Found 313 structures.
Displayed structures from 1 to 15
Next 15 structure(s)
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1. Compound ID: 3999
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a-L-Fucp-(1-2)-+
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a-D-Gulp-(1-3)-+ |
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-4)-Manp-(1-3)-a-D-Galp-(1-3)-a-D-GalpNAc-(1- |
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Structure type: polymer chemical repeating unit
Contained glycoepitopes: IEDB_130648,IEDB_130701,IEDB_136045,IEDB_136906,IEDB_137472,IEDB_137473,IEDB_137485,IEDB_1391961,IEDB_1394182,IEDB_141584,IEDB_141794,IEDB_142489,IEDB_144562,IEDB_144983,IEDB_144990,IEDB_151528,IEDB_152206,IEDB_152214,IEDB_152215,IEDB_153553,IEDB_174333,IEDB_190606,IEDB_885822,IEDB_983930,SB_154,SB_44,SB_67,SB_7,SB_72,SB_86
The structure is contained in the following publication(s):
- Article ID: 1483
Skurnik M "Molecular genetics, biochemistry and biological role of Yersinia lipopolysaccharide" -
Book: The Genus Yersinia (series: Advances in Experimental Medicine and Biolog) (2003) 187-198
Lipopolysaccharide (LPS) is the major component of the outer leaflet of the outer membrane of Gram-negative bacteria. The LPS molecule is composed of two biosynthetic entities: the lipid A--core and the O-polysaccharide (O-antigen). Most biological effects of LPS are due to the lipid A part, however, there is an increasing body of evidence also with Yersinia indicating that O-antigen plays an important role in effective colonization of host tissues, resistance to complement-mediated killing and in the resistance to cationic antimicrobial peptides that are key elements of the innate immune system. The biosynthesis of O-antigen requires numerous enzymatic activities and includes the biosynthesis of individual NDP-activated precursor sugars in the cytoplasm, linkage and sugar-specific transferases, O-unit flippase, O-antigen polymerase and O-chain length determinant. Based on this enzymatic mode of O-antigen biosynthesis LPS isolated from bacteria is a heterologous population of molecules; some do not carry any O-antigen while others that do have variation in the O-antigen chain lengths. The genes required for the O-antigen biosynthesis are located in O-antigen gene clusters that in genus Yersinia is located between the hemH and gsk genes. Temperature regulates the O-antigen expression in Y. enterocolitica and Y. pseudotuberculosis; bacteria grown at room temperature (RT, 22-25 degrees C) produce in abundance O-antigen while only trace amounts are present in bacteria grown at 37 degrees C. Even though the amount of O-antigen is known to fluctuate under different growth conditions in many bacteria very little detailed information is available on the control of the O-antigen biosynthetic machinery.
Lipopolysaccharide, genetic, lipopolysaccharides, structure, core, genetics, role, strain, cell, molecular, biological, cell wall, biochemistry, PAGE, function, genus, bacteriophage, Yersinia, molecular genetics, Yersinia pestis, influence, Bacteriophages, growth, temperature
NCBI PubMed ID: 12756756Publication DOI: 10.1007/0-306-48416-1_38Publisher: Springer US.
Editors: Skurnik M, Bengoechea JA, Granfors K
Institutions: Department of Bacteriology and Immunology, Haartman Institute, University of Helsinki, Finland
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2. Compound ID: 5515
Structure type: polymer chemical repeating unit
Compound class: K-antigen
Contained glycoepitopes: IEDB_115136,IEDB_130701,IEDB_131187,IEDB_136044,IEDB_136906,IEDB_137472,IEDB_137485,IEDB_1394182,IEDB_140630,IEDB_141794,IEDB_144983,IEDB_151528,IEDB_152206,IEDB_190606,IEDB_423153,IEDB_983930,SB_165,SB_166,SB_187,SB_195,SB_44,SB_67,SB_7,SB_72,SB_88
The structure is contained in the following publication(s):
- Article ID: 2338
Hungerer D, Jann K, Jann B, Orskov F, Orskov I "Immunochemistry of K antigens of Escherichia coli 4. The K antigen of E. coli O9:K30:H12" -
European Journal of Biochemistry 2 (1967) 115-126
Journal NLM ID: 0107600Publisher: Oxford, UK: Blackwell Science Ltd. on behalf of the Federation of European Biochemical Societies
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3. Compound ID: 5522
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-6)-Manp-(1-3)-Glcp-(1-6)-Manp-(1-3)-Glcp-(1-3)-b-GlcpA-(1-3)-a-Galp-(1- |
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Structure type: polymer chemical repeating unit
Compound class: K-antigen
Contained glycoepitopes: IEDB_115136,IEDB_130701,IEDB_136906,IEDB_137472,IEDB_137485,IEDB_1394182,IEDB_140630,IEDB_141794,IEDB_141836,IEDB_142488,IEDB_144983,IEDB_144998,IEDB_146664,IEDB_151528,IEDB_152206,IEDB_190606,IEDB_423153,IEDB_983930,IEDB_983931,SB_192,SB_44,SB_67,SB_7,SB_72
The structure is contained in the following publication(s):
- Article ID: 2343
Nhan LB, Jann B, Jann K "Immunochemistry of K antigens of Escherichia coli. The K29 antigen of E. coli O9:K29(A):H-" -
European Journal of Biochemistry 21 (1971) 226-234
Journal NLM ID: 0107600Publisher: Oxford, UK: Blackwell Science Ltd. on behalf of the Federation of European Biochemical Societies
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4. Compound ID: 6064
Structure type: polymer chemical repeating unit
Trivial name: gellan, NW11
Contained glycoepitopes: IEDB_115136,IEDB_1394182,IEDB_140630,IEDB_142488,IEDB_146664,IEDB_423153,IEDB_983930,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 2707
Pollock TJ "Gellan-related polysaccharides and the genus Sphingomonas" -
Journal of General Microbiology 139 (1993) 1939-1945
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5. Compound ID: 8324
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GalpA6NH2-(1--P--?)--+
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Manp-(1-?)-Manp-(1-?)-Glcp-(1-?)-Manp-(1-?)-Kdop-(2--/lipid A/ |
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Structure type: oligomer
Aglycon: lipid A
Trivial name: core region
Compound class: core oligosaccharide
Contained glycoepitopes: IEDB_130650,IEDB_130701,IEDB_133966,IEDB_136104,IEDB_137485,IEDB_1394182,IEDB_141793,IEDB_141836,IEDB_142488,IEDB_143632,IEDB_144983,IEDB_144995,IEDB_144998,IEDB_146664,IEDB_152206,IEDB_153219,IEDB_153220,IEDB_164174,IEDB_164479,IEDB_474450,IEDB_983930,IEDB_983931,SB_136,SB_192,SB_196,SB_197,SB_198,SB_44,SB_67,SB_72
The structure is contained in the following publication(s):
- Article ID: 3623
Knirel YA, Kochetkov NK "The structure of lipopolysaccharides of gram-negative bacteria. II. The structure of the core region" -
Biochemistry (Moscow) 58(2) (1993) 84-99
This review summarizes data on the structure of the core of bacterial lipopolysaccharides (LPS), an oligosaccharide which binds the lipid moiety of LPS to the O-antigenic polysaccharide chain. Both S-strains with complete LPS and R-mutants having various defects of core biosynthesis are considered. The role of the core in the functioning of the outer membrane and in the manifestation of antigenic specificity of LPS is discussed.
Lipopolysaccharide, antigen, lipopolysaccharides, LPS, structure, core, bacteria, core region, region, Gram-negative bacteria, gram negative bacteria, Gram-negative, review, outer membrane, bacterial lipopolysaccharide
Journal NLM ID: 0376536Publisher: Nauka/Interperiodica
Institutions: N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow (Russian Federation)
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6. Compound ID: 8362
Structure type: polymer chemical repeating unit
Compound class: O-polysaccharide, O-antigen
Contained glycoepitopes: IEDB_130660,IEDB_130701,IEDB_136044,IEDB_136105,IEDB_136906,IEDB_137472,IEDB_1394181,IEDB_1394182,IEDB_139421,IEDB_141794,IEDB_144983,IEDB_151528,IEDB_152206,IEDB_174033,IEDB_190606,IEDB_225177,IEDB_885823,IEDB_983930,SB_165,SB_166,SB_187,SB_195,SB_44,SB_67,SB_7,SB_72,SB_88
The structure is contained in the following publication(s):
- Article ID: 3635
Fukuda M, Egami F, Hammerling G, Luderitz O, Bagdian G, Staub AM "A reinvestigation of the anomeric configuration of mannose in the antigens of Salmonella groups B, D and E" -
European Journal of Biochemistry 20(3) (1971) 438-441
The anomeric configuration of mannose is a in the 0 antigens of Salmonella groups Band D, and b in group E, i.e. directly opposite to what was anticipated earlier from data obtained with mannosidase from rat epididymis. The present results were obtained with the aid of a-mannosidase from jack bean meal and of purified a- and b-mannosidases from a marine gastropod, which were allowed to act upon the disaccharides mannosyl-rhamnose isolated from partial hydrolysates of the respective antigens. The new findings, however, do not alter the validity of previous conclusions.
antigen, chemistry, analysis, group, antigens, immunology, Salmonella, Salmonella typhimurium, chromatography, Mannose, configuration, reinvestigation, anomeric, anomeric configuration, Glycoside Hydrolases, D, Mollusca, Plant Extracts
NCBI PubMed ID: 4931954Journal NLM ID: 0107600Publisher: Oxford, UK: Blackwell Science Ltd. on behalf of the Federation of European Biochemical Societies
Institutions: Department of Biophysics and Biochemistry, Faculty of Science, Univwersity of Tokyo.
Methods: biochemical methods
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7. Compound ID: 8363
Structure type: polymer chemical repeating unit
Compound class: O-polysaccharide, O-antigen
Contained glycoepitopes: IEDB_136044,IEDB_136105,IEDB_136906,IEDB_137472,IEDB_137485,IEDB_1394181,IEDB_1394182,IEDB_139420,IEDB_139421,IEDB_141794,IEDB_144983,IEDB_151528,IEDB_152206,IEDB_190606,IEDB_225177,IEDB_885823,IEDB_983930,SB_165,SB_166,SB_187,SB_195,SB_44,SB_7,SB_72,SB_88
The structure is contained in the following publication(s):
- Article ID: 3635
Fukuda M, Egami F, Hammerling G, Luderitz O, Bagdian G, Staub AM "A reinvestigation of the anomeric configuration of mannose in the antigens of Salmonella groups B, D and E" -
European Journal of Biochemistry 20(3) (1971) 438-441
The anomeric configuration of mannose is a in the 0 antigens of Salmonella groups Band D, and b in group E, i.e. directly opposite to what was anticipated earlier from data obtained with mannosidase from rat epididymis. The present results were obtained with the aid of a-mannosidase from jack bean meal and of purified a- and b-mannosidases from a marine gastropod, which were allowed to act upon the disaccharides mannosyl-rhamnose isolated from partial hydrolysates of the respective antigens. The new findings, however, do not alter the validity of previous conclusions.
antigen, chemistry, analysis, group, antigens, immunology, Salmonella, Salmonella typhimurium, chromatography, Mannose, configuration, reinvestigation, anomeric, anomeric configuration, Glycoside Hydrolases, D, Mollusca, Plant Extracts
NCBI PubMed ID: 4931954Journal NLM ID: 0107600Publisher: Oxford, UK: Blackwell Science Ltd. on behalf of the Federation of European Biochemical Societies
Institutions: Department of Biophysics and Biochemistry, Faculty of Science, Univwersity of Tokyo.
Methods: biochemical methods
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8. Compound ID: 8365
Structure type: polymer chemical repeating unit
Compound class: O-polysaccharide, O-antigen
Contained glycoepitopes: IEDB_130701,IEDB_136044,IEDB_136105,IEDB_137472,IEDB_1394181,IEDB_1394182,IEDB_141794,IEDB_144983,IEDB_152206,IEDB_190606,IEDB_225177,IEDB_885823,IEDB_983930,SB_165,SB_166,SB_187,SB_195,SB_44,SB_67,SB_7,SB_72,SB_88
The structure is contained in the following publication(s):
- Article ID: 3637
Ryan JM, Conrad HE "Structural heterogeneity in the lipopolysaccharide of Salmonella newington" -
Archives of Biochemistry and Biophysics 162(2) (1974) 530-535
Salmonella newington lipopolysaccharide extracted from a cell paste grown up from a single smooth clone was fractionated by chromatography on DEAE-cellulose in the presence of 1% Triton X-100 into seven lipopolysaccharide fractions which differed in their degrees of polymerization of the repeating unit of the O-antigen side chain and in their substitution with ester phosphate. Several of the lipopolysaccharide fractions were hydrolyzed in 1% acetic acid at 100 °C to cleave the linkage between the polysaccharide and lipid A parts of the structure. The polysaccharide fractions from each of the purified lipopolysaccharides could be further fractionated on DEAE-cellulose columns to yield a number of peaks of polysaccharide having monosaccharide ratios quite distinct from those of the parent lipopolysaccharide. The results show a high degree of structural heterogeneity in the original lipopolysaccharide.
Lipopolysaccharide, carbohydrates, lipopolysaccharides, structural, analysis, Salmonella, glucose, rhamnose, galactose, chromatography, Mannose, PDF, Glucosamine, heterogeneity, gel, Phosphates, DEAE-Cellulose, Salmonella newington, Surface-Active Agents
NCBI PubMed ID: 4407306Journal NLM ID: 0372430Institutions: Department of Biochemistry, University of Illinois, Urbana, IL, USA
Methods: sugar analysis
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9. Compound ID: 8366
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EtN-(1--P--?)--Kdop-(?-?)-+
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a-GlcpNAc-(1-2)-+ a-Galp-(1-6)-+ EtN-(1-?)-+ EtN-(1-?)-+ |
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Subst-(1-6)-a-Manp-(1-4)-b-Rhap-(1-3)-b-Galp-(1-4)-a-Glcp-(1-2)-a-Galp-(1-3)-Glcp-(1-3)-b-Hepp-(1-3)-b-Hepp-(1-5)-Kdop-(?-?)-Kdop-(2--/lipid A/
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P-?)-+ P-?)-+
Subst = O-antigen |
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Structure type: oligomer
Aglycon: lipid A
Compound class: core oligosaccharide with O-unit
Contained glycoepitopes: IEDB_120354,IEDB_123890,IEDB_130650,IEDB_130658,IEDB_130659,IEDB_130693,IEDB_130701,IEDB_136044,IEDB_136906,IEDB_137340,IEDB_137472,IEDB_137777,IEDB_137778,IEDB_1394181,IEDB_1394182,IEDB_140529,IEDB_141794,IEDB_141807,IEDB_142487,IEDB_142488,IEDB_144983,IEDB_144998,IEDB_146664,IEDB_151528,IEDB_151531,IEDB_152206,IEDB_167069,IEDB_190606,IEDB_225177,IEDB_885823,IEDB_983930,IEDB_983931,SB_165,SB_166,SB_187,SB_192,SB_195,SB_44,SB_6,SB_67,SB_7,SB_72,SB_88
The structure is contained in the following publication(s):
- Article ID: 3637
Ryan JM, Conrad HE "Structural heterogeneity in the lipopolysaccharide of Salmonella newington" -
Archives of Biochemistry and Biophysics 162(2) (1974) 530-535
Salmonella newington lipopolysaccharide extracted from a cell paste grown up from a single smooth clone was fractionated by chromatography on DEAE-cellulose in the presence of 1% Triton X-100 into seven lipopolysaccharide fractions which differed in their degrees of polymerization of the repeating unit of the O-antigen side chain and in their substitution with ester phosphate. Several of the lipopolysaccharide fractions were hydrolyzed in 1% acetic acid at 100 °C to cleave the linkage between the polysaccharide and lipid A parts of the structure. The polysaccharide fractions from each of the purified lipopolysaccharides could be further fractionated on DEAE-cellulose columns to yield a number of peaks of polysaccharide having monosaccharide ratios quite distinct from those of the parent lipopolysaccharide. The results show a high degree of structural heterogeneity in the original lipopolysaccharide.
Lipopolysaccharide, carbohydrates, lipopolysaccharides, structural, analysis, Salmonella, glucose, rhamnose, galactose, chromatography, Mannose, PDF, Glucosamine, heterogeneity, gel, Phosphates, DEAE-Cellulose, Salmonella newington, Surface-Active Agents
NCBI PubMed ID: 4407306Journal NLM ID: 0372430Institutions: Department of Biochemistry, University of Illinois, Urbana, IL, USA
Methods: sugar analysis
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10. Compound ID: 9004
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a-Galp-(1-4)-+
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a-GalpA-(1-5)-Kdop-(2-4)-+
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a-GalpA-(1-4)-+ |
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Fucp-(1-?)-Manp-(1-?)-QuipNAc-(1-?)-Kdop-(2-6)-a-Galp-(1-6)-a-Manp-(1-5)-Kdop-(2--/lipid A/ |
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Structure type: oligomer
Aglycon: lipid A
Compound class: core oligosaccharide
Contained glycoepitopes: IEDB_115015,IEDB_130650,IEDB_130659,IEDB_130701,IEDB_136045,IEDB_136906,IEDB_137472,IEDB_137485,IEDB_1394182,IEDB_141794,IEDB_142489,IEDB_144562,IEDB_144983,IEDB_149135,IEDB_151528,IEDB_152206,IEDB_152214,IEDB_174333,IEDB_190606,IEDB_983930,SB_44,SB_67,SB_7,SB_72,SB_86
The structure is contained in the following publication(s):
- Article ID: 3869
Kabanov DS, Prokhorenko IR "Structural analysis of lipopolysaccharides from Gram-negative bacteria" -
Biochemistry (Moscow) 75(4) (2010) 383-404
This review covers data on composition and structure of lipid A, core, and O-polysaccharide of the known lipopolysaccharides from Gram-negative bacteria. The relationship between the structure and biological activity of lipid A is discussed. The data on roles of core and O-polysaccharide in biological activities of lipopolysaccharides are presented. The structural homology of some oligosaccharide sequences of lipopolysaccharides to gangliosides of human cell membranes is considered.
core, Lipooligosaccharide, O-antigen, lipid A, gangliosides, cytokines, lipopolysaccharide (endotoxin)
NCBI PubMed ID: 20618127Publication DOI: 10.1134/S0006297910040012Journal NLM ID: 0376536Publisher: Nauka/Interperiodica
Correspondence: kabanovd1@rambler.ru
Institutions: Institute of Basic Biological Problems, Russian Academy of Sciences, Pushchino, Russia
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11. Compound ID: 9989
Structure type: oligomer
Contained glycoepitopes: IEDB_115136,IEDB_1394182,IEDB_140630,IEDB_142488,IEDB_146664,IEDB_423153,IEDB_983930,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 4159
O'Neill MA, Darvill AG, Albersheim P, Chou KJ "Structural analysis of an acidic polysaccharide secreted by Xanthobacter sp. (ATCC 53272)" -
Carbohydrate Research 206 (1990) 289-296
The structure of an acidic polysaccharide secreted by a Xanthobacter sp. has been investigated by glycosyl-residue and glycosyl-linkage composition analyses, and the characterization of oligoglycosyl fragments of the polysaccharide has been carried out by chemical analyses, 1H-n.m.r. spectroscopy, fast-atom bombardment mass spectrometry, and electron-impact mass spectrometry. The polysaccharide, which contains O-acetyl groups (approximately 5%) that have not been located, has the tetraglycosyl repeating unit 1 and belongs to a group of structurally related polysaccharides synthesized by both Alcaligenes and Pseudomonas species.
NCBI PubMed ID: 2073637Publication DOI: 10.1016/0008-6215(90)80068-EJournal NLM ID: 0043535Publisher: Elsevier
Institutions: University of Georgia Complex Carbohydrate Center, Athens, USA
Methods: 1H NMR, GLC-MS, gel filtration, FAB-MS, partial acid hydrolysis, acid hydrolysis, GLC, methanolysis
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12. Compound ID: 10034
Structure type: oligomer
Trivial name: arabinogalactan
Contained glycoepitopes: IEDB_114706,IEDB_130701,IEDB_136907,IEDB_137485,IEDB_1394182,IEDB_144983,IEDB_152206,IEDB_983930,SB_44,SB_67,SB_72
The structure is contained in the following publication(s):
- Article ID: 2277
Daffé M, McNeil M, Brennan PJ "Major structural features of the cell wall arabinogalactans of Mycobacterium, Rhodococcus, and Nocardia spp." -
Carbohydrate Research 249 (1993) 383-398
The cell wall arabinogalactans of strains of Mycobacterium, Rhodococcus, and Nocardia were per-O-methylated, partially hydrolyzed with acid, and the resulting oligosaccharides were reduced and per-O-ethylated to yield per-O-alkylated oligoglycosyl alditol fragments. Analyses of these fragments by gas chromatography-mass spectrometry and of the intact solubilized polysaccharides by 1H and 13C NMR revealed the major structural features of the different arabinogalactans from representatives of the different genera. All of the mycobacterial products contained a homogalactan segment of alternating 5-linked α-Galactofuranosyl (Galf) and 6-linked β-Galf residues. The arabinan segment consisted of three major domains, linear 5-linked α-arabinofuranosyl (Araf) residues and branched (3→5)-linked Araf units substituted with either 5-linked Araf or the disaccharide β-Araf-(1→2)-α-Araf at both branched positions. The recognition of these features in in vivo grown Mycobacterium leprae is an important development. The arabinan from strains of Nocardia contains a nonreducing-end motif composed of the linear trisaccharide, β-Araf-(1→2)-α-Araf-(1→5)-Araf, attached to linear 5-linked α-Araf units. The galactan segment of the arabinogalactan of Nocardia sp. is composed of linear 5-linked β-Galf units substituted in part at O-6 with terminal β-glucosyl units. The two representative strains of Rhodococcus also differed in the composition of the galactan moiety; in addition to the 5-linked Galf, 2- and 3-linked β-Galf units are present. The reducing end of the galactans, and therefore, apparently, of the entire arabinogalactans from all species from all genera, are apparently composed of the unit, rhamnosyl-(1→3)-N-acetyl-glucosamine, which, in turn, is apparently attached to peptidoglycan via phosphodiester linkage.
NCBI PubMed ID: 8275507Publication DOI: 10.1016/0008-6215(93)84102-CJournal NLM ID: 0043535Publisher: Elsevier
Institutions: Department of Microbiology, Colorado State University, Fort Collins 80523
Methods: 13C NMR, 1H NMR, GLC-MS
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13. Compound ID: 10208
Structure type: oligomer
Compound class: glycolipid, glycoglycerolipid, archaeol lipid, glycosyl diphytanyl glycerol, sulfatide
Contained glycoepitopes: IEDB_130701,IEDB_1394182,IEDB_142488,IEDB_144983,IEDB_144998,IEDB_146664,IEDB_152206,IEDB_983930,IEDB_983931,SB_192,SB_44,SB_67,SB_72
The structure is contained in the following publication(s):
- Article ID: 4236
Ishizuka I "Chemistry and functional distribution of sulfoglycolipids" -
Progress in Lipid Research 36 (1997) 245-319
No abstract
NCBI PubMed ID: 9640458Publication DOI: 10.1016/S0163-7827(97)00011-8Journal NLM ID: 7900832Publisher: Oxford; Elmsford, NY, Pergamon Press
Institutions: Teikyo University School of Medicine, Tokyo, Japan
Methods: 1H NMR, IR, FAB-MS, Azure A assay
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14. Compound ID: 10209
Structure type: oligomer
Compound class: glycolipid, glycoglycerolipid, archaeol lipid, glycosyl diphytanyl glycerol, sulfatide
Contained glycoepitopes: IEDB_130701,IEDB_1394182,IEDB_142488,IEDB_144983,IEDB_144998,IEDB_146664,IEDB_152206,IEDB_983930,IEDB_983931,SB_192,SB_44,SB_67,SB_72
The structure is contained in the following publication(s):
- Article ID: 4236
Ishizuka I "Chemistry and functional distribution of sulfoglycolipids" -
Progress in Lipid Research 36 (1997) 245-319
No abstract
NCBI PubMed ID: 9640458Publication DOI: 10.1016/S0163-7827(97)00011-8Journal NLM ID: 7900832Publisher: Oxford; Elmsford, NY, Pergamon Press
Institutions: Teikyo University School of Medicine, Tokyo, Japan
Methods: 1H NMR, IR, FAB-MS, Azure A assay
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15. Compound ID: 10210
Structure type: oligomer
Compound class: glycolipid, glycoglycerolipid, archaeol lipid, glycosyl diphytanyl glycerol, sulfatide
Contained glycoepitopes: IEDB_130701,IEDB_1394182,IEDB_142488,IEDB_144983,IEDB_144998,IEDB_146664,IEDB_152206,IEDB_983930,IEDB_983931,SB_192,SB_44,SB_67,SB_72
The structure is contained in the following publication(s):
- Article ID: 4236
Ishizuka I "Chemistry and functional distribution of sulfoglycolipids" -
Progress in Lipid Research 36 (1997) 245-319
No abstract
NCBI PubMed ID: 9640458Publication DOI: 10.1016/S0163-7827(97)00011-8Journal NLM ID: 7900832Publisher: Oxford; Elmsford, NY, Pergamon Press
Institutions: Teikyo University School of Medicine, Tokyo, Japan
Methods: 1H NMR, IR, FAB-MS, Azure A assay
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Next 15 structure(s)
Total list of structure IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
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