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16  structures 1279  species 0  interactions 18500  sequences 313  architectures

Family: RasGAP (PF00616)

Summary: GTPase-activator protein for Ras-like GTPase

Pfam includes annotations and additional family information from a range of different sources. These sources can be accessed via the tabs below.

This is the Wikipedia entry entitled "GTPase-activator protein for Ras-like GTPase". More...

GTPase-activator protein for Ras-like GTPase Edit Wikipedia article

GTPase-activator protein for Ras-like GTPase
Identifiers
SymbolRasGAP
PfamPF00616
InterProIPR001936
SMARTRasGAP
SCOP21wer / SCOPe / SUPFAM

GTPase-activator protein for Ras-like GTPase is a family of evolutionarily related proteins.

Ras proteins are membrane-associated molecular switches that bind GTP and GDP and slowly hydrolyze GTP to GDP.[1] This intrinsic GTPase activity of ras is stimulated by a family of proteins collectively known as 'GAP' or GTPase-activating proteins.[2][3] As it is the GTP bound form of ras which is active, these proteins are said to be down-regulators of ras.

The Ras GTPase-activating proteins are quite large (from 765 residues for sar1 to 3079 residues for IRA2) but share only a limited (about 250 residues) region of sequence similarity, referred to as the 'catalytic domain' or rasGAP domain.

Note: There are distinctly different GAPs for the rap and rho/rac subfamilies of ras-like proteins (reviewed in reference[4]) that do not share sequence similarity with ras GAPs.


Examples

Human genes encoding proteins containing this domain include:

References

  1. ^ McCormick F, Bourne HR, Sanders DA (1991). "The GTPase superfamily: conserved structure and molecular mechanism". Nature. 349 (6305): 117–127. PMID 1898771.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^ Wang Y, Riggs M, Rodgers L, Wigler M, Boguski M (1991). "sar1, a gene from Schizosaccharomyces pombe encoding a protein that regulates ras1". Cell Regul. 2 (6): 453–465. PMID 1883874.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^ Maruta H, Burgess AW (1994). "Regulation of the Ras signalling network". Bioessays. 16 (7): 489–496. PMID 7945277.
  4. ^ McCormick F, Boguski MS (1993). "Proteins regulating Ras and its relatives". Nature. 366 (6456): 643–654. PMID 8259209.
This article incorporates text from the public domain Pfam and InterPro: IPR001936

This page is based on a Wikipedia article. The text is available under the Creative Commons Attribution/Share-Alike License.

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.

GTPase-activator protein for Ras-like GTPase Provide feedback

All alpha-helical domain that accelerates the GTPase activity of Ras, thereby "switching" it into an "off" position.

Literature references

  1. Scheffzek K, Lautwein A, Kabsch W, Ahmadian MR, Wittinghofer A; , Nature 1996;384:591-596.: Crystal structure of the GTPase-activating domain of human p120GAP and implications for the interaction with Ras. PUBMED:8955277 EPMC:8955277

  2. Wittinghofer A, Scheffzek K, Ahmadian MR; , FEBS Lett 1997;410:63-67.: The interaction of Ras with GTPase-activating proteins. PUBMED:9247124 EPMC:9247124

  3. Xu GF, O'Connell P, Viskochil D, Cawthon R, Robertson M, Culver M, Dunn D, Stevens J, Gesteland R, White R, et al; , Cell 1990;62:599-608.: The neurofibromatosis type 1 gene encodes a protein related to GAP. PUBMED:2116237 EPMC:2116237


External database links

This tab holds annotation information from the InterPro database.

InterPro entry IPR001936

This entry represents a conserved domain in the RasGAPs (Ras GTPase-activating proteins). This domain is also known as the RasGAP domain.

Ras proteins are membrane-associated molecular switches that bind GTP and GDP and slowly hydrolyze GTP to GDP [ PUBMED:1898771 ]. This intrinsic GTPase activity of Ras is regulated by a family of proteins collectively known as 'GAP' or GTPase-activating proteins [ PUBMED:1883874 , PUBMED:7945277 ]. RasGAP proteins are usually quite large (from 765 residues for sar1 to 3079 residues for IRA2) but share only a limited (about 250 residues) region of sequence similarity, referred to as the 'catalytic domain' or RasGAP domain. The most conserved region within this domain contains a 15 residue motif which seems to be characteristic of this family of proteins [ PUBMED:1883874 ].

Note: There are distinctly different GAPs for the rap and rho/rac subfamilies of Ras-like proteins (reviewed in reference [ PUBMED:8259209 ]) that do not share sequence similarity with ras GAPs.

Gene Ontology

The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.

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 GAP (CL0409), which has the following description:

Superfamily contains BCR-homology GTPase activation domain (BH-domain) and p120GAP domain-like, including the GAP related domain of neurofibromin, families.

The clan contains the following 3 members:

Msb1-Mug8_dom RasGAP RhoGAP

Alignments

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...

View options

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
(50)
Full
(18500)
Representative proteomes UniProt
(27567)
RP15
(2199)
RP35
(5549)
RP55
(13216)
RP75
(18580)
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HTML View             
PP/heatmap 1            

1Cannot generate PP/Heatmap alignments for seeds; no PP data available

Key: ✓ available, x not generated, not available.

Format an alignment

  Seed
(50)
Full
(18500)
Representative proteomes UniProt
(27567)
RP15
(2199)
RP35
(5549)
RP55
(13216)
RP75
(18580)
Alignment:
Format:
Order:
Sequence:
Gaps:
Download/view:

Download options

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
(50)
Full
(18500)
Representative proteomes UniProt
(27567)
RP15
(2199)
RP35
(5549)
RP55
(13216)
RP75
(18580)
Raw Stockholm Download   Download   Download   Download   Download   Download   Download  
Gzipped Download   Download   Download   Download   Download   Download   Download  

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 View help on the curation process

Seed source: SMART
Previous IDs: none
Type: Family
Sequence Ontology: SO:0100021
Author: Ponting CP , Schultz J, Bork P
Number in seed: 50
Number in full: 18500
Average length of the domain: 127.7 aa
Average identity of full alignment: 23 %
Average coverage of the sequence by the domain: 13.41 %

HMM information View help on HMM parameters

HMM build commands:
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 61295632 -E 1000 --cpu 4 HMM pfamseq
Model details:
Parameter Sequence Domain
Gathering cut-off 28.3 28.3
Trusted cut-off 28.4 28.3
Noise cut-off 28.0 28.2
Model length: 208
Family (HMM) version: 22
Download: download the raw HMM for this family

Species distribution

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Viroids Viroids Unclassified sequence Unclassified sequence

Selections

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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. More...

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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 RasGAP domain has been found. There are 16 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.

Protein Predicted structure External Information
A0A044S7R6 View 3D Structure Click here
A0A044SH27 View 3D Structure Click here
A0A044SQF3 View 3D Structure Click here
A0A077Z4Q8 View 3D Structure Click here
A0A077Z7J6 View 3D Structure Click here
A0A077ZBJ1 View 3D Structure Click here
A0A0A2V1E0 View 3D Structure Click here
A0A0D2E3L4 View 3D Structure Click here
A0A0D2EKW8 View 3D Structure Click here
A0A0D2G787 View 3D Structure Click here
A0A0G2JTA7 View 3D Structure Click here
A0A0G2KFQ1 View 3D Structure Click here
A0A0H5S004 View 3D Structure Click here
A0A0K0E8N7 View 3D Structure Click here
A0A0K0EAI7 View 3D Structure Click here
A0A0K0EHZ2 View 3D Structure Click here
A0A0N4U6C5 View 3D Structure Click here
A0A0N4UCE7 View 3D Structure Click here
A0A0N4UEC3 View 3D Structure Click here
A0A0R4IE78 View 3D Structure Click here
A0A175VSC9 View 3D Structure Click here
A0A175VUG7 View 3D Structure Click here
A0A175WB12 View 3D Structure Click here
A0A175WB59 View 3D Structure Click here
A0A1C1CM41 View 3D Structure Click here
A0A1C1CWK0 View 3D Structure Click here
A0A1C1CX94 View 3D Structure Click here
A0A1D8PFE8 View 3D Structure Click here
A0A286YAN7 View 3D Structure Click here
A0A2R8Q0N0 View 3D Structure Click here
A0A2R8Q516 View 3D Structure Click here
A0A2R8QCJ5 View 3D Structure Click here
A0A3P7DMX7 View 3D Structure Click here
A0A3P7DS25 View 3D Structure Click here
A0A3P7FEU5 View 3D Structure Click here
A0A3P7GDR8 View 3D Structure Click here
A0A3Q0KRW4 View 3D Structure Click here
A0A5K4EPU0 View 3D Structure Click here
A0A5K4EQF8 View 3D Structure Click here
A0A5K4EV20 View 3D Structure Click here