Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

3ZPV

Crystal structure of Drosophila Pygo PHD finger in complex with Legless HD1 domain

Summary for 3ZPV
Entry DOI10.2210/pdb3zpv/pdb
DescriptorPROTEIN BCL9 HOMOLOG, PROTEIN PYGOPUS, ZINC ION, ... (5 entities in total)
Functional Keywordstranscription, wnt signaling pathway, zn finger, histone h3 tail binding
Biological sourceDROSOPHILA MELANOGASTER (FRUIT FLY)
More
Cellular locationNucleus: Q961D9 Q9V9W8 Q9V9W8
Total number of polymer chains36
Total formula weight199415.08
Authors
Miller, T.C.R.,Mieszczanek, J.,Sanchez-Barrena, M.J.,Rutherford, T.J.,Fiedler, M.,Bienz, M. (deposition date: 2013-03-02, release date: 2013-10-30, Last modification date: 2023-12-20)
Primary citationMiller, T.C.R.,Mieszczanek, J.,Sanchez-Barrena, M.J.,Rutherford, T.J.,Fiedler, M.,Bienz, M.
Evolutionary Adaptation of the Fly Pygo Phd Finger Towards Recognizing Histone H3 Tail Methylated at Arginine 2
Structure, 21:2208-, 2013
Cited by
PubMed Abstract: Pygo proteins promote Armadillo- and β-catenin-dependent transcription, by relieving Groucho-dependent repression of Wnt targets. Their PHD fingers bind histone H3 tail methylated at lysine 4, and to the HD1 domain of their Legless/BCL9 cofactors, linking Pygo to Armadillo/β-catenin. Intriguingly, fly Pygo orthologs exhibit a tryptophan > phenylalanine substitution in their histone pocket-divider which reduces their affinity for histones. Here, we use X-ray crystallography and NMR, to discover a conspicuous groove bordering this phenylalanine in the Drosophila PHD-HD1 complex--a semi-aromatic cage recognizing asymmetrically methylated arginine 2 (R2me2a), a chromatin mark of silenced genes. Our structural model of the ternary complex reveals a distinct mode of dimethylarginine recognition, involving a polar interaction between R2me2a and its groove, the structural integrity of which is crucial for normal tissue patterning. Notably, humanized fly Pygo derepresses Notch targets, implying an inherent Notch-related function of classical Pygo orthologs, disabled in fly Pygo, which thus appears dedicated to Wnt signaling.
PubMed: 24183574
DOI: 10.1016/J.STR.2013.09.013
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.68 Å)
Structure validation

226707

数据于2024-10-30公开中

PDB statisticsPDBj update infoContact PDBjnumon