Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
GlycoNAVI Proteins
GlycoNAVI-Proteins is dataset of glycan and protein information. This is the content of GlycoNAVI.
| Source | Last Updated |
|---|---|
| GlycoNAVI Proteins | November 28, 2024 |
| PDB ID | UniProt ID ▲ | Title | Descriptor |
|---|---|---|---|
| 2C10 | Q16853 | The structure of a truncated, soluble version of semicarbazide- sensitive amine oxidase | |
| 2C11 | Q16853 | Crystal structure of the 2-hydrazinopyridine of semicarbazide- sensitive amine oxidase | MEMBRANE COPPER AMINE OXIDASE (E.C.1.4.3.6) |
| 2Y73 | Q16853 | THE NATIVE STRUCTURES OF SOLUBLE HUMAN PRIMARY AMINE OXIDASE AOC3 | |
| 2Y74 | Q16853 | THE CRYSTAL STRUCTURE OF HUMAN SOLUBLE PRIMARY AMINE OXIDASE AOC3 IN THE OFF-COPPER CONFORMATION | |
| 3ALA | Q16853 | Crystal structure of vascular adhesion protein-1 in space group C2 | |
| 4BTW | Q16853 | Crystal structure of human vascular adhesion protein-1 in complex with pyridazinone inhibitors | |
| 4BTX | Q16853 | Crystal structure of human vascular adhesion protein-1 in complex with pyridazinone inhibitors | |
| 4BTY | Q16853 | Crystal structure of human vascular adhesion protein-1 in complex with pyridazinone inhibitors | |
| 6WM3 | Q16864 | Human V-ATPase in state 2 with SidK and ADP | V-type proton ATPase 116 kDa subunit a isoform 1, V-type proton ATPase subunit C 1, V-type proton ATPase subunit E 1, V-type proton ATPase subunit G 1, V-type proton ATPase subunit e 1, Ribonuclease kappa (E.C.3.1.-.-), V-type proton ATPase subunit H, V-type proton ATPase subunit S1, Renin receptor, V-type proton ATPase 21 kDa proteolipid subunit, V-type proton ATPase 16 kDa proteolipid subunit, V-type proton ATPase subunit d 1, V-type proton ATPase catalytic subunit A (E.C.7.1.2.2), V-type proton ATPase subunit B, brain isoform, V-type proton ATPase subunit D, V-type proton ATPase subunit F |
| 7U4T | Q16864 | Human V-ATPase in state 2 with SidK and mEAK-7 | |
| 6WM2 | Q16864 | Human V-ATPase in state 1 with SidK and ADP | V-type proton ATPase 116 kDa subunit a isoform 1, V-type proton ATPase subunit C 1, V-type proton ATPase subunit E 1, V-type proton ATPase subunit G 1, V-type proton ATPase subunit e 1, Ribonuclease kappa (E.C.3.1.-.-), V-type proton ATPase subunit H, V-type proton ATPase catalytic subunit A (E.C.7.1.2.2), V-type proton ATPase subunit B, brain isoform, k, V-type proton ATPase subunit D, V-type proton ATPase subunit F, V-type proton ATPase subunit S1, Renin receptor, V-type proton ATPase 21 kDa proteolipid subunit, V-type proton ATPase 16 kDa proteolipid subunit, V-type proton ATPase subunit d 1 |
| 6WM4 | Q16864 | Human V-ATPase in state 3 with SidK and ADP | V-type proton ATPase catalytic subunit A (E.C.7.1.2.2), V-type proton ATPase subunit B, brain isoform, SidK, V-type proton ATPase 116 kDa subunit a isoform 1, V-type proton ATPase subunit C 1, V-type proton ATPase subunit E 1, V-type proton ATPase subunit G 1, V-type proton ATPase subunit D, V-type proton ATPase subunit F, V-type proton ATPase subunit S1, Renin receptor, V-type proton ATPase 21 kDa proteolipid subunit, V-type proton ATPase 16 kDa proteolipid subunit, V-type proton ATPase subunit d 1, V-type proton ATPase subunit e 1, Ribonuclease kappa (E.C.3.1.-.-), V-type proton ATPase subunit H |
| 7UNF | Q16864 | CryoEM structure of a mEAK7 bound human V-ATPase complex | |
| 6R7D | Q16873 | Crystal structure of LTC4S in complex with AZ13690257 | |
| 2PNO | Q16873 | Crystal structure of human leukotriene C4 synthase | |
| 2UUH | Q16873 | Crystal structure of Human Leukotriene C4 Synthase in complex with substrate glutathione | |
| 2UUH | Q16873 | Crystal structure of Human Leukotriene C4 Synthase in complex with substrate glutathione | |
| 2UUI | Q16873 | Crystal structure of Human Leukotriene C4 Synthase | |
| 2UUI | Q16873 | Crystal structure of Human Leukotriene C4 Synthase | |
| 3B29 | Q16873 | Human leukotriene C4 synthase in complex with dodecyl-beta-D-selenomaltoside | |
| 3LEO | Q16873 | Structure of human Leukotriene C4 synthase mutant R31Q in complex with glutathione | |
| 3PCV | Q16873 | Crystal structure analysis of human leukotriene C4 synthase at 1.9 angstrom resolution | |
| 6HVJ | Q16875 | Human PFKFB3 in complex with a N-Aryl 6-Aminoquinoxaline inhibitor 3 | |
| 6IBX | Q16875 | Human PFKFB3 in complex with a N-Aryl 6-Aminoquinoxaline inhibitor 5 | |
| 6IBY | Q16875 | Human PFKFB3 in complex with a N-Aryl 6-Aminoquinoxaline inhibitor 6 | |
| 6IBZ | Q16875 | Human PFKFB3 in complex with a N-Aryl 6-Aminoquinoxaline inhibitor 7 | |
| 6ETJ | Q16875 | HUMAN PFKFB3 IN COMPLEX WITH KAN0438241 | 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (E.C.2.7.1.105,3.1.3.46) |
| 6IC0 | Q16875 | Human PFKFB3 in complex with a N-Aryl 6-Aminoquinoxaline inhibitor 4 | |
| 6HVH | Q16875 | Human PFKFB3 in complex with a N-Aryl 6-Aminoquinoxaline inhibitor 1 | |
| 6HVI | Q16875 | Human PFKFB3 in complex with a N-Aryl 6-Aminoquinoxaline inhibitor 2 | |
| 2AXN | Q16875 | Crystal structure of the human inducible form 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase | |
| 2DWO | Q16875 | PFKFB3 in complex with ADP and PEP | |
| 2DWP | Q16875 | A pseudo substrate complex of 6-phosphofructo-2-kinase of PFKFB | |
| 2I1V | Q16875 | Crystal structure of PFKFB3 in complex with ADP and Fructose-2,6-bisphosphate | |
| 3QPV | Q16875 | PFKFB3 trapped in a phospho-enzyme intermediate state | |
| 4D4J | Q16875 | human PFKFB3 in complex with a pyrrolopyrimidone compound | |
| 4D4K | Q16875 | human PFKFB3 in complex with a pyrrolopyrimidone compound | |
| 4D4L | Q16875 | human PFKFB3 in complex with a pyrrolopyrimidone compound | |
| 4D4M | Q16875 | human PFKFB3 in complex with a pyrrolopyrimidone compound | |
| 4MA4 | Q16875 | S-glutathionylated PFKFB3 | 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (E.C.2.7.1.105, 3.1.3.46) |
| 5AJV | Q16875 | Human PFKFB3 in complex with an indole inhibitor 1 | |
| 5AJW | Q16875 | Human PFKFB3 in complex with an indole inhibitor 2 | |
| 5AJX | Q16875 | Human PFKFB3 in complex with an indole inhibitor 3 | |
| 5AJY | Q16875 | Human PFKFB3 in complex with an indole inhibitor 4 | |
| 5AJZ | Q16875 | Human PFKFB3 in complex with an indole inhibitor 5 | |
| 5AK0 | Q16875 | Human PFKFB3 in complex with an indole inhibitor 6 | |
| 4PF6 | Q16C67 | CRYSTAL STRUCTURE OF A TRAP PERIPLASMIC SOLUTE BINDING PROTEIN FROM ROSEOBACTER DENITRIFICANS (RD1_0742, TARGET EFI-510239) WITH BOUND 3-DEOXY-D-MANNO-OCT-2-ULOSONIC ACID (KDO) | |
| 6DU6 | Q16F38 | Crystal structure of the pyruvate kinase (PK1) from the mosquito Aedes aegypti | |
| 7B1B | Q16J57 | Cryo-EM of Aedes Aegypti Toll5A dimer bound to Spz1C | |
| 7B1C | Q16J57 | Cryo-EM of Aedes Aegypti Toll5A trimer bound to Spz1C |
