KEGG   Leptonychotes weddellii (Weddell seal): 102745503
Entry
102745503         CDS       T08708                                 
Symbol
SLC25A31
Name
(RefSeq) ADP/ATP translocase 4
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
lww  Leptonychotes weddellii (Weddell seal)
Pathway
lww04020  Calcium signaling pathway
lww04022  cGMP-PKG signaling pathway
lww04217  Necroptosis
lww04218  Cellular senescence
lww04613  Neutrophil extracellular trap formation
lww05010  Alzheimer disease
lww05012  Parkinson disease
lww05016  Huntington disease
lww05017  Spinocerebellar ataxia
lww05020  Prion disease
lww05022  Pathways of neurodegeneration - multiple diseases
lww05164  Influenza A
lww05166  Human T-cell leukemia virus 1 infection
lww05208  Chemical carcinogenesis - reactive oxygen species
lww05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:lww00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    102745503 (SLC25A31)
   04022 cGMP-PKG signaling pathway
    102745503 (SLC25A31)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    102745503 (SLC25A31)
   04218 Cellular senescence
    102745503 (SLC25A31)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    102745503 (SLC25A31)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    102745503 (SLC25A31)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    102745503 (SLC25A31)
   05164 Influenza A
    102745503 (SLC25A31)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102745503 (SLC25A31)
   05012 Parkinson disease
    102745503 (SLC25A31)
   05016 Huntington disease
    102745503 (SLC25A31)
   05017 Spinocerebellar ataxia
    102745503 (SLC25A31)
   05020 Prion disease
    102745503 (SLC25A31)
   05022 Pathways of neurodegeneration - multiple diseases
    102745503 (SLC25A31)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    102745503 (SLC25A31)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:lww03029]
    102745503 (SLC25A31)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:lww02000]
    102745503 (SLC25A31)
Mitochondrial biogenesis [BR:lww03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    102745503 (SLC25A31)
Transporters [BR:lww02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   102745503 (SLC25A31)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 102745503
NCBI-ProteinID: XP_030884418
UniProt: A0A7F8QVN0
LinkDB
Position
Unknown
AA seq 267 aa
MQREPPKKKQEKKSEKRLFDPASFGKDLLAGGIAAAVSKTAVAPIERVKLLLQVQASSKQ
ISAEAQYKGMVDCLVRIPREQGFFSYWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVN
KEKQFWRWFLANLASGGAAGATSLCVVYPLDFARTRLGADIGKGPEERQFKGLGDCIIKI
AKSDGIVGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFLVSFFIAQVVTTCS
GILSYPFDTVRRRMMMQVFYIIICKFN
NT seq 804 nt   +upstreamnt  +downstreamnt
atgcagcgtgaacctccgaagaagaagcaagagaagaagtcggaaaagcggctctttgac
cccgcatccttcgggaaggacctgctggcaggcgggatcgcagcggctgtgtccaagact
gccgtggcccccatcgaacgggtgaagctgctgctgcaggtgcaggcgtcgtccaagcag
atcagtgccgaggcgcagtacaaaggcatggtggactgcctggtgcggattccccgcgag
caaggtttcttcagttattggcgtggcaatttggcaaatgttatccgatattttccaaca
caagctctaaattttgcttttaaagacaaatacaaacaactcttcatgtctggagtaaat
aaagaaaaacagttctggaggtggtttttggcaaacctggcttctggtggagctgctgga
gcaacatccttatgtgtagtttatccgctagactttgcccgaacccgattaggtgctgat
attggaaaaggtcctgaagagcgacaattcaagggtttaggtgactgtattataaaaata
gcaaaatcagacggaattgttggtttgtaccaaggatttggtgtttcagttcagggtatc
attgtgtaccgagcctcctattttggagcatatgacacagttaagggcttattaccaaaa
ccaaaggaaaccccatttcttgtctcctttttcattgctcaagttgtgaccacatgctct
ggaattctctcttatccctttgacacagttagaagacgcatgatgatgcaggtattttat
attattatttgcaagtttaattga

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