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Showing 1-50 of 81 results
PDB Identifier Description Ligand Receptor SCOP pdb.org
2QOS Crystal structure of complement protein C8 in complex with a peptide containing the C8 binding site on C8 A C
2R0L Short Form HGFA with Inhibitory Fab75 B A
2R2M 2-(2-Chloro-6-Fluorophenyl)Acetamides as Potent Thrombin Inhibitors H B
2RFX Crystal Structure of HLA-B*5701, presenting the self peptide, LSSPVTKSF C A MHC antigen-recognition domain
2RIV Crystal structure of the reactive loop cleaved human Thyroxine Binding Globulin B A
2RIW The Reactive loop cleaved human Thyroxine Binding Globulin complexed with thyroxine B A
2RKY Crystal structure of the fourth and fifth fibronectin F1 modules in complex with a fragment of staphylococcus aureus fnbpa-1 D BAC FnI-like domain
2UUF THROMBIN-HIRUGEN BINARY COMPLEX AT 1.26A RESOLUTION A B
2VLJ THE STRUCTURAL DYNAMICS AND ENERGETICS OF AN IMMUNODOMINANT T-CELL RECEPTOR ARE PROGRAMMED BY ITS VBETA DOMAIN C DEA Immunoglobulin-like beta-sandwich
2VLK THE STRUCTURAL DYNAMICS AND ENERGETICS OF AN IMMUNODOMINANT T-CELL RECEPTOR ARE PROGRAMMED BY ITS VBETA DOMAIN C DEA Immunoglobulin-like beta-sandwich
2VLL THE STRUCTURAL DYNAMICS AND ENERGETICS OF AN IMMUNODOMINANT T-CELL RECEPTOR ARE PROGRAMMED BY ITS VBETA DOMAIN C A MHC antigen-recognition domain
2VLR THE STRUCTURAL DYNAMICS AND ENERGETICS OF AN IMMUNODOMINANT T-CELL RECEPTOR ARE PROGRAMMED BY ITS VBETA DOMAIN C DEA Immunoglobulin-like beta-sandwich
2VR3 STRUCTURAL AND BIOCHEMICAL CHARACTERIZATION OF FIBRINOGEN BINDING TO CLFA FROM STAPHYLOCCCUS AUREUS C BA
2VU8 CRYSTAL STRUCTURE OF AN INSECT INHIBITOR WITH A FUNGAL TRYPSIN I E
2ZC9 Thrombin in complex with Inhibitor L H
2ZDA Exploring Thrombin S1 pocket L H
2ZDV Exploring Thrombin S1 pocket L H
2ZF0 Exploring Thrombin S1 Pocket L H
2ZFF Exploring Thrombin S1-pocket L H
2ZFP Thrombin Inibition L H
2ZFQ Exploring thrombin S3 pocket L H
2ZFR Exploring thrombin S3 pocket L H
2ZG0 Exploring thrombin S3 pocket L H
2ZGB Thrombin Inhibition L H
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
2ZGX Thrombin Inhibition L H
2ZHE Exploring thrombin S3 pocket L H
2ZHF Exploring thrombin S3 pocket L H
2ZHQ Thrombin Inhibition L H
2ZHW Exploring thrombin S3 pocket L H
2ZI2 Thrombin Inhibition L H
2ZIQ Thrombin Inhibition L H
2ZNK Thrombin Inhibition L H
2ZO3 Bisphenylic Thrombin Inhibitors L H
3BEF Crystal structure of thrombin bound to the extracellular fragment of PAR1 C B
3BEV 11mer Structure of an MHC class I molecule from B21 chickens illustrate promiscuous peptide binding C A
3BF6 Thrombin:suramin complex 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
3BO8 The High Resolution Crystal Structure of HLA-A1 Complexed with the MAGE-A1 Peptide C A
3BP4 The high resolution crystal structure of HLA-B*2705 in complex with a Cathepsin A signal sequence peptide pCatA C A
3BP7 The high resolution crystal structure of HLA-B*2709 in complex with a Cathepsin A signal sequence peptide, pCatA C A
3BV9 Structure of Thrombin Bound to the Inhibitor FM19 A B
3BW9 Crystal Structure of HLA B*3508 in complex with a HCMV 12-mer peptide from the pp65 protein C A MHC antigen-recognition domain
3BWA Crystal Structure of HLA B*3508 in complex with a HCMV 8-mer peptide from the pp65 protein C A MHC antigen-recognition domain
3BZF The human non-classical major histocompatibility complex molecule HLA-E P A MHC antigen-recognition domain
3C27 Cyanofluorophenylacetamides as Orally Efficacious Thrombin Inhibitors H B
3C4M Structure of human parathyroid hormone in complex with the extracellular domain of its G-protein-coupled receptor (PTH1R) C A