IPTig-like, plexins, transcription factors |
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| SMART accession number: | SM00429 |
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| Description: | |
| Interpro abstract (IPR002909): | This family consists of a domain that has an immunoglobulin like fold. These domains are found in cell surface receptors such as Met and Ron as well as in intracellular transcription factors where it is involved in DNA binding. The Ron tyrosine kinase receptor shares with the members of its subfamily (Met and Sea) a unique functional feature: the control of cell dissociation, motility, and invasion of extracellular matrices (scattering) [(PUBMED:8816464)]. |
| GO function: | protein binding (GO:0005515) |
| Family alignment: |
There are 3673 IPT domains in 1384 proteins in SMART's nrdb database.
Click on the following links for more information.
- Evolution (species in which this domain is found)
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Go to specific node: Anopheles gambiae, Caenorhabditis elegans, Drosophila melanogaster, Homo sapiens, Mus musculus, Rattus norvegicus, Saccharomyces cerevisiae, Takifugu rubripes - Literature (relevant references for this domain)
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Primary literature is listed below; Automatically-derived, secondary literature is also avaliable.
- Aravind L, Koonin EV
- Gleaning non-trivial structural, functional and evolutionary information about proteins by iterative database searches.
- J Mol Biol. 1999; 287: 1023-40
- Display abstract
Using a number of diverse protein families as test cases, we investigate the ability of the recently developed iterative sequence database search method, PSI-BLAST, to identify subtle relationships between proteins that originally have been deemed detectable only at the level of structure-structure comparison. We show that PSI-BLAST can detect many, though not all, of such relationships, but the success critically depends on the optimal choice of the query sequence used to initiate the search. Generally, there is a correlation between the diversity of the sequences detected in the first pass of database screening and the ability of a given query to detect subtle relationships in subsequent iterations. Accordingly, a thorough analysis of protein superfamilies at the sequence level is necessary in order to maximize the chances of gleaning non-trivial structural and functional inferences, as opposed to a single search, initiated, for example, with the sequence of a protein whose structure is available. This strategy is illustrated by several findings, each of which involves an unexpected structural prediction: (i) a number of previously undetected proteins with the HSP70-actin fold are identified, including a highly conserved and nearly ubiquitous family of metal-dependent proteases (typified by bacterial O-sialoglycoprotease) that represent an adaptation of this fold to a new type of enzymatic activity; (ii) we show that, contrary to the previous conclusions, ATP-dependent and NAD-dependent DNA ligases are confidently predicted to possess the same fold; (iii) the C-terminal domain of 3-phosphoglycerate dehydrogenase, which binds serine and is involved in allosteric regulation of the enzyme activity, is shown to typify a new superfamily of ligand-binding, regulatory domains found primarily in enzymes and regulators of amino acid and purine metabolism; (iv) the immunoglobulin-like DNA-binding domain previously identified in the structures of transcription factors NFkappaB and NFAT is shown to be a member of a distinct superfamily of intracellular and extracellular domains with the immunoglobulin fold; and (v) the Rag-2 subunit of the V-D-J recombinase is shown to contain a kelch-type beta-propeller domain which rules out its evolutionary relationship with bacterial transposases.
- Metabolism (metabolic pathways involving proteins which contain this domain)
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% proteins involved KEGG pathway ID Description 14.26 map04360 Axon guidance 8.56 map04662 B cell receptor signaling pathway 8.56 map04660 T cell receptor signaling pathway 5.87 map04370 VEGF signaling pathway 5.87 map04310 Wnt signaling pathway 5.87 map04650 Natural killer cell mediated cytotoxicity 5.70 map05120 Epithelial cell signaling in Helicobacter pylori infection 4.19 map05222 Small cell lung cancer 4.19 map04620 Toll-like receptor signaling pathway 4.19 map05212 Pancreatic cancer 4.19 map04210 Apoptosis 4.19 map05220 Chronic myeloid leukemia 4.19 map04920 Adipocytokine signaling pathway 4.19 map05215 Prostate cancer 4.19 map05221 Acute myeloid leukemia 2.68 map04010 MAPK signaling pathway 1.51 map04520 Adherens junction 1.51 map04060 Cytokine-cytokine receptor interaction 1.51 map05210 Colorectal cancer 1.51 map04510 Focal adhesion 1.51 map05211 Renal cell carcinoma 1.51 map05218 Melanoma This information is based on mapping of SMART genomic protein database to KEGG orthologous groups. Percentage points are related to the number of proteins with IPT domain which could be assigned to a KEGG orthologous group, and not all proteins containing IPT domain. Please note that proteins can be included in multiple pathways, ie. the numbers above will not always add up to 100%.
- Structure (3D structures containing this domain)
3D Structures of IPT domains in PDB
PDB code Main view Title 1a02 
Structure of the dna binding domains of nfat, fos and jun bound to dna 1a3q 
Human nf-kappa-b p52 bound to dna 1bfs 
Structure of nf-kb p50 homodimer bound to a kb site 1bft 
Structure of nf-kb p50 homodimer bound to a kb site 1gji 
Crystal structure of c-rel bound to dna 1ikn 
Ikappabalpha/nf-kappab complex 1imh 
Tonebp/dna complex 1k3z 
X-ray crystal structure of the ikbb/nf-kb p65 homodimer complex 1le5 
Crystal structure of a nf-kb heterodimer bound to an ifnb-kb 1le9 
Crystal structure of a nf-kb heterodimer bound to the ig/hiv-kb siti 1lei 
The kb dna sequence from the hlv-ltr functions as an allosteric regulator of hiv transcription 1my5 
Nf-kappab p65 subunit dimerization domain homodimer 1my7 
Nf-kappab p65 subunit dimerization domain homodimer n202r mutation 1nfi 
I-kappa-b-alpha/nf-kappa-b complex 1nfk 
Structure of the nuclear factor kappa-b (nf-kb) p50 homodimer 1ooa 
Crystal structure of nf-kb(p50)2 complexed to a high- affinity rna aptamer 1owr 
Crystal structure of human nfat1 bound monomerically to dna 1oy3 
Crystal structure of an ikbbeta/nf-kb p65 homodimer complex 1p7h 
Structure of nfat1 bound as a dimer to the hiv-1 ltr kb element 1pzu 
An asymmetric nfat1-rhr homodimer on a pseudo-palindromic, kappa-b site 1qho 
Five-domain alpha-amylase from bacillus stearothermophilus, maltose/acarbose complex 1qhp 
Five-domain alpha-amylase from bacillus stearothermophilus, maltose complex 1ram 
A novel dna recognition mode by nf-kb p65 homodimer 1s9k 
Crystal structure of human nfat1 and fos-jun on the il-2 arre1 site 1svc 
Nfkb p50 homodimer bound to dna 1u36 
Crystal stucture of wlac mutant of dimerisation domain of nf-kb p50 transcription factor 1u3j 
Crystal stucture of mlav mutant of dimerisation domain of nf-kb p50 transcription factor 1u3y 
Crystal stucture of ilac mutant of dimerisation domain of nf-kb p50 transcription factor 1u3z 
Crystal stucture of mlac mutant of dimerisation domain of nf-kb p50 transcription factor 1u41 
Crystal stucture of ylgv mutant of dimerisation domain of nf-kb p50 transcription factor 1u42 
Crystal stucture of mlam mutant of dimerisation domain of nf-kb p50 transcription factor 1vkx 
Crystal structure of the nfkb p50/p65 heterodimer complexed to the immunoglobulin kb dna 1zk9 
Nf-kb relb forms an intertwined homodimer 1zka 
Nf-kb relb forms an intertwined homodimer, y300s mutant 2as5 
Structure of the dna binding domains of nfat and foxp2 bound specifically to dna. 2i9t 
Structure of nf-kb p65-p50 heterodimer bound to prdii element of b-interferon promoter 2o61 
Crystal structure of nfkb, irf7, irf3 bound to the interferon-b enhancer 2o93 
Crystal structure of nfat bound to the hiv-1 ltr tandem kappab enhancer element 2ram 
A novel dna recognition mode by nf-kb p65 homodimer 2uzx 
Structure of the human receptor tyrosine kinase met in complex with the listeria monocytogenes invasion protein inlb: crystal form i 2uzy 
Structure of the human receptor tyrosine kinase met in complex with the listeria monocytogenes invasion protein inlb: low resolution, crystal form ii 2v2t 
X-ray structure of a nf-kb p50-relb-dna complex 2yrp 
Solution structure of the tig domain from human nuclear factor of activated t-cells, cytoplasmic 4 3do7 
X-ray structure of a nf-kb p52/relb/dna complex 3gut 
Crystal structure of a higher-order complex of p50:rela bound to the hiv-1 ltr - Links (links to other resources describing this domain)
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INTERPRO IPR002909
