Summary: Alanine racemase, C-terminal domain
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This is the Wikipedia entry entitled "Alanine racemase". More...
Alanine racemase Edit Wikipedia article
| alanine racemase | |||||||||
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| The 1.45Ã a crystal structure of alanine racemase from Pseudomonas aeruginosa, PDB 1rcq | |||||||||
| Identifiers | |||||||||
| EC number | 5.1.1.1 | ||||||||
| CAS number | 9024-06-0 | ||||||||
| Databases | |||||||||
| IntEnz | IntEnz view | ||||||||
| BRENDA | BRENDA entry | ||||||||
| ExPASy | NiceZyme view | ||||||||
| KEGG | KEGG entry | ||||||||
| MetaCyc | metabolic pathway | ||||||||
| PRIAM | profile | ||||||||
| PDB structures | RCSB PDB PDBe PDBsum | ||||||||
| Gene Ontology | AmiGO / EGO | ||||||||
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| Ala_racemase_N | |||||||||
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| the 1.45Ã a crystal structure of alanine racemase from a pathogenic bacterium, pseudomonas aeruginosa, contains both internal and external aldimine forms | |||||||||
| Identifiers | |||||||||
| Symbol | Ala_racemase_N | ||||||||
| Pfam | PF01168 | ||||||||
| Pfam clan | CL0036 | ||||||||
| InterPro | IPR001608 | ||||||||
| PROSITE | PDOC00332 | ||||||||
| SCOP | 1sft | ||||||||
| SUPERFAMILY | 1sft | ||||||||
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| Ala_racemase_C | |||||||||
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| Identifiers | |||||||||
| Symbol | Ala_racemase_C | ||||||||
| Pfam | PF00842 | ||||||||
| InterPro | IPR011079 | ||||||||
| PROSITE | PDOC00332 | ||||||||
| SCOP | 1sft | ||||||||
| SUPERFAMILY | 1sft | ||||||||
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In enzymology, an alanine racemase (EC 5.1.1.1) is an enzyme that catalyzes the chemical reaction
- L-alanine
D-alanine
Hence, this enzyme has one substrate, L-alanine, and one product, D-alanine.
This enzyme belongs to the family of isomerases, specifically those racemases and epimerases acting on amino acids and derivatives. The systematic name of this enzyme class is alanine racemase. This enzyme is also called L-alanine racemase. This enzyme participates in alanine and aspartate metabolism and D-alanine metabolism. It employs one cofactor, pyridoxal phosphate. At least two compounds, 3-Fluoro-D-alanine and D-Cycloserine are known to inhibit this enzyme.
[edit] Structural studies
The structure of alanine racemase from Bacillus stearothermophilus (Geobacillus stearothermophilus) was determined by X-ray crystallography to a resolution of 1.9 A.[1] The alanine racemase monomer is composed of two domains, an eight-stranded alpha/beta barrel at the N terminus, and a C-terminal domain essentially composed of beta-strand. The N-terminal domain is also found in the PROSC (proline synthetase co-transcribed bacterial homolog) family of proteins, which are not known to have alanine racemase activity. The pyridoxal 5'-phosphate (PLP) cofactor lies in and above the mouth of the alpha/beta barrel and is covalently linked via an aldimine linkage to a lysine residue, which is at the C terminus of the first beta-strand of the alpha/beta barrel.
[edit] References
- ^ Shaw JP, Petsko GA, Ringe D (February 1997). "Determination of the structure of alanine racemase from Bacillus stearothermophilus at 1.9-A resolution". Biochemistry 36 (6): 1329â42. doi:10.1021/bi961856c. PMID 9063881.
[edit] Further reading
- MARR AG, WILSON PW (1954). "The alanine racemase of Brucella abortus". Arch. Biochem. Biophys. 49 (2): 424â33. doi:10.1016/0003-9861(54)90211-8. PMID 13159289.
- Wood WA (1955). "Amino acid racemases". Methods Enzymol. 2: 212â217. doi:10.1016/S0076-6879(55)02189-7.
- WOOD WA, GUNSALUS IC (1951). "D-Alanine formation; a racemase in Streptococcus faecalis". J. Biol. Chem. 190 (1): 403â16. PMID 14841188.
This article incorporates text from the public domain Pfam and InterPro IPR011079
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Alanine racemase, C-terminal domain Provide feedback
No Pfam abstract.
Literature references
-
Shaw JP, Petsko GA, Ringe D; , Biochemistry 1997;36:1329-1342.: Determination of the structure of alanine racemase from Bacillus stearothermophilus at 1.9-A resolution. PUBMED:9063881 EPMC:9063881
External database links
| PANDIT: | PF00842 |
| PROSITE: | PDOC00332 |
| Pseudofam: | PF00842 |
| SCOP: | 1sft |
| SYSTERS: | Ala_racemase_C |
This tab holds annotation information from the InterPro database.
InterPro entry IPR011079
Alanine racemase (EC) plays a role in providing the D-alanine required for cell wall biosynthesis by isomerising L-alanine to D-alanine.
The molecular structure of alanine racemase from Bacillus stearothermophilus (Geobacillus stearothermophilus) was determined by X-ray crystallography to a resolution of 1.9 A [PUBMED:9063881]. The alanine racemase monomer is composed of two domains, an eight-stranded alpha/beta barrel at the N terminus, and a C-terminal domain essentially composed of beta-strand. This entry represents the C-terminal domain.
Domain organisation
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Alignments
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| Seed (121) |
Full (5638) |
Representative proteomes | NCBI (3928) |
Meta (1372) |
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| RP15 (358) |
RP35 (686) |
RP55 (893) |
RP75 (1060) |
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| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
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| Seed (121) |
Full (5638) |
Representative proteomes | NCBI (3928) |
Meta (1372) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (358) |
RP35 (686) |
RP55 (893) |
RP75 (1060) |
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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
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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.
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Curation and family details
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Curation
| Seed source: | Pfam-B_1496 (release 2.1) |
| Previous IDs: | Ala_racemase; |
| Type: | Domain |
| Author: | Bateman A, Finn RD |
| Number in seed: | 121 |
| Number in full: | 5638 |
| Average length of the domain: | 125.90 aa |
| Average identity of full alignment: | 36 % |
| Average coverage of the sequence by the domain: | 32.58 % |
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: | 129 | ||||||||||||
| Family (HMM) version: | 16 | ||||||||||||
| 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 Ala_racemase_C domain has been found. There are 90 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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D-alanine
Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence