Homo sapiens Protein: BRIP1
Summary
InnateDB Protein IDBP-759437.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BRIP1
Protein Name
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000464654
InnateDB Gene IDBG-62607 (BRIP1)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 32 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 32 [view]
Protein-Protein 28 [view]
Protein-DNA 4 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003676 nucleic acid binding
GO:0003677 DNA binding
GO:0004003 ATP-dependent DNA helicase activity
GO:0005524 ATP binding
GO:0008026 ATP-dependent helicase activity
GO:0016817 hydrolase activity, acting on acid anhydrides
GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides
Biological Process
GO:0006139 nucleobase-containing compound metabolic process
GO:0006200 ATP catabolic process
GO:0008152 metabolic process
GO:0032508 DNA duplex unwinding
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR002919 Trypsin Inhibitor-like, cysteine rich domain
IPR006554 Helicase-like, DEXD box c2 type
IPR006555 ATP-dependent helicase, C-terminal
IPR010614 DEAD2
IPR011545 DEAD/DEAH box helicase domain
IPR013020 DNA helicase (DNA repair), Rad3 type
IPR014001 Helicase, superfamily 1/2, ATP-binding domain
IPR014013 Helicase, superfamily 1/2, ATP-binding domain, DinG/Rad3-type
IPR027417 P-loop containing nucleoside triphosphate hydrolase
PFAM PF01826
PF13307
PF06733
PF00270
PRINTS
PIRSF
SMART SM00488
SM00491
SM00487
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt
PhosphoSite PhosphoSite-
TrEMBL J3QSE8
UniProt Splice Variant
Entrez Gene 83990
UniGene Hs.128903
RefSeq
HUGO HGNC:20473
OMIM 605882
CCDS
HPRD 05797
IMGT
EMBL AC002994 AC005969 AC060798
GenPept