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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 | March 05, 2025 |
| PDB ID | UniProt ID ▲ | Title | Descriptor |
|---|---|---|---|
| 4V45 | P00722 | E. COLI (lacZ) BETA-GALACTOSIDASE-TRAPPED 2-F-GALACTOSYL-ENZYME INTERMEDIATE | |
| 5A1A | P00722 | 2.2 A resolution cryo-EM structure of beta-galactosidase in complex with a cell-permeant inhibitor | |
| 3OB8 | P00723 | Structure of the beta-galactosidase from Kluyveromyces lactis in complex with galactose | |
| 7CEL | P00725 | CBH1 (E217Q) IN COMPLEX WITH CELLOHEXAOSE AND CELLOBIOSE | |
| 1CEL | P00725 | THE THREE-DIMENSIONAL CRYSTAL STRUCTURE OF THE CATALYTIC CORE OF CELLOBIOHYDROLASE I FROM TRICHODERMA REESEI | |
| 6CEL | P00725 | CBH1 (E212Q) CELLOPENTAOSE COMPLEX | |
| 1Q2E | P00725 | CELLOBIOHYDROLASE CEL7A WITH LOOP DELETION 245-252 AND BOUND NON-HYDROLYSABLE CELLOTETRAOSE | |
| 3CEL | P00725 | ACTIVE-SITE MUTANT E212Q DETERMINED AT PH 6.0 WITH CELLOBIOSE BOUND IN THE ACTIVE SITE | |
| 5CEL | P00725 | CBH1 (E212Q) CELLOTETRAOSE COMPLEX | |
| 1CPY | P00729 | SITE-DIRECTED MUTAGENESIS ON (SERINE) CARBOXYPEPTIDASE Y FROM YEAST. THE SIGNIFICANCE OF THR 60 AND MET 398 IN HYDROLYSIS AND AMINOLYSIS REACTIONS | |
| 1WPX | P00729 | Crystal structure of carboxypeptidase Y inhibitor complexed with the cognate proteinase | |
| 1YSC | P00729 | 2.8 ANGSTROMS STRUCTURE OF YEAST SERINE CARBOXYPEPTIDASE | |
| 6C2W | P00734 | Crystal structure of human prothrombin mutant S101C/A470C | |
| 6GBW | P00734 | Thrombin in complex with MI2100 ((S)-N-(2-(aminomethyl)-5-chlorobenzyl)-1-((benzylsulfonyl)-L-arginyl)pyrrolidine-2-carboxamide) | |
| 6YSJ | P00734 | Thrombin in complex with 2-amino-1-(4-bromophenyl)ethan-1-one (j10) | |
| 6ZUH | P00734 | Crystal Structure of Thrombin in complex with compound17 | |
| 6ZUU | P00734 | Crystal structure of Thrombin in complex with compound30 | |
| 7NTU | P00734 | X-ray structure of the complex between human alpha thrombin and two duplex/quadruplex aptamers: NU172 and HD22_27mer | |
| 8ASE | P00734 | Crystal structure of Thrombin in complex with macrocycle T3 | |
| 6FJT | P00734 | 4-chloro-benzamidine in complex with thrombin | |
| 6GWE | P00734 | Crystal structure of Thrombin bound to P2 macrocycle | |
| 6HSX | P00734 | Thrombin in Complex with a D-Phe-Pro-diaminopyridine derivative | |
| 6P9U | P00734 | Crystal structure of human thrombin mutant W215A | |
| 6YQV | P00734 | Thrombin in complex with 5-chlorothiophene-2-sulfonamide (j94) | |
| 7SR9 | P00734 | Human alpha-thrombin with 180- and 220- loops replaced with homologous loops from protein C | |
| 6TKI | P00734 | Tsetse thrombin inhibitor in complex with human alpha-thrombin - tetragonal form at 12.7keV | |
| 6YHG | P00734 | Thrombin in complex with D-Phe-Pro-m-methoxybenzylamide derivative (16a) | |
| 6ZUN | P00734 | Crystal Structure of Thrombin in complex with compound20a | |
| 5TO3 | P00734 | Crystal structure of thrombin mutant W215A/E217A fused to EGF456 of thrombomodulin via a 31-residue linker and bound to PPACK | |
| 6EVV | P00734 | X-ray structure of the complex between human alpha thrombin and NU172, a duplex/quadruplex 26-mer DNA aptamer, in the presence of potassium ions. | |
| 1AE8 | P00734 | HUMAN ALPHA-THROMBIN INHIBITION BY EOC-D-PHE-PRO-AZALYS-ONP | |
| 1AFE | P00734 | HUMAN ALPHA-THROMBIN INHIBITION BY CBZ-PRO-AZALYS-ONP | |
| 1BA8 | P00734 | THROMBIN INHIBITOR WITH A RIGID TRIPEPTIDYL ALDEHYDES | |
| 6PX5 | P00734 | CRYSTAL STRUCTURE OF HUMAN MEIZOTHROMBIN DESF1 MUTANT S195A bound with PPACK | |
| 6PXQ | P00734 | Crystal structure of human thrombin mutant D194A | |
| 6ROT | P00734 | Thrombin in complex with MI2105 | |
| 6T3M | P00734 | Thrombin in Complex with a D-Phe-Pro-p-phenol derivative | |
| 6T3Q | P00734 | Thrombin in Complex with a D-Phe-Pro-2-aminopyridine derivative | |
| 6T4A | P00734 | Thrombin in Complex with a D-Phe-Pro-p-aminopyridine derivative | |
| 6T52 | P00734 | Thrombin in Complex with a D-Phe-Pro-imidazole derivative | |
| 6T53 | P00734 | Thrombin in Complex with a D-Phe-Pro-p-benzylamine derivative | |
| 6T54 | P00734 | Thrombin in Complex with a D-Phe-Pro-2-bromothiophene Derivative | |
| 6T55 | P00734 | Thrombin in Complex with Methylbenzylamine | |
| 6T56 | P00734 | Thrombin in Complex with Benzylamine | |
| 6T57 | P00734 | Thrombin in Complex with a D-Phe-Pro-N-amidinopiperidine Derivative | |
| 6T7H | P00734 | Crystal structure of Thrombin in complex with macrocycle N14-PR4-A | |
| 6T89 | P00734 | Thrombin in complex with (S)-N-(tert-butyl)-4-(3-(3-carbamimidoylphenyl)-2-((2',4'-dimethoxy-[1,1'-biphenyl])-3-sulfonamido)propanoyl)piperazine-1-carboxamide (MI-498) | |
| 6T8A | P00734 | Thrombin in complex with diphenyl ((4-carbamimidoylphenyl)((S)-1-((R)-3-cyclohexyl 2-((phenylmethyl)sulfonamido)propanoyl)pyrrolidine-2-carboxamido)methyl)phosphonate (MI-492) | |
| 6TDT | P00734 | Thrombin in Complex with a D-DiPhe-Pro-p-pyridine derivative | |
| 6TKG | P00734 | Tsetse thrombin inhibitor in complex with human alpha-thrombin - orthorhombic form at 12keV |
