GlycoNAVI-Proteins is dataset of glycan and protein information. This is the content of GlycoNAVI.
Source | Last Updated |
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GlycoNAVI Proteins | September 04, 2024 |
PDB ID | UniProt ID ▲ | Title | Descriptor |
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3T2P | P00722 | E. coli (lacZ) beta-galactosidase (S796D) in complex with IPTG | |
3T2Q | P00722 | E. coli (lacZ) beta-galactosidase (S796D) in complex with galactonolactone | |
3VD4 | P00722 | E. coli (lacZ) beta-galactosidase (N460D) in complex with IPTG | |
3VD9 | P00722 | E. coli (lacZ) beta-galactosidase (N460S) in complex with IPTG | |
3VDB | P00722 | E. coli (lacZ) beta-galactosidase (N460T) in complex with galactonolactone | |
3VDC | P00722 | E. coli (lacZ) beta-galactosidase (N460T) in complex with IPTG | |
4DUV | P00722 | E. coli (lacZ) beta-galactosidase (G974A) 2-deoxy-galactosyl-enzyme and bis-Tris complex | |
4DUW | P00722 | E. coli (lacZ) beta-galactosidase (G974A) in complex with allolactose | |
4DUX | P00722 | E. coli (lacZ) beta-galactosidase (N460S) in complex with L-ribose | |
4V44 | P00722 | E. COLI (lacZ) BETA-GALACTOSIDASE IN COMPLEX WITH 2-F-LACTOSE | |
4V45 | P00722 | E. COLI (lacZ) BETA-GALACTOSIDASE-TRAPPED 2-F-GALACTOSYL-ENZYME INTERMEDIATE | |
5A1A | P00722 | 2.2 A resolution cryo-EM structure of beta-galactosidase in complex with a cell-permeant inhibitor | |
3OB8 | P00723 | Structure of the beta-galactosidase from Kluyveromyces lactis in complex with galactose | |
7CEL | P00725 | CBH1 (E217Q) IN COMPLEX WITH CELLOHEXAOSE AND CELLOBIOSE | |
1CEL | P00725 | THE THREE-DIMENSIONAL CRYSTAL STRUCTURE OF THE CATALYTIC CORE OF CELLOBIOHYDROLASE I FROM TRICHODERMA REESEI | 1,4-BETA-D-GLUCAN CELLOBIOHYDROLASE I (CELLULASE) (E.C.3.2.1.91) |
6CEL | P00725 | CBH1 (E212Q) CELLOPENTAOSE COMPLEX | |
1Q2E | P00725 | CELLOBIOHYDROLASE CEL7A WITH LOOP DELETION 245-252 AND BOUND NON-HYDROLYSABLE CELLOTETRAOSE | EXOCELLOBIOHYDROLASE I (E.C.3.2.1.91) |
3CEL | P00725 | ACTIVE-SITE MUTANT E212Q DETERMINED AT PH 6.0 WITH CELLOBIOSE BOUND IN THE ACTIVE SITE | |
5CEL | P00725 | CBH1 (E212Q) CELLOTETRAOSE COMPLEX | |
1CPY | P00729 | SITE-DIRECTED MUTAGENESIS ON (SERINE) CARBOXYPEPTIDASE Y FROM YEAST. THE SIGNIFICANCE OF THR 60 AND MET 398 IN HYDROLYSIS AND AMINOLYSIS REACTIONS | SERINE CARBOXYPEPTIDASE |
1WPX | P00729 | Crystal structure of carboxypeptidase Y inhibitor complexed with the cognate proteinase | Carboxypeptidase Y (E.C.3.4.16.5)/Carboxypeptidase Y inhibitor |
1YSC | P00729 | 2.8 ANGSTROMS STRUCTURE OF YEAST SERINE CARBOXYPEPTIDASE | SERINE CARBOXYPEPTIDASE (CPY, CPD-Y, OR PROTEINASE C) (E.C.3.4.16.5) |
6C2W | P00734 | Crystal structure of human prothrombin mutant S101C/A470C | |
6GBW | P00734 | Thrombin in complex with MI2100 ((S)-N-(2-(aminomethyl)-5-chlorobenzyl)-1-((benzylsulfonyl)-L-arginyl)pyrrolidine-2-carboxamide) | |
6YSJ | P00734 | Thrombin in complex with 2-amino-1-(4-bromophenyl)ethan-1-one (j10) | |
6ZUH | P00734 | Crystal Structure of Thrombin in complex with compound17 | |
6ZUU | P00734 | Crystal structure of Thrombin in complex with compound30 | |
7NTU | P00734 | X-ray structure of the complex between human alpha thrombin and two duplex/quadruplex aptamers: NU172 and HD22_27mer | |
8ASE | P00734 | Crystal structure of Thrombin in complex with macrocycle T3 | |
6FJT | P00734 | 4-chloro-benzamidine in complex with thrombin | |
6GWE | P00734 | Crystal structure of Thrombin bound to P2 macrocycle | |
6HSX | P00734 | Thrombin in Complex with a D-Phe-Pro-diaminopyridine derivative | |
6P9U | P00734 | Crystal structure of human thrombin mutant W215A | |
6YQV | P00734 | Thrombin in complex with 5-chlorothiophene-2-sulfonamide (j94) | |
7SR9 | P00734 | Human alpha-thrombin with 180- and 220- loops replaced with homologous loops from protein C | |
6TKI | P00734 | Tsetse thrombin inhibitor in complex with human alpha-thrombin - tetragonal form at 12.7keV | |
6YHG | P00734 | Thrombin in complex with D-Phe-Pro-m-methoxybenzylamide derivative (16a) | |
6ZUN | P00734 | Crystal Structure of Thrombin in complex with compound20a | |
5TO3 | P00734 | Crystal structure of thrombin mutant W215A/E217A fused to EGF456 of thrombomodulin via a 31-residue linker and bound to PPACK | |
6EVV | P00734 | X-ray structure of the complex between human alpha thrombin and NU172, a duplex/quadruplex 26-mer DNA aptamer, in the presence of potassium ions. | |
1AE8 | P00734 | HUMAN ALPHA-THROMBIN INHIBITION BY EOC-D-PHE-PRO-AZALYS-ONP | |
1AFE | P00734 | HUMAN ALPHA-THROMBIN INHIBITION BY CBZ-PRO-AZALYS-ONP | |
1BA8 | P00734 | THROMBIN INHIBITOR WITH A RIGID TRIPEPTIDYL ALDEHYDES | |
6PX5 | P00734 | CRYSTAL STRUCTURE OF HUMAN MEIZOTHROMBIN DESF1 MUTANT S195A bound with PPACK | |
6PXQ | P00734 | Crystal structure of human thrombin mutant D194A | |
6ROT | P00734 | Thrombin in complex with MI2105 | |
6T3M | P00734 | Thrombin in Complex with a D-Phe-Pro-p-phenol derivative | |
6T3Q | P00734 | Thrombin in Complex with a D-Phe-Pro-2-aminopyridine derivative | |
6T4A | P00734 | Thrombin in Complex with a D-Phe-Pro-p-aminopyridine derivative | |
6T52 | P00734 | Thrombin in Complex with a D-Phe-Pro-imidazole derivative |
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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: August 19, 2024