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 | September 04, 2024 |
| PDB ID | UniProt ID ▼ | Title | Descriptor |
|---|---|---|---|
| 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 | CATHEPSIN D (E.C.3.4.23.5) |
| 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 | Cathepsin D light chain (E.C.3.4.23.5), Cathepsin D heavy chain (E.C.3.4.23.5) |
| 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 | Cathepsin D light chain (E.C.3.4.23.5), Cathepsin D heavy chain (E.C.3.4.23.5) |
| 4OD9 | P07339 | Structure of Cathepsin D with inhibitor N-(3,4-dimethoxybenzyl)-Nalpha-{N-[(3,4-dimethoxyphenyl)acetyl]carbamimidoyl}-D-phenylalaninamide | Cathepsin D (E.C.3.4.23.5) |
| 4DKD | P07333 | Crystal Structure of Human Interleukin-34 Bound to Human CSF-1R | Human Interleukin-34, Human CSF-1R (E.C.2.7.10.1) |
| 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 | Voltage-dependent L-type calcium channel subunit alpha-1S, Voltage-dependent L-type calcium channel subunit beta-2, Voltage-dependent calcium channel gamma-1 subunit, Voltage-dependent calcium channel subunit alpha-2/delta-1 |
| 3JBR | P07293 | Cryo-EM structure of the rabbit voltage-gated calcium channel Cav1.1 complex at 4.2 angstrom | Voltage-dependent L-type calcium channel subunit alpha-1S, Voltage-dependent L-type calcium channel subunit beta-2, Voltage-dependent calcium channel gamma-1 subunit, Voltage-dependent calcium channel subunit alpha-2/delta-1 |
| 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 | SACCHAROPEPSIN (E.C. 3.4.23.25) |
| 1FQ4 | P07267 | CRYSTAL STRUCTURE OF A COMPLEX BETWEEN HYDROXYETHYLENE INHIBITOR CP-108,420 AND YEAST ASPARTIC PROTEINASE A | SACCHAROPEPSIN (E.C.3.4.23.25) |
| 1FQ5 | P07267 | X-ray structure of a cyclic statine inhibitor PD-129,541 bound to yeast proteinase A | SACCHAROPEPSIN (E.C.3.4.23.25) |
| 1FQ6 | P07267 | X-RAY STRUCTURE OF GLYCOL INHIBITOR PD-133,450 BOUND TO SACCHAROPEPSIN | SACCHAROPEPSIN (E.C.3.4.23.25) |
| 1FQ7 | P07267 | X-RAY STRUCTURE OF INHIBITOR CP-72,647 BOUND TO SACCHAROPEPSIN | SACCHAROPEPSIN (E.C.3.4.23.25) |
| 1FQ8 | P07267 | X-RAY STRUCTURE OF DIFLUOROSTATINE INHIBITOR CP81,198 BOUND TO SACCHAROPEPSIN | SACCHAROPEPSIN (E.C.3.4.23.25) |
| 1G0V | P07267 | THE STRUCTURE OF PROTEINASE A COMPLEXED WITH A IA3 MUTANT, MVV | |
| 2JXR | P07267 | STRUCTURE OF YEAST PROTEINASE A | |
| 3CX5 | P07257 | Structure of complex III with bound cytochrome c in reduced state and definition of a minimal core interface for electron transfer. | |
| 3CXH | P07257 | Structure of yeast complex III with isoform-2 cytochrome c bound and definition of a minimal core interface for electron transfer. | |
| 3CX5 | P07256 | Structure of complex III with bound cytochrome c in reduced state and definition of a minimal core interface for electron transfer. | |
| 3CXH | P07256 | Structure of yeast complex III with isoform-2 cytochrome c bound and definition of a minimal core interface for electron transfer. | |
| 1X6N | P07254 | Crystal structure of S. marcescens chitinase A mutant W167A in complex with allosamidin | |
| 3TRQ | P07221 | Crystal structure of native rabbit skeletal calsequestrin | |
| 3V1W | P07221 | Molecular Basis for Multiple Ligand Binding of Calsequestrin and Potential Inhibition by Caffeine and Gallocatecin | |
| 7ALJ | P07207 | Structure of Drosophila Notch EGF domains 11-13 | |
| 5TO3 | P07204 | Crystal structure of thrombin mutant W215A/E217A fused to EGF456 of thrombomodulin via a 31-residue linker and bound to PPACK | |
| 1DQB | P07204 | NMR STRUCTURE OF THROMBOMODULIN EGF(4-5) | THROMBOMODULIN |
| 1DX5 | P07204 | Crystal structure of the thrombin-thrombomodulin complex | |
| 7T4R | P07204 | CryoEM structure of the HCMV Pentamer gH/gL/UL128/UL130/UL131A in complex with THBD and neutralizing fabs MSL-109 and 13H11 | |
| 5VQF | P07200 | Crystal Structure of pro-TGF-beta 1 |
