Synthesis and evaluation of phosphopeptides containing iminodiacetate groups as binding ligands of the Src SH2 domain. - Wikidata - wikimedia - TriplyDB

Synthesis and evaluation of phosphopeptides containing iminodiacetate groups as binding ligands of the Src SH2 domain.

Synthesis and evaluation of phosphopeptides containing iminodiacetate groups as binding ligands of the Src SH2 domain.

http://www.wikidata.org/entity/Q37367562

about

Enhanced cellular uptake of short polyarginine peptides through fatty acylation and cyclization.SH2 Ligand-Like Effects of Second Cytosolic Domain of Na/K-ATPase α1 Subunit on Src Kinase.

P2860

Q34089281-56FB365E-6597-413F-B950-F3B02DE576B3 Q35836087-A19D31AE-0D47-4F63-A64F-B844C14B1702

P2860

Synthesis and evaluation of phosphopeptides containing iminodiacetate groups as binding ligands of the Src SH2 domain.

http://www.wikidata.org/entity/Q37367562

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 21 May 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Synthesis and evaluation of ph ...... ligands of the Src SH2 domain.

@en

Synthesis and evaluation of ph ...... ligands of the Src SH2 domain.

@nl

type

label

Synthesis and evaluation of ph ...... ligands of the Src SH2 domain.

@en

Synthesis and evaluation of ph ...... ligands of the Src SH2 domain.

@nl

prefLabel

Synthesis and evaluation of ph ...... ligands of the Src SH2 domain.

@en

Synthesis and evaluation of ph ...... ligands of the Src SH2 domain.

@nl

P1433

Q37367562-2AC60AAB-E0DF-4661-AF68-DE56B95719B8

P1476

Q37367562-298D14AE-E1D2-4F9E-BE9C-3F061D5F2D9E

P2093

Q37367562-069C391C-CB61-4DDF-8658-B5AE065DAA0B

Q37367562-396F0AA9-24E2-407B-86DC-012162226BDA

Q37367562-4F033E19-1A1D-4081-BF52-874EAE3254B4

Q37367562-5053F415-84C5-4408-9BE5-C32D2B937ED9

Q37367562-761348C8-B9BE-446D-AE92-9B9EFC2EFDA9

Q37367562-B4ED686D-8466-4DA5-A734-502AE82B7E5C

Q37367562-B728864A-F2F0-4770-A976-84343D8B51C7

Q37367562-CD36B43B-8E6F-4CC2-B3E0-E40627CB9821

Q37367562-E2A07036-C6C7-4974-AE9B-3B13888A7147

P2860

Q37367562-01364FF4-0466-4BFE-A832-2B078915086D

Q37367562-25605E30-8885-4843-B5D1-83778F5BDFB5

Q37367562-39399E0E-ADD9-4098-B622-02BF3D184EF6

Q37367562-448223E7-5E3D-4079-A3DD-74DCA27554D2

Q37367562-53C0975D-87A2-4A85-9260-A72A609F42C0

Q37367562-707450E7-6481-4BD3-9FF5-40A1A6770CE8

Q37367562-981A031B-146D-428B-BDFA-0039883C58C3

Q37367562-B39E3571-097B-4032-A21F-DEA2FAB52DE2

Q37367562-BBDAE342-E484-48B1-B828-4F8BFF1C1498

Q37367562-C1652418-FBBF-400F-BE07-220A85B76D72

P304

Q37367562-FC3B57FF-AA45-48AB-8255-05F3BE156922

P31

Q37367562-A188E331-DC76-4004-BCAD-5BDEDD27FD09

P356

Q37367562-D2C62E72-A7C5-4BAF-BADE-428A081EF873

P433

Q37367562-19B9849E-07E9-475D-B505-33BB271251D3

P478

Q37367562-0F0BBFAF-48A0-47AA-B84C-39EBEF269B94

P577

Q37367562-9F7B66C9-5F54-40D5-860B-2A0A45088FF0

P5875

Q37367562-E9C14F0E-620C-437A-808D-C5DEC5E4023F

P698

Q37367562-D8662B60-06AE-4E36-BE2F-990339D5C236

P932

Q37367562-B007CAFF-8CDE-4F51-ADD1-52480A5968CE

P356

J.BIOORG.2009.05.003

P1433

Bioorganic Chemistry

P1476

Synthesis and evaluation of ph ...... ligands of the Src SH2 domain.

@en

P2093

Aaron D Schuler

http://www.w3.org/2001/XMLSchema#string

Absar Faruqui

http://www.w3.org/2001/XMLSchema#string

Gongqin Sun

http://www.w3.org/2001/XMLSchema#string

Guofeng Ye

http://www.w3.org/2001/XMLSchema#string

Joel R Morgan

http://www.w3.org/2001/XMLSchema#string

John A Zebala

http://www.w3.org/2001/XMLSchema#string

Keykavous Parang

http://www.w3.org/2001/XMLSchema#string

Kezhen Huang

http://www.w3.org/2001/XMLSchema#string

Yousef Ahmadibeni

http://www.w3.org/2001/XMLSchema#string

P2860

Structure-based design of an osteoclast-selective, nonpeptide src homology 2 inhibitor with in vivo antiresorptive activity

A novel phosphotyrosine mimetic 4'-carboxymethyloxy-3'-phosphonophenylalanine (Cpp): exploitation in the design of nonpeptide inhibitors of pp60(Src) SH2 domain

Calorimetric and structural studies of 1,2,3-trisubstituted cyclopropanes as conformationally constrained peptide inhibitors of Src SH2 domain binding

Lowering the entropic barrier for binding conformationally flexible inhibitors to enzymes

SH2 domains recognize specific phosphopeptide sequences

c-Src, receptor tyrosine kinases, and human cancer.

Metal-chelating amino acids as building blocks for synthetic receptors sensing metal ions and histidine-tagged proteins.

Phosphoryltyrosyl mimetics in the design of peptide-based signal transduction inhibitors.

Targeting protein kinases for bone disease: discovery and development of Src inhibitors.

Snap-to-it probes: chelate-constrained nucleobase oligomers with enhanced binding specificity.

P304

133-142

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/J.BIOORG.2009.05.003

http://www.w3.org/2001/XMLSchema#string

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

37

http://www.w3.org/2001/XMLSchema#string

P577

2009-05-21T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

26304152

http://www.w3.org/2001/XMLSchema#string

P698

19539345

http://www.w3.org/2001/XMLSchema#string

P932

2754053

http://www.w3.org/2001/XMLSchema#string