Myotis davidii (David's myotis): 102759877
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Entry
102759877 CDS
T02992
Name
(RefSeq) cytochrome c
KO
K08738
cytochrome c
Organism
myd
Myotis davidii (David's myotis)
Pathway
myd00190
Oxidative phosphorylation
myd01100
Metabolic pathways
myd01524
Platinum drug resistance
myd04115
p53 signaling pathway
myd04210
Apoptosis
myd04215
Apoptosis - multiple species
myd04932
Non-alcoholic fatty liver disease
myd05010
Alzheimer disease
myd05012
Parkinson disease
myd05014
Amyotrophic lateral sclerosis
myd05016
Huntington disease
myd05017
Spinocerebellar ataxia
myd05020
Prion disease
myd05022
Pathways of neurodegeneration - multiple diseases
myd05132
Salmonella infection
myd05134
Legionellosis
myd05145
Toxoplasmosis
myd05152
Tuberculosis
myd05160
Hepatitis C
myd05161
Hepatitis B
myd05162
Measles
myd05163
Human cytomegalovirus infection
myd05164
Influenza A
myd05167
Kaposi sarcoma-associated herpesvirus infection
myd05168
Herpes simplex virus 1 infection
myd05169
Epstein-Barr virus infection
myd05170
Human immunodeficiency virus 1 infection
myd05200
Pathways in cancer
myd05210
Colorectal cancer
myd05222
Small cell lung cancer
myd05416
Viral myocarditis
myd05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
myd00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
102759877
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
102759877
04215 Apoptosis - multiple species
102759877
04115 p53 signaling pathway
102759877
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102759877
09162 Cancer: specific types
05210 Colorectal cancer
102759877
05222 Small cell lung cancer
102759877
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
102759877
05161 Hepatitis B
102759877
05160 Hepatitis C
102759877
05164 Influenza A
102759877
05162 Measles
102759877
05168 Herpes simplex virus 1 infection
102759877
05163 Human cytomegalovirus infection
102759877
05167 Kaposi sarcoma-associated herpesvirus infection
102759877
05169 Epstein-Barr virus infection
102759877
09171 Infectious disease: bacterial
05132 Salmonella infection
102759877
05134 Legionellosis
102759877
05152 Tuberculosis
102759877
09174 Infectious disease: parasitic
05145 Toxoplasmosis
102759877
09164 Neurodegenerative disease
05010 Alzheimer disease
102759877
05012 Parkinson disease
102759877
05014 Amyotrophic lateral sclerosis
102759877
05016 Huntington disease
102759877
05017 Spinocerebellar ataxia
102759877
05020 Prion disease
102759877
05022 Pathways of neurodegeneration - multiple diseases
102759877
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
102759877
05416 Viral myocarditis
102759877
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
102759877
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
102759877
BRITE hierarchy
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Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
102759877
NCBI-ProteinID:
XP_006766453
LinkDB
All DBs
Position
Un
AA seq
128 aa
AA seq
DB search
MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGQKTGQAPGFSYTDANKNKGITW
GEATLMEYLENPKKYIPGTKMIFAGIKKSAERADLIAYLKKATNEYSWPLPYLLHMSHNF
FNVYHFLN
NT seq
387 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact
gtggaaaagggaggcaagcacaagactgggccaaatctccatggtctctttgggcaaaag
acaggtcaggcccctggattttcttacacggatgccaacaagaacaaaggtatcacctgg
ggagaggctaccctgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctggcattaagaagagtgcagagagggcagacttgatagcttatctcaaa
aaagctactaatgagtatagttggccactgccttatttattacacatgtcccataatttt
tttaatgtgtaccattttttaaattga
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