Taxonomic group: fungi / Basidiomycota
(Phylum: Basidiomycota)
Organ / tissue: capsuleAssociated disease: infection due to Cryptococcus neoformans [ICD11:
XN3EH 
]
NCBI PubMed ID: 16696646Publication DOI: 10.1111/j.1567-1364.2006.00054.xJournal NLM ID: 101085384Publisher: Oxford University Press
Correspondence: Doering TL <doering

wustl.edu>
Institutions: Department of Molecular Microbiology, Washington University, School of Medicine, St. Louis, USA, Department of Pathology and Immunology, Washington University, School of Medicine, St. Louis, USA
Glycosyltransferases are specific enzymes that catalyse the transfer of monosaccharide moieties to biological substrates, including proteins, lipids and carbohydrates. These enzymes are present from prokaryotes to humans, and their glycoconjugate products are often vital for survival of the organism. Many glycosyltransferases found in fungal pathogens such as Cryptococcus neoformans do not exist in mammalian systems, making them attractive potential targets for selectively toxic agents. In this article, we present the features of this diverse class of enzymes, and review the fungal glycosyltransferases that are involved in synthesis of the cell wall, the cryptococcal capsule, glycoproteins and glycolipids. We specifically focus on enzymes that have been identified or studied in C. neoformans, and we consider future directions for research on glycosyltransferases in the context of this opportunistic pathogen.
polysaccharide, glycan, glycosyltransferase, glycosylation, fungi, Cryptococcus
Structure type: structural motif or average structure
Location inside paper: Fig. 1, b
Compound class: O-polysaccharide, xylogalactomannan
Contained glycoepitopes: IEDB_114701,IEDB_130701,IEDB_134624,IEDB_136044,IEDB_136906,IEDB_137472,IEDB_141794,IEDB_144983,IEDB_145668,IEDB_151528,IEDB_152206,IEDB_164174,IEDB_167188,IEDB_174332,IEDB_190606,IEDB_983930,SB_163,SB_165,SB_166,SB_187,SB_195,SB_197,SB_44,SB_67,SB_7,SB_72,SB_88
Related record ID(s): 44351, 44353, 44354
NCBI Taxonomy refs (TaxIDs): 5207Reference(s) to other database(s): GTC:G10258DN
Show glycosyltransferases
There is only one chemically distinct structure:
Taxonomic group: fungi / Basidiomycota
(Phylum: Basidiomycota)
Organ / tissue: fruiting body
The structure was elucidated in this paperNCBI PubMed ID: 30594621Publication DOI: 10.1016/j.ijbiomac.2018.12.246Journal NLM ID: 7909578Publisher: Butterworth-Heinemann
Correspondence: Wang CL <wangchunling

tust.edu.cn>
Institutions: Key Laboratory of Food Nutrition and Safety, Ministry of Education, College of Food Engineering and Biotechnology, Tianjin University of Science and Technology, Tianjin, China
In the study, a new triple-helix polysaccharide with favorable stability was purified from C. cornucopioides. Its structural characterization, stability and solution behavior were investigated by the GC-MS, periodate oxidation-smith degradation, FT-IR, 1D and 2D NMR spectroscopy, methylation analysis, Scanning electron microscope, Congo-red, CD, TGA and DSC analysis. The results showed that Craterellus cornucopioide polysaccharide (CCP) possessed the molecular weight of 1970 kDa, is mainly composed of mannose (48.73%), galactose (17.37%), glucose (15.97%) and xylose (17.93%), respectively. It was a heteroglycan with (1→)-linked-β-D-Manp-(1→6)-linked α-d-Galp backbone distributed by (1→4)-linked-α-D-Xylp-t-α-D-Manp and t-β-D-Glup units at O-6. The result of TGA and DSC assay indicated that CCP has a favorable thermal stability. MTT and Scanning electro microscopy (SEM) assay showed that CCP could significantly improve the proliferation activity and induce cells activation of RAW264.7 in a certain range of concentrations and period.
polysaccharide, chemical structure, stability, immunomodulatory activity, Craterellus cornucopioides
Structure type: structural motif or average structure
Location inside paper: p. 800, Table 3, p. 801, left column, paragraph 1
Compound class: polysaccharide, xylogalactomannan
Contained glycoepitopes: IEDB_114701,IEDB_130701,IEDB_131187,IEDB_136906,IEDB_137472,IEDB_137485,IEDB_141794,IEDB_142488,IEDB_144983,IEDB_146664,IEDB_151528,IEDB_152206,IEDB_190606,IEDB_983930,IEDB_983931,SB_192,SB_44,SB_67,SB_7,SB_72
Methods: 13C NMR, 1H NMR, methylation, periodate oxidation, NMR-2D, IR, acid hydrolysis, GC, Smith degradation, HPLC, extraction, acetylation, CD, methylation analysis, reduction, CC, HPGPC, spectrophotometry, SEM, evaporation, Congo Red assay, Sevag method, centrifugation, MTT, AFM, thermogravimetric analysis, proliferation assay
Biological activity: polysaccharide induced RAW264.7 cells activation
NCBI Taxonomy refs (TaxIDs): 94199
Show glycosyltransferases
NMR conditions: in D2O at 298 K
[as TSV]
13C NMR data:
Linkage Residue C1 C2 C3 C4 C5 C6
3 aDGalp 97.30 70.03 69.99 72.29 75.17 66.32
bDManp 103.66 73.18 78.98 72.79 75.41 69.45
6,4 aDManp 101.22 72.38 68.80 71.59 69.99 62.34
6 aDXylp 102.62 71.14 68.82 77.78 60.99
6 bDGlcp 98.08 74.87 73.42 70.08 72.58 60.90
1H NMR data:
Linkage Residue H1 H2 H3 H4 H5 H6
3 aDGalp 4.94 3.82 3.99 3.62 3.75 3.90
bDManp 4.72 3.67 3.66 3.55 3.41 3.83
6,4 aDManp 5.09 3.89 4.15 3.41 3.29 3.56
6 aDXylp 5.03 3.76 4.00 3.91 3.69
6 bDGlcp 4.88 3.78 3.88 3.95 3.67 3.84
1H/13C HSQC data:
Linkage Residue C1/H1 C2/H2 C3/H3 C4/H4 C5/H5 C6/H6
3 aDGalp 97.30/4.94 70.03/3.82 69.99/3.99 72.29/3.62 75.17/3.75 66.32/3.90
bDManp 103.66/4.72 73.18/3.67 78.98/3.66 72.79/3.55 75.41/3.41 69.45/3.83
6,4 aDManp 101.22/5.09 72.38/3.89 68.80/4.15 71.59/3.41 69.99/3.29 62.34/3.56
6 aDXylp 102.62/5.03 71.14/3.76 68.82/4.00 77.78/3.91 60.99/3.69
6 bDGlcp 98.08/4.88 74.87/3.78 73.42/3.88 70.08/3.95 72.58/3.67 60.90/3.84
1H NMR data:
| Linkage | Residue | H1 | H2 | H3 | H4 | H5 | H6 |
| 3 | aDGalp | 4.94 | 3.82 | 3.99 | 3.62 | 3.75 | 3.90 |
| | bDManp | 4.72 | 3.67 | 3.66 | 3.55 | 3.41 | 3.83 |
| 6,4 | aDManp | 5.09 | 3.89 | 4.15 | 3.41 | 3.29 | 3.56 |
| 6 | aDXylp | 5.03 | 3.76 | 4.00 | 3.91 | 3.69 | |
| 6 | bDGlcp | 4.88 | 3.78 | 3.88 | 3.95 | 3.67 | 3.84 |
|
13C NMR data:
| Linkage | Residue | C1 | C2 | C3 | C4 | C5 | C6 |
| 3 | aDGalp | 97.30 | 70.03 | 69.99 | 72.29 | 75.17 | 66.32 |
| | bDManp | 103.66 | 73.18 | 78.98 | 72.79 | 75.41 | 69.45 |
| 6,4 | aDManp | 101.22 | 72.38 | 68.80 | 71.59 | 69.99 | 62.34 |
| 6 | aDXylp | 102.62 | 71.14 | 68.82 | 77.78 | 60.99 | |
| 6 | bDGlcp | 98.08 | 74.87 | 73.42 | 70.08 | 72.58 | 60.90 |
|
There is only one chemically distinct structure: