beta-D-Manp-(1->2)-beta-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp

Term ID

CHEBI:59494

Synonyms

beta-D-Man-(1->2)-beta-D-Man-(1->2)-alpha-D-Man-(1->2)-alpha-D-Man-(1->2)-alpha-D-Man
beta-D-mannopyranosyl-(1->2)-beta-D-mannopyranosyl-(1->2)-alpha-D-mannopyranosyl-(1->2)-alpha-D-mannopyranosyl-(1->2)-alpha-D-mannopyranose
beta-D-mannosyl-(1->2)-beta-D-mannosyl-(1->2)-alpha-D-mannosyl-(1->2)-alpha-D-mannosyl-(1->2)-alpha-D-mannose
beta-Man-(1->2)-beta-Man-(1->2)-alpha-Man-(1->2)-alpha-Man-(1->2)-alpha-Man
LM5
Manbeta1-2Manbeta1-2Manalpha1-2Manalpha1-2Manalpha

Definition

A linear mannopentaose consisting of five D-mannose residues joined sequentially via two β(1→2) and two α(1→2) linkages with α anomeric configuration at the reducing end.

References

glygen:G53868KU
glytoucan:G53868KU
pubmed:12787022

Ontology

ChEBI ( EBI )

Relationships

Phenotype

Phenotype resulting from beta-D-Manp-(1->2)-beta-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp

Phenotype where environments contain beta-D-Manp-(1->2)-beta-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp

Phenotype modified by environments containing beta-D-Manp-(1->2)-beta-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp

Phenotype affecting beta-D-Manp-(1->2)-beta-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp-(1->2)-alpha-D-Manp

Human Disease Model