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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 |
|---|---|---|---|
| 6TKL | P00734 | Non-cleavable tsetse thrombin inhibitor in complex with human alpha-thrombin | |
| 6Y02 | P00734 | Thrombin in complex with 13k | |
| 6Y9H | P00734 | Thrombin in complex with D-Phe-Pro-m-Trifluoromethylbenzylamide derivative (phe2) | |
| 6ZGO | P00734 | Thrombin in complex with D-Phe-Pro-2-chlorofuran derivative (13l) | |
| 6ZUX | P00734 | Crystal Structure of Thrombin in complex with compound42a | |
| 6BJR | P00734 | Crystal structure of prothrombin mutant S101C/A470C | |
| 6YSX | P00734 | Thrombin in complex with 4-amino-N-(5-methylisoxazol-3-yl)benzenesulfonamide (j80) | |
| 6EO6 | P00734 | X-ray structure of the complex between human alpha-thrombin and modified 15-mer DNA aptamer containing 5-(3-(2-(1H-indol-3-yl)acetamide-N-yl)-1-propen-1-yl)-2'-deoxyuridine residue | |
| 6GN7 | P00734 | X-ray structure of the complex between human alpha thrombin and NU172, a duplex/quadruplex 26-mer DNA aptamer, in the presence of sodium ions. | |
| 6TKH | P00734 | Tsetse thrombin inhibitor in complex with human alpha-thrombin - orthorhombic form at 7keV | |
| 6TKJ | P00734 | Tsetse thrombin inhibitor in complex with human alpha-thrombin - tetragonal form at 7keV | |
| 6YB6 | P00734 | Thrombin in complex with D-Phe-Pro-3-chloro-1,3-dihydroxybenzylamide derivative (13c) | |
| 6YHJ | P00734 | Thrombin in complex with D-Phe-Pro-2-chlorothiophen derivative (16e) | |
| 6ZUG | P00734 | Crystal Structure of Thrombin in complex with compound10 | |
| 6ZV8 | P00734 | Crystal Structure of Thrombin in complex with compound51 | |
| 6CYM | P00734 | Reversible Covalent Direct Thrombin Inhibitors | |
| 6EO7 | P00734 | X-ray structure of the complex between human alpha-thrombin and modified 15-mer DNA aptamer containing 5-(3-(acetamide-N-yl)-1-propen-1-yl)-2'-deoxyuridine residue | |
| 6I51 | P00734 | Thrombin in complex with fragment J02 | |
| 6YMP | P00734 | Thrombin in complex with 3-((5-(tert-butyl)isoxazol-3-yl)methyl)oxetan-3-amine (j54) | |
| 6YN3 | P00734 | Thrombin in complex with 4-hydroxybenzamide (j89) | |
| 7MJ5 | P00734 | complex of human thrombin with XC-43 | |
| 1D3D | P00734 | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZOTHIOPHENE INHIBITOR 4 | |
| 1D3P | P00734 | CRYSTAL STRUCTURE OF HUMAN APLHA-THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 3 | |
| 1D3Q | P00734 | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 2 | |
| 1D3T | P00734 | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 1 | |
| 1D4P | P00734 | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH 5-AMIDINOINDOLE-4-BENZYLPIPERIDINE INHIBITOR | |
| 1DOJ | P00734 | Crystal structure of human alpha-thrombin*RWJ-51438 complex at 1.7 A | |
| 1DX5 | P00734 | Crystal structure of the thrombin-thrombomodulin complex | |
| 1HAG | P00734 | THE ISOMORPHOUS STRUCTURES OF PRETHROMBIN2, HIRUGEN-AND PPACK-THROMBIN: CHANGES ACCOMPANYING ACTIVATION AND EXOSITE BINDING TO THROMBIN | |
| 1HAH | P00734 | THE ISOMORPHOUS STRUCTURES OF PRETHROMBIN2, HIRUGEN-AND PPACK-THROMBIN: CHANGES ACCOMPANYING ACTIVATION AND EXOSITE BINDING TO THROMBIN | |
| 1HAI | P00734 | THE ISOMORPHOUS STRUCTURES OF PRETHROMBIN2, HIRUGEN-AND PPACK-THROMBIN: CHANGES ACCOMPANYING ACTIVATION AND EXOSITE BINDING TO THROMBIN | |
| 1JMO | P00734 | Crystal Structure of the Heparin Cofactor II-S195A Thrombin Complex | |
| 1JOU | P00734 | Crystal Structure of Native S195A Thrombin with an Unoccupied Active Site | |
| 1K21 | P00734 | HUMAN THROMBIN-INHIBITOR COMPLEX | |
| 1K22 | P00734 | HUMAN THROMBIN-INHIBITOR COMPLEX | |
| 1MH0 | P00734 | Crystal structure of the anticoagulant slow form of thrombin | |
| 1NO9 | P00734 | Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies. | |
| 1OOK | P00734 | Crystal Structure of the Complex of Platelet Receptor GPIb-alpha and Human alpha-Thrombin | |
| 1P8V | P00734 | CRYSTAL STRUCTURE OF THE COMPLEX OF PLATELET RECEPTOR GPIB-ALPHA AND ALPHA-THROMBIN AT 2.6A | |
| 1RD3 | P00734 | 2.5A Structure of Anticoagulant Thrombin Variant E217K | |
| 1RIW | P00734 | Thrombin in complex with natural product inhibitor Oscillarin | Prothrombin (E.C.3.4.21.5)/Hirudin IIB |
| 1SFQ | P00734 | Fast form of thrombin mutant R(77a)A bound to PPACK | |
| 1SG8 | P00734 | Crystal structure of the procoagulant fast form of thrombin | |
| 1SGI | P00734 | Crystal structure of the anticoagulant slow form of thrombin | |
| 1SHH | P00734 | Slow form of Thrombin Bound with PPACK | |
| 1SR5 | P00734 | ANTITHROMBIN-ANHYDROTHROMBIN-HEPARIN TERNARY COMPLEX STRUCTURE | |
| 1TB6 | P00734 | 2.5A Crystal Structure of the Antithrombin-Thrombin-Heparin Ternary Complex | |
| 1TMT | P00734 | CHANGES IN INTERACTIONS IN COMPLEXES OF HIRUDIN DERIVATIVES AND HUMAN ALPHA-THROMBIN DUE TO DIFFERENT CRYSTAL FORMS | |
| 1TMU | P00734 | Changes in interactions in complexes of hirudin derivatives and human alpha-thrombin due to different crystal forms | |
| 1TQ7 | P00734 | Crystal structure of the anticoagulant thrombin mutant W215A/E217A bound to PPACK |
