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