Summary: Tumour-suppressor protein CtIP N-terminal domain
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Tumour-suppressor protein CtIP N-terminal domain Provide feedback
CtIP is predominantly a nuclear protein that complexes with both BRCA1 and the BRCA1-associated RING domain protein (BARD1). At the protein level, CtIP expression varies with cell cycle progression in a pattern identical to that of BRCA1. Thus, the steady-state levels of CtIP polypeptides, which remain low in resting cells and G1 cycling cells, increase dramatically as Dividing cells traverse the G1/S boundary. CtIP can potentially modulate the functions ascribed to BRCA1 in transcriptional regulation, DNA repair, and/or cell cycle checkpoint control [2]. This N-terminal domain carries a coiled-coil region and is essential for homodimerisation of the protein [3]. The C-terminal domain is family PF08573.
Literature references
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Yu X, Wu LC, Bowcock AM, Aronheim A, Baer R; , J Biol Chem. 1998;273:25388-25392.: The C-terminal (BRCT) domains of BRCA1 interact in vivo with CtIP, a protein implicated in the CtBP pathway of transcriptional repression. PUBMED:9738006 EPMC:9738006
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Uanschou C, Siwiec T, Pedrosa-Harand A, Kerzendorfer C, Sanchez-Moran E, Novatchkova M, Akimcheva S, Woglar A, Klein F, Schlogelhofer P; , EMBO J. 2007; [Epub ahead of print]: A novel plant gene essential for meiosis is related to the human CtIP and the yeast COM1/SAE2 gene. PUBMED:18007598 EPMC:18007598
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Limbo O, Chahwan C, Yamada Y, de Bruin RA, Wittenberg C, Russell P; , Mol Cell. 2007;28:134-146.: Ctp1 is a cell-cycle-regulated protein that functions with Mre11 complex to control double-strand break repair by homologous recombination. PUBMED:17936710 EPMC:17936710
External database links
| PANDIT: | PF10482 |
| Pseudofam: | PF10482 |
| SYSTERS: | CtIP_N |
This tab holds annotation information from the InterPro database.
InterPro entry IPR019518
CtIP is predominantly a nuclear protein that complexes with both BRCA1 and the BRCA1-associated RING domain protein (BARD1). At the protein level, CtIP expression varies with cell cycle progression in a pattern identical to that of BRCA1. Thus, the steady-state levels of CtIP polypeptides, which remain low in resting cells and G1 cycling cells, increase dramatically as Dividing cells traverse the G1/S boundary. CtIP can potentially modulate the functions ascribed to BRCA1 in transcriptional regulation, DNA repair, and/or cell cycle checkpoint control [PUBMED:18007598]. This N-terminal domain carries a coiled-coil region and is essential for homodimerisation of the protein [PUBMED:17936710]. The C-terminal domain is family CtIP_C and carries functionally important CxxC and RHR motifs, absence of which lead cells to grow slowly and show hypersensitivity to genotoxins [PUBMED:17936710].
Domain organisation
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Alignments
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| Seed (4) |
Full (111) |
Representative proteomes | NCBI (100) |
Meta (0) |
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| RP15 (2) |
RP35 (6) |
RP55 (17) |
RP75 (55) |
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| PP/heatmap | 1 | |||||||
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1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
available,
not generated,
— not available.
Format an alignment
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We make all of our alignments available in Stockholm format. You can download them here as raw, plain text files or as gzip-compressed files.
| Seed (4) |
Full (111) |
Representative proteomes | NCBI (100) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (2) |
RP35 (6) |
RP55 (17) |
RP75 (55) |
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| Raw Stockholm | ||||||||
| Gzipped | ||||||||
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
External links
MyHits provides a collection of tools to handle multiple sequence alignments. For example, one can refine a seed alignment (sequence addition or removal, re-alignment or manual edition) and then search databases for remote homologs using HMMER3.
HMM logo
HMM logos is one way of visualising profile HMMs. Logos provide a quick overview of the properties of an HMM in a graphical form. You can see a more detailed description of HMM logos and find out how you can interpret them here. More...
Trees
This page displays the phylogenetic tree for this family's seed alignment. We use FastTree to calculate neighbour join trees with a local bootstrap based on 100 resamples (shown next to the tree nodes). FastTree calculates approximately-maximum-likelihood phylogenetic trees from our seed alignment.
Note: You can also download the data file for the tree.
Curation and family details
This section shows the detailed information about the Pfam family. You can see the definitions of many of the terms in this section in the glossary and a fuller explanation of the scoring system that we use in the scores section of the help pages.
Curation
| Seed source: | TreeFam_TF106469 |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Buljan M, Coggill P |
| Number in seed: | 4 |
| Number in full: | 111 |
| Average length of the domain: | 115.10 aa |
| Average identity of full alignment: | 67 % |
| Average coverage of the sequence by the domain: | 16.20 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
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| Model details: |
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| Model length: | 120 | ||||||||||||
| Family (HMM) version: | 4 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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