PCIDB

Ambrosia camphorata

Species

KNApSAcK Entry

Organism name Ambrosia camphorata
Genus Ambrosia
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Ambrosia
Linked NCBI taxonomy ID 4211
Linked level genus

Family

Family in NCBI taxonomy Asteraceae
ID 4210

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (2)

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
C00003838 External link 512 Pectolinarigenin
CHEMBL78010
C079207
31 / 27 / 19 No. 3 No. 15
C00003378 External link 512 Tulipinolide
CHEMBL520114
No. 249 No. 38

Human Protein / Gene in interactions

31 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00003838 1 / 1
P06746 DNA polymerase beta Enzyme C00003838 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00003838 0 / 0
O75496 Geminin Unclassified protein C00003838 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00003838 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00003838 4 / 2
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00003838 7 / 3
O15118 Niemann-Pick C1 protein Unclassified protein C00003838 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00003838 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00003838 4 / 3
O00255 Menin Unclassified protein C00003838 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003838 1 / 2
Q00653 Nuclear factor NF-kappa-B p100 subunit Transcription Factor C00003838 0 / 0
Q04206 Transcription factor p65 Transcription Factor C00003838 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00003838 0 / 0
Q13748 Tubulin alpha-3C/D chain Structural C00003838 0 / 0
P68366 Tubulin alpha-4A chain Structural C00003838 0 / 0
Q9H4B7 Tubulin beta-1 chain Structural C00003838 1 / 0
P04350 Tubulin beta-4A chain Structural C00003838 2 / 0
Q3ZCM7 Tubulin beta-8 chain Structural C00003838 0 / 0
P07437 Tubulin beta chain Structural C00003838 0 / 0
Q71U36 Tubulin alpha-1A chain Structural C00003838 1 / 1
P68371 Tubulin beta-4B chain Structural C00003838 0 / 0
Q13509 Tubulin beta-3 chain Structural C00003838 2 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00003838 0 / 0
P68363 Tubulin alpha-1B chain Unclassified protein C00003838 0 / 0
Q13885 Tubulin beta-2A chain Structural C00003838 0 / 0
Q6PEY2 Tubulin alpha-3E chain Unclassified protein C00003838 0 / 0
Q9BQE3 Tubulin alpha-1C chain Unclassified protein C00003838 0 / 0
Q9BUF5 Tubulin beta-6 chain Structural C00003838 0 / 0
Q9BVA1 Tubulin beta-2B chain Structural C00003838 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (27)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#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
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#612438 Leukodystrophy, hypomyelinating, 6; hld6 P04350
#611603 Lissencephaly 3; lis3 Q71U36
#613112 Macrothrombocytopenia, autosomal dominant, tubb1-related Q9H4B7
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#257220 Niemann-pick disease, type c1; npc1 O15118
#166350 Osseous heteroplasia, progressive; poh P63092
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#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
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (19)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00027 Ovarian cancer P38398 (related)
H00031 Breast cancer P38398 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (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)
H00838 Congenital fibrosis of the extraocular muscles (CFEOM) Q13509 (related)
H00268 Lissencephaly (LIS) Q71U36 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)