Evidence_35 |
TIGR01240 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_110 |
1-deoxy-D-xylulose 5-phosphate reductoisomerase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_113 |
2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_38 |
TIGR01833 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_54360 |
glutamine--fructose-6-phosphate transaminase (isomerizing) |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
GenProp0968 |
O-antigen polymerization/export system wzx/wzy/wzz~The Wzx/Wzy/Wzz system trnasports the O-antigen monomers from the cytoplasmic face of the plama membrane to the periplamic face and then polymerizes the monomers to form the mature O-antigen. The Wzx protein is the transporter (aka the flippase), Wzy is the polymerase and Wzz is the chain length determinant protein. |
None - {{∅}} |
None - {{∅},{t}} |
Unexplained |
|
Component_63457 |
O-antigen polymerase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85632 |
GenProp1046 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85217 |
GenProp0047 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
GenProp0971 |
biosynthesis of undecaprenyl phosphate (Und-P)~Undecaprenyl phosphate (Und-P) is synthesized de novo from farnesyl diphosphate via eight successive additions of isopentenyl diphosphate followed by a final removal of one phosphate. Und-P is used as a carrier for polysaccharide units via a pyrophosphate linkage. Removal of the polysaccharide results in Und-PP, so the phosphatase is also used in the recycling back to Und-P. |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_111 |
4-diphosphocytidyl-2C-methyl-D-erythritol kinase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85413 |
GenProp0932 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85415 |
GenProp0963 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85631 |
GenProp1045 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_105 |
hydroxymethylglutaryl-CoA reductase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_29 |
TIGR01217 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85630 |
GenProp1043 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_63456 |
O-antigen transporter (flippase) |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_32 |
TIGR01219 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
GenProp0046 |
IPP biosynthesis~Isopentenyl pyrophosphate (IPP) is the common intermediate of isoprenoid metabolism which includes the biosynthesis of terpenoid natural products, sterols, bile acids, carotenoids, vitamins K and E, isoprene and other prenylated compounds. IPP may be synthesized via one of two separate pathways, the mevalonate pathway is typical of eukaryotes while the deoxyxylulose pathway is typical of prokaryotes. This property summarizes the states of the two child properties, IPP biosynthesis via mevalonate and IPP biosynthesis from deoxyxylulose. |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85640 |
GenProp1047 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_103 |
diphosphomevalonate decarboxylase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_63451 |
O-antigen export system |
None - {{∅}} |
None - {{∅},{t}} |
Unexplained |
|
Evidence_34 |
TIGR01223 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85626 |
GenProp1035 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_63674 |
any O-antigen monomer system |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_54345 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85194 |
GenProp0913 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
GenProp0047 |
IPP biosynthesis via mevalonate~Isoprenyl pyrophosphate (IPP) is synthesized in eukaryotes, archaea and certain bacteria by the mevalonate pathway (which is in contrast to the non-mevalonate pathway found more generally in prokaryotes). The bacteria containing this pathway are believed to have acquired it by lateral transfer, possible in more than one independent event [Wilding, et. al. (2000) J. Bacteriol. 182, 4319-4327]. Archaea are believed to possess a mevalonate pathway for production of IPP, but several of the steps are divergent from the known enzymes in eukaryotes and have not yet been conclusively identified [PMID: 11042147]. In eukaryotes this pathway is highly regulated to control the production of steroids which require IPP as a precursor. IPP is also required for the synthesis of menaquinone, ubiquinone, terpenoids, isoprene and prenylated proteins. The pathway begins with synthesis of (S)-3-hydroxy-3-methylglutaryl-CoA from acetyl-CoA and acetoacetyl-CoA by HMG-CoA synthase and contains 5 steps all of which are included as required elements for the assignment of the YES state for this property. Some organisms contain a pathway-specific acetoacetyl-CoA synthase which is included in the gene lists for this property but is not a required element for the determination of the property state. Other species likely obtain acetoacetyl-CoA from beta-oxidation of fatty acids or related processes. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85216 |
TIGR00055 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_112 |
2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85219 |
GenProp0046 GENPROP |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_75315 |
TIGR00612 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85218 |
GenProp0048 GENPROP |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_63483 |
source of UDP-GlcNAc |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_2544 |
TIGR00748 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_63452 |
ligation to Lipid A core |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_75335 |
TIGR01455 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_99 |
acetoacetyl-CoA synthase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_39 |
TIGR01835 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_63449 |
Initiation: Und-PP-GlcNAc formation |
None - {{∅}} |
None - {{∅},{t}} |
Unexplained |
|
Evidence_33 |
TIGR01220 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85434 |
GenProp1018 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85212 |
TIGR02380 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_54362 |
glucosamine-1-phosphate N-acetyltransferase/UDP-N-acetylglucosamine diphosphorylase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_55132 |
TIGR00532 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85627 |
GenProp1036 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85623 |
GenProp1023 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_63458 |
O-antigen chain length determinant protein |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85831 |
TIGR04370 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85193 |
GenProp0970 GENPROP |
None - {{∅}} |
None - {{∅},{t}} |
Unexplained |
|
Evidence_85197 |
GenProp0968 GENPROP |
None - {{∅}} |
None - {{∅},{t}} |
Unexplained |
|
Evidence_45 |
TIGR00154 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_102 |
phosphomevalonate kinase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85628 |
GenProp1038 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_101 |
mevalonate kinase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
GenProp0970 |
biosynthesis of Und-PP-GlcNAc~N-acetylglucosamine-1-pyrophospho-undecaprenol (Und-PP-GlcNAc) is synthesized by the WecA enzyme in E. coli from UDP-GlcNAc and undecaprenyl phosphate. |
None - {{∅}} |
None - {{∅},{t}} |
Unexplained |
|
Evidence_75334 |
TIGR01135 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85629 |
GenProp1042 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_43 |
TIGR00204 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
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_85414 |
GenProp0949 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_54341 |
4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85667 |
GenProp1049 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85199 |
PF01943 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85214 |
GenProp0971 GENPROP |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85202 |
TIGR03007 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
GenProp0966 |
E. coli O-antigen biosynthesis~In E. coli biosynthesis of the O-antigen consists of initiation by ligation of (usually) N-acetyl-glucosamine to undecaprenylphosphate (Und-P) to form Und-PP-GlcNAc, followed by O-antigen specific ligation of several nucleotide triphosphate sugars onto the initiating GlcNAc residue. The completed Und-PP-O-antigen monomer is transferred to the periplasmic face of the membrane, polymerized and ligated to the lipid A outer core by one of three systems: The Wzy-dependent path consisting of Wzx, Wzy, and Wzz; the ABC-transporter-dependent pathway and the synthase-dependent pathway. The Wzy-pathway is most common in E. coli. |
None - {{∅}} |
None - {{∅},{t}} |
Unexplained |
|
Component_63486 |
undecaprenyl-diphosphate synthase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_109 |
deoxyxylulose-5-phosphate synthase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85624 |
GenProp1030 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75336 |
TIGR01173 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_63487 |
IPP biosynthesis |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_42 |
TIGR00533 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_84971 |
TIGR03990 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_104 |
hydroxymethylglutaryl-CoA synthase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85215 |
TIGR00753 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85213 |
GenProp0750 GENPROP |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85412 |
GenProp0953 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
GenProp0913 |
E. coli O-antigen monomer biosynthesis clusters~blast database at /usr/local/projects/GSTEC/BLAST/ gstec01 : 1.2741 : O2/H4 : GenProp0963 gstec02 : 97.0246 : O5/H- gstec03 : 5.0588 : O8/H- gstec04 : 97.0259 : O11/H- gstec05 : H30 : O26/H11 gstec06 : 95.0941 : O45/H2 gstec07 : 1.2264 : O76/H- gstec08 : 97.0264 : O88/H25 gstec09 : 96.0497 : O91/H21 gstec10 : 99.0741 : O91/H- gstec11 : 3.2608 : O103/H2 : GenProp0953 gstec12 : 93.0624 : O103/H6 : GenProp0953 gstec13 : 4.0522 : O111/H- : GenProp0949 gstec14 : JB1-95 : O111/H- : GenProp0949 gstec15 : 96.154 : O113/H12 gstec16 : 5.0959 : O121/H19 gstec17 : 9.1649 : O2/H- : GenProp0963 gstec18 : 9.0111 : O128/H2 gstec19 : 4.0967 : O145/H2 gstec20 : 2.3916 : O147/H- gstec21 : 3.3884 : O153/H- gstec22 : 2.4168 : O157/H12 gstec23 : 3.2303 : O157/H16 gstec24 : 3003 : O157/H45 gstec25 : TW07793 : O157/H39 gstec26 : B41 : O101/NHM gstec27 : 900105 (10e) : O26/H11 |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_84972 |
TIGR03991 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85622 |
GenProp1020 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85832 |
PF04932 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_54361 |
phosphoglucosamine mutase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_63488 |
source of isopentenyl diphosphate (IPP) |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_31 |
TIGR00549 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85417 |
GenProp0947 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_63484 |
source of undecaprenyl phosphate (Und-P) |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85620 |
GenProp1019 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_47 |
TIGR00453 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85621 |
GenProp1014 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_85201 |
PF02706 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_63450 |
O-antigen monomer biosynthesis |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_44 |
TIGR00243 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85625 |
GenProp1031 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_63485 |
undecaprenyl-diphosphate phosphohydrolase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_63482 |
UDP-GlcNAc:undecaprenylphosphate GlcNAc-1-phosphate transferase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
GenProp0048 |
IPP biosynthesis via deoxyxylulose~The pathway for the biosynthesis of isoprenyl pyrophosphate (IPP) in most bacteria has been variously referred to as the non-mevalonate pathway (in contrast to the pathway found in eukaryotes), the glyceraldehyde-3-phosphate(GAP)-pyruvate pathway and the deoxyxylulose pathway. This pathway contains six characterized enzymes and may involve additional proteins as well. |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_46 |
TIGR00151 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_75319 |
TIGR00216 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_85416 |
GenProp0974 GENPROP |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|