PDBsum entry 4ohe

Hydrolase

PDB id: 4ohe

Contents

Protein chain

489 a.a.

Waters ×131

PDB id:

4ohe

Name:

Hydrolase

Title:

Leopard syndrome-associated shp2/g464a mutant

Structure:

Tyrosine-protein phosphatase non-receptor type 11. Chain: a. Fragment: n-sh2, c-sh2 and ptp domain. Synonym: protein-tyrosine phosphatase 1d, ptp-1d, protein-tyrosine phosphatase 2c, ptp-2c, sh-ptp2, shp-2, shp2, sh-ptp3. Engineered: yes. Mutation: yes

Source:

Homo sapiens. Human. Organism_taxid: 9606. Gene: ptp2c, ptpn11, shptp2. Expressed in: escherichia coli. Expression_system_taxid: 469008.

Resolution:

2.51Å R-factor: 0.190 R-free: 0.256

Authors:

Z.H.Yu,R.Y.Zhang,C.D.Walls,L.Chen,S.Zhang,L.Wu,L.Wang,S.Liu,Z.Y.Zhang

Key ref:

Z.H.Yu et al. (2014). Molecular basis of gain-of-function LEOPARD syndrome-associated SHP2 mutations. Biochemistry, 53, 4136-4151. PubMed id: 24935154 DOI: 10.1021/bi5002695

Date:

17-Jan-14 Release date: 24-Sep-14

Protein chain

Q06124  (PTN11_HUMAN) -  Tyrosine-protein phosphatase non-receptor type 11 from Homo sapiens

Seq: 593 a.a.

Struc: 489 a.a.*

* PDB and UniProt seqs differ at 1 residue position (black cross)

Enzyme reactions

• Enzyme class: E.C.3.1.3.48 - protein-tyrosine-phosphatase.
• Reaction: O-phospho-L-tyrosyl-[protein] + H2O = L-tyrosyl-[protein] + phosphate

Molecule diagrams generated from .mol files obtained from the KEGG ftp site

Key reference

DOI no: 10.1021/bi5002695

Biochemistry 53:4136-4151 (2014)

PubMed id: 24935154

Molecular basis of gain-of-function LEOPARD syndrome-associated SHP2 mutations.

Z.H.Yu, R.Y.Zhang, C.D.Walls, L.Chen, S.Zhang, L.Wu, S.Liu, Z.Y.Zhang.

ABSTRACT

The Src homology 2 (SH2) domain-containing protein tyrosine phosphatase 2 (SHP2) is a critical signal transducer downstream of growth factors that promotes the activation of the RAS-ERK1/2 cascade. In its basal state, SHP2 exists in an autoinhibited closed conformation because of an intramolecular interaction between its N-SH2 and protein tyrosine phosphatase (PTP) domains. Binding to pTyr ligands present on growth factor receptors and adaptor proteins with its N-SH2 domain localizes SHP2 to its substrates and frees the active site from allosteric inhibition. Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders. NS-associated SHP2 mutants display elevated phosphatase activity, while LS-associated SHP2 mutants exhibit reduced catalytic activity. A conundrum in how clinically similar diseases result from mutations to SHP2 that have opposite effects on this enzyme's catalytic functionality exists. Here we report a comprehensive investigation of the kinetic, structural, dynamic, and biochemical signaling properties of the wild type as well as all reported LS-associated SHP2 mutants. The results reveal that LS-causing mutations not only affect SHP2 phosphatase activity but also induce a weakening of the intramolecular interaction between the N-SH2 and PTP domains, leading to mutants that are more readily activated by competing pTyr ligands. Our data also indicate that the residual phosphatase activity associated with the LS SHP2 mutant is required for enhanced ERK1/2 activation. Consequently, catalytically impaired SHP2 mutants could display gain-of-function properties because of their ability to localize to the vicinity of substrates for longer periods of time, thereby affording the opportunity for prolonged substrate turnover and sustained RAS-ERK1/2 activation.