Organism name | Bahia xylopoda |
---|---|
Genus | Bahia |
Family | Asteraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Bahia |
---|---|
Linked NCBI taxonomy ID | 41489 |
Linked level | genus |
Family in NCBI taxonomy | Asteraceae |
---|---|
ID | 4210 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | asterids |
---|---|
ID | 71274 |
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
---|---|---|---|---|---|---|---|---|
C00004694
![]() |
Centaureidin
/ Desmethoxycentaureidine / Quercetagetin 3,4',6-trimethyl ether / 5,7,3'-Trihydroxy-3,6,4'-trimethoxyflavone / 5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,6-dimethoxy-4H-1-benzopyran-4-one |
CHEMBL77552
|
C083161
|
24 / 14 / 6 | No. 3 | No. 15 |
![]() |
|
C00004706
![]() |
Bonanzin
/ Quercetagetin 3,6,3',4'-tetramethyl ether / 5,7-Dihydroxy-3,6,3',4'-tetramethoxyflavone / 2-(3,4-Dimethoxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4H-1-benzopyran-4-one |
No. 8 | No. 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | C00004694 | 1 / 1 |
P39748 | Flap endonuclease 1 | Enzyme | C00004694 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00004694 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00004694 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00004694 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00004694 | 1 / 1 |
P51843 | Nuclear receptor subfamily 0 group B member 1 | Nuclear hormone receptor subfamily 0 group B member 1 | C00004694 | 2 / 2 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00004694 | 1 / 0 |
Q13748 | Tubulin alpha-3C/D chain | Structural | C00004694 | 0 / 0 |
P68366 | Tubulin alpha-4A chain | Structural | C00004694 | 0 / 0 |
Q9H4B7 | Tubulin beta-1 chain | Structural | C00004694 | 1 / 0 |
P04350 | Tubulin beta-4A chain | Structural | C00004694 | 2 / 0 |
Q3ZCM7 | Tubulin beta-8 chain | Structural | C00004694 | 0 / 0 |
P07437 | Tubulin beta chain | Structural | C00004694 | 0 / 0 |
Q71U36 | Tubulin alpha-1A chain | Structural | C00004694 | 1 / 1 |
P68371 | Tubulin beta-4B chain | Structural | C00004694 | 0 / 0 |
Q13509 | Tubulin beta-3 chain | Structural | C00004694 | 2 / 1 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00004694 | 0 / 0 |
P68363 | Tubulin alpha-1B chain | Unclassified protein | C00004694 | 0 / 0 |
Q13885 | Tubulin beta-2A chain | Structural | C00004694 | 0 / 0 |
Q6PEY2 | Tubulin alpha-3E chain | Unclassified protein | C00004694 | 0 / 0 |
Q9BQE3 | Tubulin alpha-1C chain | Unclassified protein | C00004694 | 0 / 0 |
Q9BUF5 | Tubulin beta-6 chain | Structural | C00004694 | 0 / 0 |
Q9BVA1 | Tubulin beta-2B chain | Structural | C00004694 | 1 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300018 | 46,xy sex reversal 2; srxy2 |
P51843
|
#300200 | Adrenal hypoplasia, congenital; ahc |
P51843
|
#114500 | Colorectal cancer; crc |
P84022
|
#614039 | Cortical dysplasia, complex, with other brain malformations 1; cdcbm1 |
Q13509
|
#128101 | Dystonia 4, torsion, autosomal dominant; dyt4 |
P04350
|
#600638 | Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement; cfeom3a |
Q13509
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#612438 | Leukodystrophy, hypomyelinating, 6; hld6 |
P04350
|
#611603 | Lissencephaly 3; lis3 |
Q71U36
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#613112 | Macrothrombocytopenia, autosomal dominant, tubb1-related |
Q9H4B7
|
#610031 | Polymicrogyria, symmetric or asymmetric; pmgysa |
Q9BVA1
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00552 | Glycerol kinase deficiency (GKD) |
P51843
(related)
|
H00607 | 46,XY disorders of sex development (Disorders of gonadal development) |
P51843
(related)
|
H00838 | Congenital fibrosis of the extraocular muscles (CFEOM) |
Q13509
(related)
|
H00268 | Lissencephaly (LIS) |
Q71U36
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|