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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 18, 2024 |
| PDB ID | UniProt ID ▲ | Title | Descriptor |
|---|---|---|---|
| 4WNH | P00740 | Crystal structure of mouse Xyloside xylosyltransferase 1 complexed with manganese,acceptor ligand and UDP-Xylose | |
| 5F84 | P00740 | Crystal structure of Drosophila Poglut1 (Rumi) complexed with its glycoprotein product (glucosylated EGF repeat) and UDP | |
| 8EPH | P00740 | Crystal structure of human coagulation factor IXa (S195A), apo-form, DES-GLA | |
| 2GD4 | P00742 | Crystal Structure of the Antithrombin-S195A Factor Xa-Pentasaccharide Complex | |
| 8EOK | P00742 | Structure of the C3bB proconvertase in complex with lufaxin and factor Xa | |
| 9CTH | P00742 | Preliminary map of the Prothrombin-prothrombinase complex on nano discs | |
| 2XWB | P00746 | Crystal Structure of Complement C3b in complex with Factors B and D | |
| 4A5T | P00747 | STRUCTURAL BASIS FOR THE CONFORMATIONAL MODULATION | |
| 4DUR | P00747 | The X-ray Crystal Structure of Full-Length type II Human Plasminogen | |
| 6QF7 | P00748 | Crystal structures of the recombinant beta-Factor XIIa protease with bound Thr-Arg and Pro-Arg substrate mimetics | |
| 6B77 | P00748 | Structures of the two-chain human plasma factor XIIa co-crystallized with potent inhibitors | |
| 6GT6 | P00748 | Crystal structure of recombinant coagulation factor beta-XIIa | |
| 6L63 | P00748 | Human Coagulation Factor XIIa (FXIIa) bound with the macrocyclic peptide F3 containing two (1S,2S)-2-ACHC residues | |
| 4XE4 | P00748 | Coagulation Factor XII protease domain crystal structure | |
| 6B74 | P00748 | Structures of the two-chain human plasma Factor XIIa co-crystallized with potent inhibitors | |
| 8R8D | P00748 | Cryo-EM structure of coagulation factor beta-XIIa in complex with the garadacimab Fab fragment (symmetric dimer) | |
| 7FBP | P00748 | FXIIa-cMCoFx1 complex | |
| 1URK | P00749 | SOLUTION STRUCTURE OF THE AMINO TERMINAL FRAGMENT OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR | |
| 2FD6 | P00749 | Structure of Human Urokinase Plasminogen Activator in Complex with Urokinase Receptor and an anti-upar antibody at 1.9 A | |
| 2I9B | P00749 | Crystal structure of ATF-urokinase receptor complex | |
| 3BT1 | P00749 | Structure of urokinase receptor, urokinase and vitronectin complex | |
| 3BT2 | P00749 | Structure of urokinase receptor, urokinase and vitronectin complex | |
| 3U73 | P00749 | Crystal structure of stabilized human uPAR mutant in complex with ATF | |
| 4K24 | P00749 | Structure of anti-uPAR Fab ATN-658 in complex with uPAR | |
| 8ENU | P00751 | Structure of the C3bB proconvertase in complex with lufaxin | |
| 6RUR | P00751 | Structure of the SCIN stabilized C3bBb convertase bound to properdin | |
| 6RUV | P00751 | Structure of the SCIN stabilized C3bBb convertase bound to Properdin and a the non-inhibitory nanobody hFPNb1 | |
| 8UIN | P00751 | Structure of the C3bBb-albicin complex | |
| 2OK5 | P00751 | Human Complement factor B | |
| 2WIN | P00751 | C3 convertase (C3bBb) stabilized by SCIN | |
| 2WIN | P00751 | C3 convertase (C3bBb) stabilized by SCIN | |
| 2XWB | P00751 | Crystal Structure of Complement C3b in complex with Factors B and D | |
| 2XWJ | P00751 | Crystal Structure of Complement C3b in Complex with Factor B | |
| 3HRZ | P00751 | Cobra Venom Factor (CVF) in complex with human factor B | |
| 3HS0 | P00751 | Cobra Venom Factor (CVF) in complex with human factor B | |
| 7NOZ | P00751 | Structure of the nanobody stablized properdin bound alternative pathway proconvertase C3b:FB:FP | |
| 8EOK | P00751 | Structure of the C3bB proconvertase in complex with lufaxin and factor Xa | |
| 1SGF | P00756 | CRYSTAL STRUCTURE OF 7S NGF: A COMPLEX OF NERVE GROWTH FACTOR WITH FOUR BINDING PROTEINS (SERINE PROTEINASES) | |
| 1SGF | P00757 | CRYSTAL STRUCTURE OF 7S NGF: A COMPLEX OF NERVE GROWTH FACTOR WITH FOUR BINDING PROTEINS (SERINE PROTEINASES) | |
| 6B6P | P00760 | Orthorhombic trypsin cryocooled to 100 K with 30% xylose as cryoprotectant | |
| 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 | |
| 6AVL | P00760 | Orthorhombic Trypsin (295 K) in the presence of 50% xylose | |
| 6B6Q | P00760 | Orthorhombic trypsin cryocooled to 100 K with 50% xylose as cryoprotectant | |
| 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 | |
| 5TMK | P00797 | Optimization of 3,5-Disubstitued Piperidine: Discovery of Non-Peptide mimetics as an Orally Active Renin Inhibitor | |
| 5SXN | P00797 | Structure-based design of a new series of N-piperidin-3-ylpyrimidine-5-carboxamides as renin inhibitors | |
| 5SY2 | P00797 | Structure-based design of a new series of N-piperidin-3-ylpyrimidine-5-carboxamides as renin inhibitors |
