1BHH

FREE P56LCK SH2 DOMAIN

1BHH の概要

• エントリーDOI: 10.2210/pdb1bhh/pdb
• 分子名称: T-LYMPHOCYTE-SPECIFIC PROTEIN TYROSINE KINASE P56LCK, P56 LCK TYROSINE KINASE SH2 DOMAIN (3 entities in total)
• 機能のキーワード: sh2 domain, phosphorylation, transferase
• 由来する生物種: Homo sapiens (human); 詳細
• 細胞内の位置: Cytoplasm: P06239 P06239
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 24000.73

構造登録者

Tong, L.,Warren, T.C.,Lukas, S.,Schembri-King, J.,Betageri, R.,Proudfoot, J.R.,Jakes, S. (登録日: 1998-06-08, 公開日: 1998-10-21, 最終更新日: 2024-02-07)

主引用文献

Tong, L.,Warren, T.C.,Lukas, S.,Schembri-King, J.,Betageri, R.,Proudfoot, J.R.,Jakes, S.
Carboxymethyl-phenylalanine as a replacement for phosphotyrosine in SH2 domain binding.
J.Biol.Chem., 273:20238-20242, 1998

PubMed Abstract: The crystal structure of human p56(lck) SH2 domain in complex with an inhibitor containing the singly charged p-(carboxymethyl)phenylalanine residue (cmF) as a phosphotyrosine (Tyr(P) or pY) replacement has been determined at 1.8 A resolution. The binding mode of the acetyl-cmF-Glu-Glu-Ile (cmFEEI) inhibitor is very similar to that of the pYEEI inhibitor, confirming that the cmFEEI inhibitor has a similar mechanism of SH2 domain inhibition despite its significantly reduced potency. Observed conformational differences in the side chain of the cmF residue can be interpreted in terms of maintaining similar interactions with the SH2 domain as the Tyr(P) residue. The crystal structure of the free p56(lck) SH2 domain has been determined at 1.9 A resolution and shows an open conformation for the BC loop and an open phosphotyrosine binding pocket, in contrast to earlier studies on the src SH2 domain that showed mostly closed conformation. The structural information presented here suggests that the carboxymethyl-phenylalanine residue may be a viable Tyr(P) replacement and represents an attractive starting point for the design and development of SH2 domain inhibitors with better pharmaceutical profiles.

PubMed: 9685372
DOI: 10.1074/jbc.273.32.20238

実験手法

X-RAY DIFFRACTION (1.9 Å)