Search PepX: PDB
Results 1 - 50 of 1431
Results
| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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1A1M | MHC CLASS I MOLECULE B*5301 COMPLEXED WITH PEPTIDE TPYDINQML FROM GAG PROTEIN OF HIV2 | C | A | MHC antigen-recognition domain |
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1A1N | MHC CLASS I MOLECULE B*3501 COMPLEXED WITH PEPTIDE VPLRPMTY FROM THE NEF PROTEIN (75-82) OF HIV1 | C | A | MHC antigen-recognition domain |
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1A1O | MHC CLASS I MOLECULE B*5301 COMPLEXED WITH PEPTIDE LS6 (KPIVQYDNF) FROM THE MALARIA PARASITE P. FALCIPARUM | C | A | MHC antigen-recognition domain |
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1A1R | HCV NS3 PROTEASE DOMAIN:NS4A PEPTIDE COMPLEX | C | DAB | Trypsin-like serine proteases |
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1A2X | COMPLEX OF TROPONIN C WITH A 47 RESIDUE (1-47) FRAGMENT OF TROPONIN I | B | A | EF Hand-like |
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1A3B | COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG1 | I | H |
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1A3E | COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG2 | I | H |
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1A3R | FAB FRAGMENT (ANTIBODY 8F5) COMPLEXED WITH PEPTIDE FROM HUMAN RHINOVIRUS (SEROTYPE 2) VIRAL CAPSID PROTEIN VP2 (RESIDUES 156-170) | P | LH | Immunoglobulin-like beta-sandwich |
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1A46 | THROMBIN COMPLEXED WITH HIRUGEN AND A BETA-STRAND MIMETIC INHIBITOR | L | A |
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1A4W | CRYSTAL STRUCTURES OF THROMBIN WITH THIAZOLE-CONTAINING INHIBITORS: PROBES OF THE S1\' BINDING SITE | L | H |
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1A5G | HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN | L | A |
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1A61 | THROMBIN COMPLEXED WITH A BETA-MIMETIC THIAZOLE-CONTAINING INHIBITOR | L | A |
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1A8K | CRYSTALLOGRAPHIC ANALYSIS OF HUMAN IMMUNODEFICIENCY VIRUS 1 PROTEASE WITH AN ANALOG OF THE CONSERVED CA-P2 SUBSTRATE: INTERACTIONS WITH FREQUENTLY OCCURRING GLUTAMIC ACID RESIDUE AT P2\' POSITION OF SUBSTRATES | C | AB | Acid proteases |
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1A94 | STRUCTURAL BASIS FOR SPECIFICITY OF RETROVIRAL PROTEASES | C | AB | Acid proteases |
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1A9E | DECAMER-LIKE CONFORMATION OF A NANO-PEPTIDE BOUND TO HLA-B3501 DUE TO NONSTANDARD POSITIONING OF THE C-TERMINUS | C | A | MHC antigen-recognition domain |
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1AB9 | CRYSTAL STRUCTURE OF BOVINE GAMMA-CHYMOTRYPSIN | D | CB |
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1ABI | STRUCTURE OF THE HIRULOG 3-THROMBIN COMPLEX AND NATURE OF THE S\' SUBSITES OF SUBSTRATES AND INHIBITORS | L | H |
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1ABJ | STRUCTURE OF THE HIRULOG 3-THROMBIN COMPLEX AND NATURE OF THE S\' SUBSITES OF SUBSTRATES AND INHIBITORS | L | H |
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1ABO | CRYSTAL STRUCTURE OF THE COMPLEX OF THE ABL TYROSINE KINASE SH3 DOMAIN WITH 3BP-1 SYNTHETIC PEPTIDE | C | A | SH3-like barrel |
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1AD8 | COMPLEX OF THROMBIN WITH AND INHIBITOR CONTAINING A NOVEL P1 MOIETY | L | H |
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1AFQ | CRYSTAL STRUCTURE OF BOVINE GAMMA-CHYMOTRYPSIN COMPLEXED WITH A SYNTHETIC INHIBITOR | A | BC |
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1AGB | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGRKKYKL-3R MUTATION) | C | A | MHC antigen-recognition domain |
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1AGC | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKKYQL-7Q MUTATION) | C | A | MHC antigen-recognition domain |
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1AGD | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKKYKL-INDEX PEPTIDE) | C | A | MHC antigen-recognition domain |
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1AGE | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKKYRL-7R MUTATION) | C | A | MHC antigen-recognition domain |
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1AGF | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKRYKL-5R MUTATION) | C | A | MHC antigen-recognition domain |
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1AHT | CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH HIRUGEN AND P-AMIDINOPHENYLPYRUVATE) AT 1.6 ANGSTROMS RESOLUTION | L | H |
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1AI8 | HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH THE EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROMPG | L | H |
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1AIK | HIV GP41 CORE STRUCTURE | C | N | Stalk segment of viral fusion proteins |
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1AIX | HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROVAL | L | H |
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1APM | 2.0 ANGSTROM REFINED CRYSTAL STRUCTURE OF THE CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH A PEPTIDE INHIBITOR AND DETERGENT | I | E | Protein kinase-like (PK-like) |
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1AQC | X11 PTB DOMAIN-10MER PEPTIDE COMPLEX | C | A | PH domain-like barrel |
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1AS4 | CLEAVED ANTICHYMOTRYPSIN A349R | B | A | Serpins |
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1ATP | 2.2 angstrom refined crystal structure of the catalytic subunit of cAMP-dependent protein kinase complexed with MNATP and a peptide inhibitor | I | E |
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1AVF | ACTIVATION INTERMEDIATE 2 OF HUMAN GASTRICSIN FROM HUMAN STOMACH | P | A |
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1AW8 | PYRUVOYL DEPENDENT ASPARTATE DECARBOXYLASE | A | BDE | Double psi beta-barrel |
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1AWF | NOVEL COVALENT THROMBIN INHIBITOR FROM PLANT EXTRACT | L | H |
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1AWI | HUMAN PLATELET PROFILIN COMPLEXED WITH THE L-PRO10 PEPTIDE | P | A | Profilin-like |
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1AWQ | CYPA COMPLEXED WITH HAGPIA (PSEUDO-SYMMETRIC MONOMER) | B | A | Cyclophilin-like |
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1AWU | CYPA COMPLEXED WITH HVGPIA (PSEUDO-SYMMETRIC MONOMER) | B | A | Cyclophilin-like |
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1AY6 | THROMBIN INHIBITOR FROM THEONALLA, CYCLOTHEANAMIDE-BASED MACROCYCLIC TRIPEPTIDE MOTIF | L | H |
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1B07 | CRK SH3 DOMAIN COMPLEXED WITH PEPTOID INHIBITOR | C | A | SH3-like barrel |
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1B0G | CLASS I HISTOCOMPATIBILITY ANTIGEN (HLA-A2.1)/BETA 2-MICROGLOBULIN/PEPTIDE P1049 COMPLEX | C | A | MHC antigen-recognition domain |
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1B5G | HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN | L | H |
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1B7X | STRUCTURE OF HUMAN ALPHA-THROMBIN Y225I MUTANT BOUND TO D-PHE-PRO-ARG-CHLOROMETHYLKETONE | A | B |
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1BA8 | THROMBIN INHIBITOR WITH A RIGID TRIPEPTIDYL ALDEHYDES | A | B |
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1BAI | Crystal structure of Rous sarcoma virus protease in complex with inhibitor | C | A | Acid proteases |
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1BB0 | THROMBIN INHIBITORS WITH RIGID TRIPEPTIDYL ALDEHYDES | A | D |
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1BBR | THE STRUCTURE OF RESIDUES 7-16 OF THE A ALPHA CHAIN OF HUMAN FIBRINOGEN BOUND TO BOVINE THROMBIN AT 2.3 ANGSTROMS RESOLUTION | F | HE |
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1BBZ | CRYSTAL STRUCTURE OF THE ABL-SH3 DOMAIN COMPLEXED WITH A DESIGNED HIGH-AFFINITY PEPTIDE LIGAND: IMPLICATIONS FOR SH3-LIGAND INTERACTIONS | B | A | SH3-like barrel |
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