Entry |
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Symbol |
RECQL4
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Name |
ATP-dependent DNA helicase Q4 [EC: 5.6.2.4]
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Disease |
H00296 | Defects in RecQ helicases |
H00458 | Syndromic craniosynostoses |
H01734 | Rothmund-Thomson syndrome |
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Brite |
KEGG Orthology (KO) [BR:ko00001]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03032 DNA replication proteins
K10730 RECQL4; ATP-dependent DNA helicase Q4
03400 DNA repair and recombination proteins
K10730 RECQL4; ATP-dependent DNA helicase Q4
Enzymes [BR:ko01000]
5. Isomerases
5.6 Isomerases altering macromolecular conformation
5.6.2 Enzymes altering nucleic acid conformation
5.6.2.4 DNA 3'-5' helicase
K10730 RECQL4; ATP-dependent DNA helicase Q4
DNA replication proteins [BR:ko03032]
Eukaryotic type
DNA Replication Initiation Factors
Other initiation factors
K10730 RECQL4; ATP-dependent DNA helicase Q4
DNA repair and recombination proteins [BR:ko03400]
Eukaryotic type
DSBR (double strand breaks repair)
HR (homologous recombination)
RecQ family DNA helicases
K10730 RECQL4; ATP-dependent DNA helicase Q4
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Genes |
» show all
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Reference |
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Authors |
Rossi ML, Ghosh AK, Kulikowicz T, Croteau DL, Bohr VA |
Title |
Conserved helicase domain of human RecQ4 is required for strand annealing-independent DNA unwinding. |
Journal |
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Sequence |
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Reference |
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Authors |
Yin J, Kwon YT, Varshavsky A, Wang W |
Title |
RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway. |
Journal |
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Sequence |
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LinkDB |
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