Component_60637 |
pseudaminic acid CMP-transferase |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Evidence_82208 |
TIGR03590 HMM |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Evidence_75336 |
TIGR01173 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_82203 |
TIGR03587 HMM |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Evidence_84971 |
TIGR03990 HMM |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Component_54360 |
glutamine--fructose-6-phosphate transaminase (isomerizing) |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_82206 |
TIGR03588 HMM |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Evidence_84972 |
TIGR03991 HMM |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Component_60633 |
pseudaminic acid biosynthesis aminotransferase PseC |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Evidence_75334 |
TIGR01135 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_60647 |
pseudaminic acid biosynthesis associated methylase |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Component_60635 |
possible pseudaminic acid biosynthesis UDP hydrolase |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Component_60631 |
source of UDP-N-acetyl-D-glucosamine |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_54361 |
phosphoglucosamine mutase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_82207 |
TIGR03589 HMM |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Component_60636 |
pseudaminic acid synthase (pyruvate condensing enzyme) |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Evidence_82200 |
TIGR03584 HMM |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Evidence_82201 |
TIGR03585 HMM |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
GenProp0750 |
UDP-N-acetylglucosamine biosynthesis from fructose-6-phosphate~This pathway converts fructose-6-phosphate in four steps to activated N-acetylglucosamine. GlmS produces glucosamine-6-phosphate. GlmM isomerizes this product to glucosamine-1-phosphate. GlmU, which is bifunctional, adds an acetyl group from acetyl-CoA, then acts as N-acetylglucosamine-1-phosphate uridylyltransferase. The product, UDP-N-acetyl-D-glucosamine, is then used both for murein biosynthesis and (in species with LPS) for lipopolysaccharide biosynthesis. |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_75335 |
TIGR01455 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_82202 |
TIGR03586 HMM |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Component_60634 |
possible pseudaminic acid biosynthesis N-acetyl transferase |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Evidence_82188 |
GenProp0750 GENPROP |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
GenProp0796 |
CMP-pseudaminic acid biosynthesis from UDP-N-acetylglucosamine~Pseudaminic acid is a component of the O-antigen of certain pseudomonas strains [1] as well as the glycosylation modification of Campylobacter and Helicobacter flagellins [2], but is clearly more widely distributed. The proposed biosynthetic pathway involves the dehydration/isomerization of UDP-D-GlcNAc to UDP-4-keto-6-deoxy-GlcNAc by PseB, a transamination at position 4 by PseC. The PseH protein is similar to acetyltransferases and is presumed to carry out transfer to the C-4 amine. PseH itself is occasionally missing. Often in this case, the PseG protein contains an passable acetyltransferase domain. The function of PseG when PseH is present is unknown, it may complex with PseH, or ot may be responsible for the UDP-hydrolysis that clearly must happen but is not currently assigned to an enzyme with a conserved domain for this reaction. PseI carries out the condensation with phosphoenolpyruvate to create pseudaminic acid, a reaction analagous to the carried out by NeuB in the biosynthesis of neuraminic acid (GenProp0792). PseF carries out the transfer of CMP onto pseudaminic acid to yield the most common product. In Campylobacter, the biosynthetic cluster is accompanied by the PseA protein, a homolog of WbuX and is responsible for the conversion of the N-acetyl group at position 7 into the acetimidino group. PseA is accompanied by two genes, WbuY and WbuZ which are reported to provide ammonia for the reaction (GenProp0794). Other proteins are found associated with this cluster including methylases and possible formyltransferases and deacetylases. Thus, a range of closely related structures are likely produced as mature products in various lineages. |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Component_60632 |
UDP-GlcNAc C6-dehydratase/C4-reductase |
None - {{∅}} |
False - {{f}} |
Unconfirmed absence |
|
Component_54362 |
glucosamine-1-phosphate N-acetyltransferase/UDP-N-acetylglucosamine diphosphorylase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|