BacMap pathways

Pathways for Stigmatella aurantiaca DW4/3-1 gsam_325

Search and browse metabolic pathways associated with this bacterium.

1329 pathways

Displaying pathways 126–150 of 1329

ThumbnailPathwayIdentifiersDescription
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid  and Lithocholic Acid (LCA) (bai operon) via 3?,5?,7?,15?,21?,25?-hexahydroxy-Deoxycholate-24-CoA thumbnail
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid and Lithocholic Acid (LCA) (bai operon) via 3?,5?,7?,15?,21?,25?-hexahydroxy-Deoxycholate-24-CoA
SMPDBPBK0650438
PathWhizPW688217
The bai operon, responsible for bile acid metabolism, particularly the 7-?-dehydroxylation process, encodes a series of key enzymes involved in the transformation of primary bile acids like chenodeoxycholic acid (CDCA) into secondary bile acids such as lithocholic acid (LCA) and ultimately ursodeoxycholic acid (UDCA). This operon is activated by the presence of bile acids, which induce its expression, thereby facilitating the efficient utilization of these compounds by gut bacteria.The baiB gene encodes a bile acid-CoA ligase that activates bile acids by converting them into their CoA derivatives, a crucial step for subsequent enzymatic processing. Following this, baiF is responsible for encoding a bile acid-CoA hydrolase that removes the CoA group, yielding free bile acids necessary for further modifications. The gene baiC then encodes a 7-?-hydroxysteroid dehydratase, which catalyzes the conversion of bile acids at the C7 position, a key step in the 7-?-dehydroxylation pathway. Furthermore, baiE encodes a 7-?-dehydratase that facilitates the rate-limiting step of dehydroxylation, transforming intermediates into 3-oxo derivatives that will be later converted into LCA or UDCA.baiA additionally plays a role in converting 3-oxo bile acids back to their 7-dehydroxylated forms, aiding in the production of LCA. The subsequent enzymes, baiH and baiG, involve the complex series of transformations of the 3-oxo derivatives, ultimately leading to the biosynthesis of UDCA through a series of reductive steps facilitated by bai genes like baiN. In summary, the bai operon orchestrates a finely tuned series of enzymatic reactions that enable gut bacteria to efficiently metabolize endogenous bile acids, yielding bioactive secondary metabolites such as LCA and UDCA, which play significant roles in the modulation of lipid and glucose metabolism in the host
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid  and Lithocholic Acid (LCA) (bai operon) via 3?,5?,7?,15?,23?,28?-hexahydroxy-Deoxycholate-24-CoA thumbnail
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid and Lithocholic Acid (LCA) (bai operon) via 3?,5?,7?,15?,23?,28?-hexahydroxy-Deoxycholate-24-CoA
SMPDBPBK0650439
PathWhizPW688218
The bai operon, responsible for bile acid metabolism, particularly the 7-?-dehydroxylation process, encodes a series of key enzymes involved in the transformation of primary bile acids like chenodeoxycholic acid (CDCA) into secondary bile acids such as lithocholic acid (LCA) and ultimately ursodeoxycholic acid (UDCA). This operon is activated by the presence of bile acids, which induce its expression, thereby facilitating the efficient utilization of these compounds by gut bacteria.The baiB gene encodes a bile acid-CoA ligase that activates bile acids by converting them into their CoA derivatives, a crucial step for subsequent enzymatic processing. Following this, baiF is responsible for encoding a bile acid-CoA hydrolase that removes the CoA group, yielding free bile acids necessary for further modifications. The gene baiC then encodes a 7-?-hydroxysteroid dehydratase, which catalyzes the conversion of bile acids at the C7 position, a key step in the 7-?-dehydroxylation pathway. Furthermore, baiE encodes a 7-?-dehydratase that facilitates the rate-limiting step of dehydroxylation, transforming intermediates into 3-oxo derivatives that will be later converted into LCA or UDCA.baiA additionally plays a role in converting 3-oxo bile acids back to their 7-dehydroxylated forms, aiding in the production of LCA. The subsequent enzymes, baiH and baiG, involve the complex series of transformations of the 3-oxo derivatives, ultimately leading to the biosynthesis of UDCA through a series of reductive steps facilitated by bai genes like baiN. In summary, the bai operon orchestrates a finely tuned series of enzymatic reactions that enable gut bacteria to efficiently metabolize endogenous bile acids, yielding bioactive secondary metabolites such as LCA and UDCA, which play significant roles in the modulation of lipid and glucose metabolism in the host
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid  and Lithocholic Acid (LCA) (bai operon) via 3?,7?,10?,13?,23?,28?-hexahydroxy-Chenodeoxycholate-24-CoA thumbnail
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid and Lithocholic Acid (LCA) (bai operon) via 3?,7?,10?,13?,23?,28?-hexahydroxy-Chenodeoxycholate-24-CoA
SMPDBPBK0649905
PathWhizPW687806
The bai operon, responsible for bile acid metabolism, particularly the 7-?-dehydroxylation process, encodes a series of key enzymes involved in the transformation of primary bile acids like chenodeoxycholic acid (CDCA) into secondary bile acids such as lithocholic acid (LCA) and ultimately ursodeoxycholic acid (UDCA). This operon is activated by the presence of bile acids, which induce its expression, thereby facilitating the efficient utilization of these compounds by gut bacteria.The baiB gene encodes a bile acid-CoA ligase that activates bile acids by converting them into their CoA derivatives, a crucial step for subsequent enzymatic processing. Following this, baiF is responsible for encoding a bile acid-CoA hydrolase that removes the CoA group, yielding free bile acids necessary for further modifications. The gene baiC then encodes a 7-?-hydroxysteroid dehydratase, which catalyzes the conversion of bile acids at the C7 position, a key step in the 7-?-dehydroxylation pathway. Furthermore, baiE encodes a 7-?-dehydratase that facilitates the rate-limiting step of dehydroxylation, transforming intermediates into 3-oxo derivatives that will be later converted into LCA or UDCA.baiA additionally plays a role in converting 3-oxo bile acids back to their 7-dehydroxylated forms, aiding in the production of LCA. The subsequent enzymes, baiH and baiG, involve the complex series of transformations of the 3-oxo derivatives, ultimately leading to the biosynthesis of UDCA through a series of reductive steps facilitated by bai genes like baiN. In summary, the bai operon orchestrates a finely tuned series of enzymatic reactions that enable gut bacteria to efficiently metabolize endogenous bile acids, yielding bioactive secondary metabolites such as LCA and UDCA, which play significant roles in the modulation of lipid and glucose metabolism in the host
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid  and Lithocholic Acid (LCA) (bai operon) via 3?,7?,10?,13?,24?,28?-hexahydroxy-Chenodeoxycholate-24-CoA thumbnail
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid and Lithocholic Acid (LCA) (bai operon) via 3?,7?,10?,13?,24?,28?-hexahydroxy-Chenodeoxycholate-24-CoA
SMPDBPBK0649907
PathWhizPW687808
The bai operon, responsible for bile acid metabolism, particularly the 7-?-dehydroxylation process, encodes a series of key enzymes involved in the transformation of primary bile acids like chenodeoxycholic acid (CDCA) into secondary bile acids such as lithocholic acid (LCA) and ultimately ursodeoxycholic acid (UDCA). This operon is activated by the presence of bile acids, which induce its expression, thereby facilitating the efficient utilization of these compounds by gut bacteria.The baiB gene encodes a bile acid-CoA ligase that activates bile acids by converting them into their CoA derivatives, a crucial step for subsequent enzymatic processing. Following this, baiF is responsible for encoding a bile acid-CoA hydrolase that removes the CoA group, yielding free bile acids necessary for further modifications. The gene baiC then encodes a 7-?-hydroxysteroid dehydratase, which catalyzes the conversion of bile acids at the C7 position, a key step in the 7-?-dehydroxylation pathway. Furthermore, baiE encodes a 7-?-dehydratase that facilitates the rate-limiting step of dehydroxylation, transforming intermediates into 3-oxo derivatives that will be later converted into LCA or UDCA.baiA additionally plays a role in converting 3-oxo bile acids back to their 7-dehydroxylated forms, aiding in the production of LCA. The subsequent enzymes, baiH and baiG, involve the complex series of transformations of the 3-oxo derivatives, ultimately leading to the biosynthesis of UDCA through a series of reductive steps facilitated by bai genes like baiN. In summary, the bai operon orchestrates a finely tuned series of enzymatic reactions that enable gut bacteria to efficiently metabolize endogenous bile acids, yielding bioactive secondary metabolites such as LCA and UDCA, which play significant roles in the modulation of lipid and glucose metabolism in the host
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid  and Lithocholic Acid (LCA) (bai operon) via 3?,7?,12?,15?,23?,28?-hexahydroxy-Chenodeoxycholate-24-CoA thumbnail
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid and Lithocholic Acid (LCA) (bai operon) via 3?,7?,12?,15?,23?,28?-hexahydroxy-Chenodeoxycholate-24-CoA
SMPDBPBK0649909
PathWhizPW687810
The bai operon, responsible for bile acid metabolism, particularly the 7-?-dehydroxylation process, encodes a series of key enzymes involved in the transformation of primary bile acids like chenodeoxycholic acid (CDCA) into secondary bile acids such as lithocholic acid (LCA) and ultimately ursodeoxycholic acid (UDCA). This operon is activated by the presence of bile acids, which induce its expression, thereby facilitating the efficient utilization of these compounds by gut bacteria.The baiB gene encodes a bile acid-CoA ligase that activates bile acids by converting them into their CoA derivatives, a crucial step for subsequent enzymatic processing. Following this, baiF is responsible for encoding a bile acid-CoA hydrolase that removes the CoA group, yielding free bile acids necessary for further modifications. The gene baiC then encodes a 7-?-hydroxysteroid dehydratase, which catalyzes the conversion of bile acids at the C7 position, a key step in the 7-?-dehydroxylation pathway. Furthermore, baiE encodes a 7-?-dehydratase that facilitates the rate-limiting step of dehydroxylation, transforming intermediates into 3-oxo derivatives that will be later converted into LCA or UDCA.baiA additionally plays a role in converting 3-oxo bile acids back to their 7-dehydroxylated forms, aiding in the production of LCA. The subsequent enzymes, baiH and baiG, involve the complex series of transformations of the 3-oxo derivatives, ultimately leading to the biosynthesis of UDCA through a series of reductive steps facilitated by bai genes like baiN. In summary, the bai operon orchestrates a finely tuned series of enzymatic reactions that enable gut bacteria to efficiently metabolize endogenous bile acids, yielding bioactive secondary metabolites such as LCA and UDCA, which play significant roles in the modulation of lipid and glucose metabolism in the host
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid  and Lithocholic Acid (LCA) (bai operon) via 3?,7?,12?,15?,24?,28?-hexahydroxy-Chenodeoxycholate-24-CoA thumbnail
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid and Lithocholic Acid (LCA) (bai operon) via 3?,7?,12?,15?,24?,28?-hexahydroxy-Chenodeoxycholate-24-CoA
SMPDBPBK0649911
PathWhizPW687812
The bai operon, responsible for bile acid metabolism, particularly the 7-?-dehydroxylation process, encodes a series of key enzymes involved in the transformation of primary bile acids like chenodeoxycholic acid (CDCA) into secondary bile acids such as lithocholic acid (LCA) and ultimately ursodeoxycholic acid (UDCA). This operon is activated by the presence of bile acids, which induce its expression, thereby facilitating the efficient utilization of these compounds by gut bacteria.The baiB gene encodes a bile acid-CoA ligase that activates bile acids by converting them into their CoA derivatives, a crucial step for subsequent enzymatic processing. Following this, baiF is responsible for encoding a bile acid-CoA hydrolase that removes the CoA group, yielding free bile acids necessary for further modifications. The gene baiC then encodes a 7-?-hydroxysteroid dehydratase, which catalyzes the conversion of bile acids at the C7 position, a key step in the 7-?-dehydroxylation pathway. Furthermore, baiE encodes a 7-?-dehydratase that facilitates the rate-limiting step of dehydroxylation, transforming intermediates into 3-oxo derivatives that will be later converted into LCA or UDCA.baiA additionally plays a role in converting 3-oxo bile acids back to their 7-dehydroxylated forms, aiding in the production of LCA. The subsequent enzymes, baiH and baiG, involve the complex series of transformations of the 3-oxo derivatives, ultimately leading to the biosynthesis of UDCA through a series of reductive steps facilitated by bai genes like baiN. In summary, the bai operon orchestrates a finely tuned series of enzymatic reactions that enable gut bacteria to efficiently metabolize endogenous bile acids, yielding bioactive secondary metabolites such as LCA and UDCA, which play significant roles in the modulation of lipid and glucose metabolism in the host
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid  and Lithocholic Acid (LCA) (bai operon) via 3?,7?,12?,17?,23?,28?-hexahydroxy-Chenodeoxycholate-24-CoA thumbnail
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid and Lithocholic Acid (LCA) (bai operon) via 3?,7?,12?,17?,23?,28?-hexahydroxy-Chenodeoxycholate-24-CoA
SMPDBPBK0649915
PathWhizPW687816
The bai operon, responsible for bile acid metabolism, particularly the 7-?-dehydroxylation process, encodes a series of key enzymes involved in the transformation of primary bile acids like chenodeoxycholic acid (CDCA) into secondary bile acids such as lithocholic acid (LCA) and ultimately ursodeoxycholic acid (UDCA). This operon is activated by the presence of bile acids, which induce its expression, thereby facilitating the efficient utilization of these compounds by gut bacteria.The baiB gene encodes a bile acid-CoA ligase that activates bile acids by converting them into their CoA derivatives, a crucial step for subsequent enzymatic processing. Following this, baiF is responsible for encoding a bile acid-CoA hydrolase that removes the CoA group, yielding free bile acids necessary for further modifications. The gene baiC then encodes a 7-?-hydroxysteroid dehydratase, which catalyzes the conversion of bile acids at the C7 position, a key step in the 7-?-dehydroxylation pathway. Furthermore, baiE encodes a 7-?-dehydratase that facilitates the rate-limiting step of dehydroxylation, transforming intermediates into 3-oxo derivatives that will be later converted into LCA or UDCA.baiA additionally plays a role in converting 3-oxo bile acids back to their 7-dehydroxylated forms, aiding in the production of LCA. The subsequent enzymes, baiH and baiG, involve the complex series of transformations of the 3-oxo derivatives, ultimately leading to the biosynthesis of UDCA through a series of reductive steps facilitated by bai genes like baiN. In summary, the bai operon orchestrates a finely tuned series of enzymatic reactions that enable gut bacteria to efficiently metabolize endogenous bile acids, yielding bioactive secondary metabolites such as LCA and UDCA, which play significant roles in the modulation of lipid and glucose metabolism in the host
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid  and Lithocholic Acid (LCA) (bai operon) via 3?,7?,12?,17?,24?,28?-hexahydroxy-Chenodeoxycholate-24-CoA thumbnail
Biosynthesis of Ursodeoxycholic Acid (UDCA), Isolithocholic acid and Lithocholic Acid (LCA) (bai operon) via 3?,7?,12?,17?,24?,28?-hexahydroxy-Chenodeoxycholate-24-CoA
SMPDBPBK0649917
PathWhizPW687818
The bai operon, responsible for bile acid metabolism, particularly the 7-?-dehydroxylation process, encodes a series of key enzymes involved in the transformation of primary bile acids like chenodeoxycholic acid (CDCA) into secondary bile acids such as lithocholic acid (LCA) and ultimately ursodeoxycholic acid (UDCA). This operon is activated by the presence of bile acids, which induce its expression, thereby facilitating the efficient utilization of these compounds by gut bacteria.The baiB gene encodes a bile acid-CoA ligase that activates bile acids by converting them into their CoA derivatives, a crucial step for subsequent enzymatic processing. Following this, baiF is responsible for encoding a bile acid-CoA hydrolase that removes the CoA group, yielding free bile acids necessary for further modifications. The gene baiC then encodes a 7-?-hydroxysteroid dehydratase, which catalyzes the conversion of bile acids at the C7 position, a key step in the 7-?-dehydroxylation pathway. Furthermore, baiE encodes a 7-?-dehydratase that facilitates the rate-limiting step of dehydroxylation, transforming intermediates into 3-oxo derivatives that will be later converted into LCA or UDCA.baiA additionally plays a role in converting 3-oxo bile acids back to their 7-dehydroxylated forms, aiding in the production of LCA. The subsequent enzymes, baiH and baiG, involve the complex series of transformations of the 3-oxo derivatives, ultimately leading to the biosynthesis of UDCA through a series of reductive steps facilitated by bai genes like baiN. In summary, the bai operon orchestrates a finely tuned series of enzymatic reactions that enable gut bacteria to efficiently metabolize endogenous bile acids, yielding bioactive secondary metabolites such as LCA and UDCA, which play significant roles in the modulation of lipid and glucose metabolism in the host
Biotin-Carboxyl Carrier Protein Assembly thumbnail
Biotin-Carboxyl Carrier Protein Assembly
SMPDBSMP0002079
PathWhizPW002067
No description available
CAM (Crassulacean acid metabolism), dark thumbnail
CAM (Crassulacean acid metabolism), dark
SMPDBSMP0402427
PathWhizPW413681
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/10:0(3-OH)/10:0(3-OH)/10:0(3-OH)) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/10:0(3-OH)/10:0(3-OH)/10:0(3-OH))
SMPDBSMP0631290
PathWhizPW671192
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/10:0/10:0(3-OH)/10:0) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/10:0/10:0(3-OH)/10:0)
SMPDBSMP0641342
PathWhizPW681685
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/12:0(3-OH)/10:0(3-OH)/12:0(3-OH)) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/12:0(3-OH)/10:0(3-OH)/12:0(3-OH))
SMPDBSMP0641347
PathWhizPW681690
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/12:0/10:0(3-OH)/12:0) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/12:0/10:0(3-OH)/12:0)
SMPDBSMP0641349
PathWhizPW681692
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/14:0(3-OH)/10:0(3-OH)/14:0(3-OH)) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/14:0(3-OH)/10:0(3-OH)/14:0(3-OH))
SMPDBSMP0631284
PathWhizPW671185
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/14:0/10:0(3-OH)/14:0) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/14:0/10:0(3-OH)/14:0)
SMPDBSMP0631279
PathWhizPW671176
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/15:0/10:0(3-OH)/15:0) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/15:0/10:0(3-OH)/15:0)
SMPDBSMP0631275
PathWhizPW671170
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/15:0cycw5/10:0(3-OH)/15:0cycw5) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/15:0cycw5/10:0(3-OH)/15:0cycw5)
SMPDBSMP0641351
PathWhizPW681694
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/16:0/10:0(3-OH)/16:0) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/16:0/10:0(3-OH)/16:0)
SMPDBSMP0641353
PathWhizPW681696
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/16:1(9Z)/10:0(3-OH)/16:1(9Z)) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/16:1(9Z)/10:0(3-OH)/16:1(9Z))
SMPDBSMP0641356
PathWhizPW681699
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/17:0cycw7/10:0(3-OH)/17:0cycw7) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/17:0cycw7/10:0(3-OH)/17:0cycw7)
SMPDBSMP0641358
PathWhizPW681701
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/17:0cycw7/14:0/14:0) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/17:0cycw7/14:0/14:0)
SMPDBSMP0622584
PathWhizPW661732
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/18:1(9Z)/10:0(3-OH)/18:1(9Z)) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/18:1(9Z)/10:0(3-OH)/18:1(9Z))
SMPDBSMP0631271
PathWhizPW671163
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/19:0cycw7/10:0(3-OH)/19:0cycw7) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/19:0cycw7/10:0(3-OH)/19:0cycw7)
SMPDBSMP0622405
PathWhizPW661553
No description available
Cardiolipin Biosynthesis CL(10:0(3-OH)/i-19:0/10:0(3-OH)/i-19:0) thumbnail
Cardiolipin Biosynthesis CL(10:0(3-OH)/i-19:0/10:0(3-OH)/i-19:0)
SMPDBSMP0641360
PathWhizPW681703
No description available

Displaying pathways 126–150 of 1329