Evidence_35 |
TIGR01240 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_110 |
1-deoxy-D-xylulose 5-phosphate reductoisomerase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_54406 |
uncharacterized syntenic membrane protein |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_113 |
2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_38 |
TIGR01833 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_45 |
TIGR00154 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_102 |
phosphomevalonate kinase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_101 |
mevalonate kinase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_111 |
4-diphosphocytidyl-2C-methyl-D-erythritol kinase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_43 |
TIGR00204 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_54341 |
4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_75410 |
TIGR03462 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_105 |
hydroxymethylglutaryl-CoA reductase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_54404 |
source of IPP |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_29 |
TIGR01217 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75399 |
TIGR02734 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75392 |
TIGR02731 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_32 |
TIGR01219 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75394 |
PF00494 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_54405 |
lycopene cyclases |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75400 |
TIGR02734 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_103 |
diphosphomevalonate decarboxylase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75401 |
TIGR01790 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75397 |
GenProp0048 GENPROP |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_34 |
TIGR01223 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_109 |
deoxyxylulose-5-phosphate synthase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_75391 |
TIGR02732 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75404 |
TIGR03460 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75396 |
TIGR02151 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_42 |
TIGR00533 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_54400 |
phytoene desaturase (1.14.99.-) |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_104 |
hydroxymethylglutaryl-CoA synthase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_54345 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
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 |
|
Component_112 |
2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_75393 |
PF00348 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_75395 |
TIGR02150 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75315 |
TIGR00612 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_54401 |
geranylgeranyl pyrophosphate synthase |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_2544 |
TIGR00748 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_54399 |
zeta-carotene desaturase (1.14.99.30) |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_75402 |
TIGR03459 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_31 |
TIGR00549 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Component_54403 |
isopentenyl-diphosphate delta-isomerase (5.3.3.2) |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Component_99 |
acetoacetyl-CoA synthase |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_47 |
TIGR00453 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_39 |
TIGR01835 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
Evidence_33 |
TIGR01220 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
GenProp0758 |
lycopene biosynthesis from IPP~ |
None - {{∅}} |
None - {{∅},{t}} |
Unexplained |
|
Component_54402 |
phytoene synthase (2.5.1.32) |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_44 |
TIGR00243 HMM |
None - {{∅}} |
True - {{t}} |
Unconfirmed presence |
|
Evidence_75398 |
GenProp0047 GENPROP |
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_55132 |
TIGR00532 HMM |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|