Local view for "http://wifo5-04.informatik.uni-mannheim.de/drugbank/resource/drugs/DB04553"
Predicate | Value (sorted: default) |
---|---|
rdfs:label |
"2-Oxobutanoic Acid"
|
rdf:type | |
drugbank:description |
"
600-18-0
experimental
This compound belongs to the alpha keto-acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the adjacent carbon.
Alpha Keto-Acids and Derivatives
Organic Compounds
Organic Acids and Derivatives
Keto-Acids and Derivatives
Alpha Keto-Acids and Derivatives
Ketones
Polyamines
Enolates
Carboxylic Acids
Keto Acids and Derivatives
ketone
enolate
polyamine
carboxylic acid
carboxylic acid derivative
carbonyl group
logP
0.07
ALOGPS
logS
-0.11
ALOGPS
Water Solubility
7.92e+01 g/l
ALOGPS
logP
0.77
ChemAxon
IUPAC Name
2-oxobutanoic acid
ChemAxon
Traditional IUPAC Name
2-oxobutanoic acid
ChemAxon
Molecular Weight
102.0886
ChemAxon
Monoisotopic Weight
102.031694058
ChemAxon
SMILES
CCC(=O)C(O)=O
ChemAxon
Molecular Formula
C4H6O3
ChemAxon
InChI
InChI=1S/C4H6O3/c1-2-3(5)4(6)7/h2H2,1H3,(H,6,7)
ChemAxon
InChIKey
InChIKey=TYEYBOSBBBHJIV-UHFFFAOYSA-N
ChemAxon
Polar Surface Area (PSA)
54.37
ChemAxon
Refractivity
22.62
ChemAxon
Polarizability
9.2
ChemAxon
Rotatable Bond Count
2
ChemAxon
H Bond Acceptor Count
3
ChemAxon
H Bond Donor Count
1
ChemAxon
pKa (strongest acidic)
3.19
ChemAxon
pKa (strongest basic)
-9.7
ChemAxon
Physiological Charge
-1
ChemAxon
Number of Rings
0
ChemAxon
Bioavailability
1
ChemAxon
Rule of Five
true
ChemAxon
Melting Point
33 °C
PhysProp
ChEBI
30831
PubChem Compound
58
PubChem Substance
46504977
KEGG Compound
C00109
PDB
2KT
SMP00452
Threonine and 2-Oxobutanoate Degradation
DB00121
Biotin
DB00156
L-Threonine
DB04553
2-Oxobutanoic Acid
P20132
P11182
P09622
P21953
P12694
P05165
P05166
Q96PE7
P22033
SMP00721
3-Phosphoglycerate dehydrogenase deficiency
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00119
Pyruvic acid
DB00133
L-Serine
DB00134
L-Methionine
DB00142
L-Glutamic Acid
DB00145
Glycine
DB00148
Creatine
DB00151
L-Cysteine
DB00160
L-Alanine
DB01593
Zinc
DB02951
3-Hydroxypyruvic Acid
DB02957
Orotidine-5'-Monophosphate
DB04343
Glyoxalate, Glyoxylate
DB04553
2-Oxobutanoic Acid
P21397
P05091
O75600
Q9UI17
Q9UL12
P23378
P48728
P34897
P09622
P21549
P50440
Q14353
P13196
Q93088
Q14749
Q8IVS8
O43175
Q9Y617
P78330
P20132
P49591
P34896
P41250
Q9GZT4
P35520
P32929
SMP00029
Selenoamino Acid Metabolism
DB00133
L-Serine
DB00160
L-Alanine
DB00640
Adenosine
DB02345
Selenocysteine
DB04553
2-Oxobutanoic Acid
Q96I15
Q99611
P32929
P35520
P23526
Q8TCB7
P31153
Q9NZL9
P56192
O43252
P19440
SMP00214
S-Adenosylhomocysteine (SAH) Hydrolase Deficiency
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00133
L-Serine
DB00134
L-Methionine
DB00145
Glycine
DB00151
L-Cysteine
DB00640
Adenosine
DB01345
Potassium
DB01593
Zinc
DB01917
Putrescine
DB02238
4-(Methylsulfanyl)-2-Oxobutanoic Acid
DB03566
Spermidine
DB04193
L-Homoserine
DB04553
2-Oxobutanoic Acid
P34896
P42898
Q99707
P32929
P35520
Q93088
P26358
P17707
P19623
Q13126
P23526
Q96RQ9
P56192
Q96DP5
P31153
Q9NZL9
Q8NE62
Q8IXL7
Q9Y3D2
SMP00221
Methionine Adenosyltransferase Deficiency
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00133
L-Serine
DB00134
L-Methionine
DB00145
Glycine
DB00151
L-Cysteine
DB00640
Adenosine
DB01345
Potassium
DB01593
Zinc
DB01917
Putrescine
DB02238
4-(Methylsulfanyl)-2-Oxobutanoic Acid
DB03566
Spermidine
DB04193
L-Homoserine
DB04553
2-Oxobutanoic Acid
P34896
P42898
Q99707
P32929
P35520
Q93088
P26358
P17707
P19623
Q13126
P23526
Q96RQ9
P56192
Q96DP5
P31153
Q9NZL9
Q8NE62
Q8IXL7
Q9Y3D2
SMP00004
Glycine and Serine Metabolism
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00119
Pyruvic acid
DB00133
L-Serine
DB00134
L-Methionine
DB00142
L-Glutamic Acid
DB00145
Glycine
DB00148
Creatine
DB00151
L-Cysteine
DB00160
L-Alanine
DB01593
Zinc
DB02951
3-Hydroxypyruvic Acid
DB02957
Orotidine-5'-Monophosphate
DB04343
Glyoxalate, Glyoxylate
DB04553
2-Oxobutanoic Acid
P21397
P05091
O75600
Q9UI17
Q9UL12
P23378
P48728
P34897
P09622
P21549
P50440
Q14353
P13196
Q93088
Q14749
Q8IVS8
O43175
Q9Y617
P78330
P20132
P49591
P34896
P41250
Q9GZT4
P35520
P32929
SMP00570
Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00133
L-Serine
DB00134
L-Methionine
DB00145
Glycine
DB00151
L-Cysteine
DB00640
Adenosine
DB01345
Potassium
DB01593
Zinc
DB01917
Putrescine
DB02238
4-(Methylsulfanyl)-2-Oxobutanoic Acid
DB03566
Spermidine
DB04193
L-Homoserine
DB04553
2-Oxobutanoic Acid
P34896
P42898
Q99707
P32929
P35520
Q93088
P26358
P17707
P19623
Q13126
P23526
Q96RQ9
P56192
Q96DP5
P31153
Q9NZL9
Q8NE62
Q8IXL7
Q9Y3D2
SMP00177
Cystathionine Beta-Synthase Deficiency
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00133
L-Serine
DB00134
L-Methionine
DB00145
Glycine
DB00151
L-Cysteine
DB00640
Adenosine
DB01345
Potassium
DB01593
Zinc
DB01917
Putrescine
DB02238
4-(Methylsulfanyl)-2-Oxobutanoic Acid
DB03566
Spermidine
DB04193
L-Homoserine
DB04553
2-Oxobutanoic Acid
P34896
P42898
Q99707
P32929
P35520
Q93088
P26358
P17707
P19623
Q13126
P23526
Q96RQ9
P56192
Q96DP5
P31153
Q9NZL9
Q8NE62
Q8IXL7
Q9Y3D2
SMP00515
Homocystinuria, cystathionine beta-synthase deficiency
DB00133
L-Serine
DB00151
L-Cysteine
DB04553
2-Oxobutanoic Acid
P35520
P32929
SMP00514
Gamma-cystathionase deficiency (CTH)
DB00133
L-Serine
DB00151
L-Cysteine
DB04553
2-Oxobutanoic Acid
P35520
P32929
SMP00179
Dihydropyrimidine Dehydrogenase Deficiency (DHPD)
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00119
Pyruvic acid
DB00133
L-Serine
DB00134
L-Methionine
DB00142
L-Glutamic Acid
DB00145
Glycine
DB00148
Creatine
DB00151
L-Cysteine
DB00160
L-Alanine
DB01593
Zinc
DB02951
3-Hydroxypyruvic Acid
DB02957
Orotidine-5'-Monophosphate
DB04343
Glyoxalate, Glyoxylate
DB04553
2-Oxobutanoic Acid
P21397
P05091
O75600
Q9UI17
Q9UL12
P23378
P48728
P34897
P09622
P21549
P50440
Q14353
P13196
Q93088
Q14749
Q8IVS8
O43175
Q9Y617
P78330
P20132
P49591
P34896
P41250
Q9GZT4
P35520
P32929
SMP00340
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00133
L-Serine
DB00134
L-Methionine
DB00145
Glycine
DB00151
L-Cysteine
DB00640
Adenosine
DB01345
Potassium
DB01593
Zinc
DB01917
Putrescine
DB02238
4-(Methylsulfanyl)-2-Oxobutanoic Acid
DB03566
Spermidine
DB04193
L-Homoserine
DB04553
2-Oxobutanoic Acid
P34896
P42898
Q99707
P32929
P35520
Q93088
P26358
P17707
P19623
Q13126
P23526
Q96RQ9
P56192
Q96DP5
P31153
Q9NZL9
Q8NE62
Q8IXL7
Q9Y3D2
SMP00242
Dimethylglycine Dehydrogenase Deficiency
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00119
Pyruvic acid
DB00133
L-Serine
DB00134
L-Methionine
DB00142
L-Glutamic Acid
DB00145
Glycine
DB00148
Creatine
DB00151
L-Cysteine
DB00160
L-Alanine
DB01593
Zinc
DB02951
3-Hydroxypyruvic Acid
DB02957
Orotidine-5'-Monophosphate
DB04343
Glyoxalate, Glyoxylate
DB04553
2-Oxobutanoic Acid
P21397
P05091
O75600
Q9UI17
Q9UL12
P23378
P48728
P34897
P09622
P21549
P50440
Q14353
P13196
Q93088
Q14749
Q8IVS8
O43175
Q9Y617
P78330
P20132
P49591
P34896
P41250
Q9GZT4
P35520
P32929
SMP00222
Glycine N-methyltransferase Deficiency
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00133
L-Serine
DB00134
L-Methionine
DB00145
Glycine
DB00151
L-Cysteine
DB00640
Adenosine
DB01345
Potassium
DB01593
Zinc
DB01917
Putrescine
DB02238
4-(Methylsulfanyl)-2-Oxobutanoic Acid
DB03566
Spermidine
DB04193
L-Homoserine
DB04553
2-Oxobutanoic Acid
P34896
P42898
Q99707
P32929
P35520
Q93088
P26358
P17707
P19623
Q13126
P23526
Q96RQ9
P56192
Q96DP5
P31153
Q9NZL9
Q8NE62
Q8IXL7
Q9Y3D2
SMP00455
Homocysteine Degradation
DB00133
L-Serine
DB00151
L-Cysteine
DB04553
2-Oxobutanoic Acid
P35520
P32929
SMP00484
Dimethylglycinuria
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00119
Pyruvic acid
DB00133
L-Serine
DB00134
L-Methionine
DB00142
L-Glutamic Acid
DB00145
Glycine
DB00148
Creatine
DB00151
L-Cysteine
DB00160
L-Alanine
DB01593
Zinc
DB02951
3-Hydroxypyruvic Acid
DB02957
Orotidine-5'-Monophosphate
DB04343
Glyoxalate, Glyoxylate
DB04553
2-Oxobutanoic Acid
P21397
P05091
O75600
Q9UI17
Q9UL12
P23378
P48728
P34897
P09622
P21549
P50440
Q14353
P13196
Q93088
Q14749
Q8IVS8
O43175
Q9Y617
P78330
P20132
P49591
P34896
P41250
Q9GZT4
P35520
P32929
SMP00223
Non Ketotic Hyperglycinemia
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00119
Pyruvic acid
DB00133
L-Serine
DB00134
L-Methionine
DB00142
L-Glutamic Acid
DB00145
Glycine
DB00148
Creatine
DB00151
L-Cysteine
DB00160
L-Alanine
DB01593
Zinc
DB02951
3-Hydroxypyruvic Acid
DB02957
Orotidine-5'-Monophosphate
DB04343
Glyoxalate, Glyoxylate
DB04553
2-Oxobutanoic Acid
P21397
P05091
O75600
Q9UI17
Q9UL12
P23378
P48728
P34897
P09622
P21549
P50440
Q14353
P13196
Q93088
Q14749
Q8IVS8
O43175
Q9Y617
P78330
P20132
P49591
P34896
P41250
Q9GZT4
P35520
P32929
SMP00485
Hyperglycinemia, non-ketotic
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00119
Pyruvic acid
DB00133
L-Serine
DB00134
L-Methionine
DB00142
L-Glutamic Acid
DB00145
Glycine
DB00148
Creatine
DB00151
L-Cysteine
DB00160
L-Alanine
DB01593
Zinc
DB02951
3-Hydroxypyruvic Acid
DB02957
Orotidine-5'-Monophosphate
DB04343
Glyoxalate, Glyoxylate
DB04553
2-Oxobutanoic Acid
P21397
P05091
O75600
Q9UI17
Q9UL12
P23378
P48728
P34897
P09622
P21549
P50440
Q14353
P13196
Q93088
Q14749
Q8IVS8
O43175
Q9Y617
P78330
P20132
P49591
P34896
P41250
Q9GZT4
P35520
P32929
SMP00341
Hypermethioninemia
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00133
L-Serine
DB00134
L-Methionine
DB00145
Glycine
DB00151
L-Cysteine
DB00640
Adenosine
DB01345
Potassium
DB01593
Zinc
DB01917
Putrescine
DB02238
4-(Methylsulfanyl)-2-Oxobutanoic Acid
DB03566
Spermidine
DB04193
L-Homoserine
DB04553
2-Oxobutanoic Acid
P34896
P42898
Q99707
P32929
P35520
Q93088
P26358
P17707
P19623
Q13126
P23526
Q96RQ9
P56192
Q96DP5
P31153
Q9NZL9
Q8NE62
Q8IXL7
Q9Y3D2
SMP00033
Methionine Metabolism
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00133
L-Serine
DB00134
L-Methionine
DB00145
Glycine
DB00151
L-Cysteine
DB00640
Adenosine
DB01345
Potassium
DB01593
Zinc
DB01917
Putrescine
DB02238
4-(Methylsulfanyl)-2-Oxobutanoic Acid
DB03566
Spermidine
DB04193
L-Homoserine
DB04553
2-Oxobutanoic Acid
P34896
P42898
Q99707
P32929
P35520
Q93088
P26358
P17707
P19623
Q13126
P23526
Q96RQ9
P56192
Q96DP5
P31153
Q9NZL9
Q8NE62
Q8IXL7
Q9Y3D2
SMP00244
Sarcosinemia
DB00116
Tetrahydrofolic acid
DB00118
S-Adenosylmethionine
DB00119
Pyruvic acid
DB00133
L-Serine
DB00134
L-Methionine
DB00142
L-Glutamic Acid
DB00145
Glycine
DB00148
Creatine
DB00151
L-Cysteine
DB00160
L-Alanine
DB01593
Zinc
DB02951
3-Hydroxypyruvic Acid
DB02957
Orotidine-5'-Monophosphate
DB04343
Glyoxalate, Glyoxylate
DB04553
2-Oxobutanoic Acid
P21397
P05091
O75600
Q9UI17
Q9UL12
P23378
P48728
P34897
P09622
P21549
P50440
Q14353
P13196
Q93088
Q14749
Q8IVS8
O43175
Q9Y617
P78330
P20132
P49591
P34896
P41250
Q9GZT4
P35520
P32929
BE0001641
Methylmalonyl-CoA carboxyltransferase 5S subunit
Propionibacterium freudenreichii subsp. shermanii
# Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17139284
# Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17016423
unknown
Methylmalonyl-CoA carboxyltransferase 5S subunit
Energy production and conversion
The 5S subunit specifically catalyzes the transfer of the carboxyl group from biotin of the 1.3S subunit to pyruvate to form oxaloacetate and 1.3S biotin
None
5.51
55650.0
Propionibacterium freudenreichii subsp. shermanii
GenBank Gene Database
AJ606310
GenBank Protein Database
38304072
UniProtKB
Q70AC7
UniProt Accession
5S_PROFR
EC 2.1.3.1
Transcarboxylase 5S subunit
>Methylmalonyl-CoA carboxyltransferase 5S subunit
MSPREIEVSEPREVGITELVLRDAHQSLMATRMAMEDMVGACADIDAAGYWSVECWGGAT
YDSCIRFLNEDPWERLRTFRKLMPNSRLQMLLRGQNLLGYRHYNDEVVDRFVDKSAENGM
DVFRVFDAMNDPRNMAHAMAAVKKAGKHAQGTICYTISPVHTVEGYVKLAGQLLDMGADS
IALKDMAALLKPQPAYDIIKAIKDTYGQKTQINLHCHSTTGVTEVSLMKAIEAGVDVVDT
AISSMSLGPGHNPTESVAEMLEGTGYTTNLDYDRLHKIRDHFKAIRPKYKKFESKTLVDT
SIFKSQIPGGMLSNMESQLRAQGAEDKMDEVMAEVPRVRKAAGFPPLVTPSSQIVGTQAV
FNVMMGEYKRMTGEFADIMLGYYGASPADRDPKVVKLAEEQSGKKPITQRPADLLPPEWE
KQSKEAATLKGFNGTDEDVLTYALFPQVAPVFFEHRAEGPHSVALTDAQLKAEAEGDEKS
LAVAGPVTYNVNVGGTVREVTVQQA
>1560 bp
ATGAGTCCGCGAGAAATTGAGGTTTCCGAGCCGCGCGAGGTTGGTATCACCGAGCTCGTG
CTGCGCGATGCCCATCAGAGCCTGATGGCCACACGAATGGCAATGGAAGACATGGTCGGC
GCCTGTGCAGACATTGATGCTGCCGGGTACTGGTCAGTGGAGTGTTGGGGTGGTGCCACG
TATGACTCGTGTATCCGCTTCCTCAACGAGGATCCTTGGGAGCGTCTGCGCACGTTCCGC
AAGCTGATGCCCAACAGCCGTCTCCAGATGCTGCTGCGTGGCCAGAACCTGCTGGGTTAC
CGCCACTACAACGACGAGGTCGTCGATCGTTTCGTCGACAAGTCCGCTGAGAACGGCATG
GACGTGTTCCGTGTCTTCGACGCCATGAATGATCCCCGCAATATGGCGCACGCCATGGCT
GCCGTCAAGAAGGCCGGCAAGCACGCGCAGGGCACCATTTGCTACACGATCAGCCCGGTC
CACACCGTTGAGGGCTATGTCAAGCTTGCTGGTCAGCTGCTCGACATGGGTGCTGATTCC
ATCGCCCTGAAGGACATGGCCGCCCTGCTCAAGCCGCAGCCGGCCTACGACATCATCAAG
GCCATCAAGGACATACGGCCAGAAGACGCAGATCAACCTGCACTGCACTCCACCACGGGT
GTCACCGAGGTCTCCCTCATGAAGGCCATCGAGGCCGGCGTCGACACCGCCATCTCGTCC
ATGTCGCTCGGCCCGGGCCACAACCCCACCGAGTCGGTTGCCGAGATGCTCGAGGGCACC
GGGTACACCACCAACCTTGACTACGATCGCCTGCACAAGATCCGCGATCACTTCAAGGCC
ATCCGCCCGAAGTACAAGAAGTTCGAGTCGAAGACGCTTGTCGACACCTCGATCTTCAAG
TCGCAGATCCCCGGCGGCATGCTGTCCAACATGGAGTCGCAGCTGCGCGCCCAGGGCGCC
GAGGACAAGATGGACGAGGTCATGGCAGAGGTGCCGCGCGTCCGAAGGCCGGCGCCGGTT
TTCCCCGCCCCTGGTCACCCCGTCCAGCCAGATCGTCGGCACGCAGGCCTGTTCAACGTG
ATGATGGGCGAGTACAAGAGGATGACCGGCGAGTTCGCAGATATCATGCTCGGCTACTAC
GGCGCCACGCCGGCCGATCGCGATCCGAAGTGGTCAGTTGGCGAGGAGCATCGCAGAGCG
ATCACCCAGCGCCCGGCCGATCACGATCCGAAGGTGGTCAAGTTGGCCGAGGAGCAGTCC
GGCAAGAAGCCGATCACCCAGCGCCCGGCCGATCTGCTGCCCCCCGAGTGGGAGGAGCAG
TCCAAGGAGCCGCGCCCTAAGGGCTTCAACGGCACCGACGAGGACGTGCTCACCTATGCA
CTGTTCCCGCAGGTCGCTCCGGTCTTCTTCGAGAGTCGGCCGAGGGCCGCAGAGGTGGCT
CTCACCGATGCCCAGCTGAAGGCCGAGGCGAGGGCGACGAGAAGTGTCGCCGTGGCCGGT
CCCGTCACCTACAACGTGAACGTGCGGAACCGTCCGCAAGTCACCGTTCAGCAGGCGTGA
PF00682
HMGL-like
PF02436
PYC_OADA
function
catalytic activity
BE0001378
1-aminocyclopropane-1-carboxylate deaminase
Pseudomonas sp. (strain ACP)
# Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17139284
# Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17016423
unknown
1-aminocyclopropane-1-carboxylate deaminase
Amino acid transport and metabolism
Catalyzes a cyclopropane ring-opening reaction, the irreversible conversion of 1-aminocyclopropane-1-carboxylate (ACC) to ammonia and alpha-ketobutyrate. Allows growth on ACC as a nitrogen source
acdS
Cytoplasmic
None
6.52
36672.0
Pseudomonas sp. (strain ACP)
GenBank Gene Database
M73488
GenBank Protein Database
150963
UniProtKB
Q00740
UniProt Accession
1A1D_PSEUD
ACC deaminase
ACCD
EC 3.5.99.7
>1-aminocyclopropane-1-carboxylate deaminase
MNLQRFPRYPLTFGPTPIQPLARLSKHLGGKVHLYAKREDCNSGLAFGGNKTRKLEYLIP
EALAQGCDTLVSIGGIQSNQTRQVAAVAAHLGMKCVLVQENWVNYSDAVYDRVGNIQMSR
ILGADVRLVPDGFDIGFRRSWEDALESVRAAGGKPYAIPAGCSDHPLGGLGFVGFAEEVR
AQEAELGFKFDYVVVCSVTGSTQAGMVVGFAADGRADRVIGVDASAKPAQTREQITRIAR
QTAEKVGLERDIMRADVVLDERFAGPEYGLPNEGTLEAIRLCARTEGMLTDPVYEGKSMH
GMIEMVRNGEFPEGSRVLYAHLGGVPALNGYSFIFRDG
>1017 bp
ATGAACCTGCAACGATTCCCTCGTTACCCGCTGACTTTCGGGCCGACGCCAATCCAACCG
CTAGCGCGTCTGAGCAAGCACCTCGGCGGCAAAGTGCATCTGTATGCGAAACGCGAAGAC
TGCAACAGCGGCCTGGCGTTCGGTGGCAACAAGACACGCAAGCTCGAATATCTGATCCCT
GAAGCGCTTGCTCAGGGTTGCGACACGCTCGTGTCGATCGGCGGCATTCAGTCGAACCAG
ACGCGCCAGGTGGCGGCCGTGGCGGCTCATCTGGGCATGAAGTGCGTGCTGGTGCAGGAG
AACTGGGTCAACTATTCGGACGCAGTCTACGACCGCGTCGGCAACATCCAGATGTCGCGC
ATTCTCGGCGCCGATGTTCGCCTCGTGCCCGACGGCTTCGACATCGGTTTTCGCAGGAGC
TGGGAGGATGCGCTGGAAAGCGTGCGGGCGGCCGGCGGCAAGCCGTATGCGATTCCGGCA
GGCTGCTCGGATCACCCGCTCGGCGGCCTGGGTTTCGTCGGCTTCGCGGAGGAGGTGCGG
GCGCAGGAAGCCGAATTGGGCTTCAAATTCGACTATGTCGTCGTGTGTTCCGTGACCGGC
AGCACGCAGGCCGGCATGGTGGTGGGCTTCGCCGCTGACGGCCGCGCCGATCGCGTGATC
GGCGTCGACGCTTCGGCCAAACCCGCGCAGACGCGCGAGCAGATCACCCGCATCGCGAGA
CAGACCGCGGAGAAAGTCGGCCTGGAGCGCGATATCATGCGGGCCGACGTGGTGCTCGAC
GAGCGCTTCGCGGGTCCGGAATACGGATTGCCGAACGAAGGCACGCTGGAAGCGATCCGC
TTGTGCGCGCGCACGGAGGGCATGCTGACCGATCCCGTCTACGAAGGCAAATCGATGCAC
GGCATGATCGAAATGGTGCGCAACGGCGAATTTCCGGAAGGCTCGCGCGTGCTGTATGCG
CACCTCGGCGGGGTGCCGGCGTTGAACGGCTACAGCTTTATCTTCCGAGACGGCTGA
PF00291
PALP
function
catalytic activity
function
hydrolase activity
function
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
function
1-aminocyclopropane-1-carboxylate deaminase activity
process
methionine metabolism
process
physiological process
process
ethylene biosynthesis
process
metabolism
process
cellular metabolism
process
amino acid metabolism
process
amino acid and derivative metabolism
process
sulfur amino acid metabolism
"
|
owl:sameAs |
All properties reside in the graph file:///home/swish/src/ClioPatria/guidelines3/drugbank_small.nt
The resource appears as object in 24 triples