EC 3 - Hydrolases
EC 3.6 - Acting on acid anhydrides
EC 3.6.4 - Acting on ATP; involved in cellular and subcellular movement
EC 3.6.4.12 - DNA helicase
IntEnz view
ENZYME view
IntEnz Enzyme Nomenclature
EC 3.6.4.12
Names
Accepted name:
DNA helicase
Other
names:
3' to 5' DNA helicase
3'-5' DNA helicase
3'-5' PfDH
5' to 3' DNA helicase
AvDH1
BACH1 helicase
BcMCM
BLM protein
BRCA1-associated C-terminal helicase
CeWRN-1
Dbp9p
DmRECQ5
DNA helicase 120
DNA helicase A
DNA helicase E
DNA helicase II
DNA helicase III
DNA helicase RECQL5'
DNA helicase VI
dnaB
DnaB helicase E1
helicase HDH IV
Hel E
helicase DnaB
helicase domain of bacteriophage T7 gene 4 protein helicase
PcrA helicase
UvrD
hHcsA
Hmi1p
hPif1
MCM helicase
MCM protein
MER3 helicase
MER3 protein
MPH1
PcrA
PDH120
PfDH A
Pfh1p
PIF1
3'-5' DNA helicase
3'-5' PfDH
5' to 3' DNA helicase
AvDH1
BACH1 helicase
BcMCM
BLM protein
BRCA1-associated C-terminal helicase
CeWRN-1
Dbp9p
DmRECQ5
DNA helicase 120
DNA helicase A
DNA helicase E
DNA helicase II
DNA helicase III
DNA helicase RECQL5'
DNA helicase VI
dnaB
DnaB helicase E1
helicase HDH IV
Hel E
helicase DnaB
helicase domain of bacteriophage T7 gene 4 protein helicase
PcrA helicase
UvrD
hHcsA
Hmi1p
hPif1
MCM helicase
MCM protein
MER3 helicase
MER3 protein
MPH1
PcrA
PDH120
PfDH A
Pfh1p
PIF1
Systematic name:
ATP phosphohydrolase (DNA helix unwinding)
Reaction
- ATP + H2O = ADP + phosphate
Comments:
DNA helicases utilize the energy from ATP hydrolysis to unwind double-stranded DNA. Some of them unwind duplex DNA with a 3' to 5' polarity, other show 5' to 3' polarity or unwind DNA in both directions. Some helicases unwind DNA as well as RNA. May be identical with EC 3.6.4.13.
Links to other databases
Protein domains and families:
PROSITE:PDOC00039
,
PROSITE:PDOC51192
,
PROSITE:PDOC51198
,
PROSITE:PDOC51199
,
PROSITE:PDOC51206
,
PROSITE:PDOC51413
Gene Ontology:
GO:0003678
ADDA_ACET2
ADDA_ALKMQ
ADDA_ALKOO
ADDA_ANOFW
ADDA_BACAH
ADDA_BACC0
ADDA_BACC2
ADDA_BACC4
ADDA_BACC7
ADDA_BACCN
ADDA_BACCQ
ADDA_BACMK
ADDA_BACP2
ADDA_BACVZ
ADDA_CLOB1
ADDA_CLOB6
ADDA_CLOB8
ADDA_CLOBA
ADDA_CLOBB
ADDA_CLOBH
ADDA_CLOBJ
ADDA_CLOBK
ADDA_CLOBL
ADDA_CLOBM
ADDA_CLOK1
ADDA_CLOK5
ADDA_CLONN
ADDA_DESAP
ADDA_DESHD
ADDA_DESRM
ADDA_EXIS2
ADDA_GEOTN
ADDA_HELMI
ADDA_LACCB
ADDA_LACH4
ADDA_LACLM
ADDA_LACP7
ADDA_LEUCK
ADDA_LIMF3
ADDA_LIMRD
ADDA_LIMRJ
ADDA_LISMH
ADDA_LISW6
ADDA_LYSSC
ADDA_NATTJ
ADDA_PELTS
ADDA_RUMCH
ADDA_STAA1
ADDA_STAA2
ADDA_STAA9
ADDA_STAAE
ADDA_STAAT
ADDA_STACT
ADDA_STREM
ADDA_STRGC
ADDA_STRP4
ADDA_STRPG
ADDA_STRPI
ADDA_STRPJ
ADDA_STRPS
ADDA_STRPZ
ADDA_STRS2
ADDA_STRS7
ADDA_STRSV
ADDA_STRSY
ADDA_STRU0
ADDA_THEP3
ADDA_THEPX
ADDB_ACET2
ADDB_ALKMQ
ADDB_ALKOO
ADDB_ANOFW
ADDB_BACAH
ADDB_BACC0
ADDB_BACC2
ADDB_BACC4
ADDB_BACC7
ADDB_BACCN
ADDB_BACCQ
ADDB_BACMK
ADDB_BACP2
ADDB_BACVZ
ADDB_CLOB1
ADDB_CLOB8
ADDB_CLOBA
ADDB_CLOBB
ADDB_CLOBH
ADDB_CLOBK
ADDB_CLOBL
ADDB_CLOBM
ADDB_CLOK1
ADDB_CLONN
ADDB_DESAP
ADDB_DESHD
ADDB_DESRM
ADDB_EXIS2
ADDB_GEOTN
ADDB_HELMI
ADDB_LACCB
ADDB_LACH4
ADDB_LACLM
ADDB_LACP7
ADDB_LEUCK
ADDB_LIMF3
ADDB_LIMRD
ADDB_LIMRJ
ADDB_LISMH
ADDB_LISW6
ADDB_LYSSC
ADDB_NATTJ
ADDB_PELTS
ADDB_RUMCH
ADDB_STAA1
ADDB_STAA2
ADDB_STAA9
ADDB_STAAE
ADDB_STAAT
ADDB_STACT
ADDB_STREM
ADDB_STRGC
ADDB_STRP4
ADDB_STRPG
ADDB_STRPI
ADDB_STRPJ
ADDB_STRPS
ADDB_STRPZ
ADDB_STRS2
ADDB_STRS7
ADDB_STRSV
ADDB_STRSY
ADDB_STRU0
ADDB_THEP3
ADDB_THEPX
ARIP4_XENTR
CHD1_BOMMO
CHD1_CHICK
CHD5_MOUSE
CHD6-2_MOUSE
CHD6_MOUSE
CHD7-2_MOUSE
CHD7-3_MOUSE
CHD7_MOUSE
CHD8_DANRE
CHD8_XENTR
CHL1_ASPCL
CHL1_ASPNC
CHL1_LODEL
CHL1_NEOFI
CHL1_NEUCR
CHL1_PICGU
CHL1_PICST
CHL1_SCLS1
CHL1_VANPO
CHL1_YEAS7
ERC6L_BOVIN
ERC6L_DANRE
ERCC2_BOVIN
GP1D_CHLT2
HELS_CALMQ
HELS_HALS3
HELS_METB6
HELS_METVS
HELS_PYRCJ
HFM1-2_HUMAN
HFM1_HUMAN
HFM1_XENTR
INO80_NEOFI
JBP2_LEIBR
JBP2_LEIIN
JBP2_LEITA
JHS1-2_ARATH
JHS1-3_ARATH
JHS1_ARATH
MCM2_ORYSI
MCM3_BOVIN
MCM3_ORYSI
MCM5_ORYSI
MCM6_ORYSI
MCM7_ORYSI
MCM8_ORYSI
MCM8_ORYSJ
MCM9_ORYSI
MER3_ORYSJ
MPH1_ASPCL
MPH1_ASPFC
MPH1_ASPNC
MPH1_BOTFB
MPH1_MAGO7
MPH1_NEOFI
MPH1_PICST
MPH1_SCLS1
MPH1_VANPO
MPH1_YEAS7
NS1-2_HBOC2
NS1-2_HBOC3
NS1-2_HBOC4
NS1_HBOC2
NS1_HBOC3
NS1_HBOC4
PIF1-2_YEAS7
PIF1_PSYWF
PIF1_YEAS7
RAD25_ENTBH
RAD25_NOSCE
RDH54_YEAS1
RDH54_YEAS6
RDH54_YEAS7
RECQ1_CAEBR
RPOA-2_PRRSS
RPOA_PRRSS
RTEL1-2_BOVIN
RTEL1-3_BOVIN
RTEL1-4_BOVIN
RTEL1-5_BOVIN
RTEL1_BOVIN
RTEL1_CAEBR
RTEL1_CULQU
RTEL1_DROAN
RTEL1_DROER
RTEL1_DROGR
RTEL1_DROMO
RTEL1_DROPE
RTEL1_DROSE
RTEL1_DROVI
RTEL1_DROWI
RTEL1_DROYA
RTEL1_ORYSJ
RUVA_ACAM1
RUVA_ACET2
RUVA_ACHLI
RUVA_ACIAC
RUVA_ACIB3
RUVA_ACIB5
RUVA_ACIBC
RUVA_ACIBS
RUVA_ACIBT
RUVA_ACIBY
RUVA_ACIC1
RUVA_ACIC5
RUVA_ACICJ
RUVA_ACIET
RUVA_ACIF2
RUVA_ACIF5
RUVA_ACISJ
RUVA_ACTP2
RUVA_ACTP7
RUVA_ACTSZ
RUVA_AERHH
RUVA_AERS4
RUVA_AFIC5
RUVA_AGRRK
RUVA_AGRVS
RUVA_ALIB4
RUVA_ALIFM
RUVA_ALISL
RUVA_ALKMQ
RUVA_ALKOO
RUVA_AMOA5
RUVA_ANAD2
RUVA_ANADF
RUVA_ANAMF
RUVA_ANASK
RUVA_ANOFW
RUVA_ARTS2
RUVA_AZOC5
RUVA_AZOPC
RUVA_AZOSB
RUVA_BACAA
RUVA_BACAC
RUVA_BACAH
RUVA_BACC2
RUVA_BACC3
RUVA_BACC4
RUVA_BACC7
RUVA_BACCN
RUVA_BACMK
RUVA_BACP2
RUVA_BACVZ
RUVA_BARBK
RUVA_BART1
RUVA_BEII9
RUVA_BEUC1
RUVA_BIFA0
RUVA_BIFAA
RUVA_BIFLD
RUVA_BIFLS
RUVA_BORBZ
RUVA_BORDL
RUVA_BORHD
RUVA_BORPD
RUVA_BORRA
RUVA_BORT9
RUVA_BRASB
RUVA_BRASO
RUVA_BREBN
RUVA_BRUA1
RUVA_BRUA4
RUVA_BRUC2
RUVA_BRUMB
RUVA_BRUO2
RUVA_BRUSI
RUVA_BURA4
RUVA_BURCC
RUVA_BURCH
RUVA_BURCJ
RUVA_BURM1
RUVA_BURM7
RUVA_BURM9
RUVA_BURMS
RUVA_BURP0
RUVA_BURP6
RUVA_BURVG
RUVA_CALBD
RUVA_CALS8
RUVA_CAMC1
RUVA_CAMC5
RUVA_CAMFF
RUVA_CAMHC
RUVA_CAMJ8
RUVA_CAMJD
RUVA_CAMJJ
RUVA_CAMLR
RUVA_CAUSK
RUVA_CAUVN
RUVA_CELJU
RUVA_CERS5
RUVA_CHLAA
RUVA_CHLAD
RUVA_CHLL2
RUVA_CHLP8
RUVA_CHLPB
RUVA_CHLPD
RUVA_CHLPM
RUVA_CHLSY
RUVA_CHLT2
RUVA_CHLT3
RUVA_CHLTB
RUVA_CITBB
RUVA_CITK8
RUVA_CLAM3
RUVA_CLAMS
RUVA_CLOB1
RUVA_CLOB6
RUVA_CLOB8
RUVA_CLOBA
RUVA_CLOBB
RUVA_CLOBH
RUVA_CLOBJ
RUVA_CLOBK
RUVA_CLOBL
RUVA_CLOBM
RUVA_CORA7
RUVA_CORGB
RUVA_CORK4
RUVA_CORU7
RUVA_COXB1
RUVA_COXB2
RUVA_COXBN
RUVA_COXBR
RUVA_CROS5
RUVA_CROS8
RUVA_CUPTR
RUVA_DELAS
RUVA_DESAH
RUVA_DESAL
RUVA_DESAP
RUVA_DESMR
RUVA_DESOH
RUVA_DESRM
RUVA_DESVM
RUVA_DESVV
RUVA_DICNV
RUVA_DINSH
RUVA_ECO24
RUVA_ECO27
RUVA_ECO45
RUVA_ECO55
RUVA_ECO5E
RUVA_ECO7I
RUVA_ECO81
RUVA_ECO8A
RUVA_ECOBW
RUVA_ECODH
RUVA_ECOHS
RUVA_ECOK1
RUVA_ECOLC
RUVA_ECOLU
RUVA_ECOSE
RUVA_ECOSM
RUVA_ELUMP
RUVA_ENDTX
RUVA_ENT38
RUVA_ERWT9
RUVA_ESCF3
RUVA_EXIS2
RUVA_EXISA
RUVA_FERNB
RUVA_FINM2
RUVA_FLAPJ
RUVA_FRATF
RUVA_FRATM
RUVA_FRATN
RUVA_FRATW
RUVA_GEMAT
RUVA_GEODF
RUVA_GEOLS
RUVA_GEOSM
RUVA_GEOSW
RUVA_GEOTN
RUVA_GLOC7
RUVA_GLUDA
RUVA_GRAFK
RUVA_HAEIE
RUVA_HAEIG
RUVA_HALHL
RUVA_HALOH
RUVA_HAMD5
RUVA_HELPG
RUVA_HELPS
RUVA_HERA2
RUVA_HERAR
RUVA_HISS2
RUVA_JANMA
RUVA_KLEP3
RUVA_KLEP7
RUVA_KOCRD
RUVA_KOSOT
RUVA_LACCB
RUVA_LACE2
RUVA_LACH4
RUVA_LACLM
RUVA_LACP7
RUVA_LARHH
RUVA_LEGPC
RUVA_LEPBA
RUVA_LEPBP
RUVA_LEPCP
RUVA_LEUCK
RUVA_LIMF3
RUVA_LIMRD
RUVA_LIMRJ
RUVA_LISMC
RUVA_LISMH
RUVA_LISW6
RUVA_LYSSC
RUVA_MACCJ
RUVA_MAGMM
RUVA_MARMS
RUVA_MARN8
RUVA_MARSD
RUVA_METC4
RUVA_METEP
RUVA_METNO
RUVA_METPB
RUVA_METPP
RUVA_METRJ
RUVA_METS4
RUVA_METSB
RUVA_MICAN
RUVA_MICLC
RUVA_MYCA1
RUVA_MYCA5
RUVA_MYCA9
RUVA_MYCAP
RUVA_MYCBP
RUVA_MYCBT
RUVA_MYCGI
RUVA_MYCLB
RUVA_MYCMM
RUVA_MYCS2
RUVA_MYCSJ
RUVA_MYCSK
RUVA_MYCTA
RUVA_MYCUA
RUVA_MYCVP
RUVA_NATTJ
RUVA_NAUPA
RUVA_NEIG2
RUVA_NEIM0
RUVA_NEIMF
RUVA_NITSB
RUVA_NOCSJ
RUVA_OPITP
RUVA_ORITB
RUVA_ORITI
RUVA_PARD8
RUVA_PARDP
RUVA_PARL1
RUVA_PARP8
RUVA_PARPJ
RUVA_PECCP
RUVA_PELPB
RUVA_PELPD
RUVA_PETMO
RUVA_PHEZH
RUVA_PHOV8
RUVA_PHYMT
RUVA_POLAQ
RUVA_POLNS
RUVA_PORG3
RUVA_PROA2
RUVA_PROM0
RUVA_PROM1
RUVA_PROM2
RUVA_PROM4
RUVA_PROMH
RUVA_PROMS
RUVA_PSEA7
RUVA_PSEA8
RUVA_PSECP
RUVA_PSEFS
RUVA_PSEP1
RUVA_PSEPG
RUVA_PSEPW
RUVA_PSEU5
RUVA_PSYIN
RUVA_PSYWF
RUVA_RALPJ
RUVA_RENSM
RUVA_RHIE6
RUVA_RHILW
RUVA_RHOCS
RUVA_RHOE4
RUVA_RHOOB
RUVA_RHOPT
RUVA_RHOS1
RUVA_RHOSK
RUVA_RICAE
RUVA_RICAH
RUVA_RICB8
RUVA_RICCK
RUVA_RICPU
RUVA_RICRO
RUVA_RICRS
RUVA_RIPO1
RUVA_ROSCS
RUVA_ROSS1
RUVA_RUMCH
RUVA_SACEN
RUVA_SALA4
RUVA_SALAI
RUVA_SALDC
RUVA_SALEP
RUVA_SALG2
RUVA_SALHS
RUVA_SALNS
RUVA_SALPB
RUVA_SALPC
RUVA_SALPK
RUVA_SALSV
RUVA_SALTO
RUVA_SERP5
RUVA_SHEAM
RUVA_SHEB2
RUVA_SHEB5
RUVA_SHEB8
RUVA_SHEB9
RUVA_SHEHH
RUVA_SHELP
RUVA_SHEPA
RUVA_SHEPC
RUVA_SHEPW
RUVA_SHESA
RUVA_SHESH
RUVA_SHESW
RUVA_SHEWM
RUVA_SHIB3
RUVA_SINFN
RUVA_SINMW
RUVA_SPHWW
RUVA_STAA1
RUVA_STAA2
RUVA_STAA9
RUVA_STAAE
RUVA_STAAT
RUVA_STACT
RUVA_STRE4
RUVA_STREM
RUVA_STRGC
RUVA_STRGG
RUVA_STRM5
RUVA_STRMK
RUVA_STRP4
RUVA_STRP7
RUVA_STRPG
RUVA_STRPI
RUVA_STRPJ
RUVA_STRPS
RUVA_STRPZ
RUVA_STRS2
RUVA_STRS7
RUVA_STRSV
RUVA_STRSY
RUVA_STRU0
RUVA_STRZJ
RUVA_STRZP
RUVA_STRZT
RUVA_SULNB
RUVA_SYNFM
RUVA_SYNP2
RUVA_SYNPW
RUVA_SYNR3
RUVA_TERTT
RUVA_THEAB
RUVA_THEM4
RUVA_THEP1
RUVA_THEP3
RUVA_THEPX
RUVA_THERP
RUVA_THEYD
RUVA_THISH
RUVA_TOLAT
RUVA_TREPS
RUVA_UREP2
RUVA_UREU1
RUVA_VARPS
RUVA_VEREI
RUVA_VIBA3
RUVA_VIBC3
RUVA_VIBCM
RUVA_WOLPP
RUVA_WOLWR
RUVA_XANCB
RUVA_XANOP
RUVA_XANP2
RUVA_XYLF2
RUVA_XYLFM
RUVA_YERE8
RUVA_YERP3
RUVA_YERPB
RUVA_YERPG
RUVA_YERPY
RUVB_ACAM1
RUVB_ACET2
RUVB_ACHLI
RUVB_ACIAC
RUVB_ACIB3
RUVB_ACIB5
RUVB_ACIBC
RUVB_ACIBS
RUVB_ACIBT
RUVB_ACIBY
RUVB_ACIC1
RUVB_ACISJ
RUVB_ACTP2
RUVB_ACTSZ
RUVB_AERHH
RUVB_AERS4
RUVB_AGRVS
RUVB_AKKM8
RUVB_ALIB4
RUVB_ALIFM
RUVB_ALISL
RUVB_ALKMQ
RUVB_ALKOO
RUVB_AMOA5
RUVB_ANAD2
RUVB_ANADF
RUVB_ANAMF
RUVB_ANASK
RUVB_ARTS2
RUVB_AZOC5
RUVB_AZOSB
RUVB_AZOVD
RUVB_BACAA
RUVB_BACAC
RUVB_BACAH
RUVB_BACC2
RUVB_BACC3
RUVB_BACC4
RUVB_BACC7
RUVB_BACCN
RUVB_BACCQ
RUVB_BACMK
RUVB_BACP2
RUVB_BACVZ
RUVB_BARBK
RUVB_BART1
RUVB_BEII9
RUVB_BIFAA
RUVB_BIFLD
RUVB_BIFLS
RUVB_BORHD
RUVB_BRAHW
RUVB_BRASB
RUVB_BRASO
RUVB_BREBN
RUVB_BRUA1
RUVB_BRUA4
RUVB_BRUC2
RUVB_BRUMB
RUVB_BRUO2
RUVB_BRUSI
RUVB_BURA4
RUVB_BURCC
RUVB_BURCH
RUVB_BURCJ
RUVB_BURM1
RUVB_BURM7
RUVB_BURM9
RUVB_BURMS
RUVB_BURP0
RUVB_BURP6
RUVB_BURVG
RUVB_CALBD
RUVB_CALS8
RUVB_CAMC1
RUVB_CAMC5
RUVB_CAMFF
RUVB_CAMHC
RUVB_CAMJ8
RUVB_CAMJD
RUVB_CAMJJ
RUVB_CAMLR
RUVB_CAUSK
RUVB_CAUVN
RUVB_CELJU
RUVB_CERS5
RUVB_CHLAA
RUVB_CHLAD
RUVB_CHLL2
RUVB_CHLP8
RUVB_CHLPD
RUVB_CHLPM
RUVB_CHLSY
RUVB_CHLT2
RUVB_CHLTB
RUVB_CITBB
RUVB_CITK8
RUVB_CLAM3
RUVB_CLOB1
RUVB_CLOB6
RUVB_CLOB8
RUVB_CLOBA
RUVB_CLOBB
RUVB_CLOBH
RUVB_CLOBJ
RUVB_CLOBK
RUVB_CLOBL
RUVB_CLOBM
RUVB_CLOK1
RUVB_CLOK5
RUVB_CLONN
RUVB_CORA7
RUVB_CORGB
RUVB_COXB1
RUVB_COXB2
RUVB_COXBN
RUVB_COXBR
RUVB_CROS5
RUVB_CROS8
RUVB_CUPTR
RUVB_CYAP4
RUVB_DEHMB
RUVB_DELAS
RUVB_DESAH
RUVB_DESHD
RUVB_DESOH
RUVB_DESRM
RUVB_DESVV
RUVB_DICNV
RUVB_ECO24
RUVB_ECO27
RUVB_ECO45
RUVB_ECO55
RUVB_ECO5E
RUVB_ECO7I
RUVB_ECO81
RUVB_ECO8A
RUVB_ECOBW
RUVB_ECODH
RUVB_ECOHS
RUVB_ECOK1
RUVB_ECOLC
RUVB_ECOLU
RUVB_ECOSE
RUVB_ECOSM
RUVB_EDWI9
RUVB_ENT38
RUVB_ERWT9
RUVB_ESCF3
RUVB_EXIS2
RUVB_EXISA
RUVB_FERNB
RUVB_FLAJ1
RUVB_FLAPJ
RUVB_FRAP2
RUVB_FRASN
RUVB_FRATF
RUVB_FRATM
RUVB_FRATN
RUVB_FRATW
RUVB_GEMAT
RUVB_GEODF
RUVB_GEOLS
RUVB_GEOSM
RUVB_GEOSW
RUVB_GEOTN
RUVB_GEOUR
RUVB_GLOC7
RUVB_GRAFK
RUVB_HAEIE
RUVB_HALHL
RUVB_HAMD5
RUVB_HELMI
RUVB_HELP2
RUVB_HELPG
RUVB_HELPS
RUVB_HERAR
RUVB_HISS2
RUVB_JANMA
RUVB_KLEP3
RUVB_KLEP7
RUVB_KOSOT
RUVB_LACCB
RUVB_LACH4
RUVB_LACLM
RUVB_LACP7
RUVB_LARHH
RUVB_LEGPC
RUVB_LEPCP
RUVB_LIMRD
RUVB_LIMRJ
RUVB_LISMC
RUVB_LISMH
RUVB_LISW6
RUVB_MACCJ
RUVB_MAGMM
RUVB_MARMS
RUVB_MARN8
RUVB_METB6
RUVB_METPP
RUVB_METSB
RUVB_MICAN
RUVB_MYCA1
RUVB_MYCBP
RUVB_MYCBT
RUVB_MYCGI
RUVB_MYCLB
RUVB_MYCMM
RUVB_MYCS2
RUVB_MYCSJ
RUVB_MYCSK
RUVB_MYCTA
RUVB_MYCUA
RUVB_MYCVP
RUVB_NEIG2
RUVB_NEIM0
RUVB_NEIMF
RUVB_NITSB
RUVB_NOCSJ
RUVB_NOSP7
RUVB_ORITB
RUVB_ORITI
RUVB_PAEAT
RUVB_PARD8
RUVB_PARDP
RUVB_PARL1
RUVB_PARPJ
RUVB_PECCP
RUVB_PELPB
RUVB_PELPD
RUVB_PELTS
RUVB_PHEZH
RUVB_PHOV8
RUVB_PHYMT
RUVB_POLNA
RUVB_PROA2
RUVB_PROM0
RUVB_PROM1
RUVB_PROM2
RUVB_PROM3
RUVB_PROM5
RUVB_PROMH
RUVB_PROMS
RUVB_PSEA7
RUVB_PSEA8
RUVB_PSECP
RUVB_PSEFS
RUVB_PSELT
RUVB_PSEMY
RUVB_PSEP1
RUVB_PSEPG
RUVB_PSEPW
RUVB_PSEU5
RUVB_PSYIN
RUVB_PSYWF
RUVB_RALPJ
RUVB_RHIE6
RUVB_RHILW
RUVB_RHOCS
RUVB_RHOE4
RUVB_RHOOB
RUVB_RHOPT
RUVB_RHOS1
RUVB_RHOSK
RUVB_RICAE
RUVB_RICAH
RUVB_RICB8
RUVB_RICCK
RUVB_RICM5
RUVB_RICPU
RUVB_RICRS
RUVB_RIPO1
RUVB_ROSCS
RUVB_ROSS1
RUVB_SACEN
RUVB_SALA4
RUVB_SALAI
RUVB_SALAR
RUVB_SALDC
RUVB_SALHS
RUVB_SALNS
RUVB_SALPB
RUVB_SALPC
RUVB_SALPK
RUVB_SALSV
RUVB_SALTO
RUVB_SERP5
RUVB_SHEAM
RUVB_SHEB2
RUVB_SHEB5
RUVB_SHEB8
RUVB_SHEB9
RUVB_SHEHH
RUVB_SHELP
RUVB_SHEPA
RUVB_SHEPC
RUVB_SHEPW
RUVB_SHESA
RUVB_SHESH
RUVB_SHESW
RUVB_SHEWM
RUVB_SHIB3
RUVB_SINMW
RUVB_SPHWW
RUVB_STAA1
RUVB_STAA2
RUVB_STAA9
RUVB_STAAE
RUVB_STAAT
RUVB_STACT
RUVB_STRE4
RUVB_STREM
RUVB_STRGC
RUVB_STRGG
RUVB_STRM5
RUVB_STRMK
RUVB_STRP4
RUVB_STRP7
RUVB_STRPG
RUVB_STRPI
RUVB_STRPS
RUVB_STRPZ
RUVB_STRS2
RUVB_STRS7
RUVB_STRSV
RUVB_STRSY
RUVB_STRU0
RUVB_STRZJ
RUVB_STRZP
RUVB_STRZT
RUVB_SULNB
RUVB_SYNFM
RUVB_SYNP2
RUVB_SYNPW
RUVB_SYNR3
RUVB_TERTT
RUVB_THEM4
RUVB_THEP1
RUVB_THEP3
RUVB_THEPX
RUVB_THERP
RUVB_THESQ
RUVB_THEYD
RUVB_THISH
RUVB_TOLAT
RUVB_UREP2
RUVB_UREU1
RUVB_VARPS
RUVB_VEREI
RUVB_VESOH
RUVB_VIBA3
RUVB_VIBC3
RUVB_VIBCB
RUVB_VIBCM
RUVB_WOLPP
RUVB_WOLWR
RUVB_XANCB
RUVB_XANOP
RUVB_XYLF2
RUVB_XYLFM
RUVB_YERE8
RUVB_YERP3
RUVB_YERPB
RUVB_YERPG
RUVB_YERPP
RUVB_YERPY
SMRDA_DANRE
TWIH_ARATH
References
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Ozsoy, A. Z., Sekelsky, J. J., Matson, S. W.Biochemical characterization of the small isoform of Drosophila melanogaster RECQ5 helicase.Nucleic Acids Res. 29 : 2986-2993 (2001). [PMID: 11452023]
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Tanner, J. A., Watt, R. M., Chai, Y. B., Lu, L. Y., Lin, M. C., Peiris, J. S., Poon, L. L., Kung, H. F., Huang, J. D.The severe acute respiratory syndrome (SARS) coronavirus NTPase/helicase belongs to a distinct class of 5' to 3' viral helicases.J. Biol. Chem. 278 : 39578-39582 (2003). [PMID: 12917423]
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Nakagawa, T., Flores-Rozas, H., Kolodner, R. D.The MER3 helicase involved in meiotic crossing over is stimulated by single-stranded DNA-binding proteins and unwinds DNA in the 3' to 5' direction.J. Biol. Chem. 276 : 31487-31493 (2001). [PMID: 11376001]
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Lee, C., Seo, Y. S.Isolation and characterization of a processive DNA helicase from the fission yeast Schizosaccharomyces pombe that translocates in a 5'-to-3' direction.Biochem. J. 334 : 377-386 (1998). [PMID: 9716495]
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Phan, T. N., Ehtesham, N. Z., Tuteja, R., Tuteja, N.A novel nuclear DNA helicase with high specific activity from Pisum sativum catalytically translocates in the 3'→5' direction.Eur. J. Biochem. 270 : 1735-1745 (2003). [PMID: 12694186]
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Bernstein, D. A., Zittel, M. C., Keck, J. L.High-resolution structure of the E.coli RecQ helicase catalytic core.EMBO J. 22 : 4910-4921 (2003). [PMID: 14517231]
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Pike, A. C., Shrestha, B., Popuri, V., Burgess-Brown, N., Muzzolini, L., Costantini, S., Vindigni, A., Gileadi, O.Structure of the human RECQ1 helicase reveals a putative strand-separation pin.Proc. Natl. Acad. Sci. USA 106 : 1039-1044 (2009). [PMID: 19151156]
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Frick, D. N.The hepatitis C virus NS3 protein: a model RNA helicase and potential drug target.Curr. issues Mol. Biol. 9 : 1-20 (2007). [PMID: 17263143]
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Ivanov, K. A., Ziebuhr, J.Human coronavirus 229E nonstructural protein 13: characterization of duplex-unwinding, nucleoside triphosphatase, and RNA 5'-triphosphatase activities.J. Virol. 78 : 7833-7838 (2004). [PMID: 15220459]
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Ivessa, A. S., Zhou, J. Q., Schulz, V. P., Monson, E. K., Zakian, V. A.Saccharomyces Rrm3p, a 5' to 3' DNA helicase that promotes replication fork progression through telomeric and subtelomeric DNA.Genes Dev. 16 : 1383-1396 (2002). [PMID: 12050116]
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Zhou, J. Q., Qi, H., Schulz, V. P., Mateyak, M. K., Monson, E. K., Zakian, V. A.Schizosaccharomyces pombe pfh1+ encodes an essential 5' to 3' DNA helicase that is a member of the PIF1 subfamily of DNA helicases.Mol. Biol. Cell 13 : 2180-2191 (2002). [PMID: 12058079]
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George, T., Wen, Q., Griffiths, R., Ganesh, A., Meuth, M., Sanders, C. M.Human Pif1 helicase unwinds synthetic DNA structures resembling stalled DNA replication forks.Nucleic Acids Res. 37 : 6491-6502 (2009). [PMID: 19700773]
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Naqvi, A., Tinsley, E., Khan, S. A.Purification and characterization of the PcrA helicase of Bacillus anthracis.J. Bacteriol. 185 : 6633-6639 (2003). [PMID: 14594837]
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Ruiz-Maso, J. A., Anand, S. P., Espinosa, M., Khan, S. A., del Solar, G.Genetic and biochemical characterization of the Streptococcus pneumoniae PcrA helicase and its role in plasmid rolling circle replication.J. Bacteriol. 188 : 7416-7425 (2006). [PMID: 16936036]
[EC 3.6.4.12 created 2009]