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1. (Organism ID: 472)

Mycobacterium leprae

(NCBI TaxID 1769, species name lookup)

Taxonomic group: bacteria
Phylum: Actinobacteria

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

Compound ID: 830

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Structure type: oligomer
Compound class: glycolipid
Reference(s) to other database(s): GlycomeDB:5564

Carbohydrate Research 1998, "Synthesis and NMR analysis of 13C-labeled oligosaccharides corresponding to the major glycolipid from Mycobacterium leprae"
CSDB ID 5597 (all data & tools)
Compound ID: 831

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:1893

Carbohydrate Research 1998, "Synthesis and NMR analysis of 13C-labeled oligosaccharides corresponding to the major glycolipid from Mycobacterium leprae"
CSDB ID 5735 (all data & tools)
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: 4468

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Structure type: oligomer
Aglycon: phenolphthiocerol dimycocerosate
Compound class: glycolipid
Reference(s) to other database(s): GTC:G42251UW, GlycomeDB:1893

Analytical Chemistry 1989, "Plasma desorption mass spectrometric analysis of mycobacterial glycolipids"
CSDB ID 103203 (all data & tools)

Biochimica et Biophysica Acta 1989, "Diglycosyl phenol phthiocerol diester of Mycobacterium leprae"
CSDB ID 109223 (all data & tools)

Biological Mass Spectrometry 1994, "Fast atom bombardment mass spectrometry of mycobacterial phenolic glycolipids"
CSDB ID 110032 (all data & tools)
Compound ID: 4479

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Structure type: oligomer
Aglycon: (->4) Phenolphthiocerol dimycocerosate
Reference(s) to other database(s): GTC:G42251UW, GlycomeDB:1893

Annual Review of Microbiology 1987, "Leprosy and the leprosy bacillus: Recent developments in characterization of antigens and immunology of the disease"
CSDB ID 103830 (all data & tools)
Compound ID: 4788

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Structure type: oligomer
Aglycon: Phenolphthiocerol dimycocerosate
Compound class: glycolipid
Reference(s) to other database(s): GTC:G09397XW, GlycomeDB:3762

Biochimica et Biophysica Acta 1989, "Diglycosyl phenol phthiocerol diester of Mycobacterium leprae"
CSDB ID 109222 (all data & tools)
Compound ID: 5105

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Structure type: oligomer
Compound class: glycolipid
Reference(s) to other database(s): GTC:G36046MS, GlycomeDB:5232

Carbohydrate Research 1984, "Structure of the oligosaccharide component of a serologically active phenolic glycolipid isolated from Mycobacterium leprae"
CSDB ID 114263 (all data & tools)
Compound ID: 5258

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Structure type: oligomer
Reference(s) to other database(s): GlycomeDB:1893

Carbohydrate Research 1990, "An NMR and conformational analysis of the terminal trisaccharide from the serologically active glycolipid of Mycobacterium leprae in different solvents"
CSDB ID 115890 (all data & tools)
Compound ID: 5439

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Structure type: fragment of a bigger structure
Reference(s) to other database(s): GlycomeDB:16260

Carbohydrate Research 1993, "Major structural features of the cell wall arabinogalactans of Mycobacterium, Rhodococcus, and Nocardia spp."
CSDB ID 117492 (all data & tools)
Compound ID: 5442

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Structure type: fragment of a bigger structure
Reference(s) to other database(s): GTC:G27434VY, GlycomeDB:10681

Carbohydrate Research 1993, "Major structural features of the cell wall arabinogalactans of Mycobacterium, Rhodococcus, and Nocardia spp."
CSDB ID 117496 (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: 5914

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Structure type: oligomer
Aglycon: Phenol
Trivial name: phenolic glycolipid-I
Reference(s) to other database(s): GTC:G42251UW

Journal of Biological Chemistry 1982, "Structure and antigenicity of the major specific glycolipid antigen of Mycobacterium leprae"
CSDB ID 133938 (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: 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: 10022

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Structure type: oligomer
Trivial name: arabinogalactan
Reference(s) to other database(s): CCSD:30210, CBank-STR:7356

Carbohydrate Research 1993, "Major structural features of the cell wall arabinogalactans of Mycobacterium, Rhodococcus, and Nocardia spp."
CSDB ID 117494 (all data & tools)
Compound ID: 12209

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Structure type: oligomer
Aglycon: phenolic lipid
Trivial name: PGL-I, phenolic glycolipid (PGL-I)
Compound class: glycolipid
Reference(s) to other database(s): GTC:G42251UW

Russian Chemical Bulletin = Izvestiia Akademii nauk. Seriia khimicheskaia 2015, "Synthesis of a disaccharide of phenolic glycolipid from Mycobacterium leprae (PGL-I) and its conjugates with bovine serum albumin"
CSDB ID 11035 (all data & tools)

ACS Central Science 2023, "PGL-III, a Rare Intermediate of Mycobacterium leprae Phenolic Glycolipid Biosynthesis, Is a Potent Mincle Ligand"
CSDB ID 22250 (all data & tools)

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: 16487

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Structure type: oligomer
Aglycon: phenolic lipid
Trivial name: phenolic glycolipid (PGL-III)
Compound class: glycolipid

ACS Central Science 2023, "PGL-III, a Rare Intermediate of Mycobacterium leprae Phenolic Glycolipid Biosynthesis, Is a Potent Mincle Ligand"
CSDB ID 20284 (all data & tools)
Compound ID: 16731

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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 26417 (all data & tools)

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