Skip to main content

Table 6 Identification of principal enzymes and pathways contributing to the first sPLSDA’s first component and signatures of low score of fibrosis

From: Human liver microbiota modeling strategy at the early onset of fibrosis

 

Name

Function

Enzymes

EC:4.1.2.52

4-hydroxy-2-oxoheptanedioate aldolase

EC:3.5.4.1

Cytosine deaminase

EC:3.2.2.4

AMP nucleosidase

EC:4.1.3.3

N-acetylneuraminate lyase

EC:3.1.21.4

Type II site-specific deoxyribonuclease

EC:3.2.1.89

Arabinogalactan endo-beta-1,4-galactanase

EC:3.5.99.6

Glucosamine-6-phosphate deaminase

FAO-PWY

fatty acid &beta,-oxidation I

PROTOCATECHUATE-ORTHO-CLEAVAGE-PWY

protocatechuate degradation II (ortho-cleavage pathway)

Pathways

GLYCOCAT-PWY

glycogen degradation I (bacterial)

PWY-6737

starch degradation V

PWY-7323

superpathway of GDP-mannose-derived O-antigen building blocks biosynthesis

COLANSYN-PWY

colanic acid building blocks biosynthesis

LACTOSECAT-PWY

lactose and galactose degradation I

PWY-6629

superpathway of L-tryptophan biosynthesis

GLCMANNANAUT-PWY

superpathway of N-acetylglucosamine, N-acetylmannosamine and N-acetylneuraminate degradation

P441-PWY

superpathway of N-acetylneuraminate degradation

PWY0-1533

methylphosphonate degradation I