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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 ▼ |
|---|---|---|---|
| 3OVN | Q72498 | Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase | |
| 3OVQ | Q96AT9 | Crystal Structure of hRPE and D-Ribulose-5-Phospate Complex | |
| 3OVR | Q96AT9 | Crystal Structure of hRPE and D-Xylulose 5-Phosphate Complex | |
| 3OVW | P46237 | ENDOGLUCANASE I NATIVE STRUCTURE | |
| 3OXH | P0A5N8 | Mycobacterium tuberculosis kinase inhibitor homolog RV0577 | |
| 3P13 | Q2G1A5 | Complex Structure of D-ribose Pyranase Sa240 with D-ribose | |
| 3P17 | P00734 | Thrombin Inhibition by Pyridin Derivatives | |
| 3P17 | P09945 | Thrombin Inhibition by Pyridin Derivatives | |
| 3P4W | Q7NDN8 | Structure of desflurane bound to a pentameric ligand-gated ion channel, GLIC | |
| 3P50 | Q7NDN8 | Structure of propofol bound to a pentameric ligand-gated ion channel, GLIC | |
| 3P5K | P47811 | P38 inhibitor-bound | |
| 3P5S | Q9TTF5 | Structural insights into the catalytic mechanism of CD38: Evidence for a conformationally flexible covalent enzyme-substrate complex | |
| 3P6Z | P00734 | Structural basis of thrombin mediated factor V activation: essential role of the hirudin-like sequence Glu666-Glu672 for processing at the heavy chain-B domain junction | |
| 3P6Z | P12259 | Structural basis of thrombin mediated factor V activation: essential role of the hirudin-like sequence Glu666-Glu672 for processing at the heavy chain-B domain junction | |
| 3P70 | P00734 | Structural basis of thrombin-mediated factor V activation: essential role of the hirudin-like sequence Glu666-Glu672 for processing at the heavy chain-B domain junction | |
| 3P70 | P12259 | Structural basis of thrombin-mediated factor V activation: essential role of the hirudin-like sequence Glu666-Glu672 for processing at the heavy chain-B domain junction | |
| 3P78 | P47811 | P38 inhibitor-bound | |
| 3P79 | P47811 | P38 inhibitor-bound | |
| 3P7A | P47811 | p38 inhibitor-bound | |
| 3P7B | P47811 | p38 inhibitor-bound | |
| 3P7C | P47811 | p38 inhibitor-bound | |
| 3P7H | Q9UJ71 | Structure of the human Langerin carbohydrate recognition domain in complex with maltose | |
| 3PA1 | Q5F4T5 | Crystal Structure of P Domain from Norwalk Virus Strain Vietnam 026 in complex with HBGA type A | |
| 3PA2 | Q5F4T5 | Crystal Structure of P Domain from Norwalk Virus Strain Vietnam 026 in complex with HBGA type Ley | |
| 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 | |
| 3PBL | P00720 | Structure of the human dopamine D3 receptor in complex with eticlopride | |
| 3PBL | P35462 | Structure of the human dopamine D3 receptor in complex with eticlopride | |
| 3PCV | Q16873 | Crystal structure analysis of human leukotriene C4 synthase at 1.9 angstrom resolution | |
| 3PDF | P53634 | Discovery of Novel Cyanamide-Based Inhibitors of Cathepsin C | |
| 3PEQ | Q03181 | PPARd complexed with a phenoxyacetic acid partial agonist | |
| 3PFJ | Q8TFL9 | Crystal structure of Cel7A from Talaromyces emersonii | |
| 3PFX | Q8TFL9 | Crystal structure of Cel7A from Talaromyces emersonii in complex with cellobiose | |
| 3PFZ | Q8TFL9 | Crystal structure of Cel7A from Talaromyces emersonii in complex with cellotetraose | |
| 3PG3 | Q16539 | Human p38 MAP Kinase in Complex with RL182 | |
| 3PGB | Q5B038 | Crystal structure of Aspergillus nidulans amine oxidase | |
| 3PGF | P0AEX9 | Crystal structure of maltose bound MBP with a conformationally specific synthetic antigen binder (sAB) | |
| 3PGF | P0DOX5 | Crystal structure of maltose bound MBP with a conformationally specific synthetic antigen binder (sAB) | |
| 3PGF | 3PGF | Crystal structure of maltose bound MBP with a conformationally specific synthetic antigen binder (sAB) | |
| 3PGF | P0DOX5 | Crystal structure of maltose bound MBP with a conformationally specific synthetic antigen binder (sAB) | |
| 3PGF | 3PGF | Crystal structure of maltose bound MBP with a conformationally specific synthetic antigen binder (sAB) | |
| 3PGF | Q8TCD0 | Crystal structure of maltose bound MBP with a conformationally specific synthetic antigen binder (sAB) | |
| 3PGF | Q8TCD0 | Crystal structure of maltose bound MBP with a conformationally specific synthetic antigen binder (sAB) | |
| 3PGH | Q05769 | CYCLOOXYGENASE-2 (PROSTAGLANDIN SYNTHASE-2) COMPLEXED WITH A NON-SELECTIVE INHIBITOR, FLURBIPROFEN | |
| 3PH3 | A3DIL8 | Clostridium thermocellum Ribose-5-Phosphate Isomerase B with d-ribose | |
| 3PH4 | A3DIL8 | Clostridium thermocellum Ribose-5-Phosphate Isomerase B with d-allose | |
| 3PHA | A5ZY13 | The crystal structure of the W169Y mutant of alpha-glucosidase (gh31 family) from Ruminococcus obeum atcc 29174 in complex with acarbose | |
| 3PHZ | Q75WT9 | Crystal Structure Analysis of Polyporus squamosus lectin bound to human-type influenza-binding epitope Neu5Aca2-6Galb1-4GlcNAc | |
| 3PIJ | A2TLS9 | beta-fructofuranosidase from Bifidobacterium longum - complex with fructose | |
| 3PL3 | Q8TFL9 | Crystal structure of Cel7A from Talaromyces emersonii in complex with cellopentaose |
