEPTIDE ZAP.14  |   TRYPSIN HOMOLOGY, RECEPTOR ACTIVATION, TRANSFERASE-GROWTH FACTOR COMPLEX 
3a8b:A    (LYS87) to   (SER240)  CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-4-((4- BROMOPHENYLIMINO)METHYL)BENZIMIDAMIDE  |   IN-CRYSTAL CHEMICAL LIGATION, DISULFIDE BOND, HYDROLASE, METAL- BINDING, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN 
3atk:A    (SER86) to   (ASN241)  CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH CYCLOHEPTANAMINE  |   HYDROLASE, SERINE PROTEASE, PROTEIN, INHIBITOR, BOVINE PANCREAS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3beu:B    (THR86) to   (LEU245)  NA+-DEPENDENT ALLOSTERY MEDIATES COAGULATION FACTOR PROTEASE ACTIVE SITE SELECTIVITY  |   BETA SHEETS, SERINE PROTEASE, HYDROLASE, ZYMOGEN 
4bnr:B    (SER86) to   (ASN242)  EXTREMELY STABLE COMPLEX OF CRAYFISH TRYPSIN WITH BOVINE TRYPSIN INHIBITOR  |   HYDOLASE-INHIBITOR COMPLEX, PROTEASE, INHIBITION, ARTHROPODA, HEAT STABILITY, COMPLEX FORMATION 
4cbn:A    (LEU73) to   (ALA228)  CRYSTAL STRUCTURE OF COMPLEMENT FACTOR D MUTANT R202A AFTER CONVENTIONAL REFINEMENT  |   HYDROLASE, COMPLEMENT SYSTEM, ENSEMBLE REFINEMENT 
4dva:U    (GLU86) to   (LYS243)  THE CRYSTAL STRUCTURE OF HUMAN UROKINASE-TYPE PLASMINOGEN ACTIVATOR CATALYTIC DOMAIN  |   HYDROLASE, PLASMINOGEN ACTIVATION, PROTEASE, SERINE PROTEASE 
4fuc:A    (ALA93) to   (THR245)  CRYSTAL STRUCTURE OF THE UROKINASE  |   HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4fug:A    (ALA94) to   (LYS247)  CRYSTAL STRUCTURE OF THE UROKINASE  |   HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4fuh:A    (ALA93) to   (THR245)  CRYSTAL STRUCTURE OF THE UROKINASE  |   HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
5tcc:E    (LEU88) to   (ALA243)  COMPLEMENT FACTOR D INHIBITED WITH JH4  |   SERINE PROTEASE, INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2o9q:A    (SER86) to   (ASN241)  THE CRYSTAL STRUCTURE OF BOVINE TRYPSIN COMPLEXED WITH A SMALL INHIBITION PEPTIDE ORB2K  |   TRYPSIN, INHIBITOR, PEPTIDE, HYDROLASE 
1o2o:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o36:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o38:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3b:A    (SER86) to   (VAL235)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1os8:A    (THR86) to   (ALA235)  RECOMBINANT STREPTOMYCES GRISEUS TRYPSIN  |   TRYPSIN, SERINE PROTEASE, HYDROLASE 
4iw4:E   (ARG519) to   (GLY697)  CRYSTAL STRUCTURE OF THE SERINE PROTEASE DOMAIN OF MASP-3 IN COMPLEX WITH ECOTIN  |   TRYPSIN-LIKE FOLD, PROTEASE, INHIBITOR, EXTRACELLULAR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3uqv:A    (LYS87) to   (ASN245)  BOVINE TRYPSIN VARIANT X(TRIPLEPHE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR  |   TRYPSIN-LIKE SERINE PROTEASE, HYDROLASE, PROTEIN BINDING, DUODENUM, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1w12:U    (GLU86) to   (THR242)  UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   UROKINASE, HYDROLASE, PLASMINOGEN ACTIVATOR 
4fu9:A    (ALA93) to   (THR245)  CRYSTAL STRUCTURE OF THE UROKINASE  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX