Homo sapiens (human): 56919
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Entry
56919 CDS
T01001
Symbol
DHX33, DDX33
Name
(RefSeq) ATP-dependent RNA helicase DHX33 isoform 1
KO
K17820
ATP-dependent RNA helicase DHX33 [EC:
5.6.2.6
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa04621
NOD-like receptor signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09151 Immune system
04621 NOD-like receptor signaling pathway
56919 (DHX33)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03009 Ribosome biogenesis [BR:
hsa03009
]
56919 (DHX33)
Enzymes [BR:
hsa01000
]
5. Isomerases
5.6 Isomerases altering macromolecular conformation
5.6.2 Enzymes altering nucleic acid conformation
5.6.2.6 RNA 3'-5' helicase
56919 (DHX33)
Ribosome biogenesis [BR:
hsa03009
]
Eukaryotic type
Other ribosome biogenesis factors
56919 (DHX33)
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SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
OB_NTP_bind
Helicase_C
HA2_C
WHD_HA2
DEAD
AAA_22
AAA_19
Motif
Other DBs
NCBI-GeneID:
56919
NCBI-ProteinID:
NP_064547
OMIM:
614405
HGNC:
16718
Ensembl:
ENSP00000225296.3
UniProt:
Q9H6R0
B4DIS6
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All DBs
Position
17:complement(5440917..5468982)
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AA seq
707 aa
AA seq
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MPEEAGFPPAKRFRPGSGPPSRAGSFPPGRQVVMLLTAGSGGRGGGGGRRQQPPLAQPSA
SPYPEAVELQRRSLPIFQARGQLLAQLRNLDNAVLIGETGSGKTTQIPQYLYEGGISRQG
IIAVTQPRRVAAISLATRVSDEKRTELGKLVGYTVRFDDVTSEDTRIKFLTDGMLLREAI
SDSLLRKYSCVILDEAHERTIHTDVLFGVVKAAQKRRKELGKLPLKVIVMSATMDVDLFS
QYFNGAPVLYLEGRQHPIQVFYTKQPQNDYLHAALVSVFQIHQEAPSSQDILVFLTGQEE
IEAMSKTCRDIAKHLPDGCPAMLVLPLYASLPYAQQLRVFQGAPKGYRKVIISTNIAETS
ITITGIKYVVDTGMVKAKKYNPDSGLEVLAVQRVSKTQAWQRTGRAGREDSGICYRLYTE
DEFEKFDKMTVPEIQRCNLASVMLQLLAMKVPNVLTFDFMSKPSPDHIQAAIAQLDLLGA
LEHKDDQLTLTPMGRKMAAFPLEPKFAKTILMSPKFHCTEEILTIVSLLSVDSVLHNPPS
RREEVQGVRKKFISSEGDHMTLLNIYRTFKNLGGNKDWCKENFVNSKNMTLVAEVRAQLR
DICLKMSMPIASSRGDVESVRRCLAHSLFMSTAELQPDGTYATTDTHQPVAIHPSSVLFH
CKPACVVYTELLYTNKCYMRDLCVIDAQWLYEAAPEYFRRKLRTARN
NT seq
2124 nt
NT seq
+upstream
nt +downstream
nt
atgccggaggaggcgggcttcccgccggccaagagattccggccaggctctggacctccg
agccgcgctgggtccttccctcccgggaggcaagtggtgatgctgctgactgcgggcagc
ggcggcagaggaggaggaggaggccggaggcagcagccgcccctggcccagccctcggcc
agtccctaccctgaagctgtggagctgcagcgccggagtctgcccatcttccaagcgcgg
gggcaactgttggcccagctccgaaacctggacaacgcggtcctcatcggggaaactggc
tctgggaagacaactcagatccctcagtacctgtatgaaggagggatcagccgccagggc
atcattgctgtgacccagcctcgtcgagtagctgccatctctcttgctactagagtctca
gatgagaagagaactgaacttgggaagctggttggctatacagtgcgctttgatgatgtc
acctcagaagacaccaggatcaagtttctgacagatggcatgcttctgcgtgaagcaatt
tcagactctttgcttcggaaatacagctgtgtcattttggatgaagctcacgaacggact
atccacacagatgtgctctttggagtggtgaaagctgcacagaagaggagaaaggaactc
gggaaacttcctctgaaagtgattgtgatgtcagctacgatggatgtggacctgttctct
cagtatttcaatggcgcccccgtcctctacctagagggtcggcagcatccgatccaggtg
ttttacaccaaacagcctcagaatgattacctgcacgccgcgcttgtctccgtcttccag
atccaccaggaagccccttcttcacaggacatcctggtgttcctcactgggcaggaggag
atcgaagccatgagcaagacgtgccgagacattgcaaagcacctcccagacggctgccct
gcgatgctggtccttcctctgtacgcctccctgccctatgcacagcagctccgagtcttc
caaggggccccaaagggctatcgcaaagtgatcatttcaaccaacatcgctgaaacctcc
ataaccattacaggaataaaatatgtagttgacacgggcatggttaaagcaaagaagtat
aaccctgacagtggtcttgaggtgttagcagtgcagcgggtatcgaagacgcaggcttgg
cagcgcacagggagggctggcagagaggacagtggcatctgctaccggctctacacggag
gacgagtttgagaagtttgataagatgaccgtgccagagatccagaggtgtaacctggcc
agtgtgatgcttcagcttctagcaatgaaagtcccaaatgtgctcacctttgacttcatg
tcgaagccatctccagatcacattcaggcggccattgcccaactggacctgttaggtgct
cttgaacataaggatgaccagcttaccctgactccaatgggaagaaagatggcagcattt
cctttagaacccaaatttgccaaaaccatcctcatgtcccccaaattccactgtacagag
gagatcctgaccattgtctccctgctgtctgtggacagcgtcctccacaaccctccttcc
cggcgagaggaagtgcaaggggtccgcaagaagttcatatccagcgagggggatcacatg
accctgctcaatatctatcggaccttcaaaaacctaggcggaaataaggattggtgcaaa
gagaattttgtcaacagcaagaatatgacgctggtagcagaagtcagagcacagctgagg
gacatctgcttaaagatgtcaatgccaatcgcatcatcccgaggagacgtggagagtgtc
cgccgctgcctggctcacagcctcttcatgagcaccgccgagcttcagccagatggcacc
tatgccaccacggacacccaccagccagtggccatccacccgtcgtctgtcctcttccac
tgcaagccggcctgcgtcgtgtacactgagctgctctacaccaacaagtgctacatgcgg
gacctctgcgtcatagatgcacagtggctgtacgaggctgcccctgagtactttaggagg
aagctgagaaccgccagaaactga
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