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PDBsum entry 2bij

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Hydrolase PDB id
2bij
Jmol
Contents
Protein chain
284 a.a.
Ligands
SO4
Waters ×103

References listed in PDB file
Key reference
Title Crystal structures and inhibitor identification for ptpn5, Ptprr and ptpn7: a family of human mapk-Specific protein tyrosine phosphatases.
Authors J.Eswaran, J.P.Von kries, B.Marsden, E.Longman, J.E.Debreczeni, E.Ugochukwu, A.Turnbull, W.H.Lee, S.Knapp, A.J.Barr.
Ref. Biochem J, 2006, 395, 483-491. [DOI no: 10.1042/BJ20051931]
PubMed id 16441242
Abstract
Protein tyrosine phosphatases PTPN5, PTPRR and PTPN7 comprise a family of phosphatases that specifically inactivate MAPKs (mitogen-activated protein kinases). We have determined high-resolution structures of all of the human family members, screened them against a library of 24000 compounds and identified two classes of inhibitors, cyclopenta[c]quinolinecarboxylic acids and 2,5-dimethylpyrrolyl benzoic acids. Comparative structural analysis revealed significant differences within this conserved family that could be explored for the design of selective inhibitors. PTPN5 crystallized, in two distinct crystal forms, with a sulphate ion in close proximity to the active site and the WPD (Trp-Pro-Asp) loop in a unique conformation, not seen in other PTPs, ending in a 3(10)-helix. In the PTPN7 structure, the WPD loop was in the closed conformation and part of the KIM (kinase-interaction motif) was visible, which forms an N-terminal aliphatic helix with the phosphorylation site Thr66 in an accessible position. The WPD loop of PTPRR was open; however, in contrast with the structure of its mouse homologue, PTPSL, a salt bridge between the conserved lysine and aspartate residues, which has been postulated to confer a more rigid loop structure, thereby modulating activity in PTPSL, does not form in PTPRR. One of the identified inhibitor scaffolds, cyclopenta[c]quinoline, was docked successfully into PTPRR, suggesting several possibilities for hit expansion. The determined structures together with the established SAR (structure-activity relationship) propose new avenues for the development of selective inhibitors that may have therapeutic potential for treating neurodegenerative diseases in the case of PTPRR or acute myeloblastic leukaemia targeting PTPN7.
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