Summary: PI3-kinase family, ras-binding domain
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PI3-kinase family, ras-binding domain
Certain members of the PI3K family possess Ras-binding domains in their N-termini. These regions show some similarity (although not highly significant similarity) to Ras-binding PF00788 domains (unpublished observation).
Literature references
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Rodriguez-Viciana P, Warne PH, Vanhaesebroeck B, Waterfield MD, Downward J; , EMBO J 1996;15:2442-2451.: Activation of phosphoinositide 3-kinase by interaction with Ras and by point mutation. PUBMED:8665852
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Kodaki T, Woscholski R, Hallberg B, Rodriguez-Viciana P, Downward J, Parker PJ; , Curr Biol 1994;4:798-806.: The activation of phosphatidylinositol 3-kinase by Ras. PUBMED:7820549
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Rodriguez-Viciana P, Warne PH, Dhand R, Vanhaesebroeck B, Gout I, Fry MJ, Waterfield MD, Downward J; , Nature 1994;370:527-532.: Phosphatidylinositol-3-OH kinase as a direct target of Ras. PUBMED:8052307
Clan
This family is a member of clan Ubiquitin (CL0072), which has a total of 36 members.
External database links
| PANDIT: | PF00794 |
| Pseudofam: | PF00794 |
| SCOP: | 1qmm |
| SMART: | PI3K_rbd |
| SYSTERS: | PI3K_rbd |
This tab holds annotation information from the InterPro database.
InterPro entry IPR000341
Phosphatidylinositol 3-kinase (PI3K) (EC) is an enzyme that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring. A subset of PI3Ks has the capacity to bind and be activated by the GTP-bound small GTPase p21Ras (Ras). PI3Ks are recognised as one of the principal effectors of Ras signalling to the cell-cycle control machinery.
In the structure of the Ras-PI3K gamma complex, contacts between the two molecules are made primarily via the so-called switch I region of Ras and the PI3K RBD. The RBD fold comprises a five-stranded mixed beta-sheet, flanked by two alpha-helices. Interaction between Ras and the PI3K RBD is primarily polar in character and, as characterised by kinetic measurements, is reversible and transient [PUBMED:12151228].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Cellular component | phosphatidylinositol 3-kinase complex (GO:0005942) |
| Molecular function | 1-phosphatidylinositol-3-kinase activity (GO:0016303) |
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 Ubiquitin (CL0072), which contains the following 36 members:
APG12 Atg8 Bac_multiUb Blt1 Caps_synth_GfcC CIDE-N DUF1315 DUF2407 DWNN FERM_N Lambda_tail_I NQRA_SLBB PB1 PI3K_rbd Plug Prok_Ub RA Rad60-SLD Rad60-SLD_2 RBD SLBB Telomere_Sde2 TGS ThiS ThiS-like TmoB TUG Ub-Mut7C Ub-RnfH ubiquitin UBX Ufm1 UN_NPL4 Urm1 YchF-GTPase_C YukDAlignments
There are various ways to view or download the sequence alignments that we store. You can use a sequence viewer to look at either the seed or full alignment for the family, or you can look at a plain text version of the sequence in a variety of different formats. More...
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Very large alignments can often cause problems for the formatting tool above. If you find that downloading or viewing a large alignment is problematic, you can also download a gzip-compressed, Stockholm-format file containing the seed or full alignment for this family.
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
The main seed and full alignments are generated using sequences from the UniProt sequence database. However, we also generate alignments using sequences from the NCBI sequence database and the "metaseq" metagenomics dataset.
You can view alignments from these two additional datasets using the form above, or you can download alignments of NCBI or metagenomics sequences, as gzip-compressed files.
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. 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 or full alignments.
Note: You can also download the data files for the seed, full, NCBI or metagenomics trees.
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: | Alignment kindly provided by SMART |
| Previous IDs: | none |
| Type: | Family |
| Author: | SMART |
| Number in seed: | 12 |
| Number in full: | 272 |
| Average length of the domain: | 105.60 aa |
| Average identity of full alignment: | 23 % |
| Average coverage of the sequence by the domain: | 9.11 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 15929002 -E 1000 --cpu 4 HMM pfamseq
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| Model details: |
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| Model length: | 107 | ||||||||||||
| Family (HMM) version: | 13 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Colour assignments
Archea
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Eukaryota
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Bacteria
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Other sequences
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Viruses
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Unclassified
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Viroids
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Unclassified sequence
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This visualisation provides a simple graphical representation of the distribution of this family across species. You can find the original interactive tree in the adjacent tab if you need to select sub-trees and view sequence alignments. More...
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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 PI3K_rbd domain has been found. There are 34 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