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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 |
|---|---|---|---|
| 7XTG | P0A311 | Cryo-EM structure of Listeria monocytogenes man-PTS complexed with pediocin PA-1 | |
| 7XNO | P0A310 | Cryo-EM structure of the bacteriocin-receptor-immunity ternary complex from Lactobacillus sakei | |
| 7EZZ | P0A232 | Crystal structure of Salmonella typhi outer membrane phospholipase (OMPLA) dimer with bound calcium | |
| 5LDF | P0A1P7 | Maltose binding protein genetically fused to dodecameric glutamine synthetase | |
| 6CKL | P0A0Z8 | N. meningitidis CMP-sialic acid synthetase in the presence of CMP and Neu5Ac2en | |
| 2JG1 | P0A0B9 | STRUCTURE OF Staphylococcus aureus D-TAGATOSE-6-PHOSPHATE KINASE with cofactor and substrate | TAGATOSE-6-PHOSPHATE KINASE (E.C.2.7.1.144) |
| 2JG1 | P0A0B9 | STRUCTURE OF Staphylococcus aureus D-TAGATOSE-6-PHOSPHATE KINASE with cofactor and substrate | TAGATOSE-6-PHOSPHATE KINASE (E.C.2.7.1.144) |
| 1MJT | P0A004 | CRYSTAL STRUCTURE OF SANOS, A BACTERIAL NITRIC OXIDE SYNTHASE OXYGENASE PROTEIN, IN COMPLEX WITH NAD+ AND SEITU | |
| 8DMH | P09991 | Lymphocytic choriomeningitis virus glycoprotein in complex with neutralizing antibody M28 | |
| 8DMI | P09991 | Lymphocytic choriomeningitis virus glycoprotein | |
| 7O1U | P09958 | X-ray structure of furin in complex with the guanylhydrazone-based inhibitor 1 (BEV241) | |
| 7O1W | P09958 | X-ray structure of furin in complex with the guanylhydrazone-based inhibitor 2 (mi307) soaked at 1 M NaCl | |
| 7O1Y | P09958 | X-ray structure of furin in complex with the guanylhydrazone-based inhibitor 2 (mi307) soaked at 0.25 M NaCl | |
| 7O20 | P09958 | X-ray structure of furin in complex with the guanylhydrazone-based inhibitor 3 (mi300) | |
| 7O22 | P09958 | X-ray structure of furin in complex with the guanylhydrazone-based inhibitor 4 (mi359) | |
| 7QY0 | P09958 | X-ray structure of furin in complex with the dichlorophenylpyridine-based inhibitor 1 | |
| 7QY1 | P09958 | X-ray structure of furin in complex with the dichlorophenylpyridine-based inhibitor 4 | |
| 7QY2 | P09958 | X-ray structure of furin in complex with the dichlorophenylpyridine-based inhibitor 2 | |
| 5JMO | P09958 | X-ray structure of furin in complex with the inhibitory antibody Nb14 | |
| 8B4V | P09958 | X-ray structure of furin (PCSK3) in complex with benzamidine | |
| 8B4W | P09958 | X-ray structure of furin (PCSK3) in complex with 1H-isoindol-3-amine | |
| 6GBW | P09945 | Thrombin in complex with MI2100 ((S)-N-(2-(aminomethyl)-5-chlorobenzyl)-1-((benzylsulfonyl)-L-arginyl)pyrrolidine-2-carboxamide) | |
| 6YSJ | P09945 | Thrombin in complex with 2-amino-1-(4-bromophenyl)ethan-1-one (j10) | |
| 6HSX | P09945 | Thrombin in Complex with a D-Phe-Pro-diaminopyridine derivative | |
| 6YQV | P09945 | Thrombin in complex with 5-chlorothiophene-2-sulfonamide (j94) | |
| 6YHG | P09945 | Thrombin in complex with D-Phe-Pro-m-methoxybenzylamide derivative (16a) | |
| 6ROT | P09945 | Thrombin in complex with MI2105 | |
| 6T3M | P09945 | Thrombin in Complex with a D-Phe-Pro-p-phenol derivative | |
| 6T3Q | P09945 | Thrombin in Complex with a D-Phe-Pro-2-aminopyridine derivative | |
| 6T4A | P09945 | Thrombin in Complex with a D-Phe-Pro-p-aminopyridine derivative | |
| 6T52 | P09945 | Thrombin in Complex with a D-Phe-Pro-imidazole derivative | |
| 6T53 | P09945 | Thrombin in Complex with a D-Phe-Pro-p-benzylamine derivative | |
| 6T54 | P09945 | Thrombin in Complex with a D-Phe-Pro-2-bromothiophene Derivative | |
| 6T55 | P09945 | Thrombin in Complex with Methylbenzylamine | |
| 6T56 | P09945 | Thrombin in Complex with Benzylamine | |
| 6T57 | P09945 | Thrombin in Complex with a D-Phe-Pro-N-amidinopiperidine Derivative | |
| 6T89 | P09945 | 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 | P09945 | Thrombin in complex with diphenyl ((4-carbamimidoylphenyl)((S)-1-((R)-3-cyclohexyl 2-((phenylmethyl)sulfonamido)propanoyl)pyrrolidine-2-carboxamido)methyl)phosphonate (MI-492) | |
| 6TDT | P09945 | Thrombin in Complex with a D-DiPhe-Pro-p-pyridine derivative | |
| 6Y02 | P09945 | Thrombin in complex with 13k | |
| 6Y9H | P09945 | Thrombin in complex with D-Phe-Pro-m-Trifluoromethylbenzylamide derivative (phe2) | |
| 6ZGO | P09945 | Thrombin in complex with D-Phe-Pro-2-chlorofuran derivative (13l) | |
| 6YSX | P09945 | Thrombin in complex with 4-amino-N-(5-methylisoxazol-3-yl)benzenesulfonamide (j80) | |
| 6YB6 | P09945 | Thrombin in complex with D-Phe-Pro-3-chloro-1,3-dihydroxybenzylamide derivative (13c) | |
| 6YHJ | P09945 | Thrombin in complex with D-Phe-Pro-2-chlorothiophen derivative (16e) | |
| 6I51 | P09945 | Thrombin in complex with fragment J02 | Prothrombin (E.C.3.4.21.5), Hirudin variant-2 |
| 6YMP | P09945 | Thrombin in complex with 3-((5-(tert-butyl)isoxazol-3-yl)methyl)oxetan-3-amine (j54) | |
| 6YN3 | P09945 | Thrombin in complex with 4-hydroxybenzamide (j89) | |
| 1DOJ | P09945 | Crystal structure of human alpha-thrombin*RWJ-51438 complex at 1.7 A | |
| 1K21 | P09945 | HUMAN THROMBIN-INHIBITOR COMPLEX | Prothrombin (E.C.3.4.21.5), Hirudin variant-2 |
