Summary: Pyridoxine 5'-phosphate oxidase C-terminal dimerisation region
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Pyridoxine 5'-phosphate oxidase C-terminal dimerisation region Provide feedback
Pyridoxine 5'-phosphate oxidase (PNPOx) catalyses the terminal step in the biosynthesis of pyridoxal 5'-phosphate (PLP), a cofactor used by many enzymes involved in amino acid metabolism. The enzyme oxidises either the 4'-hydroxyl group of pyridoxine 5'-phosphate (PNP) or the 4'-primary amine of pyridoxamine 5'-phosphate (PMP) to an aldehyde. PNPOx is a homodimeric enzyme with one flavin mononucleotide (FMN) molecule non-covalently bound to each subunit. This domain represents one of the two dimerisation regions of the protein, located at the edge of the dimer interface, at the C-terminus, being the last three beta strands, S6, S7, and S8 along with the last three residues to the end. In P21159 S6 runs from residues 178-192, S7 from 200-206 and S8 from 211-215. the extended loop, of residues 167-177 may well be involved in the pocket formed between the two dimers that positions the FMN molecule [2].
Literature references
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di Salvo ML, Safo MK, Musayev FN, Bossa F, Schirch V; , Biochim Biophys Acta. 2003;1647:76-82.: Structure and mechanism of Escherichia coli pyridoxine 5'-phosphate oxidase. PUBMED:12686112 EPMC:12686112
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Safo MK, Mathews I, Musayev FN, di Salvo ML, Thiel DJ, Abraham DJ, Schirch V; , Structure. 2000;8:751-762.: X-ray structure of Escherichia coli pyridoxine 5'-phosphate oxidase complexed with FMN at 1.8 A resolution. PUBMED:10903950 EPMC:10903950
External database links
| PANDIT: | PF10590 |
| Pseudofam: | PF10590 |
| SYSTERS: | PNPOx_C |
This tab holds annotation information from the InterPro database.
InterPro entry IPR019576
Pyridoxamine 5'-phosphate oxidase (EC) is an enzyme that is involved in the de novo synthesis of pyridoxine (vitamin B6) and pyridoxal phosphate. It oxidizes pyridoxamine-5-P (PMP) and pyridoxine-5-P (PNP) to pyridoxal-5-P. The enzyme requires the presence of flavin mononucleotide (FMN) as a cofactor, although there is some evidence that coenzyme F420 may perform this role in some species [PUBMED:20675471].
The sequences of the enzyme from bacterial (genes pdxH or fprA) [PUBMED:1356963] and fungal (gene PDX3) [PUBMED:7896706] sources show that this protein has been highly conserved throughout evolution. PdxH is evolutionary related [PUBMED:8586283] to one of the enzymes in the phenazine biosynthesis protein pathway, phzD (also known as phzG).
This entry represents one of the two dimerisation regions of the protein, located at the edge of the dimer interface, at the C terminus, being the last three beta strands, S6, S7, and S8 along with the last three residues to the end. In SWISSPROT, S6 runs from residues 178-192, S7 from 200-206 and S8 from 211-215. the extended loop, of residues 167-177 may well be involved in the pocket formed between the two dimers that positions the FMN molecule [PUBMED:10903950].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | oxidoreductase activity, acting on the CH-NH2 group of donors (GO:0016638) |
| Biological process | oxidation-reduction process (GO:0055114) |
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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We make a range of alignments for each Pfam-A family. You can see a description of each above. You can view these alignments in various ways but please note that some types of alignment are never generated while others may not be available for all families, most commonly because the alignments are too large to handle.
| Seed (243) |
Full (2399) |
Representative proteomes | NCBI (1792) |
Meta (1629) |
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| RP15 (211) |
RP35 (437) |
RP55 (608) |
RP75 (735) |
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| PP/heatmap | 1 | |||||||
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1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
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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 (243) |
Full (2399) |
Representative proteomes | NCBI (1792) |
Meta (1629) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (211) |
RP35 (437) |
RP55 (608) |
RP75 (735) |
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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: | Pfam-B_685 (release 22.0), PROSITE_PS01064 |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Finn R, Coggill P |
| Number in seed: | 243 |
| Number in full: | 2399 |
| Average length of the domain: | 42.50 aa |
| Average identity of full alignment: | 54 % |
| Average coverage of the sequence by the domain: | 19.13 % |
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: | 42 | ||||||||||||
| Family (HMM) version: | 4 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Interactions
There is 1 interaction for this family. More...
Pyridox_oxidaseStructures
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 PNPOx_C domain has been found. There are 18 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