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- Table of Contents
Facts about Fanconi anemia group M protein.
In complicated with CENPS and CENPX, binds double-stranded DNA (dsDNA), fork-structured DNA (fsDNA) and Holliday junction substrates (PubMed:20347428, PubMed:20347429). Its ATP-dependent DNA branch migration activity can process branched DNA structures like a movable replication fork.
Human | |
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Gene Name: | FANCM |
Uniprot: | Q8IYD8 |
Entrez: | 57697 |
Belongs to: |
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DEAD box helicase family |
ATP-dependent RNA helicase FANCM; EC 3.6.1; FAAP250EC 3.6.4.13; Fanconi anemia, complementation group M; Fanconi anemia-associated polypeptide of 250 kDa; KIAA1596Fanconi anemia group M protein; MGC176453; Protein FACM; Protein Hef ortholog
Mass (kDA):
232.191 kDA
Human | |
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Location: | 14q21.2 |
Sequence: | 14; NC_000014.9 (45135930..45200890) |
Nucleus.
PMID: 16116422 by Meetei A.R., et al. A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.
PMID: 16116434 by Mosedale G., et al. The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway.