Summary: Formiminotransferase domain
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This is the Wikipedia entry entitled "Glutamate formimidoyltransferase". More...
Glutamate formimidoyltransferase Edit Wikipedia article
| Formiminotransferase domain, N-terminal subdomain | |||||||||
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| the crystal structure of the formiminotransferase domain of formiminotransferase-cyclodeaminase. | |||||||||
| Identifiers | |||||||||
| Symbol | FTCD_N | ||||||||
| Pfam | PF07837 | ||||||||
| InterPro | IPR012886 | ||||||||
| SCOP | 1qd1 | ||||||||
| SUPERFAMILY | 1qd1 | ||||||||
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| Formiminotransferase domain | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| the crystal structure of the formiminotransferase domain of formiminotransferase-cyclodeaminase. | |||||||||
| Identifiers | |||||||||
| Symbol | FTCD | ||||||||
| Pfam | PF02971 | ||||||||
| InterPro | IPR013802 | ||||||||
| SCOP | 1qd1 | ||||||||
| SUPERFAMILY | 1qd1 | ||||||||
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In molecular biology, Glutamate formimidoyltransferase is a methyltransferase enzyme which uses tetrahydrofolate as part of histidine catabolism. It catalyses two reactions:
- 5-formyltetrahydrofolate + L-glutamate <=> tetrahydrofolate + N-formyl-L-glutamate
It is classified under EC 2.1.2.5 and in mammals is found as part of a bifunctional enzyme that also has formimidoyltetrahydrofolate cyclodeaminase activity.[1]
[edit] Structure
The formiminotransferase (FT) domain of formiminotransferase-cyclodeaminase (FTCD) forms a homodimer, with each protomer comprising two subdomains. The formiminotransferase domain has an N-terminal subdomain that is made up of a six-stranded mixed beta-pleated sheet and five alpha helices, which are arranged on the external surface of the beta sheet. This, in turn, faces the beta-sheet of the C-terminal subdomain to form a double beta-sheet layer. The two subdomains are separated by a short linker sequence, which is not thought to be any more flexible than the remainder of the molecule. The substrate is predicted to form a number of contacts with residues found in both the N-terminal and C-terminal subdomains.[2] In humans, deficiency of this enzyme results in a disease phenotype.[3]
[edit] References
- ^ MacKenzie RE, Aldridge M, Paquin J (10 October 1980). "The bifunctional enzyme formiminotransferase-cyclodeaminase is a tetramer of dimers". J. Biol. Chem. 255 (19): 9474â8. PMID 7410436. http://www.jbc.org/cgi/reprint/255/19/9474.
- ^ Kohls D, Sulea T, Purisima EO, MacKenzie RE, Vrielink A (January 2000). "The crystal structure of the formiminotransferase domain of formiminotransferase-cyclodeaminase: implications for substrate channeling in a bifunctional enzyme". Structure 8 (1): 35â46. doi:10.1016/S0969-2126(00)00078-2. PMID 10673422.
- ^ Hilton JF, Christensen KE, Watkins D, Raby BA, Renaud Y, de la Luna S, Estivill X, MacKenzie RE, Hudson TJ, Rosenblatt DS (July 2003). "The molecular basis of glutamate formiminotransferase deficiency". Hum. Mutat. 22 (1): 67â73. doi:10.1002/humu.10236. PMID 12815595.
[edit] External links
- Glutamate formimidoyltransferase at the US National Library of Medicine Medical Subject Headings (MeSH)
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This article incorporates text from the public domain Pfam and InterPro IPR013802
This article incorporates text from the public domain Pfam and InterPro IPR012886
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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.
Formiminotransferase domain Provide feedback
No Pfam abstract.
Literature references
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Kohls D, Sulea T, Purisima EO, MacKenzie RE, Vrielink A; , Structure Fold Des 2000;8:35-46.: The crystal structure of the formiminotransferase domain of formiminotransferase-cyclodeaminase: implications for substrate channeling in a bifunctional enzyme. PUBMED:10673422 EPMC:10673422
External database links
| PANDIT: | PF02971 |
| Pseudofam: | PF02971 |
| SCOP: | 1qd1 |
| SYSTERS: | FTCD |
This tab holds annotation information from the InterPro database.
InterPro entry IPR013802
The formiminotransferase (FT) domain of formiminotransferase-cyclodeaminase (FTCD) forms a homodimer, with each protomer being comprised of two subdomains. The formiminotransferase domain has an N-terminal subdomain that is made up of a six-stranded mixed beta-pleated sheet and five alpha helices, which are arranged on the external surface of the beta sheet. This, in turn, faces the beta-sheet of the C-terminal subdomain to form a double beta-sheet layer. The two subdomains are separated by a short linker sequence, which is not thought to be any more flexible than the remainder of the molecule. The substrate is predicted to form a number of contacts with residues found in both the N-terminal and C-terminal subdomains [PUBMED:10673422]. In humans, deficiency of this enzyme results in a disease phenotype [PUBMED:12815595].
This entry represents the C-terminal subdomain of the formiminotransferase domain.
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | folic acid binding (GO:0005542) |
| transferase activity (GO:0016740) | |
| Biological process | metabolic process (GO:0008152) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Alignments
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| Seed (4) |
Full (394) |
Representative proteomes | NCBI (337) |
Meta (180) |
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| RP15 (62) |
RP35 (84) |
RP55 (104) |
RP75 (124) |
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| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
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| Seed (4) |
Full (394) |
Representative proteomes | NCBI (337) |
Meta (180) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (62) |
RP35 (84) |
RP55 (104) |
RP75 (124) |
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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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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: | Structural domain |
| Previous IDs: | formiminotr; |
| Type: | Domain |
| Author: | Griffiths-Jones SR |
| Number in seed: | 4 |
| Number in full: | 394 |
| Average length of the domain: | 124.30 aa |
| Average identity of full alignment: | 43 % |
| Average coverage of the sequence by the domain: | 33.96 % |
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: | 145 | ||||||||||||
| Family (HMM) version: | 9 | ||||||||||||
| 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 FTCD domain has been found. There are 6 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