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 18, 2024 |
PDB ID | UniProt ID | Title | Descriptor ▲ |
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1QW9 | Q9XBQ3 | Crystal structure of a family 51 alpha-L-arabinofuranosidase in complex with 4-nitrophenyl-Ara | |
1QWN | Q24451 | GOLGI ALPHA-MANNOSIDASE II Covalent Intermediate Complex with 5-fluoro-gulosyl-fluoride | |
1QWU | Q24451 | Golgi alpha-mannosidase II D341N mutant complex with 5-F-guloside | |
1QX1 | Q24451 | Golgi alpha-mannosidase II D341N mutant complex with 2-F-mannosyl-F | |
1QXR | P83194 | Crystal structure of phosphoglucose isomerase from Pyrococcus furiosus in complex with 5-phosphoarabinonate | |
1QY4 | P83194 | Crystal structure of phosphoglucose isomerase from Pyrococcus furiosus in complex with gluconate 6-phosphate | |
1QYY | P07359 | Crystal Structure of N-Terminal Domain of Human Platelet Receptor Glycoprotein Ib-alpha at 2.8 Angstrom Resolution | |
1R0A | P03366 | Crystal structure of HIV-1 reverse transcriptase covalently tethered to DNA template-primer solved to 2.8 angstroms | |
1R0A | 1R0A | Crystal structure of HIV-1 reverse transcriptase covalently tethered to DNA template-primer solved to 2.8 angstroms | |
1R1A | P23008 | CRYSTAL STRUCTURE OF HUMAN RHINOVIRUS SEROTYPE 1A (HRV1A) | |
1R1H | P08473 | STRUCTURAL ANALYSIS OF NEPRILYSIN WITH VARIOUS SPECIFIC AND POTENT INHIBITORS | |
1R1J | P08473 | STRUCTURAL ANALYSIS OF NEPRILYSIN WITH VARIOUS SPECIFIC AND POTENT INHIBITORS | |
1R1L | 1R1L | Structure of dimeric antithrombin complexed with a P14-P9 reactive loop peptide and an exogenous tripeptide (formyl-norleucine-LF) | |
1R1L | P01008 | Structure of dimeric antithrombin complexed with a P14-P9 reactive loop peptide and an exogenous tripeptide (formyl-norleucine-LF) | |
1R33 | Q24451 | Golgi alpha-mannosidase II complex with 5-thio-D-mannopyranosylamine | |
1R34 | Q24451 | Golgi alpha-mannosidase II complex with 5-thio-D-mannopyranosylamidinium salt | |
1R42 | 11225609 | Native Human Angiotensin Converting Enzyme-Related Carboxypeptidase (ACE2) | |
1R42 | 1R42 | Native Human Angiotensin Converting Enzyme-Related Carboxypeptidase (ACE2) | |
1R46 | P06280 | Structure of human alpha-galactosidase | |
1R47 | P06280 | Structure of human alpha-galactosidase | |
1R4L | Q9BYF1 | Inhibitor Bound Human Angiotensin Converting Enzyme-Related Carboxypeptidase (ACE2) | |
1R4L | 1R4L | Inhibitor Bound Human Angiotensin Converting Enzyme-Related Carboxypeptidase (ACE2) | |
1R54 | Q9BZ11 | Crystal structure of the catalytic domain of human ADAM33 | |
1R55 | Q9BZ11 | Crystal structure of the catalytic domain of human ADAM 33 | |
1R64 | P13134 | The 2.2 A crystal structure of Kex2 protease in complex with Ac-Arg-Glu-Lys-boroArg peptidyl boronic acid inhibitor | |
1R64 | 1R64 | The 2.2 A crystal structure of Kex2 protease in complex with Ac-Arg-Glu-Lys-boroArg peptidyl boronic acid inhibitor | |
1R6Z | P02928 | The Crystal Structure of the Argonaute2 PAZ domain (as a MBP fusion) | |
1R6Z | 23093413 | The Crystal Structure of the Argonaute2 PAZ domain (as a MBP fusion) | |
1R6Z | P02928 | The Crystal Structure of the Argonaute2 PAZ domain (as a MBP fusion) | |
1R6Z | 23093413 | The Crystal Structure of the Argonaute2 PAZ domain (as a MBP fusion) | |
1R7T | P16442 | Glycosyltransferase A in complex with 3-deoxy-acceptor analog inhibitor | |
1R7U | P16442 | Glycosyltransferase B in complex with 3-deoxy-acceptor analog inhibitor | |
1R7V | P16442 | Glycosyltransferase A in complex with 3-amino-acceptor analog inhibitor | |
1R7X | P16442 | Glycosyltransferase B in complex with 3-amino-acceptor analog inhibitor | |
1R7Y | P16442 | Glycosyltransferase A in complex with 3-amino-acceptor analog inhibitor and uridine diphosphate | |
1R80 | P16442 | Glycosyltransferase B in complex with 3-amino-acceptor analog inhibitor and uridine diphosphate | |
1R81 | P16442 | Glycosyltransferase A in complex with 3-amino-acceptor analog inhibitor and uridine diphosphate-N-acetyl-galactose | |
1R82 | P16442 | Glycosyltransferase B in complex with 3-amino-acceptor analog inhibitor, and uridine diphosphate-galactose | |
1R87 | P40943 | Crystal structure of the extracellular xylanase from Geobacillus stearothermophilus T-6 (XT6, monoclinic form): The complex of the WT enzyme with xylopentaose at 1.67A resolution | |
1R9M | P27487 | Crystal Structure of Human Dipeptidyl Peptidase IV at 2.1 Ang. Resolution. | |
1R9N | P27487 | Crystal Structure of human dipeptidyl peptidase IV in complex with a decapeptide (tNPY) at 2.3 Ang. Resolution | |
1R9N | Q9XSW6 | Crystal Structure of human dipeptidyl peptidase IV in complex with a decapeptide (tNPY) at 2.3 Ang. Resolution | |
1RBL | P00880 | STRUCTURE DETERMINATION AND REFINEMENT OF RIBULOSE 1,5 BISPHOSPHATE CARBOXYLASE(SLASH)OXYGENASE FROM SYNECHOCOCCUS PCC6301 | |
1RBL | P04716 | STRUCTURE DETERMINATION AND REFINEMENT OF RIBULOSE 1,5 BISPHOSPHATE CARBOXYLASE(SLASH)OXYGENASE FROM SYNECHOCOCCUS PCC6301 | |
1RBO | P00875 | SPINACH RUBISCO IN COMPLEX WITH THE INHIBITOR 2-CARBOXYARABINITOL-1,5-DIPHOSPHATE | |
1RBO | P00870 | SPINACH RUBISCO IN COMPLEX WITH THE INHIBITOR 2-CARBOXYARABINITOL-1,5-DIPHOSPHATE | |
1RC2 | P60844 | 2.5 Angstrom Resolution X-ray Structure of Aquaporin Z | |
1RCO | P00875 | SPINACH RUBISCO IN COMPLEX WITH THE INHIBITOR D-XYLULOSE-2,2-DIOL-1,5-BISPHOSPHATE | |
1RCO | P00870 | SPINACH RUBISCO IN COMPLEX WITH THE INHIBITOR D-XYLULOSE-2,2-DIOL-1,5-BISPHOSPHATE | |
1RCX | P00875 | NON-ACTIVATED SPINACH RUBISCO IN COMPLEX WITH ITS SUBSTRATE RIBULOSE-1,5-BISPHOSPHATE |
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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