Physeter catodon (sperm whale): 102986675
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Entry
102986675 CDS
T06011
Name
(RefSeq) cytochrome c-like
KO
K08738
cytochrome c
Organism
pcad
Physeter catodon (sperm whale)
Pathway
pcad00190
Oxidative phosphorylation
pcad01100
Metabolic pathways
pcad01524
Platinum drug resistance
pcad04115
p53 signaling pathway
pcad04210
Apoptosis
pcad04215
Apoptosis - multiple species
pcad04932
Non-alcoholic fatty liver disease
pcad05010
Alzheimer disease
pcad05012
Parkinson disease
pcad05014
Amyotrophic lateral sclerosis
pcad05016
Huntington disease
pcad05017
Spinocerebellar ataxia
pcad05020
Prion disease
pcad05022
Pathways of neurodegeneration - multiple diseases
pcad05132
Salmonella infection
pcad05134
Legionellosis
pcad05145
Toxoplasmosis
pcad05152
Tuberculosis
pcad05160
Hepatitis C
pcad05161
Hepatitis B
pcad05162
Measles
pcad05163
Human cytomegalovirus infection
pcad05164
Influenza A
pcad05167
Kaposi sarcoma-associated herpesvirus infection
pcad05168
Herpes simplex virus 1 infection
pcad05169
Epstein-Barr virus infection
pcad05170
Human immunodeficiency virus 1 infection
pcad05200
Pathways in cancer
pcad05210
Colorectal cancer
pcad05222
Small cell lung cancer
pcad05416
Viral myocarditis
pcad05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
pcad00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
102986675
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
102986675
04215 Apoptosis - multiple species
102986675
04115 p53 signaling pathway
102986675
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102986675
09162 Cancer: specific types
05210 Colorectal cancer
102986675
05222 Small cell lung cancer
102986675
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
102986675
05161 Hepatitis B
102986675
05160 Hepatitis C
102986675
05164 Influenza A
102986675
05162 Measles
102986675
05168 Herpes simplex virus 1 infection
102986675
05163 Human cytomegalovirus infection
102986675
05167 Kaposi sarcoma-associated herpesvirus infection
102986675
05169 Epstein-Barr virus infection
102986675
09171 Infectious disease: bacterial
05132 Salmonella infection
102986675
05134 Legionellosis
102986675
05152 Tuberculosis
102986675
09174 Infectious disease: parasitic
05145 Toxoplasmosis
102986675
09164 Neurodegenerative disease
05010 Alzheimer disease
102986675
05012 Parkinson disease
102986675
05014 Amyotrophic lateral sclerosis
102986675
05016 Huntington disease
102986675
05017 Spinocerebellar ataxia
102986675
05020 Prion disease
102986675
05022 Pathways of neurodegeneration - multiple diseases
102986675
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
102986675
05416 Viral myocarditis
102986675
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
102986675
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
102986675
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
102986675
NCBI-ProteinID:
XP_007118006
Ensembl:
ENSPCTG00005016773
UniProt:
A0A2Y9F9I0
LinkDB
All DBs
Position
13:complement(8439817..8440670)
Genome browser
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPSLHGLFGRKTGQAVGFSYTDANKNKGITW
GEETLMEYLENPKKYIPGTKMIFAGIKKKGERADLIAYLKKATNE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact
gtggaaaagggaggcaagcacaagactgggccaagtctccatggtctgtttgggcgaaag
acaggtcaggctgtcggattctcttacacagatgccaacaagaacaaaggcatcacctgg
ggagaggagacgctgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctggcattaagaagaagggagaaagggcagacttgatagcttatctcaaa
aaagctactaatgagtaa
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integrated database retrieval system