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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 |
|---|---|---|---|
| 6MMN | P35439 | Diheteromeric NMDA receptor GluN1/GluN2A in the '2-Knuckle-Symmetric' conformation, in complex with glycine and glutamate, in the presence of 1 micromolar zinc chloride, and at pH 8.0 | Glutamate receptor ionotropic, NMDA 1, Glutamate receptor ionotropic, NMDA 2A |
| 6WI0 | P35439 | GluN1b-GluN2B NMDA receptor in complex with GluN1 antagonist L689,560, class 2 | Glutamate receptor ionotropic, NMDA 1, Glutamate receptor ionotropic, NMDA 2B |
| 3Q41 | P35439 | Crystal structure of the GluN1 N-terminal domain (NTD) | Glutamate [NMDA] receptor subunit zeta-1 |
| 4PE5 | P35439 | Crystal Structure of GluN1a/GluN2B NMDA Receptor Ion Channel | |
| 6MMV | P35439 | Triheteromeric NMDA receptor GluN1/GluN2A/GluN2A* Extracellular Domain in the '2-Knuckle-Asymmetric' conformation, in complex with glycine and glutamate, in the presence of 1 micromolar zinc chloride, and at pH 7.4 | Glutamate receptor ionotropic, NMDA 1, Glutamate receptor ionotropic, NMDA 2A |
| 6WHS | P35439 | GluN1b-GluN2B NMDA receptor in non-active 1 conformation at 3.95 angstrom resolution | Glutamate receptor ionotropic, NMDA 1, Glutamate receptor ionotropic, NMDA 2B |
| 7YFG | P35439 | Structure of the Rat GluN1-GluN2C NMDA receptor in complex with glycine and glutamate (major class in asymmetry) | |
| 7YFH | P35439 | Structure of the Rat GluN1-GluN2C NMDA receptor in complex with glycine, glutamate and (R)-PYD-106 | |
| 7YFI | P35439 | Structure of the Rat tri-heteromeric GluN1-GluN2A-GluN2C NMDA receptor in complex with glycine and glutamate | |
| 8HDK | P35439 | Structure of the Rat GluN1-GluN2C NMDA receptor in complex with glycine and glutamate (minor class in symmetry) | |
| 9ARF | P35439 | Rat GluN1-GluN2B NMDA receptor channel in complex with glycine, glutamate, and EU-1622-A, in nonactive1 conformation | |
| 9ARH | P35439 | Rat GluN1-GluN2B NMDA receptor channel in complex with glycine | |
| 7SAA | P35439 | Glycine and glutamate bound GluN1a-GluN2B NMDA receptors in non-active 1 conformation at 2.97 Angstrom resolution | |
| 7SAB | P35439 | Phencyclidine-bound GluN1a-GluN2B NMDA receptors | |
| 7SAC | P35439 | S-(+)-ketamine bound GluN1a-GluN2B NMDA receptors at 3.69 Angstrom resolution | |
| 7SAD | P35439 | Memantine-bound GluN1a-GluN2B NMDA receptors | |
| 1YO8 | P35442 | Structure of the C-terminal domain of human thrombospondin-2 | thrombospondin-2 |
| 2RHP | P35442 | The Thrombospondin-1 Polymorphism Asn700Ser Associated with Cornoary Artery Disease Causes Local and Long-Ranging Changes in Protein Structure | |
| 6AEX | P35456 | Crystal structure of unoccupied murine uPAR | |
| 3LAQ | P35456 | Structure-based engineering of species selectivity in the uPA-uPAR interaction | Urokinase-type plasminogen activator (E.C.3.4.21.73), Urokinase plasminogen activator surface receptor |
| 3PBL | P35462 | Structure of the human dopamine D3 receptor in complex with eticlopride | |
| 6I6R | P35475 | New Irreversible a-l-Iduronidase Inhibitors and Activity-Based Probes | |
| 6I6X | P35475 | New Irreversible a-l-Iduronidase Inhibitors and Activity-Based Probes | |
| 3W81 | P35475 | Human alpha-l-iduronidase | Alpha-L-iduronidase (E.C.3.2.1.76) |
| 3W82 | P35475 | Human alpha-L-iduronidase in complex with iduronic acid | |
| 4KGJ | P35475 | Crystal structure of human alpha-L-iduronidase complex with 5-fluoro-alpha-L-idopyranosyluronic acid fluoride | |
| 4KGL | P35475 | Crystal structure of human alpha-L-iduronidase complex with [2R,3R,4R,5S]-2-carboxy-3,4,5-trihydroxy-piperidine | |
| 4KH2 | P35475 | Crystal structure of human alpha-L-iduronidase complex with 2-deoxy-2-fluoro-alpha-L-idopyranosyluronic acid fluoride | |
| 4MJ2 | P35475 | Crystal structure of apo-iduronidase in the R3 form | Alpha-L-iduronidase (E.C.3.2.1.76) |
| 4MJ4 | P35475 | Human iduronidase apo structure P21 form | |
| 4OBR | P35475 | Crystal structure of human alpha-L-iduronidase complex with alpha-L-iduronic acid | |
| 4OBS | P35475 | Crystal structure of human alpha-L-iduronidase in the P212121 form | |
| 7DTD | P35498 | Voltage-gated sodium channel Nav1.1 and beta4 | Sodium channel subunit beta-4, Sodium channel protein type 1 subunit alpha |
| 6AGF | P35499 | Structure of the human voltage-gated sodium channel Nav1.4 in complex with beta1 | Sodium channel protein PaFPC1, Mu-diguetoxin-Dc1a |
| 6E0E | P35557 | Crystal structure of Glucokinase in complex with compound 6 | |
| 6E0I | P35557 | Crystal structure of Glucokinase in complex with compound 72 | |
| 5V4W | P35557 | Human glucokinase in complex with novel indazole activator. | |
| 5V4X | P35557 | Human glucokinase in complex with novel pyrazole activator. | |
| 1V4S | P35557 | Crystal structure of human glucokinase | |
| 3A0I | P35557 | Human glucokinase in complex with a synthetic activator | |
| 3F9M | P35557 | Human pancreatic glucokinase in complex with glucose and activator showing a mobile flap | |
| 3FGU | P35557 | Catalytic complex of Human Glucokinase | |
| 3FR0 | P35557 | Human glucokinase in complex with 2-amino benzamide activator | |
| 3H1V | P35557 | Human glucokinase in complex with a synthetic activator | |
| 3ID8 | P35557 | Ternary complex of human pancreatic glucokinase crystallized with activator, glucose and AMP-PNP | |
| 3IDH | P35557 | Human pancreatic glucokinase in complex with glucose | |
| 3QIC | P35557 | The structure of human glucokinase E339K mutation | |
| 3S41 | P35557 | Glucokinase in complex with activator and glucose | |
| 3VEV | P35557 | Glucokinase in complex with an activator and glucose | |
| 3VEY | P35557 | glucokinase in complex with glucose and ATPgS |
