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GlycoNAVI Proteins
GlycoNAVI-Proteins is dataset of glycan and protein information. This is the content of GlycoNAVI.
| Source | Last Updated |
|---|---|
| GlycoNAVI Proteins | September 04, 2024 |
| PDB ID | UniProt ID ▲ | Title | Descriptor |
|---|---|---|---|
| 6B6P | P00760 | Orthorhombic trypsin cryocooled to 100 K with 30% xylose as cryoprotectant | Cationic trypsin (E.C.3.4.21.4) |
| 6DZF | P00760 | Orthorhombic trypsin cryocooled to 100 K with 20% xylose as cryoprotectant | |
| 6B6O | P00760 | Orthorhombic trypsin cryocooled to 100 K with 20% xylose as cryoprotectant | Cationic trypsin (E.C.3.4.21.4) |
| 6AVL | P00760 | Orthorhombic Trypsin (295 K) in the presence of 50% xylose | Cationic trypsin (E.C.3.4.21.4) |
| 6B6Q | P00760 | Orthorhombic trypsin cryocooled to 100 K with 50% xylose as cryoprotectant | Cationic trypsin (E.C.3.4.21.4) |
| 1Z7K | P00761 | Crystal Structure of Trypsin- Ovomucoid turkey egg white inhibitor complex | |
| 5V8V | P00797 | Crystal Structure of Human Renin in Complex with a biphenylpipderidinylcarbinol | |
| 5TMG | P00797 | Optimization of 3,5-Disubstitued Piperidine: Discovery of Non-Peptide mimetics as an Orally Active Renin Inhibitor | Renin (E.C.3.4.23.15) |
| 5TMK | P00797 | Optimization of 3,5-Disubstitued Piperidine: Discovery of Non-Peptide mimetics as an Orally Active Renin Inhibitor | Renin (E.C.3.4.23.15) |
| 5SXN | P00797 | Structure-based design of a new series of N-piperidin-3-ylpyrimidine-5-carboxamides as renin inhibitors | Renin (E.C.3.4.23.15) |
| 5SY2 | P00797 | Structure-based design of a new series of N-piperidin-3-ylpyrimidine-5-carboxamides as renin inhibitors | Renin (E.C.3.4.23.15) |
| 5SY3 | P00797 | Structure-based design of a new series of N-piperidin-3-ylpyrimidine-5-carboxamides as renin inhibitors | Renin (E.C.3.4.23.15) |
| 5SZ9 | P00797 | Structure-based design of a new series of N-piperidin-3-ylpyrimidine-5-carboxamides as renin inhibitors | Renin (E.C.3.4.23.15) |
| 5T4S | P00797 | Novel Approach of Fragment-Based Lead Discovery applied to Renin Inhibitors | Renin (E.C.3.4.23.15) |
| 5VPM | P00797 | Crystal Structure of Human Renin in Complex with a biphenylpipderidinylcarbinol | Renin (E.C.3.4.23.15) |
| 5VRP | P00797 | Crystal Structure of Human Renin in Complex with a biphenylpipderidinylcarbinol | Renin (E.C.3.4.23.15) |
| 6I3F | P00797 | Crystal structure of the complex of human angiotensinogen and renin at 2.55 Angstrom | |
| 1HRN | P00797 | HIGH RESOLUTION CRYSTAL STRUCTURES OF RECOMBINANT HUMAN RENIN IN COMPLEX WITH POLYHYDROXYMONOAMIDE INHIBITORS | RENIN COMPLEXED WITH POLYHYDROXYMONOAMIDE INHIBITOR BILA 980 |
| 1RNE | P00797 | THE CRYSTAL STRUCTURE OF RECOMBINANT GLYCOSYLATED HUMAN RENIN ALONE AND IN COMPLEX WITH A TRANSITION STATE ANALOG INHIBITOR | RENIN (ACTIVATED, GLYCOSYLATED, INHIBITED) (E.C.3.4.23.15) COMPLEX WITH CGP 38'560 |
| 2G1N | P00797 | Ketopiperazine-based renin inhibitors: Optimization of the "C" ring | Renin (E.C.3.4.23.15) |
| 2G1O | P00797 | Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring | Renin (E.C.3.4.23.15) |
| 2G1R | P00797 | Ketopiperazine-Based Renin Inhibitors: Optimization of the C Ring | Renin (E.C.3.4.23.15) |
| 2G1S | P00797 | Ketopiperazine-Based Renin Inhibitors: Optimization of the C Ring | Renin (E.C.3.4.23.15) |
| 2G1Y | P00797 | Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring | Renin (E.C.3.4.23.15) |
| 2G22 | P00797 | Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring | Renin (E.C.3.4.23.15) |
| 2REN | P00797 | STRUCTURE OF RECOMBINANT HUMAN RENIN, A TARGET FOR CARDIOVASCULAR-ACTIVE DRUGS, AT 2.5 ANGSTROMS RESOLUTION | RENIN (E.C.3.4.23.15) |
| 2V0Z | P00797 | Crystal Structure of Renin with Inhibitor 10 (Aliskiren) | RENIN (E.C.3.4.23.15) |
| 3G6Z | P00797 | Design and Preparation of Potent, Non-Peptidic, Bioavailable Renin Inhibitors | Renin (E.C.3.4.23.15) |
| 3G70 | P00797 | Design and Preparation of Potent, Non-Peptidic, Bioavailable Renin Inhibitors | Renin (E.C.3.4.23.15) |
| 3G72 | P00797 | Design and Preparation of Potent, Non-Peptidic, Bioavailable Renin Inhibitors | Renin (E.C.3.4.23.15) |
| 3GW5 | P00797 | Crystal structure of human renin complexed with a novel inhibitor | |
| 3K1W | P00797 | New Classes of Potent and Bioavailable Human Renin Inhibitors | Renin (E.C.3.4.23.15) |
| 3KM4 | P00797 | Optimization of Orally Bioavailable Alkyl Amine Renin Inhibitors | |
| 3O9L | P00797 | Design and optimisation of new piperidines as renin inhibitors | Renin (E.C.3.4.23.15), Renin (E.C.3.4.23.15) |
| 3OAD | P00797 | Design and optimization of new piperidines as renin inhibitors | Renin (E.C.3.4.23.15) |
| 3OAG | P00797 | Design and optimization of new piperidines as renin inhibitors | Renin (E.C.3.4.23.15) |
| 3OOT | P00797 | Crystal Structure Analysis of Renin-indole-piperazin inhibitor complexes | Renin (E.C.3.4.23.15) |
| 3OQF | P00797 | Crystal Structure Analysis of Renin-indole-piperazine inhibitor complexes | Renin (E.C.3.4.23.15) |
| 3OQK | P00797 | Crystal Structure Analysis of Renin-indole-piperazin inhibitor complexes | Renin (E.C.3.4.23.15) |
| 3Q3T | P00797 | Alkyl Amine Renin Inhibitors: Filling S1 from S3 | |
| 3Q4B | P00797 | Clinically Useful Alkyl Amine Renin Inhibitors | |
| 3Q5H | P00797 | Clinically Useful Alkyl Amine Renin Inhibitors | |
| 3SFC | P00797 | Structure-Based Optimization of Potent 4- and 6-Azaindole-3-Carboxamides as Renin Inhibitors | Renin (E.C.3.4.23.15) |
| 3VCM | P00797 | Crystal structure of human prorenin | |
| 3VSW | P00797 | Human renin in complex with compound 8 | |
| 3VSX | P00797 | Human renin in complex with compound 18 | |
| 3VUC | P00797 | Human renin in complex with compound 5 | |
| 3VYD | P00797 | Human renin in complex with inhibitor 6 | |
| 3VYE | P00797 | Human renin in complex with inhibitor 7 | |
| 3VYF | P00797 | Human renin in complex with inhibitor 9 |
