CSDB: Search results

Found 1 organism. Displayed organism 1
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1. (Organism ID: 593)

Mycobacterium tuberculosis

(NCBI TaxID 1773, species name lookup)

Previously named: Bacterium tuberculosis , Bacillus tuberculosis
Taxonomic group: bacteria
Phylum: Actinobacteria

The following compound(s) are assigned to this organism:

Compound ID: 1007

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Compound ID: 1008

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Compound ID: 1009

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Compound ID: 1010

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Structure type: oligomer
Trivial name: phospholipid (glycosylphosphopolyprenol)

BOOK: Tuberculosis (series: Current Topics in Microbiology and Immunology); Eds.: Shinnick TM; Berlin, Heidelberg: Springer. 1996, "Mycobacterium tuberculosis cell envelope"
CSDB ID 31418 (all data & tools)
Compound ID: 1011

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Structure type: oligomer
Trivial name: phospholipid (glycosylphosphopolyprenol)

BOOK: Tuberculosis (series: Current Topics in Microbiology and Immunology); Eds.: Shinnick TM; Berlin, Heidelberg: Springer. 1996, "Mycobacterium tuberculosis cell envelope"
CSDB ID 31419 (all data & tools)
Compound ID: 1012

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Structure type: fragment of a bigger structure
Trivial name: nonreducing terminal epitope of lipoarabinomannan
Reference(s) to other database(s): GTC:G46014AY

BOOK: Tuberculosis (series: Current Topics in Microbiology and Immunology); Eds.: Shinnick TM; Berlin, Heidelberg: Springer. 1996, "Mycobacterium tuberculosis cell envelope"
CSDB ID 31420 (all data & tools)

Compound ID: 1013

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Compound ID: 1014

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Compound ID: 1015

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Structure type: fragment of a bigger structure
Trivial name: nonreducing terminal epitope of lipoarabinomannan
Reference(s) to other database(s): GTC:G69949WX

BOOK: Tuberculosis (series: Current Topics in Microbiology and Immunology); Eds.: Shinnick TM; Berlin, Heidelberg: Springer. 1996, "Mycobacterium tuberculosis cell envelope"
CSDB ID 31423 (all data & tools)

Compound ID: 1016

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Compound ID: 1017

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Compound ID: 1018

-5)-a-D-Araf-(1- Show graphically

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Structure type: homopolymer
Trivial name: arabinan, arabinan fragmemnt of the lipoarabinomannan
Compound class: arabinogalactan, arabinan part of arabinogalactan
Reference(s) to other database(s): GTC:G30321MJ, GlycomeDB:10680

BOOK: Tuberculosis (series: Current Topics in Microbiology and Immunology); Eds.: Shinnick TM; Berlin, Heidelberg: Springer. 1996, "Mycobacterium tuberculosis cell envelope"
CSDB ID 31426 (all data & tools)

Journal of Biological Chemistry 1990, "Predominant structural features of the cell wall arabinogalactan of Mycobacterium tuberculosis as revealed through characterization of oligoglycosyl alditol fragments by gas chromatography/mass spectrometry and by proton and carbon-13 NMR analyses"
CSDB ID 135836 (all data & tools)

BOOK: Methods in Molecular Biology; Eds.: Holst O, Walker JM, Beck A; Totowa, NJ: Humana Press 2013, "Subfractionation and analysis of the cell envelope (lipo)polysaccharides of Mycobacterium tuberculosis"
CSDB ID 29528 (all data & tools)
Compound ID: 1019

-5)-b-D-Galf-(1- Show graphically

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Structure type: homopolymer
Trivial name: galactan, PAM-galactan, galactofuranomannan
Compound class: EPS, cell wall polysaccharide, arabinogalactan, galactan
Reference(s) to other database(s): GTC:G92108RF, CCSD:7498, CBank-STR:2546

BOOK: Tuberculosis (series: Current Topics in Microbiology and Immunology); Eds.: Shinnick TM; Berlin, Heidelberg: Springer. 1996, "Mycobacterium tuberculosis cell envelope"
CSDB ID 31427 (all data & tools)

Compound ID: 1020

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Compound ID: 1577

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Compound ID: 1578

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Structure type: fragment of a bigger structure
Aglycon: (->5) arabinan
Trivial name: mannooligosaccharide cap of the LAM (ManLAM)

Applied Biochemistry and Biotechnology 2004, "Structural analysis of mycobacterial lipoglycans"
CSDB ID 31634 (all data & tools)
Compound ID: 1579

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Structure type: fragment of a bigger structure
Aglycon: (->5) arabinan
Trivial name: phospho-myo-inositol cap (PILAM)

Applied Biochemistry and Biotechnology 2004, "Structural analysis of mycobacterial lipoglycans"
CSDB ID 31635 (all data & tools)

Compound ID: 1813

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Compound ID: 1814

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Compound ID: 2068

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:25200

Journal of Organic Chemistry 2001, "Synthesis of oligosaccharides of motifs D and E of arabinogalactan present in Mycobacterium tuberculosis"
CSDB ID 469 (all data & tools)
Compound ID: 2157

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:12667

Journal of Organic Chemistry 2001, "Synthesis of oligosaccharides of motifs D and E of arabinogalactan present in Mycobacterium tuberculosis"
CSDB ID 582 (all data & tools)
Compound ID: 2330

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:11084

Journal of the American Chemical Society 2000, "Arabinofuranosyl oligosaccharides from mycobacteria: Synthesis and effect of glycosylation on ring conformation and hydroxymethyl group rotamer populations"
CSDB ID 1279 (all data & tools)
Compound ID: 2331

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:25417

Journal of the American Chemical Society 2000, "Arabinofuranosyl oligosaccharides from mycobacteria: Synthesis and effect of glycosylation on ring conformation and hydroxymethyl group rotamer populations"
CSDB ID 1344 (all data & tools)
Compound ID: 2332

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:25418

Journal of the American Chemical Society 2000, "Arabinofuranosyl oligosaccharides from mycobacteria: Synthesis and effect of glycosylation on ring conformation and hydroxymethyl group rotamer populations"
CSDB ID 1345 (all data & tools)
Compound ID: 2333

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:25419

Journal of the American Chemical Society 2000, "Arabinofuranosyl oligosaccharides from mycobacteria: Synthesis and effect of glycosylation on ring conformation and hydroxymethyl group rotamer populations"
CSDB ID 1346 (all data & tools)
Compound ID: 2334

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:25420

Journal of the American Chemical Society 2000, "Arabinofuranosyl oligosaccharides from mycobacteria: Synthesis and effect of glycosylation on ring conformation and hydroxymethyl group rotamer populations"
CSDB ID 1347 (all data & tools)
Compound ID: 2335

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:16140

Journal of the American Chemical Society 2000, "Arabinofuranosyl oligosaccharides from mycobacteria: Synthesis and effect of glycosylation on ring conformation and hydroxymethyl group rotamer populations"
CSDB ID 1348 (all data & tools)
Compound ID: 2659

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Structure type: oligomer
Aglycon: 9-decen-1-ol
Trivial name: neoglycolipid acceptor
Reference(s) to other database(s): GTC:G16870CD, GlycomeDB:12667

Journal of Biological Chemistry 2001, "Galactan biosynthesis in Mycobacterium tuberculosis. Identification of a bifunctional UDP-galactofuranosyltransferase"
CSDB ID 2888 (all data & tools)
Compound ID: 2660

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Structure type: oligomer
Aglycon: 9-decen-1-ol
Trivial name: neoglycolipid acceptor
Reference(s) to other database(s): GTC:G10721CS, GlycomeDB:3807

Journal of Biological Chemistry 2001, "Galactan biosynthesis in Mycobacterium tuberculosis. Identification of a bifunctional UDP-galactofuranosyltransferase"
CSDB ID 3081 (all data & tools)
Compound ID: 2661

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Structure type: oligomer
Aglycon: 9-decen-1-ol
Reference(s) to other database(s): GTC:G69030ZC, GlycomeDB:25786

Journal of Biological Chemistry 2001, "Galactan biosynthesis in Mycobacterium tuberculosis. Identification of a bifunctional UDP-galactofuranosyltransferase"
CSDB ID 2904 (all data & tools)
Compound ID: 2662

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Structure type: oligomer
Aglycon: 9-decen-1-ol
Reference(s) to other database(s): GTC:G07059FD, GlycomeDB:25787

Journal of Biological Chemistry 2001, "Galactan biosynthesis in Mycobacterium tuberculosis. Identification of a bifunctional UDP-galactofuranosyltransferase"
CSDB ID 2905 (all data & tools)
Compound ID: 2663

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Structure type: oligomer
Aglycon: 9-decen-1-ol
Reference(s) to other database(s): GTC:G99317XX, GlycomeDB:25788

Journal of Biological Chemistry 2001, "Galactan biosynthesis in Mycobacterium tuberculosis. Identification of a bifunctional UDP-galactofuranosyltransferase"
CSDB ID 2906 (all data & tools)
Compound ID: 3011

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Structure type: polymer chemical repeating unit ; n=15
Trivial name: galactofuran
Reference(s) to other database(s): GTC:G27434VY, GlycomeDB:26078

Journal of Bacteriology 2001, "Cell wall core galactofuran synthesis is essential for growth of mycobacteria"
CSDB ID 4006 (all data & tools)
Compound ID: 3085

a-D-Glcp-(1-1)-Dec Show graphically

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Structure type: monomer
Reference(s) to other database(s): GlycomeDB:123

Carbohydrate Research 1995, "Synthesis of a pentasaccharide fragment of polysaccharide II of Mycobacterium tuberculosis"
CSDB ID 4074 (all data & tools)
Compound ID: 3086

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:1463

Carbohydrate Research 1995, "Synthesis of a pentasaccharide fragment of polysaccharide II of Mycobacterium tuberculosis"
CSDB ID 4159 (all data & tools)
Compound ID: 3087

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:8662

Carbohydrate Research 1995, "Synthesis of a pentasaccharide fragment of polysaccharide II of Mycobacterium tuberculosis"
CSDB ID 4160 (all data & tools)
Compound ID: 3088

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:8663

Carbohydrate Research 1995, "Synthesis of a pentasaccharide fragment of polysaccharide II of Mycobacterium tuberculosis"
CSDB ID 4161 (all data & tools)
Compound ID: 3089

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:26239

Carbohydrate Research 1995, "Synthesis of a pentasaccharide fragment of polysaccharide II of Mycobacterium tuberculosis"
CSDB ID 4162 (all data & tools)

Compound ID: 4342

b-D-Galf-(1-6)-{{{-b-D-Galf-(1-5)-b-D-Galf-(1-6)-}}}+ | Mycolic-(1-5)-+ | | | Mycolic-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | Mycolic-(1-5)-+ | {{{-a-D-Araf-(1-5)-}}}/n=7/-a-D-Araf-(1-3)-+ | | | | | Mycolic-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-5)-b-D-Galf-(1-5)-{{{-b-D-Galf-(1-6)-b-D-Galf-(1-5)-}}}/n=3/-a-D-Galf-(1-4)-b-L-Rhap-(1-4)-a-D-GlcpNAc-(1---P---/peptidoglycan/

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Compound ID: 4343

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Compound ID: 4344

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Compound ID: 4392

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Structure type: oligomer
Aglycon: rest of arabinogalactan
Reference(s) to other database(s): GTC:G12037KS, GlycomeDB:10774

Glycobiology 2005, "Structural elucidation of the predominant motifs of the major cell wall arabinogalactan antigens from the borderline species Tsukamurella paurometabolum and Mycobacterium fallax"
CSDB ID 10630 (all data & tools)

Compound ID: 4395

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Compound ID: 4396

-5)-a-D-Araf-(1- Show graphically

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Structure type: polymer chemical repeating unit
Reference(s) to other database(s): GTC:G30321MJ, GlycomeDB:10680

Glycobiology 2005, "Structural elucidation of the predominant motifs of the major cell wall arabinogalactan antigens from the borderline species Tsukamurella paurometabolum and Mycobacterium fallax"
CSDB ID 10780 (all data & tools)
Compound ID: 4397

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Structure type: polymer chemical repeating unit
Trivial name: galactan, galactan core of arabinogalactan
Reference(s) to other database(s): GTC:G27434VY, GlycomeDB:10681

Glycobiology 2005, "Structural elucidation of the predominant motifs of the major cell wall arabinogalactan antigens from the borderline species Tsukamurella paurometabolum and Mycobacterium fallax"
CSDB ID 10781 (all data & tools)

Journal of Biological Chemistry 1990, "Predominant structural features of the cell wall arabinogalactan of Mycobacterium tuberculosis as revealed through characterization of oligoglycosyl alditol fragments by gas chromatography/mass spectrometry and by proton and carbon-13 NMR analyses"
CSDB ID 135837 (all data & tools)

Biochemistry 2012, "A processive carbohydrate polymerase that mediates bifunctional catalysis using a single active site"
CSDB ID 27248 (all data & tools)
Compound ID: 4569

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Structure type: oligomer
Compound class: LOS
Reference(s) to other database(s): GTC:G01875TD, GlycomeDB:3126

Biochemistry 1991, "Novel type-specific lipooligosaccharides from Mycobacterium tuberculosis"
CSDB ID 107651 (all data & tools)
Compound ID: 4599

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Structure type: oligomer
Aglycon: peptidoglycan
Compound class: peptidoglycan
Reference(s) to other database(s): GlycomeDB:16957

Biochemistry 1995, "A new interpretation of the structure of the mycolyl-arabinogalactan complex of Mycobacterium tuberculosis as revealed through characterization of oligoglycosylalditol fragments by fast-atom bombardment mass spectrometry and 1H nuclear magnetic resonance spectroscopy"
CSDB ID 108289 (all data & tools)
Compound ID: 4786

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Structure type: monomer
Aglycon: (->1) Phenolphthiocerol dimycocerosate
Reference(s) to other database(s): GTC:G62332IV, GlycomeDB:3740

Biochimica et Biophysica Acta 1988, "Monoglycosyldiacylphenol-phthiocerol of Mycobacterium tuberculosis and Mycobacterium bovis"
CSDB ID 109136 (all data & tools)
Compound ID: 4787

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Structure type: oligomer
Aglycon: Phenolphthiocerol dimycocerosate
Compound class: glycolipid
Reference(s) to other database(s): GTC:G83415MR, GlycomeDB:3760

Biochimica et Biophysica Acta 1989, "Further specific triglycosyl phenol phthiocerol diester from Mycobacterium tuberculosis"
CSDB ID 109219 (all data & tools)
Compound ID: 4792

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Structure type: oligomer
Aglycon: phenolphthiocerol A dimycocerosate
Reference(s) to other database(s): GTC:G54215YH, GlycomeDB:3796

Biochimica et Biophysica Acta 1994, "Structural elucidation of new phenolic glycolipids from Mycobacterium tuberculosis"
CSDB ID 109501 (all data & tools)
Compound ID: 4793

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Structure type: oligomer
Aglycon: phenolphthiotriol A dimycocerosate
Reference(s) to other database(s): GTC:G79798AG, GlycomeDB:3797

Biochimica et Biophysica Acta 1994, "Structural elucidation of new phenolic glycolipids from Mycobacterium tuberculosis"
CSDB ID 109502 (all data & tools)
Compound ID: 4796

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Structure type: oligomer
Aglycon: phenolphthiocerol dimycocerosate
Trivial name: phenylethanoid glycoside
Reference(s) to other database(s): GTC:G79798AG, GlycomeDB:3797

Biological Mass Spectrometry 1994, "Fast atom bombardment mass spectrometry of mycobacterial phenolic glycolipids"
CSDB ID 110030 (all data & tools)
Compound ID: 5594

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Structure type: oligomer
Aglycon: unknown
Reference(s) to other database(s): GTC:G79798AG, GlycomeDB:3797

European Journal of Biochemistry 1987, "Structure of the major triglycosyl phenol-pthiocerol of Mycobacterium tuberculosis (strain Canetti)"
CSDB ID 123048 (all data & tools)
Compound ID: 5692

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Structure type: oligomer
Trivial name: trehalose
Reference(s) to other database(s): GlycomeDB:8671

FEMS Microbiology Letters 1991, "Revised structure of a trehalose-containing immunoreactive glycolipid of Mycobacterium tuberculosis"
CSDB ID 126009 (all data & tools)
Compound ID: 5711

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Structure type: oligomer
Trivial name: ManLAM
Reference(s) to other database(s): GTC:G65672WF, GlycomeDB:8827

Glycobiology 1993, "Structural definition of the non-reducing termini of mannose-capped LAM from Mycobacterium tuberculosis through selective enzymatic degradation and fast atom bombardment-mass spectrometry"
CSDB ID 126816 (all data & tools)
Compound ID: 5712

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Structure type: oligomer
Trivial name: ManLAM
Reference(s) to other database(s): GTC:G74579IY, GlycomeDB:8828

Glycobiology 1993, "Structural definition of the non-reducing termini of mannose-capped LAM from Mycobacterium tuberculosis through selective enzymatic degradation and fast atom bombardment-mass spectrometry"
CSDB ID 126817 (all data & tools)

Compound ID: 5713

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Compound ID: 5714

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Structure type: oligomer
Trivial name: ManLAM
Reference(s) to other database(s): GTC:G09324ZP, GlycomeDB:8830

Glycobiology 1993, "Structural definition of the non-reducing termini of mannose-capped LAM from Mycobacterium tuberculosis through selective enzymatic degradation and fast atom bombardment-mass spectrometry"
CSDB ID 126819 (all data & tools)
Compound ID: 5715

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Structure type: oligomer
Trivial name: ManLAM
Reference(s) to other database(s): GTC:G41692GO, GlycomeDB:8831

Glycobiology 1993, "Structural definition of the non-reducing termini of mannose-capped LAM from Mycobacterium tuberculosis through selective enzymatic degradation and fast atom bombardment-mass spectrometry"
CSDB ID 126820 (all data & tools)

Compound ID: 5716

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Compound ID: 5717

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Structure type: oligomer
Trivial name: ManLAM
Reference(s) to other database(s): GTC:G89130CO, GlycomeDB:8833

Glycobiology 1993, "Structural definition of the non-reducing termini of mannose-capped LAM from Mycobacterium tuberculosis through selective enzymatic degradation and fast atom bombardment-mass spectrometry"
CSDB ID 126822 (all data & tools)

Compound ID: 5718

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Compound ID: 5719

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Compound ID: 5720

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Compound ID: 5721

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Compound ID: 5722

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Structure type: oligomer
Reference(s) to other database(s): GTC:G31035LI, GlycomeDB:8883

Glycobiology 1994, "Enzymatic evidence for the presence of a critical terminal hexa-arabinoside in the cell walls of Mycobacterium tuberculosis"
CSDB ID 126933 (all data & tools)

Compound ID: 5732

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Compound ID: 5733

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Compound ID: 5734

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Compound ID: 5940

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Structure type: fragment of a bigger structure
Aglycon: arabinogalactan
Compound class: arabinogalactan
Reference(s) to other database(s): GTC:G33147FH, GlycomeDB:16141

Journal of Biological Chemistry 1990, "Predominant structural features of the cell wall arabinogalactan of Mycobacterium tuberculosis as revealed through characterization of oligoglycosyl alditol fragments by gas chromatography/mass spectrometry and by proton and carbon-13 NMR analyses"
CSDB ID 135833 (all data & tools)

Compound ID: 5941

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Compound ID: 5942

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Structure type: fragment of a bigger structure
Aglycon: (1->5)aDAraf of arabinogalactan
Compound class: arabinogalactan
Reference(s) to other database(s): GTC:G57248ZN, GlycomeDB:16140

Journal of Biological Chemistry 1990, "Predominant structural features of the cell wall arabinogalactan of Mycobacterium tuberculosis as revealed through characterization of oligoglycosyl alditol fragments by gas chromatography/mass spectrometry and by proton and carbon-13 NMR analyses"
CSDB ID 135835 (all data & tools)
Compound ID: 5965

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Structure type: oligomer
Reference(s) to other database(s): GTC:G12037KS, GlycomeDB:10774

Journal of Biological Chemistry 1991, "Location of the mycolyl ester substituents in the cell walls of mycobacteria"
CSDB ID 136188 (all data & tools)

Compound ID: 5966

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Compound ID: 5695

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Structure type: oligomer
Trivial name: diacyltrehalose
Compound class: glycolipid
Reference(s) to other database(s): GlycomeDB:245

Journal of Immunological Methods 1994, "Development of an enzyme-linked immunosorbent assay (ELISA) combined with a streptavidin-biotin and enzyme amplification method to detect anti-2,3-di-O-acyltrehalose (DAT) antibodies in patients with tuberculosis"
CSDB ID 140210 (all data & tools)
Compound ID: 6355

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Structure type: oligomer
Aglycon: phosphatidylinositol, lyso-PI
Compound class: glycolipid

Glycobiology 1995, "Structural definition of acylated phosphatidylinositol mannosides from Mycobacterium tuberculosis: definition of a common anchor for lipomannan and lipoarabinomannan"
CSDB ID 127450 (all data & tools)

Compound ID: 6356

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Compound ID: 6357

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Compound ID: 6358

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Compound ID: 6394

Mycolic-(?-5)-+ | Mycolic-(?-5)-b-D-Araf-(1-2)-b-D-Araf-(1-5)-+ | Mycolic-(?-5)-+ | | | Mycolic-(?-5)-b-D-Araf-(1-2)-b-D-Araf-(1-3)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-+ | Mycolic-(?-5)-+ | | | Mycolic-(?-5)-b-D-Araf-(1-2)-b-D-Araf-(1-5)-+ | | | Mycolic-(?-5)-+ | | | | | Mycolic-(?-5)-b-D-Araf-(1-2)-b-D-Araf-(1-3)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-b-D-Araf-(1-3)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-b-D-Araf-(1-5)-D-Ara

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Compound ID: 1267

-4)-a-D-Glcp-(1- Show graphically

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Structure type: homopolymer
Trivial name: methyl glucose lipopolysaccharide, glucan, maltosaccharide, α-1,4-D-glucan, amylose, α-glucan, glycogen backbone, α-(1,4)-glucan, starch, α-(1-4)-glucan, starch, glycogen
Compound class: CPS, EPS, O-polysaccharide, cell wall polysaccharide, glucan, polysaccharide, methyl glucose lipopolysaccharide
Reference(s) to other database(s): GTC:G05740LL, GlycomeDB:12100, CCSD:4943, CBank-STR:819

Biochemical Journal 1994, "Structural features of the exocellular polysaccharides of Mycobacterium tuberculosis"
CSDB ID 106369 (all data & tools)

Molecular Microbiology 2008, "Capsular glucan and intracellular glycogen of Mycobacterium tuberculosis: Biosynthesis and Impact on the Persistence in mice"
CSDB ID 22727 (all data & tools)
Compound ID: 6635

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Structure type: cyclic polymer repeating unit ; n=2-4
Compound class: cell wall polysaccharide
Reference(s) to other database(s): GTC:G27434VY, GlycomeDB:26078

Glycobiology 1994, "Enzymatic evidence for the presence of a critical terminal hexa-arabinoside in the cell walls of Mycobacterium tuberculosis"
CSDB ID 126932 (all data & tools)
Compound ID: 6636

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Structure type: oligomer
Aglycon: phosphatidylinositol, lyso-PI
Trivial name: mannophosphoinositide, phosphatidylinositol mannoside, PIM

Glycobiology 1995, "Structural definition of acylated phosphatidylinositol mannosides from Mycobacterium tuberculosis: definition of a common anchor for lipomannan and lipoarabinomannan"
CSDB ID 127451 (all data & tools)

Compound ID: 6769

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Compound ID: 6774

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Structure type: polymer biological repeating unit ; n=11
Reference(s) to other database(s): GTC:G61425HH, GlycomeDB:26078

Biochemistry 1995, "A new interpretation of the structure of the mycolyl-arabinogalactan complex of Mycobacterium tuberculosis as revealed through characterization of oligoglycosylalditol fragments by fast-atom bombardment mass spectrometry and 1H nuclear magnetic resonance spectroscopy"
CSDB ID 108288 (all data & tools)

Compound ID: 6678

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Compound ID: 1144

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Structure type: monomer
Trivial name: dTDP-6-deoxy-D-xylohex-4-ulose, dTDP-4-keto-6-deoxy-α-D-glucose, dTDP-6-dideoxy-xylo-hexos-4-ulose, dTDP-6-deoxy-α-D-xylo-hex-4-ulose, dTDP-4-oxo-6-deoxy-α-D-glucose, dTDP-6-deoxy-D-xylo-hex-4-ulopyranose, dTDP-4-keto-6-deoxy-D-glucose, dTDP-4-keto-6-deoxyglucose
Compound class: nucleoside diphosphate sugar

Journal of Molecular Biology 2007, "RmlC, a C3' and C5' carbohydrate epimerase, appears to operate via an intermediate with an unusual twist boat conformation"
CSDB ID 21584 (all data & tools)
Compound ID: 7640

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Structure type: monomer
Trivial name: dTDP-6-dideoxy-lyxo-hexos-4-ulose

Journal of Molecular Biology 2007, "RmlC, a C3' and C5' carbohydrate epimerase, appears to operate via an intermediate with an unusual twist boat conformation"
CSDB ID 22008 (all data & tools)
Compound ID: 7680

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Structure type: oligomer
Aglycon: octyl
Reference(s) to other database(s): GTC:G49480AS, GlycomeDB:16957

Journal of Bacteriology 2008, "Galactosyl transferases in mycobacterial cell wall synthesis"
CSDB ID 22612 (all data & tools)
Compound ID: 7681

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Structure type: oligomer
Aglycon: octyl
Reference(s) to other database(s): GlycomeDB:36907

Journal of Bacteriology 2008, "Galactosyl transferases in mycobacterial cell wall synthesis"
CSDB ID 22821 (all data & tools)
Compound ID: 7682

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Structure type: oligomer
Aglycon: octyl
Reference(s) to other database(s): GTC:G40662XV, GlycomeDB:36908

Journal of Bacteriology 2008, "Galactosyl transferases in mycobacterial cell wall synthesis"
CSDB ID 22822 (all data & tools)
Compound ID: 7683

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Structure type: oligomer
Aglycon: octyl
Reference(s) to other database(s): GTC:G99153GE, GlycomeDB:36909

Journal of Bacteriology 2008, "Galactosyl transferases in mycobacterial cell wall synthesis"
CSDB ID 22823 (all data & tools)
Compound ID: 7894

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Structure type: oligomer
Aglycon: peptidoglycan
Trivial name: tetrasaccharide phosphate the linkage region of the arabinogalactan-peptidoglycan complex
Compound class: cell wall polysaccharide

Carbohydrate Research 2008, "Synthesis of a tetrasaccharide phosphate from the linkage region of the arabinogalactan-peptidoglycan complex in the mycobacterial cell wall"
CSDB ID 22683 (all data & tools)
Compound ID: 8213

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Structure type: oligomer
Aglycon: 8-aminooctanol
Trivial name: synthetic hexasaccharide
Reference(s) to other database(s): GTC:G46014AY, GlycomeDB:10679

Current Topics in Medicinal Chemistry 2008, "Recent developments in synthetic oligosaccharide-based bacterial vaccines"
CSDB ID 23502 (all data & tools)

Compound ID: 8214

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Compound ID: 8215

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Compound ID: 8500

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Structure type: monomer
Trivial name: Glucosyl-3-phosphoglycerate

PLoS One 2009, "Initiation of methylglucose lipopolysaccharide biosynthesis in mycobacteria"
CSDB ID 23736 (all data & tools)
Compound ID: 8501

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Structure type: monomer
Trivial name: Glucosylglycerate

PLoS One 2009, "Initiation of methylglucose lipopolysaccharide biosynthesis in mycobacteria"
CSDB ID 24022 (all data & tools)
Compound ID: 8669

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Structure type: oligomer
Aglycon: C8H17
Reference(s) to other database(s): GTC:G87517PM, GlycomeDB:37411

Chembiochem: a European Journal of Chemical Biology 2009, "Chemistry and biology of galactofuranose-containing polysaccharides"
CSDB ID 24202 (all data & tools)
Compound ID: 10268

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Structure type: oligomer

News in Physiological Sciences 2003, "Self glycosphingolipids: new antigens recognized by autoreactive T lymphocytes"
CSDB ID 11406 (all data & tools)
Compound ID: 10269

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Structure type: monomer
Aglycon: dolichol

News in Physiological Sciences 2003, "Self glycosphingolipids: new antigens recognized by autoreactive T lymphocytes"
CSDB ID 14406 (all data & tools)

Compound ID: 10270

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Compound ID: 10894

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Compound ID: 11210

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Compound ID: 11211

Mycolic-(1-5)-+ | Mycolic-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | Mycolic-(1-5)-+ | | | Mycolic-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-5)-+ | Mycolic-(1-5)-+ | | | Mycolic-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | Mycolic-(1-5)-+ | | | | | Mycolic-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=13/-+ | | /Variants 0/-+ | | b-D-Galf-(1-5)-{{{-b-D-Galf-(1-6)-b-D-Galf-(1-5)-}}}/n=10/-b-D-Galf-(1-6)-b-D-Galf-(1-5)-{{{-b-D-Galf-(1-6)-b-D-Galf-(1-5)-}}}/n=3/-b-D-Galf-(1-4)-a-L-Rhap-(1-3)-a-D-GlcpNAc-(1---P---/peptidoglycan/ /Variants 0/ is: Suc-(1-2)- OR (exclusively) D-GalpN-(1-2)-

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Compound ID: 11212

10b1C19-(1-3)-+ | a-D-Manp-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | a-D-Manp-(1-2)-a-D-Manp-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-3)-+ | | | a-D-Manp-(1-2)-a-D-Manp-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | | | a-D-Manp-(1-2)-a-D-Manp-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-5)-+ | a-D-Manp-(1-6)-+ a-D-Manp-(1-2)-+ Pam-(1-?)-a-D-Manp-(1-2)-+ | | | | | | | a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-2)-a-D-Manp-(1-6)-{{{-a-D-Manp-(1-6)-}}}/n=10/-a-D-Manp-(1-6)-a-D-Manp-(1-6)-INO-(1--P--1)--Gro-(?--/phosphatidylinositol anchor of LAM/ | | 10b1C19-(1-?)-+ Pam-(1-2)-+

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Compound ID: 11284

Mycolic-(1-?)-+ | Mycolic-(1-?)-a-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | Mycolic-(1-?)-+ | ANY-(1-3)-+ b-D-Galf-(1-6)-+ ANY-(1-4)-+ | | | | | Mycolic-(1-?)-a-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-5)-b-D-Galf-(1-5)-{{{-b-D-Galf-(1-6)-b-D-Galf-(1-5)-}}}/n=30/-b-D-Galf-(1-6)-b-D-Galf-(1-5)-b-D-Galf-(1-4)-a-L-Rhap-(1-3)-a-D-GlcpNAc-(1--P--6)--b-Murp2Ac-(1-4)-b-D-GlcpNAc-(1--/peptidogycan/ | PEP-(2-8)-+

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Compound ID: 11323

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Structure type: oligomer
Aglycon: (->1)decaprenol
Trivial name: lipid-linked aceptor for galactan
Compound class: cell wall polysaccharide

Journal of the American Chemical Society 2011, "Monitoring processivity and length control of a carbohydrate polymerase"
CSDB ID 29634 (all data & tools)
Compound ID: 12818

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Structure type: structural motif or average structure
Trivial name: lipomannan
Compound class: EPS, cell wall polysaccharide, glycolipid
Reference(s) to other database(s): GTC:G70811VN

Carbohydrate Polymers 2017, "Synthesis of synthetic mannan backbone polysaccharides found on the surface of Mycobacterium tuberculosis as a vaccine adjuvant and their immunological properties"
CSDB ID 12034 (all data & tools)

Compound ID: 12819

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Compound ID: 12831

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Compound ID: 12879

b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-+ | b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=12/-a-D-Araf-(1-5)-+ | | ?%Suc-(1-2)-+ | | Mycolic-(1-?)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | Mycolic-(1-?)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-5)-+ | | | Mycolic-(1-?)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | | | Mycolic-(1-?)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-3)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=12/-a-D-Araf-(1-5)-+ | | | | ?%a-D-GalpN-(1-2)-+ | | | | Subst1-(1-?)-Subst2-(1-?)-b-D-Galf-(1-5)-{{{-b-D-Galf-(1-6)-b-D-Galf-(1-5)-}}}/n=2/-b-D-Galf-(1-6)-b-D-Galf-(1-5)-b-D-Galf-(1-6)-b-D-Galf-(1-5)-b-D-Galf-(1-6)-{{{-b-D-Galf-(1-5)-}}}/n=4/-b-D-Galf-(1-5)-b-D-Galf Subst1 = peptidoglycan; Subst2 = linker

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Compound ID: 12880

a-D-Manp-(1-2)-+ | a-D-Manp-(1-2)-+ | | | a-D-Manp-(1-2)-+ | | | | | a-D-Manp-(1-2)-+ | | | | | | | a-D-Manp-(1-2)-+ | | | | | | | | | a-D-Manp-(1-2)-+ | | | | | | | | | | | a-D-Manp-(1-2)-+ | | | | | | | | | | | | | a-D-Manp-(1-6)-+ | | | | | | | | | | | | | | | a-D-Manp-(1-2)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-+ | | | | | b-D-Araf-(1-2)-a-D-Araf-(1-3)-+ | | | | | | | b-D-Araf-(1-2)-{{{-a-D-Araf-(1-5)-}}}/n=5/-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-3)-+ | | | | | | | a-D-Manp-(1-2)-a-D-Manp-(1-2)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-+ | | | | | | | | | b-D-Araf-(1-2)-{{{-a-D-Araf-(1-5)-}}}/n=6/-a-D-Araf-(1-3)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=3/-a-D-Araf-(1-3)-+ | | | | | | | b-D-Araf-(1-2)-a-D-Araf-(1-3)-+ | | | | | | | | | a-D-Manp-(1-2)-a-D-Manp-(1-2)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-5)-a-D-Araf-(1-3)-+ | | | | | | | | | a-D-Manp-(1-2)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | | | LIP-(1-?)-a-D-Manp-(1-?)-+ LIP-(1-1)-+ | | | | | | | | a-D-Xylf5S5Me-(1-4)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=11/-a-D-Araf-(1-5)-D-Araf-(1-?)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-?)-L-myoIno-(1--P--3)--Gro | | Suc-(1-2)-+ LIP-(1-2)-+ Xyl5S = 5-thio-xylose

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Compound ID: 12904

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Structure type: monomer ; 546.0883
Trivial name: dTDP-4-amino-4,6-dideoxy-d-glucose

Protein Science 2018, "The Mycobacterium tuberculosis Complex has a Pathway for the Biosynthesis of 4-Formamido-4,6-Dideoxy-D-Glucose"
CSDB ID 12875 (all data & tools)
Compound ID: 11883

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Structure type: monomer
Trivial name: dTDP-4,6-dideoxy-4-formamido-D-glucose, dTDP-4-formamido-4,6-dideoxy-d-glucose

Protein Science 2018, "The Mycobacterium tuberculosis Complex has a Pathway for the Biosynthesis of 4-Formamido-4,6-Dideoxy-D-Glucose"
CSDB ID 13059 (all data & tools)

Compound ID: 13121

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Compound ID: 13123

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Compound ID: 13124

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Compound ID: 13201

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Structure type: structural motif or average structure
Trivial name: branched hexaarabinofuranoside (Ara6), terminal epitope LAM (Ara6)
Compound class: lipoarabinomannan, mannose-capped LAM
Reference(s) to other database(s): GTC:G46014AY

Pathogens and Disease 2018, "Mannose-capped lipoarabinomannan in Mycobacterium tuberculosis pathogenesis"
CSDB ID 12989 (all data & tools)

Pathogens 2023, "Collected Thoughts on Mycobacterial Lipoarabinomannan, a Cell Envelope Lipoglycan"
CSDB ID 27051 (all data & tools)
Compound ID: 13202

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Structure type: structural motif or average structure
Trivial name: linear tetraarabinofuranoside (Ara4), terminal epitope LAM (Ara4)
Compound class: lipoarabinomannan, mannose-capped LAM
Reference(s) to other database(s): GTC:G04816FL

Pathogens and Disease 2018, "Mannose-capped lipoarabinomannan in Mycobacterium tuberculosis pathogenesis"
CSDB ID 12806 (all data & tools)

Pathogens 2023, "Collected Thoughts on Mycobacterial Lipoarabinomannan, a Cell Envelope Lipoglycan"
CSDB ID 22329 (all data & tools)
Compound ID: 13203

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Structure type: structural motif or average structure
Trivial name: terminal arabinan motif ManLAM
Compound class: lipoarabinomannan
Reference(s) to other database(s): GTC:G57959BY

Pathogens and Disease 2018, "Mannose-capped lipoarabinomannan in Mycobacterium tuberculosis pathogenesis"
CSDB ID 12807 (all data & tools)
Compound ID: 13360

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43133 (all data & tools)
Compound ID: 13361

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43134 (all data & tools)
Compound ID: 13362

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43135 (all data & tools)
Compound ID: 13363

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43136 (all data & tools)
Compound ID: 13364

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43137 (all data & tools)
Compound ID: 13365

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43138 (all data & tools)
Compound ID: 13366

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43140 (all data & tools)
Compound ID: 13367

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43141 (all data & tools)
Compound ID: 13368

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43142 (all data & tools)
Compound ID: 13369

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43144 (all data & tools)
Compound ID: 13370

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43147 (all data & tools)
Compound ID: 13371

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Structure type: oligomer

Future Science OA 2017, "Galactofuranose antigens, a target for diagnosis of fungal infections in humans"
CSDB ID 43148 (all data & tools)

Compound ID: 13388

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Compound ID: 13396

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Compound ID: 14093

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Compound ID: 14292

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Structure type: oligomer
Aglycon: (->5) cell wall
Compound class: arabinan
Reference(s) to other database(s): GTC:G46014AY

Journal of Organic Chemistry 2015, "Influence of steric crowding on diastereoselective arabinofuranosylations"
CSDB ID 47841 (all data & tools)
Compound ID: 14208

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Structure type: monomer
Trivial name: mycothiol
Compound class: glycoside

Biochemistry 2015, "Molecular determinants of N-acetylglucosamine recognition and turnover by N-acetyl-1-D-myo-inosityl-2-amino-2-deoxy-α-D-glucopyranoside deacetylase (MshB)"
CSDB ID 49296 (all data & tools)

Biometals 2015, "Identity of cofactor bound to mycothiol conjugate amidase (Mca) influenced by expression and purification conditions"
CSDB ID 49297 (all data & tools)

Journal of Bioscience and Bioengineering 2015, "Ergothioneine protects Streptomyces coelicolor A3(2) from oxidative stresses"
CSDB ID 49317 (all data & tools)

Bioorganic and Medicinal Chemistry Letters 2015, "Synthesis of mycothiol conjugate analogues and evaluation of their antimycobacterial activity"
CSDB ID 49324 (all data & tools)

Compound ID: 14339

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Compound ID: 14340

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Compound ID: 14341

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Structure type: fragment of a bigger structure
Aglycon: lipoarabinomannan
Compound class: O-antigen
Reference(s) to other database(s): GTC:G46014AY

Chemistry 2015, "Specificity of furanoside-protein recognition through antibody engineering and molecular modeling"
CSDB ID 49300 (all data & tools)

Compound ID: 14342

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Compound ID: 14351

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Compound ID: 14353

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Structure type: monomer
Compound class: glycopeptide

Tuberculosis 2015, "Structural and functional features of enzymes of Mycobacterium tuberculosis peptidoglycan biosynthesis as targets for drug development"
CSDB ID 49316 (all data & tools)

Compound ID: 14357

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Compound ID: 14364

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Structure type: oligomer
Compound class: glycolipid

Chemical Communications 2015, "Corynomycolic acid-containing glycolipids signal through the pattern recognition receptor Mincle"
CSDB ID 49331 (all data & tools)

Compound ID: 14365

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Compound ID: 14366

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Structure type: oligomer
Compound class: glycolipid

Chemical Communications 2015, "Corynomycolic acid-containing glycolipids signal through the pattern recognition receptor Mincle"
CSDB ID 49333 (all data & tools)
Compound ID: 14367

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Structure type: monomer
Compound class: glycolipid

Chemical Communications 2015, "Corynomycolic acid-containing glycolipids signal through the pattern recognition receptor Mincle"
CSDB ID 49334 (all data & tools)
Compound ID: 14368

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Structure type: monomer
Compound class: glycolipid

Chemical Communications 2015, "Corynomycolic acid-containing glycolipids signal through the pattern recognition receptor Mincle"
CSDB ID 49335 (all data & tools)
Compound ID: 14369

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Structure type: structural motif or average structure
Compound class: O-antigen, glucan, polysaccharide
Reference(s) to other database(s): GTC:G77660TL

Chembiochem: a European Journal of Chemical Biology 2015, "A murine monoclonal antibody to glycogen: characterization of epitope-fine specificity by saturation transfer difference (STD) NMR spectroscopy and its use in mycobacterial capsular α-glucan research"
CSDB ID 49336 (all data & tools)

Compound ID: 14370

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Compound ID: 14371

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Structure type: monomer
Compound class: O-antigen, phosphoglycolipid

Immunological Reviews 2015, "CD1 and mycobacterial lipids activate human T cells"
CSDB ID 49338 (all data & tools)
Compound ID: 14372

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Structure type: monomer
Compound class: O-antigen, glycolipid

Immunological Reviews 2015, "CD1 and mycobacterial lipids activate human T cells"
CSDB ID 49339 (all data & tools)
Compound ID: 14373

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Structure type: oligomer
Compound class: O-antigen, glycoinositol phospholipid

Immunological Reviews 2015, "CD1 and mycobacterial lipids activate human T cells"
CSDB ID 49340 (all data & tools)
Compound ID: 14434

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Structure type: oligomer
Trivial name: trehalose mycolate
Compound class: glycolipid

Frontiers in Microbiology 2020, "Microarray Strategies for Exploring Bacterial Surface Glycans and Their Interactions With Glycan-Binding Proteins"
CSDB ID 3284 (all data & tools)

Compound ID: 14435

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Compound ID: 15642

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Compound ID: 16005

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Structure type: oligomer
Aglycon: Ser/Thr-pilin
Compound class: O-glycoprotein

Chemical Reviews 2022, "Chemical reporters for bacterial glycans: development and applications"
CSDB ID 20830 (all data & tools)
Compound ID: 16009

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Structure type: fragment of a bigger structure
Trivial name: α-1,4-D-glucan
Compound class: CPS

Chemical Reviews 2022, "Chemical reporters for bacterial glycans: development and applications"
CSDB ID 20839 (all data & tools)

Compound ID: 16593

{{{-a-D-Manp-(1-2)-}}}/n=6-7/-a-D-Manp-(1-2)-+ | b-D-Araf-(1-2)-a-D-Araf-(1-3)-+ | | | a-D-Manp-(1-2)-a-D-Manp-(1-2)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-3)-+ | | | D-Manp-(1-?)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | | | Suc-(1-3)-+ | | | | | | | a-D-Xylf5S5Me-(1-4)-a-D-Manp-(1-2)-a-D-Manp-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-5)-+ | | | | Suc-(1-2)-+ | | | | b-D-Araf-(1-2)-a-D-Araf-(1-3)-+ | | | | | b-D-Araf-(1-2)-{{{-a-D-Araf-(1-5)-}}}/n=5/-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-3)-+ | | | | | Suc-(1-3)-+ | | | | | | | Suc-(1-3)-+ a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Araf-(1-2)-b-D-Araf-(1-5)-a-D-Araf-(1-5)-+ | | a-D-Manp-(1-2)-+ | a-D-Manp-(1-2)-+ a-D-Manp-(1-2)-+ | | | | | | | | b-D-Araf-(1-2)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-D-Araf-(1-?)-}}}a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=13/-a-D-Araf-(1-6)-a-D-Manp-(1-6)-{{{-a-D-Manp-(1-6)-}}}/n=2/-a-D-Manp-(1-6)-{{{-a-D-Manp-(1-6)-}}}a-D-Manp-(1-6)-{{{-a-D-Manp-(1-6)-}}}/n=2/-a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1--/phosphatidyl-myo-inositol anchor/ | Suc-(1-2)-+ Xyl5S = 5-thio-xylose

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Compound ID: 16594

b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-+ | | ?%Suc-(1-2)-+ | | b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=12/-a-D-Araf-(1-5)-+ | | ?%Suc-(1-2)-+ | | Mycolic-(1-?)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | Mycolic-(1-?)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-5)-+ | | | Mycolic-(1-?)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | | | Mycolic-(1-?)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}a-D-Araf-(1-3)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=12/-a-D-Araf-(1-5)-+ | | | | ?%a-D-GalpN-(1-2)-+ | | | | Subst1-(1-?)-Subst2-(1-?)-b-D-Galf-(1-5)-{{{-b-D-Galf-(1-6)-b-D-Galf-(1-5)-}}}/n=2/-b-D-Galf-(1-6)-b-D-Galf-(1-5)-b-D-Galf-(1-6)-b-D-Galf-(1-5)-{{{-b-D-Galf-(1-6)-b-D-Galf-(1-5)-}}}/n=5/-b-D-Galf-(1-6)-b-D-Galf Subst1 = peptidoglycan; Subst2 = linker

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Compound ID: 16653

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Compound ID: 16727

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Compound ID: 16728

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Compound ID: 16729

a-D-Manp-(1-2)-+ | a-D-Manp-(1-6)-a-D-Manp-(1-6)-{{{-a-D-Manp-(1-6)-}}}/n=6/-+ | SUG-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | SUG-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-a-D-Araf-(1-3)-+ b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | | | SUG-(1-5)-b-D-Araf-(1-2)-{{{-a-D-Araf-(1-5)-}}}/n=5/-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-3)-+ | | | SUG-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-a-D-Araf-(1-5)-+ | | | | | SUG-(1-5)-b-D-Araf-(1-2)-a-D-Araf-(1-5)-a-D-Araf-(1-3)-a-D-Araf-(1-5)-a-D-Araf-(1-3)-+ b-D-Araf-(1-2)-a-D-Araf-(1-5)-+ | | a-D-Manp-(1-2)-+ | | | | | SUG-(1-5)-b-D-Araf-(1-2)-{{{-a-D-Araf-(1-5)-}}}/n=5/-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=6/-a-D-Araf-(1-3)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=2/-a-D-Araf-(1-5)-a-D-Araf-(1-5)-{{{-a-D-Araf-(1-5)-}}}/n=14/-a-D-Araf-(1-2)-a-D-Manp-(1-6)-{{{-a-D-Manp-(1-6)-}}}/n=4/-a-D-Manp-(1-6)-a-D-Manp-(1--/(1->6)phosphatidylinositol mannoside (PIM) anchor/ | Suc-(1-2)-+

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Compound ID: 16730

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Structure type: oligomer
Trivial name: phenolic glycolipid (PGL)
Compound class: cell wall polysaccharide

Scandinavian Journal of Immunology 2023, "Polysaccharides and glycolipids of Mycobacterium tuberculosis and their induced immune responses"
CSDB ID 27094 (all data & tools)

Compound ID: 16732

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Compound ID: 1030

-6)-b-D-GlcpNAc-(1- Show graphically

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Structure type: homopolymer
Trivial name: poly-β-1,6-GlcNAc (PGA), biofilm, poly-b-(1-6)-N-acetyl-D-glucosamine (PNAG), poly-β-N-acetyl-glucosamine (PNAG), PNAG, poly-N-acetylglucosamine, PNAG
Compound class: CPS, EPS, O-polysaccharide, glucan, polysaccharide
Reference(s) to other database(s): GTC:G36952FI, GlycomeDB:11210

Engineering (Beijing) 2024, "Antibodies targeting a conserved surface polysaccharide are protective against a wide range of microbial pathogens producing β-1–6-linked poly-N-acetylglucosamine (PNAG)"
CSDB ID 15645 (all data & tools)
Compound ID: 21280

-2)-a-D-Manp-(1- Show graphically

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Structure type: structural motif or average structure
Compound class: cell wall polysaccharide, glucan
Reference(s) to other database(s): GTC:G88014SW

Frontiers in Immunology 2018, "Dectin-3 recognizes glucuronoxylomannan of Cryptococcus neoformans serotype AD and Cryptococcus gattii serotype B to initiate host defense against Cryptococcosis"
CSDB ID 48719 (all data & tools)

Compound ID: 23446

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