Summary: Phosphotyrosine-binding domain
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Phosphotyrosine-binding domain Edit Wikipedia article
| Phosphotyrosine-binding domain | |||||||||
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| Structure of the PTB domain of tensin1.[1] | |||||||||
| Identifiers | |||||||||
| Symbol | PTB | ||||||||
| Pfam | PF08416 | ||||||||
| InterPro | IPR013625 | ||||||||
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| PTB domain (IRS-1 type) | |||||||||
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| irs-1 ptb domain complexed with a il-4 receptor phosphopeptide, nmr, minimized average structure | |||||||||
| Identifiers | |||||||||
| Symbol | IRS | ||||||||
| Pfam | PF02174 | ||||||||
| InterPro | IPR002404 | ||||||||
| SMART | PTBI | ||||||||
| SCOP | 1cli | ||||||||
| SUPERFAMILY | 1cli | ||||||||
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In molecular biology, Phosphotyrosine-binding domains are protein domains which bind to phosphotyrosine.
The phosphotyrosine-binding domain (PTB, also phosphotyrosine-interaction or PI domain) in the protein tensin tends to be found at the C-terminus. Tensin is a multi-domain protein that binds to actin filaments and functions as a focal-adhesion molecule (focal adhesions are regions of plasma membrane through which cells attach to the extracellular matrix). Human tensin has actin-binding sites, an SH2 (Pfam PF00017) domain and a region similar to the tumour suppressor PTEN.[2] The PTB domain interacts with the cytoplasmic tails of beta integrin by binding to an NPXY motif.[3]
The phosphotyrosine-binding domain of insulin receptor substrate-1 is not related to the phosphotyrosine-binding domain of tensin. Insulin receptor substrate-1 proteins contain both a pleckstrin homology domain and a phosphotyrosine binding (PTB) domain. The PTB domains facilitate interaction with the activated tyrosine-phosphorylated insulin receptor. The PTB domain is situated towards the N terminus. Two arginines in this domain are responsible for hydrogen bonding phosphotyrosine residue]s on an Ac-LYASSNPApY-NH2 peptide in the juxtamembrane region of the insulin receptor. Further interactions via `bridged' water molecules are coordinated by residues an Asn and a Ser residue .[4] The PTB domain has a compact, 7-stranded beta-sandwich structure, capped by a C-terminal helix. The substrate peptide fits into an L-shaped surface cleft formed from the C-terminal helix and strands 5 and 6.[5]
[edit] Human proteins containing these domains
APBA1; APBA2; APBA3; EPS8; EPS8L1; EPS8L2; EPS8L3; TENC1; TNS; TNS1; TNS3; TNS4; DOK1; DOK2; DOK3; DOK4; DOK5; DOK6; DOK7; FRS2; FRS3; IRS1; IRS2; IRS4; TLN1; TLN2
[edit] References
- ^ McCleverty CJ, Lin DC, Liddington RC (June 2007). "Structure of the PTB domain of tensin1 and a model for its recruitment to fibrillar adhesions". Protein Sci. 16 (6): 1223–9. doi:10.1110/ps.072798707. PMC 2206669. PMID 17473008.
- ^ Chen H, Ishii A, Wong WK, Chen LB, Lo SH (October 2000). "Molecular characterization of human tensin". Biochem. J. 351 (2): 403–11. PMC 1221376. PMID 11023826.
- ^ Lo SH (January 2004). "Tensin". Int. J. Biochem. Cell Biol. 36 (1): 31–4. doi:10.1016/S1357-2725(03)00171-7. PMID 14592531.
- ^ Eck MJ, Dhe-Paganon S, Trub T, Nolte RT, Shoelson SE (May 1996). "Structure of the IRS-1 PTB domain bound to the juxtamembrane region of the insulin receptor". Cell 85 (5): 695–705. doi:10.1016/S0092-8674(00)81236-2. PMID 8646778.
- ^ Zhou MM, Huang B, Olejniczak ET, Meadows RP, Shuker SB, Miyazaki M, Trub T, Shoelson SE, Fesik SW (April 1996). "Structural basis for IL-4 receptor phosphopeptide recognition by the IRS-1 PTB domain". Nat. Struct. Biol. 3 (4): 388–93. doi:10.1038/nsb0496-388. PMID 8599766.
[edit] External links
- Eukaryotic Linear Motif resource motif class LIG_PTB_Phospho_1
This article incorporates text from the public domain Pfam and InterPro IPR013625
This article incorporates text from the public domain Pfam and InterPro IPR002404
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Phosphotyrosine-binding domain Provide feedback
The phosphotyrosine-binding domain (PTB, also phosphotyrosine-interaction or PI domain) in the protein tensin tends to be found at the C-terminus. Tensin is a multi-domain protein that binds to actin filaments and functions as a focal-adhesion molecule (focal adhesions are regions of plasma membrane through which cells attach to the extracellular matrix). Human tensin has actin-binding sites, an SH2 (PF00017) domain and a region similar to the tumour suppressor PTEN [1]. The PTB domain interacts with the cytoplasmic tails of beta integrin by binding to an NPXY motif [2].
Literature references
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Chen H, Ishii A, Wong WK, Chen LB, Lo SH; , Biochem J 2000;351:403-411.: Molecular characterization of human tensin. PUBMED:11023826 EPMC:11023826
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Lo SH; , Int J Biochem Cell Biol 2004;36:31-34.: Tensin. PUBMED:14592531 EPMC:14592531
External database links
| PANDIT: | PF08416 |
| Pseudofam: | PF08416 |
| SYSTERS: | PTB |
This tab holds annotation information from the InterPro database.
InterPro entry IPR013625
The phosphotyrosine-binding domain (PTB, also phosphotyrosine-interaction or PI domain) of tensin tends to be found at the C terminus of a protein. Tensin is a multi-domain protein that binds to actin filaments and functions as a focal-adhesion molecule (focal adhesions are regions of plasma membrane through which cells attach to the extracellular matrix). Human tensin has actin-binding sites, an SH2 (INTERPRO) domain and a region similar to the tumour suppressor PTEN [PUBMED:11023826]. The PTB domain interacts with the cytoplasmic tails of beta integrin by binding to an NPXY motif [PUBMED:14592531].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | protein binding (GO:0005515) |
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
Alignments
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| Seed (14) |
Full (631) |
Representative proteomes | NCBI (1087) |
Meta (1) |
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| RP15 (54) |
RP35 (78) |
RP55 (174) |
RP75 (308) |
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| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
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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 (14) |
Full (631) |
Representative proteomes | NCBI (1087) |
Meta (1) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (54) |
RP35 (78) |
RP55 (174) |
RP75 (308) |
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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.
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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.
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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: | Pfam-B_3174 (release 18.0) |
| Previous IDs: | none |
| Type: | Family |
| Author: | Wuster A |
| Number in seed: | 14 |
| Number in full: | 631 |
| Average length of the domain: | 127.00 aa |
| Average identity of full alignment: | 29 % |
| Average coverage of the sequence by the domain: | 14.53 % |
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: | 131 | ||||||||||||
| Family (HMM) version: | 8 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Interactions
There is 1 interaction for this family. More...
PTBStructures
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 PTB domain has been found. There are 7 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