KEGG   Puma concolor (puma): 112870035
Entry
112870035         CDS       T08890                                 
Symbol
CASP3
Name
(RefSeq) caspase-3 isoform X1
  KO
K02187  caspase 3 [EC:3.4.22.56]
Organism
pcoo  Puma concolor (puma)
Pathway
pcoo01524  Platinum drug resistance
pcoo04010  MAPK signaling pathway
pcoo04115  p53 signaling pathway
pcoo04148  Efferocytosis
pcoo04210  Apoptosis
pcoo04215  Apoptosis - multiple species
pcoo04623  Cytosolic DNA-sensing pathway
pcoo04650  Natural killer cell mediated cytotoxicity
pcoo04657  IL-17 signaling pathway
pcoo04668  TNF signaling pathway
pcoo04726  Serotonergic synapse
pcoo04932  Non-alcoholic fatty liver disease
pcoo04933  AGE-RAGE signaling pathway in diabetic complications
pcoo04936  Alcoholic liver disease
pcoo05010  Alzheimer disease
pcoo05012  Parkinson disease
pcoo05014  Amyotrophic lateral sclerosis
pcoo05016  Huntington disease
pcoo05020  Prion disease
pcoo05022  Pathways of neurodegeneration - multiple diseases
pcoo05132  Salmonella infection
pcoo05133  Pertussis
pcoo05134  Legionellosis
pcoo05145  Toxoplasmosis
pcoo05146  Amoebiasis
pcoo05152  Tuberculosis
pcoo05160  Hepatitis C
pcoo05161  Hepatitis B
pcoo05162  Measles
pcoo05163  Human cytomegalovirus infection
pcoo05164  Influenza A
pcoo05165  Human papillomavirus infection
pcoo05167  Kaposi sarcoma-associated herpesvirus infection
pcoo05168  Herpes simplex virus 1 infection
pcoo05169  Epstein-Barr virus infection
pcoo05170  Human immunodeficiency virus 1 infection
pcoo05200  Pathways in cancer
pcoo05203  Viral carcinogenesis
pcoo05205  Proteoglycans in cancer
pcoo05206  MicroRNAs in cancer
pcoo05210  Colorectal cancer
pcoo05222  Small cell lung cancer
pcoo05416  Viral myocarditis
pcoo05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:pcoo00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04010 MAPK signaling pathway
    112870035 (CASP3)
   04668 TNF signaling pathway
    112870035 (CASP3)
 09140 Cellular Processes
  09141 Transport and catabolism
   04148 Efferocytosis
    112870035 (CASP3)
  09143 Cell growth and death
   04210 Apoptosis
    112870035 (CASP3)
   04215 Apoptosis - multiple species
    112870035 (CASP3)
   04115 p53 signaling pathway
    112870035 (CASP3)
 09150 Organismal Systems
  09151 Immune system
   04623 Cytosolic DNA-sensing pathway
    112870035 (CASP3)
   04650 Natural killer cell mediated cytotoxicity
    112870035 (CASP3)
   04657 IL-17 signaling pathway
    112870035 (CASP3)
  09156 Nervous system
   04726 Serotonergic synapse
    112870035 (CASP3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    112870035 (CASP3)
   05206 MicroRNAs in cancer
    112870035 (CASP3)
   05205 Proteoglycans in cancer
    112870035 (CASP3)
   05203 Viral carcinogenesis
    112870035 (CASP3)
  09162 Cancer: specific types
   05210 Colorectal cancer
    112870035 (CASP3)
   05222 Small cell lung cancer
    112870035 (CASP3)
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    112870035 (CASP3)
   05161 Hepatitis B
    112870035 (CASP3)
   05160 Hepatitis C
    112870035 (CASP3)
   05164 Influenza A
    112870035 (CASP3)
   05162 Measles
    112870035 (CASP3)
   05168 Herpes simplex virus 1 infection
    112870035 (CASP3)
   05163 Human cytomegalovirus infection
    112870035 (CASP3)
   05167 Kaposi sarcoma-associated herpesvirus infection
    112870035 (CASP3)
   05169 Epstein-Barr virus infection
    112870035 (CASP3)
   05165 Human papillomavirus infection
    112870035 (CASP3)
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    112870035 (CASP3)
   05133 Pertussis
    112870035 (CASP3)
   05134 Legionellosis
    112870035 (CASP3)
   05152 Tuberculosis
    112870035 (CASP3)
  09174 Infectious disease: parasitic
   05146 Amoebiasis
    112870035 (CASP3)
   05145 Toxoplasmosis
    112870035 (CASP3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    112870035 (CASP3)
   05012 Parkinson disease
    112870035 (CASP3)
   05014 Amyotrophic lateral sclerosis
    112870035 (CASP3)
   05016 Huntington disease
    112870035 (CASP3)
   05020 Prion disease
    112870035 (CASP3)
   05022 Pathways of neurodegeneration - multiple diseases
    112870035 (CASP3)
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    112870035 (CASP3)
   05416 Viral myocarditis
    112870035 (CASP3)
  09167 Endocrine and metabolic disease
   04936 Alcoholic liver disease
    112870035 (CASP3)
   04932 Non-alcoholic fatty liver disease
    112870035 (CASP3)
   04933 AGE-RAGE signaling pathway in diabetic complications
    112870035 (CASP3)
  09176 Drug resistance: antineoplastic
   01524 Platinum drug resistance
    112870035 (CASP3)
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01002 Peptidases and inhibitors [BR:pcoo01002]
    112870035 (CASP3)
Enzymes [BR:pcoo01000]
 3. Hydrolases
  3.4  Acting on peptide bonds (peptidases)
   3.4.22  Cysteine endopeptidases
    3.4.22.56  caspase-3
     112870035 (CASP3)
Peptidases and inhibitors [BR:pcoo01002]
 Cysteine peptidases
  Family C14: caspase family
   112870035 (CASP3)
SSDB
Motif
Pfam: Peptidase_C14
Other DBs
NCBI-GeneID: 112870035
NCBI-ProteinID: XP_025788896
UniProt: A0A6P6IKZ1
LinkDB
Position
Unknown
AA seq 277 aa
MENSENSVDAKSIKNSETKIFHGSKSMDSGIYMDNSYKMDYPEMGLCIIINNKNFHESTG
MPSRSGTDVDAANLRETFTNLKYEVRNKNDLTREQIVALLDSVSREDHSKRSSFICVLLS
HGDEGIIYGTNGPVDLKKLTGFFRGDYCRSLTGKPKLFIIQACRGTELDCGIETDSGTED
DIACQKIPVEADFLYAYSTAPGYYSWRNSKDGSWFIQSLCSMLKLYAHKLEFMHILTRVN
RKVALEFESFSLDSAFHGKKQIPCIVSMLTKELYFYH
NT seq 834 nt   +upstreamnt  +downstreamnt
atggagaacagtgaaaactcagtggatgcaaaatccattaaaaattccgaaacaaagatc
ttccatggaagcaaatcaatggactctggaatatacatggacaacagttacaaaatggat
taccctgaaatgggtttatgtataataattaataataagaactttcatgaaagtaccgga
atgccatctcggtctggtacagatgtggatgcggcgaacctccgagaaacattcacaaac
ttgaaatacgaagtcaggaataaaaacgatcttacacgcgaacaaattgtggcgttgctg
gacagtgtttctagagaagatcatagcaaaaggagcagttttatttgcgtgcttctaagc
cacggtgatgaaggaatcatttatggaacaaacggacctgttgacctgaaaaaattaaca
ggtttcttcagaggggattattgtagaagtctaaccggcaaacccaaactcttcattatt
caggcctgccgaggcacggaactcgactgcggcattgagactgacagtggtaccgaggat
gacatcgcctgtcagaaaataccagtggaagccgacttcttatatgcgtattccacagcc
cctggttactactcctggcgaaattccaaggatggatcctggttcatccagtcactttgc
tcgatgctcaaactgtatgctcacaagcttgagttcatgcacattcttactcgggttaac
cgaaaggtagctctagaatttgagtccttttctcttgactctgcttttcatggaaagaaa
cagattccatgtattgtgtctatgctcacaaaagaactatatttttatcactaa

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