Metabolite

KNApSAcK Entry

id C00019347
Name AMP / Adenosine 5'-phosphate
CAS RN 61-19-8
Standard InChI InChI=1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(22-10)1-21-23(18,19)20/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)/t4-,6?,7+,10-/m1/s1
Standard InChI (Main Layer) InChI=1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(22-10)1-21-23(18,19)20/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)

Cluster

Phytochemical cluster
KCF-S cluster No. 1201

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL16720 CHEMBL752 CHEMBL603811 CHEMBL608290 CHEMBL1230732

KEGG

By LinkDB C00020

CTD

By CAS RN D000249

Species

Summary

Plant class

class name count

Family

family name count
Enterobacteriaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Escherichia coli 562 Enterobacteriaceae Bacteria

Human Protein / Gene in interaction

21 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein CHEMBL16720 CHEMBL1613842 (1)
4 / 2
P49798 Regulator of G-protein signaling 4 Unclassified protein CHEMBL752 CHEMBL1794499 (1)
2 / 0
P47900 P2Y purinoceptor 1 Purine receptor CHEMBL752 CHEMBL750157 (2)
0 / 0
P21589 5'-nucleotidase Enzyme CHEMBL752 CHEMBL1042900 (1)
1 / 1
P51582 P2Y purinoceptor 4 Purine receptor CHEMBL752 CHEMBL756884 (1) CHEMBL757041 (1)
0 / 0
P60891 Ribose-phosphate pyrophosphokinase 1 Enzyme CHEMBL603811 CHEMBL760863 (1) CHEMBL760865 (1)
CHEMBL760868 (1)
4 / 4
Q96G91 P2Y purinoceptor 11 Purine receptor CHEMBL752 CHEMBL755046 (1) CHEMBL756287 (1)
0 / 0
P41231 P2Y purinoceptor 2 Purine receptor CHEMBL752 CHEMBL753285 (2)
0 / 0
P07195 L-lactate dehydrogenase B chain Enzyme CHEMBL752 CHEMBL2060672 (1)
1 / 4
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme CHEMBL752 CHEMBL1042901 (1)
3 / 1
P00338 L-lactate dehydrogenase A chain Enzyme CHEMBL752 CHEMBL2060668 (1) CHEMBL2060670 (1)
CHEMBL2060671 (1)
1 / 5
P12931 Proto-oncogene tyrosine-protein kinase Src Src CHEMBL752 CHEMBL942401 (1)
0 / 0
P09467 Fructose-1,6-bisphosphatase 1 Enzyme CHEMBL752 CHEMBL694959 (1) CHEMBL981259 (1)
CHEMBL1074684 (1) CHEMBL1074685 (1)
CHEMBL1106396 (1)
1 / 1
Q6DHV7 Adenosine deaminase-like protein Enzyme CHEMBL752 CHEMBL1817385 (1) CHEMBL1817386 (2)
0 / 0
P30542 Adenosine receptor A1 Adenosine receptor CHEMBL752 CHEMBL2169616 (1)
0 / 0
P28329 Choline O-acetyltransferase Enzyme CHEMBL752 CHEMBL662975 (1)
1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme CHEMBL752 CHEMBL1738442 (1)
0 / 0
Q9UBF8 Phosphatidylinositol 4-kinase beta Enzyme CHEMBL752 CHEMBL758629 (1)
0 / 0
Q8TCG2 Phosphatidylinositol 4-kinase type 2-beta Enzyme CHEMBL752 CHEMBL758629 (1)
0 / 0
Q9BTU6 Phosphatidylinositol 4-kinase type 2-alpha Enzyme CHEMBL752 CHEMBL758629 (1)
0 / 0
P42356 Phosphatidylinositol 4-kinase alpha Enzyme CHEMBL752 CHEMBL758629 (1)
0 / 0

CTD interaction (6)

compound gene gene name gene description interaction interaction type form reference
pmid
D000249 216 ALDH1A1
ALDC
ALDH-E1
ALDH1
ALDH11
PUMB1
RALDH1
aldehyde dehydrogenase 1 family, member A1 (EC:1.2.1.36) [4-dimethylaminocinnamaldehyde co-treated with Adenosine Monophosphate] binds to ALDH1A1 protein affects binding
/ affects cotreatment
protein 10609638
D000249 170685 NUDT10
APS2
DIPP3a
hDIPP3alpha
nudix (nucleoside diphosphate linked moiety X)-type motif 10 (EC:3.6.1.52 3.6.1.60) [NUDT10 protein results in increased metabolism of diadenosine 5',5''''-P1,P6-hexaphosphate] which results in increased chemical synthesis of Adenosine Monophosphate increases chemical synthesis
/ increases metabolic processing
protein 12121577
D000249 170685 NUDT10
APS2
DIPP3a
hDIPP3alpha
nudix (nucleoside diphosphate linked moiety X)-type motif 10 (EC:3.6.1.52 3.6.1.60) [NUDT10 protein results in increased metabolism of P(1),P(5)-di(adenosine-5'-)pentaphosphate] which results in increased chemical synthesis of Adenosine Monophosphate increases chemical synthesis
/ increases metabolic processing
protein 12121577
D000249 55190 NUDT11
APS1
ASP1
DIPP3b
DIPP3beta
hDIPP3beta
nudix (nucleoside diphosphate linked moiety X)-type motif 11 (EC:3.6.1.52 3.6.1.60) [NUDT11 protein results in increased metabolism of diadenosine 5',5''''-P1,P6-hexaphosphate] which results in increased chemical synthesis of Adenosine Monophosphate increases chemical synthesis
/ increases metabolic processing
protein 12121577
D000249 55190 NUDT11
APS1
ASP1
DIPP3b
DIPP3beta
hDIPP3beta
nudix (nucleoside diphosphate linked moiety X)-type motif 11 (EC:3.6.1.52 3.6.1.60) [NUDT11 protein results in increased metabolism of P(1),P(5)-di(adenosine-5'-)pentaphosphate] which results in increased chemical synthesis of Adenosine Monophosphate increases chemical synthesis
/ increases metabolic processing
protein 12121577
D000249 10891 PPARGC1A
LEM6
PGC-1(alpha)
PGC-1v
PGC1
PGC1A
PPARGC1
peroxisome proliferator-activated receptor gamma, coactivator 1 alpha Adenosine Monophosphate results in increased expression of PPARGC1A mRNA increases expression
mRNA 23056435

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#301835 Arts syndrome; arts P60891
#211800 Calcification of joints and arteries; calja P21589
#311070 Charcot-marie-tooth disease, x-linked recessive, 5; cmtx5 P60891
#304500 Deafness, x-linked 1; dfnx1 P60891
#229700 Fructose-1,6-bisphosphatase deficiency P09467
#612933 Glycogen storage disease xi; gsd11 P00338
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#614128 Lactate dehydrogenase b deficiency; ldhbd P07195
#254210 Myasthenic syndrome, congenital, associated with episodic apnea P28329
#300661 Phosphoribosylpyrophosphate synthetase superactivity P60891
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637

KEGG DISEASE (14)

KEGG disease name UniProt
H00069 Glycogen storage diseases (GSD) P00338 (related)
H00010 Multiple myeloma P00338 (marker)
P07195 (marker)
H00023 Testicular cancer P00338 (marker)
P07195 (marker)
H00035 Ewing's sarcoma P00338 (marker)
P07195 (marker)
H00043 Neuroblastoma P00338 (marker)
P07195 (marker)
H00213 Hypophosphatasia P05186 (related)
H00114 Fructose-1,6-bisphosphatase deficiency P09467 (related)
H00824 Calcification of joints and arteries P21589 (related)
H00770 Congenital myasthenic syndrome P28329 (related)
H00196 Phosphoribosylpyrophosphate synthetase I superactivity P60891 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P60891 (related)
H00946 Arts syndrome P60891 (related)
H01209 Deafness, X-linked P60891 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
Q16637 (related)