ID: ENSBTAT00000071085
DBxRefs: refseq:NP_001098446 refseq:NM_001104976
Gene: ENSBTAG00000002612 FA complementation group M [Source:VGNC Symbol;Acc:VGNC:106735]
Polypeptide: ENSBTAT00000071085
21:54856782..54947082 1
Ontology | ID | Term |
---|---|---|
molecular_function | GO:0003676 | nucleic acid binding |
molecular_function | GO:0003677 | DNA binding |
molecular_function | GO:0004518 | nuclease activity |
molecular_function | GO:0005524 | ATP binding |
biological_process | GO:0006281 | DNA repair |
molecular_function | GO:0043138 | 3'-5' DNA helicase activity |
Protein database | Protein domain |
---|---|
FUNFAM | G3DSA:1.20.1320.20:FF:000001 null |
FUNFAM | G3DSA:3.40.50.300:FF:000861 null |
FUNFAM | G3DSA:3.40.50.300:FF:001333 null |
FUNFAM | G3DSA:3.40.50.10130:FF:000004 null |
SMART | SM00490 helicmild6 |
SMART | SM00891 ERCC4_2 |
SMART | SM00487 ultradead3 |
GENE3D | G3DSA:1.20.1320.20 hef helicase domain |
PFAM | PF02732 ERCC4 |
PFAM | PF00270 DEAD |
PFAM | PF16783 FANCM-MHF_bd |
GENE3D | G3DSA:1.10.150.20 |
PFAM | PF00271 Helicase_C |
GENE3D | G3DSA:3.40.50.10130 |
GENE3D | G3DSA:3.40.50.300 |
MOBIDB_LITE | mobidb-lite disorder_prediction |
PANTHER | PTHR14025 FANCONI ANEMIA GROUP M FANCM FAMILY MEMBER |
PROSITE_PROFILES | PS51194 HELICASE_CTER |
PROSITE_PROFILES | PS51192 HELICASE_ATP_BIND_1 |
CDD | cd20077 XPF_nuclease_FANCM |
CDD | cd18801 SF2_C_FANCM_Hef |
CDD | cd12091 FANCM_ID |
CDD | cd18033 DEXDc_FANCM |
SUPERFAMILY | SSF47781 RuvA domain 2-like |
SUPERFAMILY | SSF52980 Restriction endonuclease-like |
SUPERFAMILY | SSF52540 P-loop containing nucleoside triphosphate hydrolases |
TMHMM | TMhelix null |