GlycoNAVI-Proteins is dataset of glycan and protein information. This is the content of GlycoNAVI.
Source | Last Updated |
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GlycoNAVI Proteins | December 11, 2024 |
PDB ID | UniProt ID ▼ | Title | Descriptor |
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8B0F | P07357 | CryoEM structure of C5b8-CD59 | |
8B0G | P07357 | 2C9, C5b9-CD59 structure | |
7NYC | P07357 | cryoEM structure of 3C9-sMAC | |
2HYU | P07355 | Human Annexin A2 with heparin tetrasaccharide bound | |
2HYV | P07355 | Human Annexin A2 with heparin hexasaccharide bound | |
7X20 | P07340 | Crystal structure of non gastric H,K-ATPase alpha2 in (K+)E2-AlF state | |
7X21 | P07340 | Cryo-EM structure of non gastric H,K-ATPase alpha2 K794A in (K+)E2-AlF state | |
7X22 | P07340 | Cryo-EM structure of non gastric H,K-ATPase alpha2 K794S in (2K+)E2-AlF state | |
7X23 | P07340 | Cryo-EM structure of non gastric H,K-ATPase alpha2 SPWC mutant in 3Na+E1-AMPPCPF state | |
7X24 | P07340 | Cryo-EM structure of non gastric H,K-ATPase alpha2 SPWC mutant in (2K+)E2-AlF state | |
8IJM | P07340 | Cyo-EM structure of K794A non-gastric proton pump in Na+ bound E1AMPPCP state | |
8IJL | P07340 | Cyo-EM structure of wildtype non-gastric proton pump in the presence of Na+, AlF and ADP | |
6QBH | P07339 | Crystal structure of human cathepsin D in complex with macrocyclic inhibitor 33 | |
6QCB | P07339 | Crystal structure of human cathepsin D in complex with macrocyclic inhibitor 9 | |
6QBG | P07339 | Crystal structure of human cathepsin D in complex with macrocyclic inhibitor 14 | |
1LYA | P07339 | CRYSTAL STRUCTURES OF NATIVE AND INHIBITED FORMS OF HUMAN CATHEPSIN D: IMPLICATIONS FOR LYSOSOMAL TARGETING AND DRUG DESIGN | |
1LYB | P07339 | CRYSTAL STRUCTURES OF NATIVE AND INHIBITED FORMS OF HUMAN CATHEPSIN D: IMPLICATIONS FOR LYSOSOMAL TARGETING AND DRUG DESIGN | |
4OBZ | P07339 | Structure of Cathepsin D with inhibitor 2-(3,4-dimethoxyphenyl)-N-[N-(4-methylbenzyl)carbamimidoyl]acetamide | |
4OC6 | P07339 | Structure of Cathepsin D with inhibitor 2-bromo-N-[(2S,3S)-4-{[2-(2,4-dichlorophenyl)ethyl][3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propanoyl]amino}-3-hydroxy-1-(3-phenoxyphenyl)butan-2-yl]-4,5-dimethoxybenzamide | |
4OD9 | P07339 | Structure of Cathepsin D with inhibitor N-(3,4-dimethoxybenzyl)-Nalpha-{N-[(3,4-dimethoxyphenyl)acetyl]carbamimidoyl}-D-phenylalaninamide | |
4DKD | P07333 | Crystal Structure of Human Interleukin-34 Bound to Human CSF-1R | |
4LIQ | P07333 | Structure of the extracellular domain of human CSF-1 receptor in complex with the Fab fragment of RG7155 | |
4WRL | P07333 | Structure of the human CSF-1:CSF-1R complex | |
5JPV | P07306 | Efficient targeting of the asialoglycoprotein receptor by polyvalent display of a compact galactoseamine mimic | |
6JP5 | P07293 | Rabbit Cav1.1-Nifedipine Complex | |
6JPA | P07293 | Rabbit Cav1.1-Verapamil Complex | |
6JP8 | P07293 | Rabbit Cav1.1-Bay K8644 Complex | |
6JPB | P07293 | Rabbit Cav1.1-Diltiazem Complex | |
3JBR | P07293 | Cryo-EM structure of the rabbit voltage-gated calcium channel Cav1.1 complex at 4.2 angstrom | |
3JBR | P07293 | Cryo-EM structure of the rabbit voltage-gated calcium channel Cav1.1 complex at 4.2 angstrom | |
5GJV | P07293 | Structure of the mammalian voltage-gated calcium channel Cav1.1 complex at near atomic resolution | |
5GJW | P07293 | Structure of the mammalian voltage-gated calcium channel Cav1.1 complex for ClassII map | |
8E56 | P07293 | Rabbit L-type voltage-gated calcium channel Cav1.1 in the presence of Amiodarone at 2.8 Angstrom resolution | |
8E57 | P07293 | Rabbit L-type voltage-gated calcium channel Cav1.1 in the presence of Amiodarone and 100 microM MNI-1 at 2.8 Angstrom resolution | |
8E58 | P07293 | Rabbit L-type voltage-gated calcium channel Cav1.1 in the presence of Amiodarone and 1 mM MNI-1 at 3.0 Angstrom resolution | |
2ZCH | P07288 | Crystal structure of human prostate specific antigen complexed with an activating antibody | |
2ZCK | P07288 | Crystal structure of a ternary complex between PSA, a substrat-acyl intermediate and an activating antibody | |
2ZCL | P07288 | Crystal structure of human prostate specific antigen complexed with an activating antibody | |
3QUM | P07288 | Crystal structure of human prostate specific antigen (PSA) in Fab sandwich with a high affinity and a PCa selective antibody | |
7DSJ | P07285 | Anthranilate phosphoribosyltransferase from Saccharomyces cerevisiae in complex with PRPP and Mg | |
1DP5 | P07267 | THE STRUCTURE OF PROTEINASE A COMPLEXED WITH A IA3 MUTANT INHIBITOR | |
1DPJ | P07267 | THE STRUCTURE OF PROTEINASE A COMPLEXED WITH IA3 PEPTIDE INHIBITOR | |
1FMU | P07267 | STRUCTURE OF NATIVE PROTEINASE A IN P3221 SPACE GROUP. | SACCHAROPEPSIN (E.C. 3.4.23.25) |
1FMX | P07267 | STRUCTURE OF NATIVE PROTEINASE A IN THE SPACE GROUP P21 | |
1FQ4 | P07267 | CRYSTAL STRUCTURE OF A COMPLEX BETWEEN HYDROXYETHYLENE INHIBITOR CP-108,420 AND YEAST ASPARTIC PROTEINASE A | |
1FQ5 | P07267 | X-ray structure of a cyclic statine inhibitor PD-129,541 bound to yeast proteinase A | |
1FQ6 | P07267 | X-RAY STRUCTURE OF GLYCOL INHIBITOR PD-133,450 BOUND TO SACCHAROPEPSIN | |
1FQ7 | P07267 | X-RAY STRUCTURE OF INHIBITOR CP-72,647 BOUND TO SACCHAROPEPSIN | |
1FQ8 | P07267 | X-RAY STRUCTURE OF DIFLUOROSTATINE INHIBITOR CP81,198 BOUND TO SACCHAROPEPSIN | |
1G0V | P07267 | THE STRUCTURE OF PROTEINASE A COMPLEXED WITH A IA3 MUTANT, MVV |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: December 9, 2024