KEGG   Panthera pardus (leopard): 109262802
Entry
109262802         CDS       T06062                                 
Symbol
SMAD3
Name
(RefSeq) mothers against decapentaplegic homolog 3 isoform X1
  KO
K23605  mothers against decapentaplegic homolog 3
Organism
ppad  Panthera pardus (leopard)
Pathway
ppad04068  FoxO signaling pathway
ppad04110  Cell cycle
ppad04144  Endocytosis
ppad04218  Cellular senescence
ppad04310  Wnt signaling pathway
ppad04350  TGF-beta signaling pathway
ppad04371  Apelin signaling pathway
ppad04390  Hippo signaling pathway
ppad04520  Adherens junction
ppad04550  Signaling pathways regulating pluripotency of stem cells
ppad04659  Th17 cell differentiation
ppad04933  AGE-RAGE signaling pathway in diabetic complications
ppad05161  Hepatitis B
ppad05166  Human T-cell leukemia virus 1 infection
ppad05200  Pathways in cancer
ppad05210  Colorectal cancer
ppad05212  Pancreatic cancer
ppad05220  Chronic myeloid leukemia
ppad05225  Hepatocellular carcinoma
ppad05226  Gastric cancer
ppad05321  Inflammatory bowel disease
ppad05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ppad00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    109262802 (SMAD3)
   04350 TGF-beta signaling pathway
    109262802 (SMAD3)
   04390 Hippo signaling pathway
    109262802 (SMAD3)
   04371 Apelin signaling pathway
    109262802 (SMAD3)
   04068 FoxO signaling pathway
    109262802 (SMAD3)
 09140 Cellular Processes
  09141 Transport and catabolism
   04144 Endocytosis
    109262802 (SMAD3)
  09143 Cell growth and death
   04110 Cell cycle
    109262802 (SMAD3)
   04218 Cellular senescence
    109262802 (SMAD3)
  09144 Cellular community - eukaryotes
   04520 Adherens junction
    109262802 (SMAD3)
   04550 Signaling pathways regulating pluripotency of stem cells
    109262802 (SMAD3)
 09150 Organismal Systems
  09151 Immune system
   04659 Th17 cell differentiation
    109262802 (SMAD3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    109262802 (SMAD3)
  09162 Cancer: specific types
   05210 Colorectal cancer
    109262802 (SMAD3)
   05212 Pancreatic cancer
    109262802 (SMAD3)
   05225 Hepatocellular carcinoma
    109262802 (SMAD3)
   05226 Gastric cancer
    109262802 (SMAD3)
   05220 Chronic myeloid leukemia
    109262802 (SMAD3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    109262802 (SMAD3)
   05161 Hepatitis B
    109262802 (SMAD3)
  09163 Immune disease
   05321 Inflammatory bowel disease
    109262802 (SMAD3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    109262802 (SMAD3)
  09167 Endocrine and metabolic disease
   04933 AGE-RAGE signaling pathway in diabetic complications
    109262802 (SMAD3)
SSDB
Motif
Pfam: MH2 MH1 IRF-3
Other DBs
NCBI-GeneID: 109262802
NCBI-ProteinID: XP_019297243
Ensembl: ENSPPRG00000003306
UniProt: A0A9V1F7G6
LinkDB
Position
Unknown
AA seq 425 aa
MSSILPFTPPIVKRLLGWKKGEQNGQEEKWCEKAVKSLVKKLKKTGQLDELEKAITTQNV
NTKCITIPRSLDGRLQVSHRKGLPHVIYCRLWRWPDLHSHHELRAMELCEFAFNMKKDEV
CVNPYHYQRVETPVLPPVLVPRHTEIPAEFPPLDDYSHSIPENTNFPAGIEPQSNIPETP
PPGYLSEDGETSDHQMNHSMDAGSPNLSPNPMSPAHNNLDLQPVTYCEPAFWCSISYYEL
NQRVGETFHASQPSMTVDGFTDPSNSERFCLGLLSNVNRNAAVELTRRHIGRGVRLYYIG
GEVFAECLSDSAIFVQSPNCNQRYGWHPATVCKIPPGCNLKIFNNQEFAALLAQSVNQGF
EAVYQLTRMCTIRMSFVKGWGAEYRRQTVTSTPCWIELHLNGPLQWLDKVLTQMGSPSIR
CSSVS
NT seq 1278 nt   +upstreamnt  +downstreamnt
atgtcgtccatcctgcccttcacccccccgatcgtgaagcgcctgctgggctggaagaag
ggcgagcagaacgggcaggaggagaagtggtgcgagaaggcggtcaagagtttggtcaag
aagctcaagaagaccgggcagctggacgaactggagaaggccatcaccacgcagaacgtc
aacaccaagtgcatcaccatccccaggtccctggatggccgactgcaggtgtcccatcgg
aaggggctcccccatgtcatctactgccgcctgtggcgatggcctgacctccacagccac
cacgagctgcgggccatggagctatgcgagttcgccttcaacatgaagaaggacgaggtc
tgcgtgaatccctaccactatcagagggtagagaccccagttctacctcctgtgctggta
ccacgccacacagagatcccggccgagttccccccgctggacgactacagccattccatc
cccgagaacactaacttccccgcgggcatcgagccccagagcaatattccagaaacccca
ccccctggctacctgagtgaagatggagagaccagtgaccaccagatgaaccacagcatg
gatgcaggttctccaaacctatccccgaatccgatgtccccagcacacaacaatttggac
ctgcagcctgtcacctactgcgagccagccttctggtgctccatttcctactacgagctg
aaccagcgcgtcggggagaccttccacgcctcccagccctccatgactgtggacggcttc
accgacccctccaactcggagcgcttctgcctggggctgctctccaatgtcaacaggaac
gcggctgtggagctcacacggaggcatatcgggcgaggcgtgcggctgtactacatcgga
ggggaggtcttcgccgagtgcctcagtgacagcgccatttttgtccagtctcccaactgt
aaccagcgctacggctggcacccagccaccgtctgcaagatcccgccaggatgcaacctg
aagatcttcaacaaccaggagtttgccgccctcctggctcagtctgtcaaccagggcttc
gaggcggtctaccaactgacccggatgtgcaccatccgcatgagcttcgtcaaaggctgg
ggagcagagtacaggagacagacagtgaccagcaccccctgctggattgagctgcacctg
aatgggccgttgcagtggcttgacaaggtcctcacccagatgggctccccaagcatccgc
tgttccagtgtgtcttag

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