Organism name | Sideritis jahandiezii |
---|---|
Genus | Sideritis |
Family | Labiatae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Sideritis |
---|---|
Linked NCBI taxonomy ID | 155231 |
Linked level | genus |
Family in NCBI taxonomy | Lamiaceae |
---|---|
ID | 4136 |
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 |
---|---|---|---|---|---|---|---|---|
C00003883
![]() |
Gardenin B
/ Demethyltangeretin / 5-Hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one |
CHEMBL226512
|
7 / 10 / 4 | No. 8 | No. 15 |
![]() |
||
C00003933
![]() |
Gardenin D
/ 5,3'-Dihydroxy-6,7,8,4'-tetramethoxyflavone / 5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,7,8-trimethoxy-4H-1-benzopyran-4-one |
CHEMBL495821
|
No. 8 | No. 15 |
![]() |
|||
C00003936
![]() |
Demethylnobiletin
/ 5-Hydroxy-6,7,8,3',4'-pentamethoxyflavone / 2-(3,4-Dimethoxyphenyl)-5-hydroxy-6,7,8-trimethoxy-4H-1-benzopyran-4-one |
CHEMBL75978
|
21 / 22 / 16 | No. 8 | No. 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P00352 | Retinal dehydrogenase 1 | Enzyme | C00003883 C00003936 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00003883 C00003936 | 0 / 0 |
Q9H4B7 | Tubulin beta-1 chain | Structural | C00003936 | 1 / 0 |
P15559 | NAD(P)H dehydrogenase [quinone] 1 | Enzyme | C00003883 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00003883 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00003883 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00003883 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00003883 | 7 / 3 |
O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00003936 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00003936 | 0 / 1 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00003936 | 4 / 3 |
Q13748 | Tubulin alpha-3C/D chain | Structural | C00003936 | 0 / 0 |
P68366 | Tubulin alpha-4A chain | Structural | C00003936 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00003936 | 11 / 10 |
P04350 | Tubulin beta-4A chain | Structural | C00003936 | 2 / 0 |
Q3ZCM7 | Tubulin beta-8 chain | Structural | C00003936 | 0 / 0 |
P07437 | Tubulin beta chain | Structural | C00003936 | 0 / 0 |
Q71U36 | Tubulin alpha-1A chain | Structural | C00003936 | 1 / 1 |
P68371 | Tubulin beta-4B chain | Structural | C00003936 | 0 / 0 |
Q13509 | Tubulin beta-3 chain | Structural | C00003936 | 2 / 1 |
P68363 | Tubulin alpha-1B chain | Unclassified protein | C00003936 | 0 / 0 |
Q13885 | Tubulin beta-2A chain | Structural | C00003936 | 0 / 0 |
Q6PEY2 | Tubulin alpha-3E chain | Unclassified protein | C00003936 | 0 / 0 |
Q9BQE3 | Tubulin alpha-1C chain | Unclassified protein | C00003936 | 0 / 0 |
Q9BUF5 | Tubulin beta-6 chain | Structural | C00003936 | 0 / 0 |
Q9BVA1 | Tubulin beta-2B chain | Structural | C00003936 | 1 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#114500 | Colorectal cancer; crc |
P84022
|
#614039 | Cortical dysplasia, complex, with other brain malformations 1; cdcbm1 |
Q13509
|
#128101 | Dystonia 4, torsion, autosomal dominant; dyt4 |
P04350
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#600638 | Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement; cfeom3a |
Q13509
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#612438 | Leukodystrophy, hypomyelinating, 6; hld6 |
P04350
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#611603 | Lissencephaly 3; lis3 |
Q71U36
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#613112 | Macrothrombocytopenia, autosomal dominant, tubb1-related |
Q9H4B7
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#610031 | Polymicrogyria, symmetric or asymmetric; pmgysa |
Q9BVA1
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | name | UniProt |
---|---|---|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
H00663 | Restrictive dermopathy |
P02545
(related)
|
H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00838 | Congenital fibrosis of the extraocular muscles (CFEOM) |
Q13509
(related)
|
H00268 | Lissencephaly (LIS) |
Q71U36
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|