Summary: IMP dehydrogenase / GMP reductase domain
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This is the Wikipedia entry entitled "IMPDH/GMPR family". More...
IMPDH/GMPR family Edit Wikipedia article
IMP dehydrogenase / GMP reductase domain | |||||||||
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![]() binary complex of human type-i inosine monophosphate dehydrogenase with 6-cl-imp | |||||||||
Identifiers | |||||||||
Symbol | IMPDH | ||||||||
Pfam | PF00478 | ||||||||
Pfam clan | CL0036 | ||||||||
InterPro | IPR001093 | ||||||||
PROSITE | PDOC00391 | ||||||||
SCOP2 | 1ak5 / SCOPe / SUPFAM | ||||||||
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In molecular biology, the IMPDH/GMPR family of enzymes includes IMP dehydrogenase and GMP reductase. These enzymes are involved in purine metabolism. These enzymes adopt a TIM barrel structure.[1][2]
References
- ^ Whitby FG, Luecke H, Kuhn P, Somoza JR, Huete-Perez JA, Phillips JD; et al. (1997). "Crystal structure of Tritrichomonas foetus inosine-5'-monophosphate dehydrogenase and the enzyme-product complex". Biochemistry. 36 (35): 10666–74. doi:10.1021/bi9708850. PMID 9271497.
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: Explicit use of et al. in:|author=
(help)CS1 maint: multiple names: authors list (link) - ^ Zhang R, Evans G, Rotella FJ, Westbrook EM, Beno D, Huberman E; et al. (1999). "Characteristics and crystal structure of bacterial inosine-5'-monophosphate dehydrogenase". Biochemistry. 38 (15): 4691–700. doi:10.1021/bi982858v. PMID 10200156.
{{cite journal}}
: Explicit use of et al. in:|author=
(help)CS1 maint: multiple names: authors list (link)
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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.
IMP dehydrogenase / GMP reductase domain Provide feedback
This family is involved in biosynthesis of guanosine nucleotide. Members of this family contain a TIM barrel structure. In the inosine monophosphate dehydrogenases 2 CBS domains PF00571 are inserted in the TIM barrel [2]. This family is a member of the common phosphate binding site TIM barrel family.
Literature references
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Whitby FG, Luecke H, Kuhn P, Somoza JR, Huete-Perez JA, Phillips JD, Hill CP, Fletterick RJ, Wang CC; , Biochemistry 1997;36:10666-10674.: Crystal structure of Tritrichomonas foetus inosine-5'-monophosphate dehydrogenase and the enzyme-product complex. PUBMED:9271497 EPMC:9271497
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Zhang R, Evans G, Rotella FJ, Westbrook EM, Beno D, Huberman E, Joachimiak A, Collart FR; , Biochemistry 1999;38:4691-4700.: Characteristics and crystal structure of bacterial inosine-5'-monophosphate dehydrogenase. PUBMED:10200156 EPMC:10200156
Internal database links
SCOOP: | Aldolase B12-binding CBS DeoC DHO_dh DUF561 Dus FMN_dh G3P_antiterm Glu_syn_central Glu_synthase His_biosynth IGPS NanE NMO PcrB PEP_mutase PK QRPTase_C QRPTase_N ThiG TMP-TENI Trp_syntA |
Similarity to PfamA using HHSearch: | CBS CBS His_biosynth FMN_dh Glu_synthase NMO NanE |
External database links
HOMSTRAD: | IMPDH |
PROSITE: | PDOC00391 |
SCOP: | 1ak5 |
This tab holds annotation information from the InterPro database.
InterPro entry IPR001093
Synonym(s): Inosine-5'-monophosphate dehydrogenase, Inosinic acid dehydrogenase; Synonym(s): Guanosine 5'-monophosphate oxidoreductase
This entry contains two related enzymes: IMP dehydrogenase and GMP reductase. These enzymes adopt a TIM barrel structure.
IMP dehydrogenase (
EC
) (IMPDH) catalyses the rate-limiting reaction of
de novo
GTP biosynthesis, the NAD-dependent reduction of IMP into XMP [
PUBMED:2902093
].
GMP reductase (
EC
) catalyses the irreversible and NADPH-dependent reductive deamination of GMP into IMP [
PUBMED:2904262
].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
Molecular function | catalytic activity (GO:0003824) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Pfam Clan
This family is a member of clan TIM_barrel (CL0036), which has the following description:
This large superfamily of TIM barrel enzymes all contain a common phosphate binding site. The phosphate is found in a variety of cofactors and ligands such as FMN [1,2].
The clan contains the following 61 members:
4HFCP_synth Ala_racemase_N ALAD Aldolase AP_endonuc_2 BtpA CdhD ComA CutC DAHP_synth_1 DAHP_synth_2 DeoC DHDPS DHO_dh DHquinase_I DUF2090 DUF4862 DUF561 DUF692 DUF993 Dus F_bP_aldolase FMN_dh G3P_antiterm GatZ_KbaZ-like Glu_syn_central Glu_synthase His_biosynth HMGL-like IGPS IMPDH KDGP_aldolase Lys-AminoMut_A MtrH NanE NAPRTase NeuB NMO OAM_alpha OMPdecase Orn_Arg_deC_N Oxidored_FMN PcrB PdxJ PRAI PRMT5_TIM Pterin_bind QRPTase_C Radical_SAM Radical_SAM_2 RhaA Ribul_P_3_epim SOR_SNZ TAL_FSA ThiC_Rad_SAM ThiG TIM TMP-TENI Trp_syntA UvdE UxuAAlignments
We store a range of different sequence alignments for families. As well as the seed alignment from which the family is built, we provide the full alignment, generated by searching the sequence database (reference proteomes) using the family HMM. We also generate alignments using four representative proteomes (RP) sets and the UniProtKB sequence database. More...
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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 (439) |
Full (16983) |
Representative proteomes | UniProt (67467) |
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RP15 (2201) |
RP35 (7573) |
RP55 (16313) |
RP75 (27152) |
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Jalview | |||||||
HTML | |||||||
PP/heatmap | 1 |
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
available,
not generated,
— not available.
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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 (439) |
Full (16983) |
Representative proteomes | UniProt (67467) |
||||
---|---|---|---|---|---|---|---|
RP15 (2201) |
RP35 (7573) |
RP55 (16313) |
RP75 (27152) |
||||
Raw Stockholm | |||||||
Gzipped |
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
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 |
Sequence Ontology: | SO:0000417 |
Author: |
Finn RD |
Number in seed: | 439 |
Number in full: | 16983 |
Average length of the domain: | 407.1 aa |
Average identity of full alignment: | 37 % |
Average coverage of the sequence by the domain: | 91.93 % |
HMM information
HMM build commands: |
build method: hmmbuild -o /dev/null --hand HMM SEED
search method: hmmsearch -Z 61295632 -E 1000 --cpu 4 HMM pfamseq
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Model details: |
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Model length: | 345 | ||||||||||||
Family (HMM) version: | 28 | ||||||||||||
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 IMPDH domain has been found. There are 425 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 sequence.
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AlphaFold Structure Predictions
The list of proteins below match this family and have AlphaFold predicted structures. Click on the protein accession to view the predicted structure.