Organism name | Fissistigma glaucescens |
---|---|
Genus | Fissistigma |
Family | Annonaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Fissistigma glaucescens |
---|---|
Linked NCBI taxonomy ID | 296847 |
Linked level | species |
Family in NCBI taxonomy | Annonaceae |
---|---|
ID | 22140 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Magnoliophyta |
---|---|
ID | 3398 |
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 |
---|---|---|---|---|---|---|---|---|
C00001928
![]() |
Xylopine
/ (-)-Xylopine |
CHEMBL227689
CHEMBL452201 |
C062700
|
No. 20 | No. 4 |
![]() |
||
C00026108
![]() |
Aequaline
/ Discretamine / (-)-Discretamine |
CHEMBL320397
CHEMBL2334883 |
7 / 3 / 0 | No. 37 | No. 4 |
![]() |
||
C00027404
![]() |
Kuafumine
|
No. 74 |
![]() |
|||||
C00025339
![]() |
Oxocrebanine
/ 8,9-Dimethoxyliriodenine |
No. 74 |
![]() |
|||||
C00001878
![]() |
Liriodenine
/ Oxoushinsunine / Spermatheridine |
CHEMBL37736
|
C026980
|
5 / 3 / 1 | No. 74 |
![]() |
||
C00027457
![]() |
Oxoglaucine
/ O-Methylatheroline |
CHEMBL470881
|
C111587
|
25 / 27 / 24 | No. 74 |
![]() |
||
C00027364
![]() |
Fissiceine
|
No. 74 |
![]() |
|||||
C00027282
![]() |
Aristolactam BIII
/ Aristololactam B III |
CHEMBL390715
|
No. 125 |
![]() |
||||
C00027121
![]() |
Aristolactam AII
/ Aristololactam A II |
CHEMBL390368
|
No. 125 |
![]() |
||||
C00025791
![]() |
Cepharanone B
/ Aristolactam BII / Aristololactam B II |
CHEMBL226772
|
C064674
|
No. 125 |
![]() |
|||
C00027470
![]() |
Piperolactam A
|
CHEMBL387864
|
C457227
|
No. 125 |
![]() |
|||
C00027434
![]() |
Norcepharadione B
|
CHEMBL227414
|
C457229
|
No. 125 |
![]() |
|||
C00027371
![]() |
Goniothalactam
|
CHEMBL228081
|
No. 125 |
![]() |
||||
C00028270
![]() |
Fissicesine
|
No. 639 |
![]() |
|||||
C00027417
![]() |
N-Acetylxylopine
|
No. 2511 |
![]() |
|||||
C00028271
![]() |
Fissicesine N-oxide
|
No. 8193 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00027457 | 1 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00027457 | 0 / 0 |
P21728 | D(1A) dopamine receptor | Dopamine receptor | C00026108 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00027457 | 0 / 0 |
P29466 | Caspase-1 | C14 | C00027457 | 0 / 0 |
Q92793 | CREB-binding protein | Enzyme | C00027457 | 1 / 1 |
P02545 | Prelamin-A/C | Unclassified protein | C00027457 | 11 / 10 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00027457 | 0 / 1 |
P30926 | Neuronal acetylcholine receptor subunit beta-4 | CHRN beta | C00001878 | 0 / 0 |
P32297 | Neuronal acetylcholine receptor subunit alpha-3 | CHRN alpha | C00001878 | 1 / 0 |
P17787 | Neuronal acetylcholine receptor subunit beta-2 | CHRN beta | C00001878 | 1 / 1 |
P43681 | Neuronal acetylcholine receptor subunit alpha-4 | CHRN alpha | C00001878 | 1 / 1 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00027457 | 1 / 0 |
P14416 | D(2) dopamine receptor | Dopamine receptor | C00026108 | 2 / 0 |
Q14761 | Protein tyrosine phosphatase receptor type C-associated protein | Enzyme | C00001878 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00027457 | 0 / 0 |
P42858 | Huntingtin | Unclassified protein | C00027457 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00027457 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00027457 | 0 / 0 |
P35348 | Alpha-1A adrenergic receptor | Adrenergic receptor | C00026108 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00027457 | 1 / 1 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00027457 | 1 / 2 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00027457 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00027457 | 0 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00027457 | 2 / 2 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00027457 | 0 / 0 |
P28223 | 5-hydroxytryptamine receptor 2A | Serotonin receptor | C00026108 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00027457 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00027457 | 0 / 1 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00027457 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00027457 | 4 / 3 |
P08908 | 5-hydroxytryptamine receptor 1A | Serotonin receptor | C00026108 | 1 / 0 |
P25100 | Alpha-1D adrenergic receptor | Adrenergic receptor | C00026108 | 0 / 0 |
P35368 | Alpha-1B adrenergic receptor | Adrenergic receptor | C00026108 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00027457 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00027457 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00027457 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#103780 | Alcohol dependence |
P14416
|
#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
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#600513 | Epilepsy, nocturnal frontal lobe, 1; enfl1 |
P43681
|
#605375 | Epilepsy, nocturnal frontal lobe, 3; enfl3 |
P17787
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#143100 | Huntington disease; hd |
P42858
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#159900 | Myoclonic dystonia |
P14416
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#614674 | Periodic fever, menstrual cycle-dependent |
P08908
|
#172700 | Pick disease of brain |
P10636
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#180849 | Rubinstein-taybi syndrome 1; rsts1 |
Q92793
|
#612052 | Smoking as a quantitative trait locus 3; sqtl3 |
P32297
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
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)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00807 | Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) |
P17787
(related)
P43681 (related) |
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00504 | Rubinstein-Taybi syndrome |
Q92793
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|