GlycoNAVI Proteins

GlycoNAVI-Proteins is dataset of glycan and protein information. This is the content of GlycoNAVI.

Source Last Updated
GlycoNAVI Proteins December 11, 2024
Displaying entries 22051 - 22100 of 40384 in total
PDB ID UniProt ID ▼ Title Descriptor
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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Last updated: December 9, 2024