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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5E6W | P05107 | Re-refinement of the Crystal Structure of the Plexin-Semaphorin-Integrin Domain/Hybrid Domain/I-EGF1 Segment from the Human Integrin b2 Subunit | |
5E6X | P05107 | Re-refinement of the Crystal Structure of the Plexin-Semaphorin-Integrin Domain/Hybrid Domain/I-EGF1 Segment from the Human Integrin b2 Subunit | |
5ES4 | P05107 | RE-REFINEMENT OF INTEGRIN ALPHAXBETA2 ECTODOMAIN IN THE CLOSED/BENT CONFORMATION | |
6OEL | P05112 | Engineered Fab bound to IL-4 receptor | |
3BPL | P05112 | Crystal structure of the IL4-IL4R-Common Gamma ternary complex | |
3BPN | P05112 | Crystal structure of the IL4-IL4R-IL13Ra ternary complex | |
3QT2 | P05113 | Structure of a cytokine ligand-receptor complex | |
8TLD | P05113 | Structure of the IL-5 Signaling Complex | |
1A7C | P05121 | HUMAN PLASMINOGEN ACTIVATOR INHIBITOR TYPE-1 IN COMPLEX WITH A PENTAPEPTIDE | |
3R4L | P05121 | Human very long half life Plasminogen Activator Inhibitor type-1 | |
5FSG | P05133 | Structure of the hantavirus nucleoprotein provides insights into the mechanism of RNA encapsidation and a template for drug design | |
3JCU | P05146 | Cryo-EM structure of spinach PSII-LHCII supercomplex at 3.2 Angstrom resolution | |
8Z9D | P05146 | cryo-EM structure of PSII-LHCII megacomplex from spinach | |
1LQ8 | P05154 | Crystal structure of cleaved protein C inhibitor | |
3B9F | P05154 | 1.6 A structure of the PCI-thrombin-heparin complex | |
3DY0 | P05154 | Crystal Structure of Cleaved PCI Bound to Heparin | |
2OAY | P05155 | Crystal structure of latent human C1-inhibitor | |
5DUQ | P05155 | Active human c1-inhibitor in complex with dextran sulfate | |
2XRC | P05156 | Human complement factor I | |
5O32 | P05156 | The structure of complement complex | |
1HLC | P05162 | X-RAY CRYSTAL STRUCTURE OF THE HUMAN DIMERIC S-LAC LECTIN, L-14-II, IN COMPLEX WITH LACTOSE AT 2.9 ANGSTROMS RESOLUTION | |
5DG1 | P05162 | Sugar binding protein - human galectin-2 | |
5DG2 | P05162 | Sugar binding protein - human galectin-2 (dimer) | |
5EWS | P05162 | Sugar binding protein - human galectin-2 | |
7LAE | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH Compound-4 | |
7NI1 | P05164 | CRYSTAL STRUCTURE OF NATIVE HUMAN MYELOPEROXIDASE IN COMPLEX WITH CPD 9 | |
7NI3 | P05164 | CRYSTAL STRUCTURE OF NATIVE HUMAN MYELOPEROXIDASE IN COMPLEX WITH CPD 3 | |
7LAL | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH COMPOUND-18 AKA 7-(3-(2,3-DIHYDRO-1H-INDEN-1-YLAMINO)-1-PHENYLPROPYL)-1H-[1,2,3]TRIAZOLO[4,5-B]PYRIDIN-5-AMINE | |
7LAN | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH COMPOUND-30 AKA 7-[(3~{S},4~{R},6~{R})-4-benzyl-2-oxa-7,13,14-triazatetracyclo[14.3.1.1^{3,6}.1^{11,14}]docosa-1(19),11(21),12,16(20),17-pentaen-10-yl]-3~{H}-triazolo[4,5-b]pyridin-5-amine | |
5QJ2 | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) OMPLEX WITH COMPOUND-20 AKA 7-((3-(1-METHYL-1H-PYRAZOL-3- YL)BENZYL)OXY)- 1H-[1,2,3]TRIAZOLO[4,5-B]PYRIDIN-5-AMINE | |
5QJ3 | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH COMPOUND-24 AKA 7-({4-CHLORO-3'-FLUORO-[1,1'- BIPHENYL]-3-YL}METHOXY)-3H-[1,2,3]TRIAZOLO[4,5-B]PYRIDIN- 5-AMINE | |
5UZU | P05164 | Immune evasion by a Staphylococcal Peroxidase Inhibitor that blocks myeloperoxidase | |
6WXZ | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH Compound-29 A.K.A 7-(1,2-DIPHENYLETHYL)-1H-[1,2,3]TRIAZOLO[4,5-B]PYRIDIN-5-AMINE | |
6WY0 | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH Compound-40 A.K.A 7-[(1R)-1-phenyl-3-{[(1r,4r)-4-phenylcyclohexyl]amino}propyl]-3H-[1,2,3]triazolo[4,5-b]pyridin-5-amine | |
6WY5 | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH Compound-37 A.K.A 7-(1-phenyl-3-(((1S,3S)-3-phenyl-2,3-dihydro-1H-inden-1-yl)amino)propyl)-1H-[1,2,3]triazolo[4,5-b]pyridin-5-amine | |
6WY7 | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH Compound-41 A.K.A 7-[1-phenyl-3-({4-phenylbicyclo[2.2.2]octan-1-yl}amino)propyl]-3H-[1,2,3]triazolo[4,5-b]pyridin-5-amine | |
6WYD | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH Compound-12 (AKA; 7-benzyl-1H-[1,2,3]triazolo[4,5-b]pyrid | |
7LAG | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH Compound-14 AKA 7-({1-[(3-phenoxyphenyl)methyl]-1H-pyrazol-4-yl}methyl)-3H-[1,2,3]triazolo[4,5-b]pyridin-5-amine | |
5WDJ | P05164 | CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH COMPOUND-6 AKA 7-(BENZYLOXY)-1H-[1,2, 3]TRIAZOLO[4,5-D]PYRIMIDIN-5-AMINE | |
6BMT | P05164 | Crystal Structure of a Recombinant form of Human Myeloperoxidase Bound to an Inhibitor from Staphylococcus delphini | |
7OIH | P05164 | Glycosylation in the crystal structure of neutrophil myeloperoxidase | |
1CXP | P05164 | CRYOGENIC CRYSTAL STRUCTURE OF HUMAN MYELOPEROXIDASE ISOFORM C | MYELOPEROXIDASE (E.C.1.11.1.7) |
1D2V | P05164 | CRYSTAL STRUCTURE OF BROMIDE-BOUND HUMAN MYELOPEROXIDASE ISOFORM C AT PH 5.5 | MYELOPEROXIDASE (E.C.1.11.1.7) |
1D5L | P05164 | CRYSTAL STRUCTURE OF CYANIDE-BOUND HUMAN MYELOPEROXIDASE ISOFORM C AT PH 5.5 | MYELOPEROXIDASE (E.C.1.11.1.7) |
1D7W | P05164 | CRYSTAL STRUCTURE OF HUMAN MYELOPEROXIDASE ISOFORM C COMPLEXED WITH CYANIDE AND BROMIDE AT PH 4.0 | MYELOPEROXIDASE (E.C.1.11.1.7) |
1DNU | P05164 | STRUCTURAL ANALYSES OF HUMAN MYELOPEROXIDASE-THIOCYANATE COMPLEX | MYELOPEROXIDASE (E.C.1.11.1.7)/THIOCYANATE COMPLEX |
1DNW | P05164 | HUMAN MYELOPEROXIDASE-CYANIDE-THIOCYANATE COMPLEX | MYELOPEROXIDASE (E.C.1.11.1.7)/CYANIDE-THIOCYANATE COMPLEX |
1MHL | P05164 | CRYSTAL STRUCTURE OF HUMAN MYELOPEROXIDASE ISOFORM C CRYSTALLIZED IN SPACE GROUP P2(1) AT PH 5.5 AND 20 DEG C | |
1MYP | P05164 | X-RAY CRYSTAL STRUCTURE OF CANINE MYELOPEROXIDASE AT 3 ANGSTROMS RESOLUTION | MYELOPEROXIDASE (E.C.1.11.1.7) |
3F9P | P05164 | Crystal structure of myeloperoxidase from human leukocytes |
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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