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Structure paper

TitleTargeting a Pleckstrin Homology Domain with a Lysine-Reactive Covalent Binder.
Journal, issue, pagesJ. Med. Chem., Year 2026
Publish dateJan 7, 2020 (structure data deposition date)
AuthorsWest, R.M. / Bizga Nicolescu, R.C. / Brear, P. / Wagstaff, J. / Blaszczyk, B.K. / Deingruber, T. / Sanders, M.G. / Perez-Areales, F.J. / Spring, D.R. / Hyvonen, M.
External linksJ. Med. Chem. / PubMed:42130460
MethodsX-ray diffraction
Resolution1.692 - 2.769 Å
Structure data

PDB-6tuh:
PH domain of Bruton's tyrosine kinase bound to compound 1
Method: X-RAY DIFFRACTION / Resolution: 2.25 Å

PDB-7i90:
Crystal Structure of 7 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.993 Å

PDB-7i91:
Crystal Structure of 13 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.93 Å

PDB-7i92:
Crystal Structure of 9 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 2.633 Å

PDB-7i93:
Crystal Structure of 27 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.91 Å

PDB-7i94:
Crystal Structure of 33 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.828 Å

PDB-7i95:
Crystal Structure of 25 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.991 Å

PDB-7i96:
Crystal Structure of 4 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 2.52 Å

PDB-7i97:
Crystal Structure of 8 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.692 Å

PDB-7i98:
Crystal Structure of 10 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 2.07 Å

PDB-7i99:
Crystal Structure of 22 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.97 Å

PDB-7i9a:
Crystal Structure of 24 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 2.11 Å

PDB-7i9b:
Crystal Structure of 32 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 2.769 Å

PDB-7i9c:
Crystal Structure of 30 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.939 Å

PDB-7i9d:
Crystal Structure of 14 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

PDB-7i9e:
Crystal Structure of 18 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.91 Å

PDB-7i9f:
Crystal Structure of 16 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 2.04 Å

PDB-7i9g:
Crystal Structure of 28 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.698 Å

PDB-7i9h:
Crystal Structure of 26 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 2.589 Å

PDB-7i9i:
Crystal Structure of 2 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.83 Å

PDB-9rl9:
Crystal Structure of 24 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 2.11 Å

PDB-9rmo:
Crystal Structure of 31 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

PDB-9rn5:
Crystal Structure of 33 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.83 Å

PDB-9t0t:
Crystal Structure of the correct enantiomer bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.73 Å

PDB-9t1v:
Crystal Structure of 17 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 2.41 Å

PDB-9t21:
Crystal Structure of 29 bound to the ph domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.869 Å

PDB-9t23:
Crystal Structure of 5 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.845 Å

PDB-9t3g:
Crystal Structure of 12 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.946 Å

PDB-9t3m:
Crystal Structure of 11 bound to the PH domain of Btk
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

Chemicals

ChemComp-NXT:
4,5,6,7-tetrahydro-1-benzofuran-3-carboxylic acid

ChemComp-MG:
Unknown entry

ChemComp-ZN:
Unknown entry

ChemComp-HOH:
WATER

PDB-1b6f:
BIRCH POLLEN ALLERGEN BET V 1

PDB-1b6s:
STRUCTURE OF N5-CARBOXYAMINOIMIDAZOLE RIBONUCLEOTIDE SYNTHETASE

PDB-1b6t:
PHOSPHOPANTETHEINE ADENYLYLTRANSFERASE IN COMPLEX WITH 3'-DEPHOSPHO-COA FROM ESCHERICHIA COLI

PDB-1b6u:
CRYSTAL STRUCTURE OF THE HUMAN KILLER CELL INHIBITORY RECEPTOR (KIR2DL3) SPECIFIC FOR HLA-CW3 RELATED ALLELES

PDB-1b6x:
3,N4-ETHENO-2'-DEOXYCYTIDINE OPPOSITE GUANINE IN AN 11-MER DUPLEX, SOLUTION STRUCTURE FROM NMR AND MOLECULAR DYNAMICS, 4 STRUCTURES

PDB-1b6v:
CRYSTAL STRUCTURE OF A HYBRID BETWEEN RIBONUCLEASE A AND BOVINE SEMINAL RIBONUCLEASE

PDB-1b6p:
HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 7

PDB-1b6q:
ALANINE 31 PROLINE MUTANT OF ROP PROTEIN

PDB-1b6w:
CRYSTAL STRUCTURE OF THE SELENOMETHIONINE VARIANT OF HISTONE HMFB FROM METHANOTHERMUS FERVIDUS

PDB-1b6r:
N5-CARBOXYAMINOIMIDAZOLE RIBONUCLEOTIDE SYNTHETASE FROM E. COLI

PDB-1b6k:
HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 5

PDB-1b6l:
HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 4

PDB-1b6m:
HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 6

ChemComp-CL:
Unknown entry

PDB-1b6g:
HALOALKANE DEHALOGENASE AT PH 5.0 CONTAINING CHLORIDE

PDB-1b6h:
OLIGO-PEPTIDE BINDING PROTEIN COMPLEXED WITH LYSYL-NORVALYL-LYSINE

PDB-1b6i:
T4 LYSOZYME MUTANT WITH CYS 54 REPLACED BY THR, CYS 97 REPLACED BY ALA, THR 21 REPLACED BY CYS AND LYS 124 REPLACED BY CYS (C54T,C97A,T21C,K124C)

PDB-1b6j:
HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 1

PDB-1jia:
STRUCTURE OF A BASIC PHOSPHOLIPASE A2 FROM AGKISTRODON HALYS PALLAS AT 2.13A RESOLUTION

PDB-1jr3:
Crystal Structure of the Processivity Clamp Loader Gamma Complex of E. coli DNA Polymerase III

PDB-1js1:
Crystal Structure of a new transcarbamylase from the anaerobic bacterium Bacteroides fragilis at 2.0 A resolution

PDB-1js0:
Crystal Structure of 3D Domain-swapped RNase A Minor Trimer

PDB-1js4:
ENDO/EXOCELLULASE:CELLOBIOSE FROM THERMOMONOSPORA

PDB-1js7:
Solution Structure of dAAUAA DNA Bulge

PDB-1js6:
Crystal Structure of DOPA decarboxylase

PDB-1jta:
Crystal Structure of Pectate Lyase A (C2 form)

PDB-1jtb:
LIPID TRANSFER PROTEIN COMPLEXED WITH PALMITOYL COENZYME A, NMR, 16 STRUCTURES

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / BTK / Covalent fragments / surface entrophy reduction / crystal engineering / HYDROLASE / Fragment based drug discovery / ph domain

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