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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 | December 11, 2024 |
| PDB ID | UniProt ID ▼ | Title | Descriptor |
|---|---|---|---|
| 6THP | P08473 | Neprilysin in complex with the inhibitor (R)-4-(1-carboxy-3-(3'-chlorobiphenyl-4-yl)propan-2-ylamino)-4-oxobutanoic acid | |
| 6GID | P08473 | High resolution crystal structure of substrate-free human neprilysin | |
| 1DMT | P08473 | STRUCTURE OF HUMAN NEUTRAL ENDOPEPTIDASE COMPLEXED WITH PHOSPHORAMIDON | |
| 1R1H | P08473 | STRUCTURAL ANALYSIS OF NEPRILYSIN WITH VARIOUS SPECIFIC AND POTENT INHIBITORS | |
| 1R1I | P08473 | STRUCTURAL ANALYSIS OF NEPRILYSIN WITH VARIOUS SPECIFIC AND POTENT INHIBITORS | Neprilysin (E.C.3.4.24.11) |
| 1R1J | P08473 | STRUCTURAL ANALYSIS OF NEPRILYSIN WITH VARIOUS SPECIFIC AND POTENT INHIBITORS | |
| 1Y8J | P08473 | Crystal Structure of human NEP complexed with an imidazo[4,5-c]pyridine inhibitor | |
| 2QPJ | P08473 | Human NEP complexed with a bifunctional NEP/DPP IV inhibitor | |
| 4CTH | P08473 | Neprilysin variant G399V,G714K in complex with phosphoramidon | |
| 5JMY | P08473 | NEPRILYSIN COMPLEXED WITH LBQ657 | |
| 3PAK | P08427 | Crystal Structure of Rat Surfactant Protein A neck and carbohydrate recognition domain (NCRD) complexed with Mannose | |
| 3PAQ | P08427 | Surfactant Protein A neck and carbohydrate recognition domain (NCRD) complexed with alpha-methylmannose | |
| 4WRF | P08427 | Crystal Structure of Surfactant Protein-A DEDN Mutant (E171D/P175E/R197N/K203D) Complexed with Mannose | |
| 4WUX | P08427 | Crystal Structure of Surfactant Protein-A DED Mutant (E171D/P175E/K203D) Complexed with Mannose | |
| 5MLG | P08424 | Crystal structure of rat prorenin | |
| 3INB | P08362 | Structure of the measles virus hemagglutinin bound to the CD46 receptor | |
| 3A6T | P08337 | Crystal structure of MutT-8-OXO-DGMP complex | |
| 8G24 | P08311 | Crystal Structure of Cathepsin-G and Neutrophil Elastase Inhibited by S. aureus EapH2 at pH 5.5 | |
| 8G26 | P08311 | Crystal Structure of Cathepsin-G and Neutrophil Elastase Inhibited by S. aureus EapH2 at pH 8.5 | |
| 9ASX | P08311 | BIFUNCTIONAL INHIBITION OF NEUTROPHIL ELASTASE AND CATHEPSIN G by Eap3 of S. aureus | |
| 9ATK | P08311 | BIFUNCTIONAL INHIBITION OF NEUTROPHIL ELASTASE AND CATHEPSIN G by Eap4 of S. aureus | |
| 8D4S | P08311 | Crystal Structure of Cathepsin G Inhibited by Eap1 from S. aureus | |
| 3EHB | P08306 | A D-Pathway Mutation Decouples the Paracoccus Denitrificans Cytochrome c Oxidase by Altering the side chain orientation of a distant, conserved Glutamate | |
| 3HB3 | P08306 | High resolution crystal structure of Paracoccus denitrificans cytochrome c oxidase | |
| 7CBK | P08246 | Structure of Human Neutrophil Elastase Ecotin complex | |
| 8G24 | P08246 | Crystal Structure of Cathepsin-G and Neutrophil Elastase Inhibited by S. aureus EapH2 at pH 5.5 | |
| 8G26 | P08246 | Crystal Structure of Cathepsin-G and Neutrophil Elastase Inhibited by S. aureus EapH2 at pH 8.5 | |
| 6E69 | P08246 | Ortho-substituted phenyl sulfonyl fluoride and fluorosulfate as potent elastase inhibitory fragments | |
| 1B0F | P08246 | CRYSTAL STRUCTURE OF HUMAN NEUTROPHIL ELASTASE WITH MDL 101, 146 | |
| 6SMA | P08246 | Crystal structure of Human Neutrophil Elastase (HNE) in complex with the 3-Oxo-beta-Sultam inhibitor LMC249 | |
| 6F5M | P08246 | Crystal structure of highly glycosylated human leukocyte elastase in complex with a thiazolidinedione inhibitor | |
| 1H1B | P08246 | Crystal structure of human neutrophil elastase complexed with an inhibitor (GW475151) | |
| 1PPF | P08246 | X-RAY CRYSTAL STRUCTURE OF THE COMPLEX OF HUMAN LEUKOCYTE ELASTASE (PMN ELASTASE) AND THE THIRD DOMAIN OF THE TURKEY OVOMUCOID INHIBITOR | |
| 1PPG | P08246 | The refined 2.3 angstroms crystal structure of human leukocyte elastase in a complex with a valine chloromethyl ketone inhibitor | |
| 2RG3 | P08246 | Covalent complex structure of elastase | Leukocyte elastase (E.C.3.4.21.37) |
| 2Z7F | P08246 | Crystal structure of the complex of human neutrophil elastase with 1/2SLPI | |
| 3Q76 | P08246 | Structure of human neutrophil elastase (uncomplexed) | |
| 3Q77 | P08246 | Structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor | |
| 4NZL | P08246 | Extracellular proteins of Staphylococcus aureus inhibit the neutrophil serine proteases | |
| 4WVP | P08246 | Crystal structure of an activity-based probe HNE complex | |
| 5A09 | P08246 | Crystal Structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor | |
| 5A0A | P08246 | Crystal Structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor | |
| 5A0B | P08246 | Crystal Structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor | |
| 5A0C | P08246 | Crystal Structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor | |
| 5A8X | P08246 | Crystal Structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor | |
| 5A8Y | P08246 | Crystal Structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor | |
| 5A8Z | P08246 | Crystal Structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor | |
| 5ABW | P08246 | Neutrophil elastase inhibitors for the treatment of (cardio)pulmonary diseases | |
| 7WHU | P08246 | Human Neutrophil Elastase in-complex with Ecotin Peptide | |
| 9ASS | P08246 | Crystal Structure of Neutrophil Elastase Inhibited by Eap4 from S. aureus |
