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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 |
|---|---|---|---|
| 2V5Y | P28827 | Crystal structure of the receptor protein tyrosine phosphatase mu ectodomain | |
| 8A16 | P28827 | Human PTPRM domains FN3-4, in spacegroup P212121 | |
| 8A17 | P28827 | Human PTPRM domains FN3-4, in spacegroup P3221 | |
| 8OM2 | P28817 | Small subunit of yeast mitochondrial ribosome in complex with METTL17/Rsm22. | |
| 8OM3 | P28817 | Small subunit of yeast mitochondrial ribosome in complex with IF3/Aim23. | |
| 8OM4 | P28817 | Small subunit of yeast mitochondrial ribosome. | |
| 8T8R | P28799 | Sortilin-PGRN peptide complex | |
| 8T8S | P28799 | Sortilin-PGRN peptide complex | |
| 8OM2 | P28778 | Small subunit of yeast mitochondrial ribosome in complex with METTL17/Rsm22. | |
| 8OM3 | P28778 | Small subunit of yeast mitochondrial ribosome in complex with IF3/Aim23. | |
| 8OM4 | P28778 | Small subunit of yeast mitochondrial ribosome. | |
| 5D28 | P28773 | Complex of GM-CSF/IL-2 inhibition factor with Granulocyte-macrophage colony-stimulating factor | |
| 3NDZ | P28623 | The structure of the catalytic and carbohydrate binding domain of endoglucanase D from Clostridium cellulovorans bound to cellotriose | |
| 6D67 | P28562 | Crystal structure of the human dual specificity phosphatase 1 catalytic domain (C258S) as a maltose binding protein fusion (maltose bound form) in complex with the designed AR protein mbp3_16 | |
| 5AHG | P28511 | Thrombin in complex with ((4-chlorophenyl)sulfamoyl))diemethylamine | |
| 4AZ2 | P28509 | Human thrombin - inhibitor complex | |
| 4AYV | P28508 | Human thrombin - inhibitor complex | |
| 1VIT | P28507 | THROMBIN:HIRUDIN 51-65 COMPLEX | |
| 1RIW | P28506 | Thrombin in complex with natural product inhibitor Oscillarin | |
| 4AYY | P28506 | Human thrombin - inhibitor complex | |
| 1HAG | P28505 | THE ISOMORPHOUS STRUCTURES OF PRETHROMBIN2, HIRUGEN-AND PPACK-THROMBIN: CHANGES ACCOMPANYING ACTIVATION AND EXOSITE BINDING TO THROMBIN | |
| 6ZUH | P28504 | Crystal Structure of Thrombin in complex with compound17 | |
| 6ZUU | P28504 | Crystal structure of Thrombin in complex with compound30 | |
| 6ZUN | P28504 | Crystal Structure of Thrombin in complex with compound20a | |
| 6ZUX | P28504 | Crystal Structure of Thrombin in complex with compound42a | |
| 6ZUG | P28504 | Crystal Structure of Thrombin in complex with compound10 | |
| 6ZV8 | P28504 | Crystal Structure of Thrombin in complex with compound51 | |
| 1TMT | P28504 | CHANGES IN INTERACTIONS IN COMPLEXES OF HIRUDIN DERIVATIVES AND HUMAN ALPHA-THROMBIN DUE TO DIFFERENT CRYSTAL FORMS | |
| 1TWX | P28504 | Crystal structure of the thrombin mutant D221A/D222K | |
| 4UD9 | P28504 | Thrombin in complex with 5-chlorothiophene-2-carboxamide | |
| 5AFY | P28504 | Thrombin in complex with 3-chloro-benzamide | |
| 5AFZ | P28504 | Thrombin in complex with (2R)-2-(benzylsulfonylamino)-N-(2-((4- carbamimidoylphenyl)methylamino)-2-oxo-propyl)-3-phenyl-propanamide | |
| 6ZUW | P28504 | Crystal Structure of Thrombin in complex with compound40 | |
| 6ZV7 | P28504 | Crystal Structure of Thrombin in complex with compound42b | |
| 1AE8 | P28501 | HUMAN ALPHA-THROMBIN INHIBITION BY EOC-D-PHE-PRO-AZALYS-ONP | |
| 1AFE | P28501 | HUMAN ALPHA-THROMBIN INHIBITION BY CBZ-PRO-AZALYS-ONP | |
| 1D3D | P28501 | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZOTHIOPHENE INHIBITOR 4 | |
| 1D3P | P28501 | CRYSTAL STRUCTURE OF HUMAN APLHA-THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 3 | |
| 1D3Q | P28501 | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 2 | |
| 1D3T | P28501 | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 1 | |
| 1D4P | P28501 | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH 5-AMIDINOINDOLE-4-BENZYLPIPERIDINE INHIBITOR | |
| 1NO9 | P28501 | Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies. | |
| 1UMA | P28501 | ALPHA-THROMBIN (HIRUGEN) COMPLEXED WITH NA-(N,N-DIMETHYLCARBAMOYL)-ALPHA-AZALYSINE | |
| 6A96 | P28472 | Cryo-EM structure of the human alpha5beta3 GABAA receptor in complex with GABA and Nb25 | |
| 6HUJ | P28472 | CryoEM structure of human full-length heteromeric alpha1beta3gamma2L GABA(A)R in complex with picrotoxin, GABA and megabody Mb38. | |
| 6HUK | P28472 | CryoEM structure of human full-length alpha1beta3gamma2L GABA(A)R in complex with bicuculline and megabody Mb38. | |
| 8PVB | P28472 | Structure of GABAAR determined by cryoEM at 100 keV | |
| 7A5V | P28472 | CryoEM structure of a human gamma-aminobutyric acid receptor, the GABA(A)R-beta3 homopentamer, in complex with histamine and megabody Mb25 in lipid nanodisc | |
| 7QN5 | P28472 | Cryo-EM structure of human full-length extrasynaptic alpha4beta3delta GABA(A)R in complex with nanobody Nb25 | |
| 7QN6 | P28472 | Cryo-EM structure of human full-length beta3delta GABA(A)R in complex with nanobody Nb25 |
