KEGG   Lynx rufus (bobcat): 124503169
Entry
124503169         CDS       T08475                                 
Name
(RefSeq) bcl-2-like protein 1 isoform X1
  KO
K04570  Bcl-2-like 1 (apoptosis regulator Bcl-X)
Organism
lruf  Lynx rufus (bobcat)
Pathway
lruf01521  EGFR tyrosine kinase inhibitor resistance
lruf01524  Platinum drug resistance
lruf04014  Ras signaling pathway
lruf04064  NF-kappa B signaling pathway
lruf04115  p53 signaling pathway
lruf04137  Mitophagy - animal
lruf04140  Autophagy - animal
lruf04151  PI3K-Akt signaling pathway
lruf04210  Apoptosis
lruf04215  Apoptosis - multiple species
lruf04621  NOD-like receptor signaling pathway
lruf04630  JAK-STAT signaling pathway
lruf05012  Parkinson disease
lruf05014  Amyotrophic lateral sclerosis
lruf05022  Pathways of neurodegeneration - multiple diseases
lruf05145  Toxoplasmosis
lruf05162  Measles
lruf05166  Human T-cell leukemia virus 1 infection
lruf05168  Herpes simplex virus 1 infection
lruf05170  Human immunodeficiency virus 1 infection
lruf05200  Pathways in cancer
lruf05202  Transcriptional misregulation in cancer
lruf05212  Pancreatic cancer
lruf05220  Chronic myeloid leukemia
lruf05222  Small cell lung cancer
lruf05225  Hepatocellular carcinoma
lruf05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:lruf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04014 Ras signaling pathway
    124503169
   04630 JAK-STAT signaling pathway
    124503169
   04064 NF-kappa B signaling pathway
    124503169
   04151 PI3K-Akt signaling pathway
    124503169
 09140 Cellular Processes
  09141 Transport and catabolism
   04140 Autophagy - animal
    124503169
   04137 Mitophagy - animal
    124503169
  09143 Cell growth and death
   04210 Apoptosis
    124503169
   04215 Apoptosis - multiple species
    124503169
   04115 p53 signaling pathway
    124503169
 09150 Organismal Systems
  09151 Immune system
   04621 NOD-like receptor signaling pathway
    124503169
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    124503169
   05202 Transcriptional misregulation in cancer
    124503169
  09162 Cancer: specific types
   05212 Pancreatic cancer
    124503169
   05225 Hepatocellular carcinoma
    124503169
   05220 Chronic myeloid leukemia
    124503169
   05222 Small cell lung cancer
    124503169
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    124503169
   05170 Human immunodeficiency virus 1 infection
    124503169
   05162 Measles
    124503169
   05168 Herpes simplex virus 1 infection
    124503169
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    124503169
  09164 Neurodegenerative disease
   05012 Parkinson disease
    124503169
   05014 Amyotrophic lateral sclerosis
    124503169
   05022 Pathways of neurodegeneration - multiple diseases
    124503169
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    124503169
  09176 Drug resistance: antineoplastic
   01521 EGFR tyrosine kinase inhibitor resistance
    124503169
   01524 Platinum drug resistance
    124503169
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01009 Protein phosphatases and associated proteins [BR:lruf01009]
    124503169
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:lruf03036]
    124503169
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:lruf02000]
    124503169
Protein phosphatases and associated proteins [BR:lruf01009]
 Protein serine/threonine phosphatases
  Phosphoprotein phosphatases (PPPs)
   Protein phosphatase-1
    PP1-interacting proteins (PIPs)
     124503169
Chromosome and associated proteins [BR:lruf03036]
 Eukaryotic type
  Centrosome formation proteins
   Other centrosome associated proteins
    124503169
Transporters [BR:lruf02000]
 Other transporters
  Pores ion channels [TC:1]
   124503169
SSDB
Motif
Pfam: Bcl-2 BH4 Bcl-2_3
Other DBs
NCBI-GeneID: 124503169
NCBI-ProteinID: XP_046923994
LinkDB
Position
Unknown
AA seq 233 aa
MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLA
DSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAY
QSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIATWMATYLNDHLEP
WIQENGGWDTFVELYGNNAAAESRKGQERFNRWFLTGMTVAGVVLLGSLFSRK
NT seq 702 nt   +upstreamnt  +downstreamnt
atgtctcagagcaaccgggagctggtggttgactttctctcctacaagctttcccagaaa
ggatacagctggagtcagtttagtgatgtggaagagaacagaactgaggccccagaaggg
actgaatcagagatggagacccccagtgccatcaatggcaacccatcctggcacttggcg
gacagccctgcggtgaatggagccactggccacagcagcagcttggatgcccgggaggtg
atccccatggcagcggtgaagcaggcgctgagggaggccggggatgagtttgaactgagg
taccggcgggcattcagcgacctgacatcccagcttcacatcaccccagggacagcatat
cagagctttgagcaggtagtgaatgaactcttccgggatggggtgaactggggtcgcatt
gtggcctttttctccttcggtggggcactgtgcgtggaaagcgtagacaaggagatgcag
gtattggtgagtcggatcgcaacttggatggccacttacctgaacgaccacctagagcct
tggatccaggagaacggcggctgggacacttttgtggaactctacgggaacaatgcagcg
gccgagagccggaagggccaggagcgcttcaaccgctggttcctgacaggcatgactgtg
gctggcgtggttctgctgggctcactcttcagtcggaaatga

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