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Annotation 'Hydrolase'

Showing 1-50 of 231 results
PDB Identifier Description Ligand Receptor SCOP pdb.org
8PCH CRYSTAL STRUCTURE OF PORCINE CATHEPSIN H DETERMINED AT 2.1 ANGSTROM RESOLUTION: LOCATION OF THE MINI-CHAIN C-TERMINAL CARBOXYL GROUP DEFINES CATHEPSIN H AMINOPEPTIDASE FUNCTION P A
7KME CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN INHIBITED WITH SEL2711. L H
4VGC GAMMA-CHYMOTRYPSIN D-NAPHTHYL-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX A CB
3VGC GAMMA-CHYMOTRYPSIN L-NAPHTHYL-1-ACETAMIDO BORONIC ACID ACID INHIBITOR COMPLEX A CB
3HKI Crystal structure of murine thrombin mutant W215A/E217A in complex with the extracellular fragment of human PAR1 F E
3HBV PrtC methionine mutants: M226A in-house Z P
3HDA PrtC methionine mutants: M226A_DESY Z P
3HK3 Crystal structure of murine thrombin mutant W215A/E217A (one molecule in the asymmetric unit) A B
3GZE Algal prolyl 4-hydroxylase complexed with zinc and (Ser-Pro)5 peptide substrate X A
3GME Crystal Structure of Polynucleotide Phosphorylase in complex with RNase E and manganese D A
3GIC Structure of thrombin mutant delta(146-149e) in the free form A B
3GCM Crystal Structure of E. coli polynucleotide phosphorylase bound to RNA and RNase E D A
3GCI Crystal Structure of the Complex Formed Between a New Isoform of Phospholipase A2 with C-terminal Amyloid Beta Heptapeptide at 2 A Resolution P A
3G94 Further refinement of botulinum neurotoxin type B catalytic domain with synaptobrevin-II bound C BA
3FIE Crystal structure of Clostridium botulinum neurotoxin serotype F catalytic domain with an inhibitor (inh1) C A
3FII Crystal structure of Clostridium botulinum neurotoxin serotype F catalytic domain with an inhibitor (inh2) B A
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
3FG5 Crystal structure determination of a ternary complex of phospholipase A2 with a pentapetide FLSYK and Ajmaline at 2.5 A resolution C A
3EYD Structure of HCV NS3-4A Protease with an Inhibitor Derived from a Boronic Acid D BCA
3F2O Crystal Structure of human splA/ryanodine receptor domain and SOCS box containing 1 (SPSB1) in complex with a 20-residue VASA peptide D B
3EGK KNOBLE Inhibitor L H
3EDQ Crystal structure of Caspase-3 with inhibitor AC-LDESD-CHO E AB
3DUX Understanding Thrombin Inhibition L H
3DT0 Understanding Thrombin Inhibition L H
3DDA Crystal structure of the catalytic domain of Botulinum neurotoxin serotype a with a snap-25 peptide B A
3DDB Crystal structure of the catalytic domain of Botulinum neurotoxin serotype a with a substrate analog peptide B A
3DHK Bisphenylic Thrombin Inhibitors L H
3DA9 Crystal structure of thrombin in complex with inhibitor A B
3D9T CIAP1-BIR3 in complex with N-terminal peptide from Caspase-9 (ATPFQE) C A Inhibitor of apoptosis (IAP) repeat
3C27 Cyanofluorophenylacetamides as Orally Efficacious Thrombin Inhibitors H B
3BV9 Structure of Thrombin Bound to the Inhibitor FM19 A B
3BRH Protein Tyrosine Phosphatase PTPN-22 (Lyp) bound to the mono-Phosphorylated Lck active site peptide C A
3BP7 The high resolution crystal structure of HLA-B*2709 in complex with a Cathepsin A signal sequence peptide, pCatA C A
3BP4 The high resolution crystal structure of HLA-B*2705 in complex with a Cathepsin A signal sequence peptide pCatA C A
3BG4 The crystal structure of guamerin in complex with chymotrypsin and the development of an elastase-specific inhibitor A CB
3BF6 Thrombin:suramin complex L H
3BEF Crystal structure of thrombin bound to the extracellular fragment of PAR1 C B
2ZGH Crystal Structure of active granzyme M bound to its product B A
2ZGJ Crystal Structure of D86N-GzmM Complexed with Its Optimal Synthesized Substrate B A
2ZC9 Thrombin in complex with Inhibitor L H
2WAY STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3-FDF PEPTIDE B A
2WAX STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3-FDF PEPTIDE B A
2W73 HIGH-RESOLUTION STRUCTURE OF THE COMPLEX BETWEEN CALMODULIN AND A PEPTIDE FROM CALCINEURIN A K ABF
2W10 MONA SH3C IN COMPLEX C B
2VU8 CRYSTAL STRUCTURE OF AN INSECT INHIBITOR WITH A FUNGAL TRYPSIN I E
2VGC GAMMA-CHYMOTRYPSIN D-PARA-CHLORO-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX A CB
2V3O THROMBIN WITH 3-CYCLE WITH F I H
2V3H THROMBIN WITH 3-CYCLE NO F I H
2V2F CRYSTAL STRUCTURE OF PBP1A FROM DRUG-RESISTANT STRAIN 5204 FROM STREPTOCOCCUS PNEUMONIAE A F
2UUF THROMBIN-HIRUGEN BINARY COMPLEX AT 1.26A RESOLUTION A B
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