Metabolite

KNApSAcK Entry

id C00019654
Name D-Alanine / D-2-Aminopropionic acid
CAS RN 338-69-2
Standard InChI InChI=1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m1/s1
Standard InChI (Main Layer) InChI=1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)

Cluster

Phytochemical cluster
KCF-S cluster No. 2426

Link

ChEMBL

By standard InChI CHEMBL66693
By standard InChI Main Layer CHEMBL12198 CHEMBL279597 CHEMBL66693

KEGG

By LinkDB C00133

CTD

By CAS RN

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

11 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 CHEMBL279597 CHEMBL66693 CHEMBL1741321 (2)
1 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein CHEMBL66693 CHEMBL1794499 (1)
2 / 0
P00918 Carbonic anhydrase 2 Lyase CHEMBL12198 CHEMBL657923 (1)
1 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 CHEMBL279597 CHEMBL66693 CHEMBL1741325 (2)
0 / 1
P00915 Carbonic anhydrase 1 Lyase CHEMBL12198 CHEMBL662718 (1)
0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 CHEMBL279597 CHEMBL66693 CHEMBL1741322 (2)
0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 CHEMBL279597 CHEMBL66693 CHEMBL1741323 (2)
1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 CHEMBL279597 CHEMBL66693 CHEMBL1741324 (2)
0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme CHEMBL279597 CHEMBL1614211 (1)
0 / 0
Q7Z2H8 Proton-coupled amino acid transporter 1 Unclassified protein CHEMBL12198 CHEMBL66693 CHEMBL1919336 (4)
0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme CHEMBL279597 CHEMBL1614364 (1)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (6)

KEGG disease name UniProt
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)