Homo sapiens (human): 79587
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Entry
79587 CDS
T01001
Symbol
CARS2, COXPD27, cysRS
Name
(RefSeq) cysteinyl-tRNA synthetase 2, mitochondrial
KO
K01883
cysteinyl-tRNA synthetase [EC:
6.1.1.16
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa00970
Aminoacyl-tRNA biosynthesis
Disease
H00891
Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09122 Translation
00970 Aminoacyl-tRNA biosynthesis
79587 (CARS2)
09180 Brite Hierarchies
09181 Protein families: metabolism
01007 Amino acid related enzymes [BR:
hsa01007
]
79587 (CARS2)
09182 Protein families: genetic information processing
03016 Transfer RNA biogenesis [BR:
hsa03016
]
79587 (CARS2)
Enzymes [BR:
hsa01000
]
6. Ligases
6.1 Forming carbon-oxygen bonds
6.1.1 Ligases forming aminoacyl-tRNA and related compounds
6.1.1.16 cysteine---tRNA ligase
79587 (CARS2)
Amino acid related enzymes [BR:
hsa01007
]
Aminoacyl-tRNA synthetase
Class I (G)
79587 (CARS2)
Transfer RNA biogenesis [BR:
hsa03016
]
Eukaryotic type
Aminoacyl-tRNA synthetases (AARSs)
Other AARSs
79587 (CARS2)
Prokaryotic type
79587 (CARS2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
tRNA-synt_1e
tRNA-synt_1g
tRNA-synt_1
tRNA-synt_1f
DALR_2
Motif
Other DBs
NCBI-GeneID:
79587
NCBI-ProteinID:
NP_078813
OMIM:
612800
HGNC:
25695
Ensembl:
ENSG00000134905
UniProt:
Q9HA77
B7Z7E6
LinkDB
All DBs
Position
13:complement(110641410..110713522)
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AA seq
564 aa
AA seq
DB search
MLRTTRGPGLGPPLLQAALGLGRAGWHWPAGRAASGGRGRAWLQPTGRETGVQVYNSLTG
RKEPLIVAHAEAASWYSCGPTVYDHAHLGHACSYVRFDIIRRILTKVFGCSIVMVMGITD
VDDKIIKRANEMNISPASLASLYEEDFKQDMAALKVLPPTVYLRVTENIPQIISFIEGII
ARGNAYSTAKGNVYFDLKSRGDKYGKLVGVVPGPVGEPADSDKRHASDFALWKAAKPQEV
FWASPWGPGRPGWHIECSAIASMVFGSQLDIHSGGIDLAFPHHENEIAQCEVFHQCEQWG
NYFLHSGHLHAKGKEEKMSKSLKNYITIKDFLKTFSPDVFRFFCLRSSYRSAIDYSDSAM
LQAQQLLLGLGSFLEDARAYMKGQLACGSVREAMLWERLSSTKRAVKAALADDFDTPRVV
DAILGLAHHGNGQLRASLKEPEGPRSPAVFGAIISYFEQFFETVGISLANQQYVSGDGSE
ATLHGVVDELVRFRQKVRQFALAMPEATGDARRQQLLERQPLLEACDTLRRGLTAHGINI
KDRSSTTSTWELLDQRTKDQKSAG
NT seq
1695 nt
NT seq
+upstream
nt +downstream
nt
atgttgaggactacgcgcggcccaggcctgggccccccgctgctccaggccgcgctgggc
cttgggcgggctgggtggcactggcctgcgggccgggcggcgagcggggggcgcgggcgg
gcctggctgcagcccacgggccgggagacgggtgtgcaggtgtacaacagcctcaccggg
aggaaggaacccctaatcgtggcgcacgccgaagccgcctcctggtatagctgtggacca
actgtatatgatcatgcgcaccttggccatgcttgctcatatgttagatttgatatcatt
cgaaggatcctaaccaaggtttttggatgcagcatagtcatggtgatgggtattacagat
gtagatgataaaatcatcaaaagagccaatgagatgaatatttcccccgcttccctcgcc
agtctttatgaggaagacttcaagcaggacatggcagccctgaaggttctcccacccacg
gtgtacctgagggtaaccgaaaatattcctcagataatttctttcattgaaggaatcatt
gctcgtgggaacgcttattcaacggcaaaaggcaatgtctacttcgatctgaagtctaga
ggagacaagtatggcaaattggtcggcgtggtccctggtccagtcggagagccagcggac
tctgacaagcgtcatgccagtgacttcgccctgtggaaggcggccaaaccccaggaggtg
ttctgggcctctccctggggacccgggaggccgggctggcacatcgagtgctctgccatc
gctagtatggtatttggaagtcaactggatatccattcaggtgggatagatttagctttt
ccacatcatgaaaacgaaattgcacagtgcgaagtctttcatcagtgcgagcagtgggga
aattattttctgcattctgggcatttgcacgccaaaggcaaagaagaaaaaatgtccaaa
tcattaaagaactacattactattaaggactttctgaagaccttttcccccgatgtcttc
cggttcttctgcctgcggagcagctaccgctcagccatcgactacagtgacagcgccatg
ctccaagctcagcagctgctcctggggctgggctctttcctggaggacgcacgtgcctac
atgaaggggcagctggcctgcggctccgtcagggaagcgatgctgtgggagaggctctcc
agcaccaagagggccgtgaaggcggccttggcagatgattttgacacacccagggtggtt
gatgccatcctgggccttgcacaccacgggaatggacagctcagggcgtccctgaaggaa
cctgaagggccgagaagtcctgctgtgtttggtgccatcatctcttactttgaacagttt
tttgaaactgttggaatttctctggcaaatcaacagtacgtttcaggagacggcagcgag
gctaccttgcatggtgtggtggacgagctggtgcggttccggcagaaggtccggcagttt
gcgctggccatgcccgaggccacgggggacgcccggcggcagcagctcctagaaaggcag
cccctgctggaagcatgcgacaccctgcgccggggcctgactgcccacggcatcaacatc
aaggacagaagcagtacaacatccacgtgggaactgctggatcaaaggacaaaagaccaa
aaatcagcgggctga
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