Found 2629 chains in Genus chains table. Displaying 1151 - 1200. Applied filters: Proteins

Search results query: Thrombin, subunit H

Total Genus Sequence Length pdb Title
56 223 2zhdA Exploring trypsin s3 pocket
48 242 2za5A Crystal structure of human tryptase with potent non-peptide inhibitor
59 258 2zo3H Bisphenylic thrombin inhibitors
86 305 2z9kA Complex structure of sars-cov 3c-like protease with jmf1600
91 306 2z3cA A mechanistic view of enzyme inhibition and peptide hydrolysis in the active site of the sars-cov 3c-like peptidase
59 258 2zffH Exploring thrombin s1-pocket
53 237 2zckP Crystal structure of a ternary complex between psa, a substrat-acyl intermediate and an activating antibody
42 218 2z7fE Crystal structure of the complex of human neutrophil elastase with 1/2slpi
56 257 2zhwH Exploring thrombin s3 pocket
51 231 2zgcA Crystal structure of active human granzyme m
52 237 2zclP Crystal structure of human prostate specific antigen complexed with an activating antibody
58 258 2zc9H Thrombin in complex with inhibitor
47 237 2zchP Crystal structure of human prostate specific antigen complexed with an activating antibody
50 231 2zksA Structural insights into the proteolytic machinery of apoptosis-inducing granzyme m
57 258 2zgxH Thrombin inhibition
55 258 2zfpH Thrombin inibition
59 258 2zfrH Exploring thrombin s3 pocket
57 223 2zdkA Exploring trypsin s3 pocket
60 258 2zhqH Thrombin inhibition
64 309 2z9iA Crystal structure of rv0983 from mycobacterium tuberculosis- proteolytically active form
88 306 2z3dA A mechanistic view of enzyme inhibition and peptide hydrolysis in the active site of the sars-cov 3c-like peptidase
58 257 2zhfH Exploring thrombin s3 pocket
58 258 2zgbH Thrombin inhibition
53 242 2zecA Potent, nonpeptide inhibitors of human mast cell tryptase
58 258 2zdaH Exploring thrombin s1 pocket
57 257 2zi2H Thrombin inhibition
12 74 2ymsD Structure and assembly of a b-propeller with nine blades and a new conserved repetitive sequence motif
44 228 2yolA West nile virus ns2b-ns3 protease in complex with 3,4- dichlorophenylacetyl-lys-lys-gcma
14 74 2ymsB Structure and assembly of a b-propeller with nine blades and a new conserved repetitive sequence motif
12 75 2ymsC Structure and assembly of a b-propeller with nine blades and a new conserved repetitive sequence motif
84 306 2ynaA Crystal structure of the main protease of coronavirus hku4
87 306 2ynbA Crystal structure of the main protease of coronavirus hku4 in complex with a michael acceptor sg85
63 234 2y7zA Structure and property based design of factor xa inhibitors: pyrrolidin-2-ones with aminoindane and phenylpyrrolidine p4 motifs
52 245 2y6tA Molecular recognition of chymotrypsin by the serine protease inhibitor ecotin from yersinia pestis
65 234 2y80A Structure and property based design of factor xa inhibitors: pyrrolidin-2-ones with aminoindane and phenylpyrrolidine p4 motifs
39 182 2xyaA Non-covalent inhibtors of rhinovirus 3c protease.
61 234 2y7xA The discovery of potent and long-acting oral factor xa inhibitors with tetrahydroisoquinoline and benzazepine p4 motifs
48 228 2xwbI Crystal structure of complement c3b in complex with factors b and d
62 234 2y82A Structure and property based design of factor xa inhibitors: pyrrolidin-2-ones with aminoindane and phenylpyrrolidine p4 motifs
62 233 2y5fA Factor xa - cation inhibitor complex
60 228 2xw9A Crystal structure of complement factor d mutant s183a
58 228 2xwaA Crystal structure of complement factor d mutant r202a
55 223 2xttB Bovine trypsin in complex with evolutionary enhanced schistocerca gregaria protease inhibitor 1 (sgpi-1-p02)
64 233 2y5hA Factor xa - cation inhibitor complex
62 233 2y81A Structure and property based design of factor xa inhibitors: pyrrolidin-2-ones with aminoindane and phenylpyrrolidine p4 motifs
63 233 2y5gA Factor xa - cation inhibitor complex
102 354 2xxlA Crystal structure of drosophila grass clip serine protease of toll pathway
92 548 2xrcA Human complement factor i
61 234 2xbyA Factor xa in complex with a pyrrolidine-3,4-dicarboxylic acid inhibitor
35 181 2xniA Protein-ligand complex of a novel macrocyclic hcv ns3 protease inhibitor derived from amino cyclic boronates