Ursus maritimus (polar bear): 103662923
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Entry
103662923 CDS
T03271
Name
(RefSeq) cytochrome c-like
KO
K08738
cytochrome c
Organism
umr
Ursus maritimus (polar bear)
Pathway
umr00190
Oxidative phosphorylation
umr01100
Metabolic pathways
umr01524
Platinum drug resistance
umr04115
p53 signaling pathway
umr04210
Apoptosis
umr04215
Apoptosis - multiple species
umr04932
Non-alcoholic fatty liver disease
umr05010
Alzheimer disease
umr05012
Parkinson disease
umr05014
Amyotrophic lateral sclerosis
umr05016
Huntington disease
umr05017
Spinocerebellar ataxia
umr05020
Prion disease
umr05022
Pathways of neurodegeneration - multiple diseases
umr05132
Salmonella infection
umr05134
Legionellosis
umr05145
Toxoplasmosis
umr05152
Tuberculosis
umr05160
Hepatitis C
umr05161
Hepatitis B
umr05162
Measles
umr05163
Human cytomegalovirus infection
umr05164
Influenza A
umr05167
Kaposi sarcoma-associated herpesvirus infection
umr05168
Herpes simplex virus 1 infection
umr05169
Epstein-Barr virus infection
umr05170
Human immunodeficiency virus 1 infection
umr05200
Pathways in cancer
umr05210
Colorectal cancer
umr05222
Small cell lung cancer
umr05416
Viral myocarditis
umr05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
umr00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
103662923
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
103662923
04215 Apoptosis - multiple species
103662923
04115 p53 signaling pathway
103662923
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
103662923
09162 Cancer: specific types
05210 Colorectal cancer
103662923
05222 Small cell lung cancer
103662923
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
103662923
05161 Hepatitis B
103662923
05160 Hepatitis C
103662923
05164 Influenza A
103662923
05162 Measles
103662923
05168 Herpes simplex virus 1 infection
103662923
05163 Human cytomegalovirus infection
103662923
05167 Kaposi sarcoma-associated herpesvirus infection
103662923
05169 Epstein-Barr virus infection
103662923
09171 Infectious disease: bacterial
05132 Salmonella infection
103662923
05134 Legionellosis
103662923
05152 Tuberculosis
103662923
09174 Infectious disease: parasitic
05145 Toxoplasmosis
103662923
09164 Neurodegenerative disease
05010 Alzheimer disease
103662923
05012 Parkinson disease
103662923
05014 Amyotrophic lateral sclerosis
103662923
05016 Huntington disease
103662923
05017 Spinocerebellar ataxia
103662923
05020 Prion disease
103662923
05022 Pathways of neurodegeneration - multiple diseases
103662923
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
103662923
05416 Viral myocarditis
103662923
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
103662923
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
103662923
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
PPAK
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
103662923
NCBI-ProteinID:
XP_040488599
UniProt:
A0A8M1G907
LinkDB
All DBs
Position
Unknown
AA seq
104 aa
AA seq
DB search
MGDIEKNKNFVQKCAQCHTMENGGKHKTGPNLHGLFGQKTGQPPRFSYTDANKNKGIIWG
EETLMEYLENPKKYIPETKMIFTGVKKTRKRADLIAYLKKATKE
NT seq
315 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatattgagaagaacaagaattttgttcagaaatgtgcccagtgtcataccatg
gaaaacggaggcaagcacaagactgggccaaatctccatggtttatttgggcaaaagaca
ggtcaacctcctagattttcttacacggatgccaataagaacaaaggtatcatctgggga
gaggagacactgatggagtatttggagaatcccaagaagtacatccctgaaacaaaaatg
atcttcactggcgttaagaagacaaggaaaagagcagacttgatagcttatctcaaaaaa
gctactaaggagtaa
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integrated database retrieval system