Summary: Dihydrodipicolinate reductase, C-terminus
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Dihydrodipicolinate reductase, C-terminus Provide feedback
Dihydrodipicolinate reductase (DapB) reduces the alpha,beta-unsaturated cyclic imine, dihydro-dipicolinate. This reaction is the second committed step in the biosynthesis of L-lysine and its precursor meso-diaminopimelate, which are critical for both protein and cell wall biosynthesis. The C-terminal domain of DapB has been proposed to be the substrate- binding domain.
Literature references
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Reddy SG, Scapin G, Blanchard JS; , Biochemistry 1996;35:13294-13302.: Interaction of pyridine nucleotide substrates with Escherichia coli dihydrodipicolinate reductase: thermodynamic and structural analysis of binary complexes. PUBMED:8873595 EPMC:8873595
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Scapin G, Reddy SG, Zheng R, Blanchard JS; , Biochemistry 1997;36:15081-15088.: Three-dimensional structure of Escherichia coli dihydrodipicolinate reductase in complex with NADH and the inhibitor 2,6-pyridinedicarboxylate. PUBMED:9398235 EPMC:9398235
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Scapin G, Blanchard JS, Sacchettini JC; , Biochemistry 1995;34:3502-3512.: Three-dimensional structure of Escherichia coli dihydrodipicolinate reductase. PUBMED:7893645 EPMC:7893645
External database links
| PANDIT: | PF05173 |
| PROSITE: | PDOC01000 |
| Pseudofam: | PF05173 |
| SCOP: | 1drw |
| SYSTERS: | DapB_C |
This tab holds annotation information from the InterPro database.
InterPro entry IPR022663
This entry represents the C-terminal region of Dihydrodipicolinate reductase.
Dihydrodipicolinate reductase catalyzes the second step in the biosynthesis of diaminopimelic acid and lysine, the NAD or NADP-dependent reduction of 2,3-dihydrodipicolinate into 2,3,4,5-tetrahydrodipicolinate [PUBMED:8873595, PUBMED:9398235, PUBMED:7893645].
In Escherichia coli and Mycobacterium tuberculosis, dihydrodipicolinate reductase has equal specificity for NADH and NADPH, however in Thermotoga maritima there it has a greater affinity for NADPH [PUBMED:18250105]. In addition, the enzyme is inhibited by high concentrations of its substrate, which consequently acts as a feedback control on the lysine biosynthesis pathway. In T. maritima, the enzyme also lacks N-terminal and C-terminal loops which are present in enzyme of the former two organisms.
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | dihydrodipicolinate reductase activity (GO:0008839) |
| Biological process | lysine biosynthetic process via diaminopimelate (GO:0009089) |
| 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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| Seed (189) |
Full (4343) |
Representative proteomes | NCBI (3039) |
Meta (2348) |
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| RP15 (327) |
RP35 (676) |
RP55 (865) |
RP75 (1018) |
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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 (189) |
Full (4343) |
Representative proteomes | NCBI (3039) |
Meta (2348) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (327) |
RP35 (676) |
RP55 (865) |
RP75 (1018) |
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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: | none |
| Type: | Domain |
| Author: | Studholme, DJ |
| Number in seed: | 189 |
| Number in full: | 4343 |
| Average length of the domain: | 134.50 aa |
| Average identity of full alignment: | 37 % |
| Average coverage of the sequence by the domain: | 51.96 % |
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: | 132 | ||||||||||||
| 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 DapB_C domain has been found. There are 36 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