Summary: Lyase
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This is the Wikipedia entry entitled "Fumarate lyase". More...
Fumarate lyase Edit Wikipedia article
| Lyase | |||||||||
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| Identifiers | |||||||||
| Symbol | Lyase_1 | ||||||||
| Pfam | PF00206 | ||||||||
| InterPro | IPR000362 | ||||||||
| PROSITE | PDOC00147 | ||||||||
| SCOP | 1jsw | ||||||||
| SUPERFAMILY | 1jsw | ||||||||
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A number of enzymes, belonging to the lyase class, for which fumarate is a substrate, have been shown to share a short conserved sequence around a methionine which is probably involved in the catalytic activity of this type of enzymes.[1][2] The following are examples of members of this family:
- 3-carboxymuconate lactonizing enzyme, EC 5.5.1.2 (3-carboxy-cis,cis-muconate cycloisomerase), an enzyme involved in aromatic acids catabolism.[3]
- Delta-crystallin shares around 90% sequence identity with arginosuccinate lyase, showing that it is an example of a 'hijacked' enzyme - accumulated mutations have, however, rendered the protein enzymatically inactive.
- Class I Fumarase enzyme, EC 4.2.1.2 (fumarate hydratase), which catalyzes the reversible hydration of fumarate to L-malate. Class I enzymes are thermolabile dimeric enzymes (as for example: Escherichia coli fumC).
- Arginosuccinase, EC 4.3.2.1 (argininosuccinate lyase), which catalyzes the formation of arginine and fumarate from argininosuccinate, the last step in the biosynthesis of arginine.
- Aspartate ammonia-lyase, EC 4.3.1.1 (aspartase), which catalyzes the reversible conversion of aspartate to fumarate and ammonia. This reaction is analogous to that catalyzed by fumarase, except that ammonia rather than water is involved in the trans-elimination reaction.
- class II Fumarase enzyme, EC 4.2.1.2, are thermostable and tetrameric and are found in prokaryotes (as for example: Escherichia coli fumA and fumB) as well as in eukaryotes. The sequence of the two classes of fumarases are not closely related.
- Adenylosuccinase, EC 4.3.2.2 (adenylosuccinate lyase),[4] which catalyzes the eighth step in the de novo biosynthesis of purines, the formation of 5'-phosphoribosyl-5-amino-4-imidazolecarboxamide and fumarate from 1-(5- phosphoribosyl)-4-(N-succino-carboxamide). That enzyme can also catalyze the formation of fumarate and AMP from adenylosuccinate.
[edit] References
- ^ Guest JR, Woods SA, Schwartzbach SD (1988). "Two biochemically distinct classes of fumarase in Escherichia coli". Biochim. Biophys. Acta 954 (1): 14â26. PMID 3282546.
- ^ Guest JR, Woods SA, Miles JS (1988). "Sequence homologies between arginosuccinase, aspartase and fumarase - a family of strycturally related enzymes". FEMS Microbiol. Lett. 51: 181â186.
- ^ Babbitt PC, Ransom SC, Williams SE, Woolridge EM, Landro JA, Kozarich JW (1992). "3-Carboxy-cis,cis-muconate lactonizing enzyme from Pseudomonas putida is homologous to the class II fumarase family: a new reaction in the evolution of a mechanistic motif". Biochemistry 31 (40): 9768â9776. doi:10.1021/bi00155a033. PMID 1390752.
- ^ Dixon JE, Zalkin H (1992). "De novo purine nucleotide biosynthesis". Prog. Nucleic Acid Res. Mol. Biol. 42: 259â287. PMID 1574589.
This article incorporates text from the public domain Pfam and InterPro IPR000362
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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.
Lyase Provide feedback
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External database links
| HOMSTRAD: | lyase_1 |
| PANDIT: | PF00206 |
| PRINTS: | PR00149 |
| PROSITE: | PDOC00147 |
| Pseudofam: | PF00206 |
| SCOP: | 1jsw |
| SYSTERS: | Lyase_1 |
Domain organisation
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Alignments
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| Seed (18) |
Full (16439) |
Representative proteomes | NCBI (12313) |
Meta (9223) |
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| RP15 (1294) |
RP35 (2586) |
RP55 (3471) |
RP75 (4142) |
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| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
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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 (18) |
Full (16439) |
Representative proteomes | NCBI (12313) |
Meta (9223) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (1294) |
RP35 (2586) |
RP55 (3471) |
RP75 (4142) |
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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: | Prosite |
| Previous IDs: | lyase_1; |
| Type: | Domain |
| Author: | Finn RD |
| Number in seed: | 18 |
| Number in full: | 16439 |
| Average length of the domain: | 297.30 aa |
| Average identity of full alignment: | 26 % |
| Average coverage of the sequence by the domain: | 66.01 % |
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: | 312 | ||||||||||||
| Family (HMM) version: | 15 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Interactions
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 Lyase_1 domain has been found. There are 204 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