PDBsum entry: 1wvh

Cell adhesion

PDB id: 1wvh

Contents

Protein chain

132 a.a. *

Waters ×104

* Residue conservation analysis

PDB id:

1wvh

Name:

Cell adhesion

Title:

Crystal structure of tensin1 ptb domain

Structure:

Tensin. Chain: a. Fragment: ptb domain. Synonym: tensin1. Engineered: yes

Source:

Gallus gallus. Chicken. Organism_taxid: 9031. Expressed in: escherichia coli. Expression_system_taxid: 562.

Biol. unit:

Monomer (from PQS)

Resolution:

1.50Å R-factor: 0.218 R-free: 0.236

Authors:

C.J.Mccleverty,R.C.Liddington

Key ref:

C.J.McCleverty et al. (2007). Structure of the PTB domain of tensin1 and a model for its recruitment to fibrillar adhesions. Protein Sci, 16, 1223-1229. PubMed id: 17473008 DOI: 10.1110/ps.072798707

Date:

15-Dec-04 Release date: 13-Dec-05

Protein chain

Q04205  (TENS_CHICK) -  Tensin

Seq: 1744 a.a.

Struc: 132 a.a.

DOI no: 10.1110/ps.072798707

Protein Sci 16:1223-1229 (2007)

PubMed id: 17473008

Structure of the PTB domain of tensin1 and a model for its recruitment to fibrillar adhesions.

C.J.McCleverty, D.C.Lin, R.C.Liddington.

ABSTRACT

Tensin is a cytoskeletal protein that links integrins to the actin cytoskeleton at sites of cell-matrix adhesion. Here we describe the crystal structure of the phosphotyrosine-binding (PTB) domain of tensin1, and show that it binds integrins in an NPxY-dependent fashion. Alanine mutagenesis of both the PTB domain and integrin tails supports a model of integrin binding similar to that of the PTB-like domain of talin. However, we also show that phosphorylation of the NPxY tyrosine, which disrupts talin binding, has a negligible effect on tensin binding. This suggests that tyrosine phosphorylation of integrin, which occurs during the maturation of focal adhesions, could act as a switch to promote the migration of tensin-integrin complexes into fibronectin-mediated fibrillar adhesions.

Selected figure(s)

Figure 1.
Structure of the tensin PTB domain. (A) Stereo C[alpha] plot of the tensin1 PTB domain with every 10th residue, and N and C termini, labeled. The unstructured [beta]6-[beta]7 loop is shown schematically in green. (B) Ribbon diagram of the tensin1 PTB domain, with secondary structural elements labeled. A model of the integrin peptide is also shown (in red), including the side-chains of the NPxY tyrosine and the tryptophan residue at the --8 position. (C) Structure-based sequence alignment of the PTB domains of tensin family members, the talin PTB-like domain (Garcia-Alvarez et al. 2003), and other PTB domains (X11 [Zhang et al. 1997], Numb [Li et al. 1998], Dab1 [Stolt et al. 2003], Shc [Zhou et al. 1995b], IRS-1 [Eck et al. 1996; Zhou et al. 1996], and Dok1 [Shi et al. 2004]). [beta]-strands are colored red; [alpha]-helices are blue. Residues involved in peptide binding are underlined, and those that directly bind phosphotyrosine are boxed. In the tensin homologs, two basic residues from the [beta]6-[beta]7 loop proposed to engage the phosphotyrosine are boxed in green. Numbers in parentheses for X11, Dab1, and Shc indicate the size of sequence insertions that have been removed for clarity. The asterisk in the X11 sequence marks a 19-residue insertion that is also not shown.

Figure 2.
PTB-integrin models. Surface representations of the tensin1-integrin model (A) and the talin-integrin crystal structure (B) (Garcia-Alvarez et al. 2003), colored by electrostatic potential (blue for positive, red for negative). The integrin peptides are shown as sticks and colored by atom type. Integrin residue numbers are in black (and numbered with respect to the NPxY tyrosine in parentheses); in A, tensin residue numbers are given in green. Figures were generated with MOLSCRIPT (Kraulis 1991), RASTER3D (Kraulis 1991; Merritt and Murphy 1994), and PyMol (http://www.pymol.org).

The above figures are reprinted from an Open Access publication published by the Protein Society: Protein Sci (2007, 16, 1223-1229) copyright 2007.