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Organism related
Word Map for Organism Sulfolobus acidocaldarius
- Sulfolobus acidocaldarius
- archaeon
-
thermoacidophilic
- archaebacterium
-
hyperthermophilic
- solfataricus
-
crenarchaeon
- acidophilum
- islandicus
- s-layers
-
tetraether
- sulfolobales
- thermoplasma
- methanococcus
- tokodaii
- halobium
- halobacterium
- volcanii
- quinol
- f0f1-atpases
- cyclopentane
-
hyperthermoacidophilic
-
acidothermophilic
-
archaellation
-
rieske
-
archaellum
- pyrococcus
-
haloferax
-
geranylgeranyl
-
pyre
TaxTree of Organism Sulfolobus acidocaldarius
Condensed Tree View
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EC NUMBER 
COMMENTARY 
-
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
PATHWAY
BRENDA Link
KEGG Link
MetaCyc Link
(3R)-linalool biosynthesis
-
-
PWY-7709
(3S)-linalool biosynthesis
-
-
PWY-7141
(aminomethyl)phosphonate degradation
-
-
PWY-7805
(S)-lactate fermentation to propanoate, acetate and hydrogen
-
-
PWY-8086
(S)-propane-1,2-diol degradation
-
-
PWY-7013
1,3-propanediol biosynthesis (engineered)
-
-
PWY-7385
1,5-anhydrofructose degradation
-
-
PWY-6992
2-amino-3-hydroxycyclopent-2-enone biosynthesis
-
-
PWY-7536
2-arachidonoylglycerol biosynthesis
-
-
PWY-8052
2-nitrotoluene degradation
-
-
PWY-5641
3,6-anhydro-alpha-L-galactopyranose degradation
-
-
PWY-7562
3-methylbutanol biosynthesis (engineered)
-
-
PWY-6871
4-aminobutanoate degradation V
-
-
PWY-5022
4-chlorobenzoate degradation
-
-
PWY-6215
4-coumarate degradation (aerobic)
-
-
PWY-8002
4-deoxy-L-threo-hex-4-enopyranuronate degradation
-
-
PWY-6507
4-hydroxymandelate degradation
4-methylphenol degradation to protocatechuate
-
-
PWY-7700
5-oxo-L-proline metabolism
-
-
PWY-7942
7-(3-amino-3-carboxypropyl)-wyosine biosynthesis
-
-
PWY-7286
acetaldehyde biosynthesis I
-
-
PWY-6333
acetone degradation I (to methylglyoxal)
-
-
PWY-5451
acetone degradation III (to propane-1,2-diol)
-
-
PWY-7466
acetylene degradation (anaerobic)
-
-
P161-PWY
adenosine ribonucleotides de novo biosynthesis
-
-
PWY-7219
adipate biosynthesis
-
-
PWY-8347
adipate degradation
-
-
PWY-8354
aerobic respiration I (cytochrome c)
-
-
PWY-3781
aerobic respiration II (cytochrome c) (yeast)
-
-
PWY-7279
aerobic respiration III (alternative oxidase pathway)
-
-
PWY-4302
all-trans-farnesol biosynthesis
-
-
PWY-6859
alpha-linolenate metabolites biosynthesis
-
-
PWY-8398
alpha-tomatine degradation
-
-
PWY18C3-5
Amaryllidacea alkaloids biosynthesis
-
-
PWY-7826
ammonia assimilation cycle I
-
-
PWY-6963
ammonia assimilation cycle II
-
-
PWY-6964
ammonia assimilation cycle III
-
-
AMMASSIM-PWY
anaerobic energy metabolism (invertebrates, cytosol)
-
-
PWY-7383
anaerobic energy metabolism (invertebrates, mitochondrial)
-
-
PWY-7384
anandamide biosynthesis I
-
-
PWY-8051
anandamide biosynthesis II
-
-
PWY-8053
arachidonate metabolites biosynthesis
-
-
PWY-8397
arsenite to oxygen electron transfer
-
-
PWY-4521
arsenite to oxygen electron transfer (via azurin)
-
-
PWY-7429
aspirin triggered resolvin D biosynthesis
-
-
PWY66-395
aspirin triggered resolvin E biosynthesis
-
-
PWY66-394
assimilatory sulfate reduction I
-
-
SO4ASSIM-PWY
assimilatory sulfate reduction III
-
-
PWY-6683
ATP biosynthesis
-
-
PWY-7980
bacterial bioluminescence
-
-
PWY-7723
baicalein degradation (hydrogen peroxide detoxification)
-
-
PWY-7214
betanidin degradation
-
-
PWY-5461
bisabolene biosynthesis (engineered)
-
-
PWY-7102
bisphenol A degradation
-
-
PWY-7757
brassicicene C biosynthesis
-
-
PWY-7517
bupropion degradation
-
-
PWY66-241
butanol and isobutanol biosynthesis (engineered)
-
-
PWY-7396
C20,20 CDP-archaeol biosynthesis
-
-
PWY-6349
C4 photosynthetic carbon assimilation cycle, NAD-ME type
-
-
PWY-7115
C4 photosynthetic carbon assimilation cycle, NADP-ME type
-
-
PWY-241
C4 photosynthetic carbon assimilation cycle, PEPCK type
-
-
PWY-7117
Calvin-Benson-Bassham cycle
-
-
CALVIN-PWY
catechol degradation to 2-hydroxypentadienoate I
-
-
P183-PWY
catechol degradation to 2-hydroxypentadienoate II
-
-
PWY-5419
cellulose degradation II (fungi)
-
-
PWY-6788
chitin deacetylation
-
-
PWY-7118
chitin degradation I (archaea)
-
-
PWY-6855
chlorpyrifos degradation
-
-
PWY-8065
cis-zeatin biosynthesis
-
-
PWY-2781
CO2 fixation into oxaloacetate (anaplerotic)
-
-
PWYQT-4429
coenzyme B biosynthesis
-
-
P241-PWY
coenzyme B/coenzyme M regeneration I (methanophenazine-dependent)
-
-
PWY-5207
coumarin biosynthesis (via 2-coumarate)
-
-
PWY-5176
crotonyl-CoA/ethylmalonyl-CoA/hydroxybutyryl-CoA cycle (engineered)
-
-
PWY-7854
cyclic electron flow
-
-
PWY-8270
cytosolic NADPH production (yeast)
-
-
PWY-7268
D-arabinose degradation III
-
-
PWY-5519
D-fructuronate degradation
-
-
PWY-7242
D-galactonate degradation
-
-
GALACTCAT-PWY
D-galactose degradation II
-
-
GALDEG-PWY
D-galacturonate degradation I
-
-
GALACTUROCAT-PWY
D-glucosaminate degradation
-
-
PWY-7310
D-lactate to cytochrome bo oxidase electron transfer
-
-
PWY0-1565
D-myo-inositol (1,4,5)-trisphosphate biosynthesis
-
-
PWY-6351
D-myo-inositol-5-phosphate metabolism
-
-
PWY-6367
D-xylose degradation III
-
-
PWY-6760
D-xylose degradation IV
-
-
PWY-7294
D-xylose degradation V
-
-
PWY-8020
degradation of aromatic, nitrogen containing compounds
-
-
di-homo-gamma-linolenate metabolites biosynthesis
-
-
PWY-8396
di-trans,poly-cis-undecaprenyl phosphate biosynthesis
-
-
PWY-5785
diethylphosphate degradation
-
-
PWY-5491
docosahexaenoate metabolites biosynthesis
-
-
PWY-8400
dolichol and dolichyl phosphate biosynthesis
Entner-Doudoroff pathway I
-
-
PWY-8004
Entner-Doudoroff pathway II (non-phosphorylative)
-
-
NPGLUCAT-PWY
Entner-Doudoroff pathway III (semi-phosphorylative)
-
-
PWY-2221
Entner-Doudoroff shunt
-
-
ENTNER-DOUDOROFF-PWY
ethanol degradation I
-
-
ETOH-ACETYLCOA-ANA-PWY
ethanol degradation II
-
-
PWY66-21
ethanolamine utilization
-
-
PWY0-1477
ethene biosynthesis III (microbes)
-
-
PWY-6854
ethene biosynthesis IV (engineered)
-
-
PWY-7126
ethene biosynthesis V (engineered)
-
-
PWY-7124
Fe(II) oxidation
-
-
PWY-6692
FeMo cofactor biosynthesis
-
-
PWY-7710
firefly bioluminescence
-
-
PWY-7913
formaldehyde assimilation I (serine pathway)
-
-
PWY-1622
formaldehyde assimilation II (assimilatory RuMP Cycle)
-
-
PWY-1861
formaldehyde assimilation III (dihydroxyacetone cycle)
-
-
P185-PWY
formaldehyde oxidation I
-
-
RUMP-PWY
formate to nitrite electron transfer
-
-
PWY0-1585
fructan degradation
-
-
PWY-862
fusicoccin A biosynthesis
-
-
PWY-6659
gamma-glutamyl cycle
-
-
PWY-4041
geranyl diphosphate biosynthesis
-
-
PWY-5122
geranylgeranyl diphosphate biosynthesis
-
-
PWY-5120
ginsenoside degradation I
-
-
PWY-6411
ginsenoside degradation III
-
-
PWY-6413
gluconeogenesis I
-
-
GLUCONEO-PWY
gluconeogenesis II (Methanobacterium thermoautotrophicum)
-
-
PWY-6142
gluconeogenesis III
-
-
PWY66-399
glucose and glucose-1-phosphate degradation
-
-
GLUCOSE1PMETAB-PWY
glucose degradation (oxidative)
-
-
DHGLUCONATE-PYR-CAT-PWY
glutathione-peroxide redox reactions
-
-
PWY-4081
glycerol-3-phosphate to cytochrome bo oxidase electron transfer
-
-
PWY0-1561
glycerol-3-phosphate to fumarate electron transfer
-
-
PWY0-1582
glycogen biosynthesis I (from ADP-D-Glucose)
-
-
GLYCOGENSYNTH-PWY
glycogen biosynthesis II (from UDP-D-Glucose)
-
-
PWY-5067
glycogen degradation I
-
-
GLYCOCAT-PWY
glycogen degradation II
-
-
PWY-5941
glycolate and glyoxylate degradation II
-
-
GLYOXDEG-PWY
glycolysis I (from glucose 6-phosphate)
-
-
GLYCOLYSIS
glycolysis II (from fructose 6-phosphate)
-
-
PWY-5484
glycolysis III (from glucose)
-
-
ANAGLYCOLYSIS-PWY
glycolysis IV
-
-
PWY-1042
glycolysis V (Pyrococcus)
-
-
P341-PWY
glyoxylate cycle
-
-
GLYOXYLATE-BYPASS
glyphosate degradation III
-
-
PWY-7807
heterolactic fermentation
-
-
P122-PWY
hydrogen to fumarate electron transfer
-
-
PWY0-1576
icosapentaenoate metabolites biosynthesis
-
-
PWY-8399
incomplete reductive TCA cycle
-
-
P42-PWY
ipsdienol biosynthesis
-
-
PWY-7410
isoprene biosynthesis II (engineered)
-
-
PWY-7391
isopropanol biosynthesis (engineered)
-
-
PWY-6876
justicidin B biosynthesis
-
-
PWY-6824
kauralexin biosynthesis
-
-
PWY-6887
L-alanine degradation II (to D-lactate)
-
-
ALACAT2-PWY
L-alanine degradation V (oxidative Stickland reaction)
-
-
PWY-8189
L-arabinose degradation IV
-
-
PWY-7295
L-arginine biosynthesis I (via L-ornithine)
-
-
ARGSYN-PWY
L-arginine biosynthesis II (acetyl cycle)
-
-
ARGSYNBSUB-PWY
L-arginine biosynthesis III (via N-acetyl-L-citrulline)
-
-
PWY-5154
L-arginine biosynthesis IV (archaea)
-
-
PWY-7400
L-ascorbate biosynthesis IV (animals, D-glucuronate pathway)
-
-
PWY3DJ-35471
L-ascorbate biosynthesis VI (plants, myo-inositol pathway)
-
-
PWY-8142
L-ascorbate biosynthesis VIII (engineered pathway)
-
-
PWY-7165
L-aspartate degradation II (aerobic)
-
-
PWY-8291
L-aspartate degradation III (anaerobic)
-
-
PWY-8294
L-glucose degradation
-
-
PWY-7130
L-glutamate degradation I
-
-
GLUTAMATE-DEG1-PWY
L-glutamate degradation V (via hydroxyglutarate)
-
-
P162-PWY
L-glutamate degradation VI (to pyruvate)
-
-
PWY-5087
L-glutamate degradation VII (to butanoate)
-
-
GLUDEG-II-PWY
L-glutamate degradation XI (reductive Stickland reaction)
-
-
PWY-8190
L-glutamine biosynthesis I
-
-
GLNSYN-PWY
L-isoleucine biosynthesis I (from threonine)
-
-
ILEUSYN-PWY
L-isoleucine biosynthesis III
-
-
PWY-5103
L-isoleucine degradation II
-
-
PWY-5078
L-leucine degradation III
-
-
PWY-5076
L-lysine biosynthesis IV
-
-
LYSINE-AMINOAD-PWY
L-lysine biosynthesis V
-
-
PWY-3081
L-lysine degradation V
-
-
PWY-5283
L-methionine degradation III
-
-
PWY-5082
L-phenylalanine degradation III
-
-
PWY-5079
L-tryptophan degradation V (side chain pathway)
-
-
PWY-3162
L-tyrosine degradation III
-
-
PWY3O-4108
L-valine biosynthesis
-
-
VALSYN-PWY
L-valine degradation II
-
-
PWY-5057
lactate fermentation to acetate, CO2 and hydrogen (Desulfovibrionales)
-
-
PWY-8377
linalool biosynthesis I
-
-
PWY-7182
linamarin degradation
-
-
PWY-3121
linoleate metabolites biosynthesis
-
-
PWY-8395
linustatin bioactivation
-
-
PWY-7091
lipid A-core biosynthesis (E. coli K-12)
-
-
LIPA-CORESYN-PWY
lotaustralin degradation
-
-
PWY-6002
luteolin triglucuronide degradation
-
-
PWY-7445
malate/L-aspartate shuttle pathway
-
-
MALATE-ASPARTATE-SHUTTLE-PWY
maresin biosynthesis
-
-
PWY-8356
matairesinol biosynthesis
-
-
PWY-5466
melatonin degradation I
-
-
PWY-6398
Methanobacterium thermoautotrophicum biosynthetic metabolism
-
-
PWY-6146
methyl indole-3-acetate interconversion
-
-
PWY-6303
methyl parathion degradation
-
-
PWY-5489
methyl phomopsenoate biosynthesis
-
-
PWY-7721
methylaspartate cycle
methylsalicylate degradation
-
-
PWY18C3-24
methylwyosine biosynthesis
-
-
PWY-7285
mevalonate pathway I (eukaryotes and bacteria)
-
-
PWY-922
mevalonate pathway II (haloarchaea)
-
-
PWY-6174
mevalonate pathway III (Thermoplasma)
-
-
PWY-7524
mevalonate pathway IV (archaea)
-
-
PWY-8125
mixed acid fermentation
-
-
FERMENTATION-PWY
mono-trans, poly-cis decaprenyl phosphate biosynthesis
-
-
PWY-6383
mRNA capping I
-
-
PWY-7375
NAD(P)/NADPH interconversion
-
-
PWY-5083
NADH to cytochrome bd oxidase electron transfer I
-
-
PWY0-1334
NADH to cytochrome bo oxidase electron transfer I
-
-
PWY0-1335
NADH to cytochrome bo oxidase electron transfer II
-
-
PWY0-1567
NADH to fumarate electron transfer
-
-
PWY0-1336
NADPH to cytochrome c oxidase via plastocyanin
-
-
PWY-8271
neolinustatin bioactivation
-
-
PWY-7092
nicotine degradation IV
-
-
PWY66-201
nicotine degradation V
-
-
PWY66-221
nitrate reduction X (dissimilatory, periplasmic)
-
-
PWY0-1584
nitrogen remobilization from senescing leaves
-
-
PWY-6549
noradrenaline and adrenaline degradation
-
-
PWY-6342
oleandomycin activation/inactivation
-
-
PWY-6972
ophiobolin F biosynthesis
-
-
PWY-7720
oryzalide A biosynthesis
-
-
PWY-7481
paraoxon degradation
-
-
PWY-5490
parathion degradation
-
-
PARATHION-DEGRADATION-PWY
partial TCA cycle (obligate autotrophs)
-
-
PWY-5913
paspaline biosynthesis
-
-
PWY-7492
pentose phosphate pathway (non-oxidative branch) II
-
-
PWY-8178
pentose phosphate pathway (oxidative branch) I
-
-
OXIDATIVEPENT-PWY
peptido-conjugates in tissue regeneration biosynthesis
-
-
PWY-8355
phenylethanol biosynthesis
-
-
PWY-5751
phosphate acquisition
-
-
PWY-6348
phosphatidate metabolism, as a signaling molecule
-
-
PWY-7039
phosphatidylcholine acyl editing
-
-
PWY-6803
phospholipases
-
-
LIPASYN-PWY
phospholipid remodeling (phosphatidate, yeast)
-
-
PWY-7417
phospholipid remodeling (phosphatidylcholine, yeast)
-
-
PWY-7416
phospholipid remodeling (phosphatidylethanolamine, yeast)
-
-
PWY-7409
photosynthesis light reactions
-
-
PWY-101
phytol degradation
-
-
PWY66-389
plasmalogen degradation
-
-
PWY-7783
plaunotol biosynthesis
-
-
PWY-6691
polybrominated dihydroxylated diphenyl ethers biosynthesis
-
-
PWY-7934
polyphosphate metabolism
-
-
PWY-8138
proline to cytochrome bo oxidase electron transfer
-
-
PWY0-1544
protectin biosynthesis
-
-
PWY-8357
protein N-glycosylation (Haloferax volcanii)
-
-
PWY-7661
protein N-glycosylation (Methanococcus voltae)
-
-
PWY-7658
protein N-glycosylation initial phase (eukaryotic)
-
-
MANNOSYL-CHITO-DOLICHOL-BIOSYNTHESIS
purine nucleobases degradation II (anaerobic)
-
-
PWY-5497
pyrimidine deoxyribonucleotides biosynthesis from CTP
-
-
PWY-7210
pyrimidine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7184
pyrimidine deoxyribonucleotides de novo biosynthesis III
-
-
PWY-6545
pyrimidine deoxyribonucleotides de novo biosynthesis IV
-
-
PWY-7198
pyruvate decarboxylation to acetyl CoA III
-
-
PWY-8275
pyruvate fermentation to acetate I
-
-
P142-PWY
pyruvate fermentation to acetate III
-
-
PWY-5483
pyruvate fermentation to acetate V
-
-
PWY-5537
pyruvate fermentation to acetate VI
-
-
PWY-5538
pyruvate fermentation to acetate VII
-
-
PWY-5600
pyruvate fermentation to acetone
-
-
PWY-6588
pyruvate fermentation to butanoate
-
-
CENTFERM-PWY
pyruvate fermentation to butanol I
-
-
PWY-6583
pyruvate fermentation to ethanol I
-
-
PWY-5480
pyruvate fermentation to ethanol II
-
-
PWY-5486
pyruvate fermentation to ethanol III
-
-
PWY-6587
pyruvate fermentation to hexanol (engineered)
-
-
PWY-6863
pyruvate fermentation to isobutanol (engineered)
-
-
PWY-7111
pyruvate fermentation to propanoate I
-
-
P108-PWY
pyruvate to cytochrome bo oxidase electron transfer
-
-
PWY-7544
reactive oxygen species degradation
-
-
DETOX1-PWY-1
reductive glycine pathway of autotrophic CO2 fixation
-
-
PWY-8303
reductive monocarboxylic acid cycle
-
-
PWY-5493
reductive TCA cycle I
-
-
P23-PWY
reductive TCA cycle II
-
-
PWY-5392
resolvin D biosynthesis
-
-
PWY66-397
retinol biosynthesis
-
-
PWY-6857
salidroside biosynthesis
-
-
PWY-6802
sedoheptulose bisphosphate bypass
-
-
PWY0-1517
serotonin degradation
-
-
PWY-6313
sesamin biosynthesis
-
-
PWY-5469
sorbitol biosynthesis II
-
-
PWY-5530
spongiadioxin C biosynthesis
-
-
PWY-7935
starch biosynthesis
-
-
PWY-622
starch degradation I
-
-
PWY-842
starch degradation II
-
-
PWY-6724
stellatic acid biosynthesis
-
-
PWY-7736
succinate to chytochrome c oxidase via cytochrome c6
-
-
PWY1YI0-2
succinate to cytochrome bd oxidase electron transfer
-
-
PWY0-1353
succinate to cytochrome bo oxidase electron transfer
-
-
PWY0-1329
succinate to cytochrome c oxidase via plastocyanin
-
-
PWY1YI0-3
succinate to plastoquinol oxidase
-
-
PWY1YI0-8
sucrose biosynthesis I (from photosynthesis)
-
-
SUCSYN-PWY
sucrose degradation V (sucrose alpha-glucosidase)
-
-
PWY66-373
sulfoquinovosyl diacylglycerol biosynthesis
-
-
PWYQT-4427
sulfur disproportionation II (aerobic)
-
-
PWY-5302
sulfur reduction I
-
-
PWY-5332
sulfur reduction II (via polysulfide)
-
-
PWY-5364
superoxide radicals degradation
-
-
DETOX1-PWY
superpathway of fermentation (Chlamydomonas reinhardtii)
-
-
PWY4LZ-257
superpathway of glycolysis and the Entner-Doudoroff pathway
-
-
GLYCOLYSIS-E-D
superpathway of glyoxylate cycle and fatty acid degradation
-
-
PWY-561
superpathway of methylsalicylate metabolism
-
-
PWY18C3-25
taxadiene biosynthesis (engineered)
-
-
PWY-7392
taxol biosynthesis
TCA cycle I (prokaryotic)
-
-
TCA
TCA cycle II (plants and fungi)
-
-
PWY-5690
TCA cycle III (animals)
-
-
PWY66-398
TCA cycle IV (2-oxoglutarate decarboxylase)
-
-
P105-PWY
TCA cycle V (2-oxoglutarate synthase)
-
-
PWY-6969
TCA cycle VI (Helicobacter)
-
-
REDCITCYC
TCA cycle VII (acetate-producers)
-
-
PWY-7254
TCA cycle VIII (Chlamydia)
-
-
TCA-1
tetrapyrrole biosynthesis II (from glycine)
-
-
PWY-5189
thiamine triphosphate metabolism
-
-
PWY-7369
toluene degradation II (aerobic) (via 4-methylcatechol)
-
-
TOLUENE-DEG-3-OH-PWY
toluene degradation to 2-hydroxypentadienoate (via toluene-cis-diol)
-
-
TOLUENE-DEG-DIOL-PWY
toluene degradation to 2-hydroxypentadienoate I (via o-cresol)
-
-
TOLUENE-DEG-2-OH-PWY
trans, trans-farnesyl diphosphate biosynthesis
-
-
PWY-5123
trehalose biosynthesis V
-
-
PWY-2661
trehalose biosynthesis VI
-
-
PWY-5983
trehalose degradation II (cytosolic)
-
-
PWY0-1182
trehalose degradation VI (periplasmic)
-
-
PWY0-1466
triacylglycerol degradation
-
-
LIPAS-PWY
tRNA charging
-
-
TRNA-CHARGING-PWY
tRNA methylation (yeast)
-
-
PWY-6829
tRNA processing
-
-
PWY0-1479
UMP biosynthesis I
-
-
PWY-5686
UMP biosynthesis II
-
-
PWY-7790
UMP biosynthesis III
-
-
PWY-7791
urea cycle
UTP and CTP dephosphorylation I
-
-
PWY-7185
UTP and CTP dephosphorylation II
-
-
PWY-7177
vanillin biosynthesis I
-
-
PWY-5665
viridicatumtoxin biosynthesis
-
-
PWY-7659
xanthommatin biosynthesis
-
-
PWY-8249
xyloglucan degradation II (exoglucanase)
-
-
PWY-6807
4-hydroxymandelate degradation
-
-
4-HYDROXYMANDELATE-DEGRADATION-PWY
dolichol and dolichyl phosphate biosynthesis
-
-
PWY-6129
methylaspartate cycle
-
-
PWY-6728
taxol biosynthesis
-
-
PWY-5660
urea cycle
-
-
PWY-4984
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ORGANISM
COMMENTARY
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
-
799, 3485, 3488, 3822, 134449, 134751, 137306, 137307, 137308, 137309, 137310, 209827, 210576, 286659, 286660, 286661, 286662, 286672, 392720, 396010, 485879, 488043, 488049, 638756, 638757, 638758, 638759, 642582, 642604, 645121, 649108, 651095, 651345, 651359, 659533, 662624, 674641, 677799, 677801, 678015, 678480, 679506, 679620, 679621, 679623, 679808, 679809, 680590, 680591, 681367, 681369, 684926, 694439, 706873, 718723, 718808, 719022, 719180, 719388, 719754, 719784, 720219, 720484, 720600, 720613, 720621, 721061, 722296, 723776, 724403, 724404, 724613, 724723, 724867, 724896, 724987, 724988, 725031, 725224, 725232, 725305, 725306, 725804, 725968, 726057, 726069, 726404, 726406, 727363, 727720, 727830, 728368, 729627, 733810, 746846, 750194, 750695, 753334, 754823, 764352, 764486
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-
-
637490, 678016, 678510, 713146, 719340, 719397, 719474, 719516, 720564, 722595, 723964, 725361, 725547, 725968, 726025, 728703, 729348, 736647, 754823, 756160, 756728, 757838, 759474, 763730
P11386, P14288, P39464, P95690, Q08582, Q08713, Q4J6M3, Q4J6M6, Q4J6M5
, Q4J894, Q4J8E7, Q4J8K9, Q4J989, Q4JAP9, Q4JAQ2, Q4JB80, Q4JC68, Q7M529, Q9HH76
SwissProt
-
642627, 678510, 682747, 708519, 718621, 718681, 718686, 718713, 718714, 718771, 719428, 719713, 719753, 720252, 720497, 721283, 724106, 724227, 724478, 724560, 724931, 725032, 725185, 725283, 725338, 725972, 726351, 728790, 729510, 729693, 729697, 731776, 733814, 733831, 734205, 734650, 738195, 746511, 746849, 749205, 751313, 753023, 754823, 756455, 761051
A0A2Z5U3T3, O73957, P35028, P39465, P50308, Q4J6C9, Q4J6E1, Q4J6K0, Q4J6Z8, Q4J702, Q4J7F1, Q4J7I6, Q4J9B4, Q4J9F2, Q4J9F6, Q4J9L0, Q4J9M2, Q4J9M3, Q4JA33, Q4JAQ3, Q4JB16, Q4JB37, Q4JBJ3, Q4JC35, Q4JCB7, Q53641, Q53688, Q55080, Q9HH97
UniProt
enzyme exhibits RNase activity as well as DNA-binding properties
-
-
gene agl3, or Saci0423, of the sulfoquinovose biosynthesis operon
-
-
P39480 (soxA) and P98004 (soxB) and P39479 (soxA) and P39477 (Saci_2086)
P39480, P98004, P39479, P39477
SwissProt
P39480 (soxC) and P98004 (soxB) and P39479 (soxA) and P39477 (Saci_2086)
P39480, P98004, P39479, P39477
SwissProt
P39481 (soxM), Q97UN3 (soxG), Q53765 (soxE), Q53766 (soxD), Q59825 (soxH), Q53768 (soxI)
P39481, Q97UN3, Q53765, Q53766, Q59825, Q53768
-
P77943: subunit sdhA (flavoprotein subunit), P77944: subunit sdhB, P77945: subunit sdhC, P77946: subunit sdhD
UniProt
Q4J6I9 i.e. alpha subunit, Q4J6I8 i.e. beta subunit KorB
UniProt
Q4J711: ABC-type transmembrane domain (saci_2121), Q4J710: ABC-type substrate binding protein (saci_2122), saci_2120: ABC-type nucleotide binding domain, putative ATPase. saci_2120 is cotranscribed with saci_2122 and saci_2121 as a single mRNA; strain MW001 is a pyrE deletion mutant of Sulfolubus acidocaldarius wild type strain DSM 639 missing 322 bp
Q4J711, Q4J710
UniProt
the wild type strain DSM 639 missing 322 bp called MW001
UniProt
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SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
SOURCE
additional information
the transcription level of malA is increased 3-fold upon the addition of maltose to the medium. The alpha-glucosidase activity for maltose as a substrate in cell extracts is 11-fold higher during growth in YT medium (Brocks mineral salts, 0.1% (w/v) tryptone, and 0.005% (w/v) yeast extract) containing maltose, than during growth on other sugars
the transcription level of malA is increased 3fold upon the addition of maltose or starch to the medium. The alpha-glucosidase activity for maltose as a substrate in cell extracts is 11fold higher during growth in YT medium (Brocks mineral salts, 0.1% (w/v) tryptone, and 0.005% (w/v) yeast extract) containing maltose, than during growth on other sugars
the transcription level of malA is increased 3-fold upon the addition of starch to the medium. The alpha-glucosidase activity for maltose as a substrate in cell extracts is 10-fold higher during growth in YT medium (Brocks mineral salts, 0.1% (w/v) tryptone, and 0.005% (w/v) yeast extract) containing starch, respectively, than during growth on other sugars
the transcription level of malA is increased 3fold upon the addition of maltose or starch to the medium. The alpha-glucosidase activity for maltose as a substrate in cell extracts is 10fold higher during growth in YT medium (Brocks mineral salts, 0.1% (w/v) tryptone, and 0.005% (w/v) yeast extract) containing starch, than during growth on other sugars
the transcription level of malA is increased 3fold upon the addition of maltose or starch to the medium. The alpha-glucosidase activity for starch as a substrate in cell extracts is 10fold higher during growth in YT medium (Brocks mineral salts, 0.1% (w/v) tryptone, and 0.005% (w/v) yeast extract) containing starch, than during growth on other sugars
additional information
-
optimal cell cultivation at pH 2.0 and 70°C
additional information
Sulfolobus acidocaldarius is able to grow on 24 mM 5-oxo-L-proline, reaching a maximum cell dry weight of 0.64 g/l and a maximum growth rate of 0.055/h within 96 h of cultivation
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LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY
GeneOntology No.
LITERATURE
SOURCE
archaellum, soluble motor ATPase FlaI localizes to the membrane, possibly via an interaction of the archaellum membrane components
-
it comprises at least 11% of the cytosolic protein
Q4J6M3 AND Q4J6M6 AND Q4J6M5
present in the cytosol to at least 0.4% of the soluble protein
contains cell-associated and secreted alpha-amylase. Inactivation of the amyA gene results in a complete loss of activity, suggesting that the same protein is responsible for the alpha-amylase activity at both locations
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contains cell-associated and secreted alpha-amylase. Inactivation of the amyA gene results in a complete loss of activity, suggesting that the same protein is responsible for the alpha-amylase activity at both locations
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AglH possesses ten transmembrane helices separated by five internal and four external hydrophilic loops
LINKS TO OTHER DATABASES (specific for Sulfolobus acidocaldarius)
SILVA: 16S/18S rRNA, 23S/28S rRNA
: 16649
