Summary: GCM motif protein
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This is the Wikipedia entry entitled "GCM transcription factors". More...
GCM transcription factors Edit Wikipedia article
| structure of the gcm domain bound to dna | |||||||||
| Identifiers | |||||||||
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| Symbol | GCM | ||||||||
| Pfam | PF03615 | ||||||||
| Pfam clan | CL0274 | ||||||||
| InterPro | IPR003902 | ||||||||
| SCOP | 1odh | ||||||||
| SUPERFAMILY | 1odh | ||||||||
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In molecular biology, the GCM transcription factors are a family of proteins which contain a GCM motif. The GCM motif is a domain that has been identified in proteins belonging to a family of transcriptional regulators involved in fundamental developmental processes which comprise Drosophila melanogaster GCM and its mammalian homologues.[1][2][3][4] In GCM transcription factors the N-terminal moiety contains a DNA-binding domain of 150 amino acids. Sequence conservation is highest in this GCM domain. In contrast, the C-terminal moiety contains one or two transactivating regions and is only poorly conserved.
The GCM motif has been shown to be a DNA binding domain that recognises preferentially the nonpalindromic octamer 5'-ATGCGGGT-3'.[1][2][3] The GCM motif contains many conserved basic amino acid residues, seven cysteine residues, and four histidine residues.[1] The conserved cysteines are involved in shaping the overall conformation of the domain, in the process of DNA binding and in the redox regulation of DNA binding.[3] The GCM domain as a new class of Zn-containing DNA-binding domain with no similarity to any other DNA-binding domain.[5] The GCM domain consists of a large and a small domain tethered together by one of the two Zn ions present in the structure. The large and the small domains comprise five- and three-stranded beta-sheets, respectively, with three small helical segments packed against the same side of the two beta-sheets. The GCM domain exercises a novel mode of sequence-specific DNA recognition, where the five-stranded beta-pleated sheet inserts into the major groove of the DNA. Residues protruding from the edge strand of the beta-pleated sheet and the following loop and strand contact the bases and backbone of both DNA strands, providing specificity for its DNA target site.
[edit] References
- ^ a b c Akiyama Y, Hosoya T, Poole AM, Hotta Y (December 1996). "The gcm-motif: a novel DNA-binding motif conserved in Drosophila and mammals". Proc. Natl. Acad. Sci. U.S.A. 93 (25): 14912–6. DOI:10.1073/pnas.93.25.14912. PMC 26236. PMID 8962155. //www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=26236.
- ^ a b Schreiber J, Sock E, Wegner M (April 1997). "The regulator of early gliogenesis glial cells missing is a transcription factor with a novel type of DNA-binding domain". Proc. Natl. Acad. Sci. U.S.A. 94 (9): 4739–44. DOI:10.1073/pnas.94.9.4739. PMC 20794. PMID 9114061. //www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=20794.
- ^ a b c Schreiber J, Enderich J, Wegner M (May 1998). "Structural requirements for DNA binding of GCM proteins". Nucleic Acids Res. 26 (10): 2337–43. DOI:10.1093/nar/26.10.2337. PMC 147556. PMID 9580683. //www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=147556.
- ^ Tuerk EE, Schreiber J, Wegner M (February 2000). "Protein stability and domain topology determine the transcriptional activity of the mammalian glial cells missing homolog, GCMb". J. Biol. Chem. 275 (7): 4774–82. PMID 10671510.
- ^ Cohen SX, Moulin M, Hashemolhosseini S, Kilian K, Wegner M, Muller CW (April 2003). "Structure of the GCM domain-DNA complex: a DNA-binding domain with a novel fold and mode of target site recognition". EMBO J. 22 (8): 1835–45. DOI:10.1093/emboj/cdg182. PMC 154474. PMID 12682016. //www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=154474.
This article incorporates text from the public domain Pfam and InterPro IPR003902
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This tab holds the annotation information that is stored in the Pfam database. As we move to using Wikipedia as our main source of annotation, the contents of this tab will be gradually replaced by the Wikipedia tab.
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External database links
| PANDIT: | PF03615 |
| Pseudofam: | PF03615 |
| SCOP: | 1odh |
| SYSTERS: | GCM |
This tab holds annotation information from the InterPro database.
InterPro entry IPR003902
GCM transcription factors are a family of proteins which contain a GCM motif. The GCM motif is a domain that has been identified in proteins belonging to a family of transcriptional regulators involved in fundamental developmental processes which comprise Drosophila melanogaster GCM and its mammalian homologs [PUBMED:8962155, PUBMED:9114061, PUBMED:9580683, PUBMED:10671510]. IN GCM transcription factors the N-terminal moiety contains a DNA-binding domain of 150 residues. Sequence conservation is highest in this GCM domain. In contrast, the C-terminal moiety contains one or two transactivating regions and is only poorly conserved.
The GCM motif has been shown to be a DNA binding domain that recognises preferentially the nonpalindromic octamer 5'-ATGCGGGT-3' [PUBMED:8962155, PUBMED:9114061, PUBMED:9580683]. The GCM motif contains many conserved basic amino acid residues, seven cysteine residues, and four histidine residues [PUBMED:8962155]. The conserved cysteines are involved in shaping the overall conformation of the domain, in the process of DNA binding and in the redox regulation of DNA binding [PUBMED:9580683]. The GCM domain as a new class of Zn-containing DNA-binding domain with no similarity to any other DNA-binding domain [PUBMED:12682016]. The GCM domain consists of a large and a small domain tethered together by one of the two Zn ions present in the structure. The large and the small domains comprise five- and three-stranded beta-sheets, respectively, with three small helical segments packed against the same side of the two beta-sheets. The GCM domain exercises a novel mode of sequence-specific DNA recognition, where the five-stranded beta-pleated sheet inserts into the major groove of the DNA. Residues protruding from the edge strand of the beta-pleated sheet and the following loop and strand contact the bases and backbone of both DNA strands, providing specificity for its DNA target site.
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | DNA binding (GO:0003677) |
| Biological process | regulation of transcription, DNA-dependent (GO:0006355) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Pfam Clan
Alignments
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| Seed (6) |
Full (146) |
Representative proteomes | NCBI (148) |
Meta (0) |
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| RP15 (21) |
RP35 (27) |
RP55 (55) |
RP75 (94) |
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| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
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| Seed (6) |
Full (146) |
Representative proteomes | NCBI (148) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (21) |
RP35 (27) |
RP55 (55) |
RP75 (94) |
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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.
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Trees
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Curation and family details
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Curation
| Seed source: | PROSITE |
| Previous IDs: | none |
| Type: | Family |
| Author: | Griffiths-Jones SR |
| Number in seed: | 6 |
| Number in full: | 146 |
| Average length of the domain: | 139.50 aa |
| Average identity of full alignment: | 68 % |
| Average coverage of the sequence by the domain: | 28.86 % |
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: | 143 | ||||||||||||
| Family (HMM) version: | 10 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Structures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the GCM domain has been found. There are 1 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein seqence.
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Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence