PDBsum entry 2kft

Transcription/protein binding

PDB id: 2kft

Contents

Protein chains

56 a.a. *

21 a.a. *

Metals

_ZN ×2

* Residue conservation analysis

PDB id:

2kft

Name:

Transcription/protein binding

Title:

Nmr solution structure of the first phd finger domain of human autoimmune regulator (aire) in complex with histone h3(1-20cys) peptide

Structure:

Autoimmune regulator. Chain: a. Fragment: aire phd-type 1 zinc finger. Synonym: autoimmune polyendocrinopathy candidiasis ectodermal dystrophy protein, apeced protein. Engineered: yes. Histone h3. Chain: b. Fragment: histone h3 1-20cys n-terminal domain.

Source:

Homo sapiens. Human. Organism_taxid: 9606. Gene: aire, apeced. Expressed in: escherichia coli. Expression_system_taxid: 562. Synthetic: yes

NMR struc:

20 models

Authors:

S.Chakravarty,L.Zeng,M.Zhou

Key ref:

S.Chakravarty et al. (2009). Structure and Site-Specific Recognition of Histone H3 by the PHD Finger of Human Autoimmune Regulator. Structure, 17, 670-679. PubMed id: 19446523 DOI: 10.1016/j.str.2009.02.017

Date:

27-Feb-09 Release date: 28-Apr-09

Protein chain

O43918  (AIRE_HUMAN) -  Autoimmune regulator from Homo sapiens

Seq: 545 a.a.

Struc: 56 a.a.*

Protein chain

No UniProt id for this chain

Struc: 21 a.a.

* PDB and UniProt seqs differ at 2 residue positions (black crosses)

Enzyme reactions

• Enzyme class: Chain A: E.C.?

DOI no: 10.1016/j.str.2009.02.017

Structure 17:670-679 (2009)

PubMed id: 19446523

Structure and Site-Specific Recognition of Histone H3 by the PHD Finger of Human Autoimmune Regulator.

S.Chakravarty, L.Zeng, M.M.Zhou.

ABSTRACT

Human autoimmune regulator (AIRE) functions to control thymic expression of tissue-specific antigens via sequence-specific histone H3 recognition by its plant homeodomain (PHD) finger. Mutations in the AIRE PHD finger have been linked to autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). Here we report the three-dimensional solution structure of the first PHD finger of human AIRE bound to a histone H3 peptide. The structure reveals a detailed network of interactions between the protein and the amino-terminal residues of histone H3, and particularly key electrostatic interactions of a conserved aspartic acid 297 in AIRE with the unmodified lysine 4 of histone H3 (H3K4). NMR binding study with H3 peptides carrying known posttranslational modifications flanking H3K4 confirms that transcriptional regulation by AIRE through its interactions with histone H3 is confined to the first N-terminal eight residues in H3. Our study offers a molecular explanation for the APECED mutations and helps define a subclass of the PHD finger family proteins that recognize histone H3 in a sequence-specific manner.

Selected figure(s)

Figure 1.
Figure 1. Three-Dimensional Solution Structure of the AIRE-PHD1/H3K4me0 Peptide Complex
(A) Schematic representation of the functional domains in the human AIRE protein. Grey boxes represent HSR (homogenously staining region), PHD (plant homeodomain), and SAND (Sp100, AIRE-1, NucP41/P75, and Drosophila DEAF-1). PHD and SAND domain boundaries are based on Pfam HMM (Bateman et al., 1999) and remaining segments are based on Meloni et al. (2008). AIRE-PHD1 studied here is shown in blue.
(B) Backbone atoms (N, Cα, and C′) of the 20 superposed NMR structures of the AIRE-PHD1 where protein and peptide are gray and yellow, respectively (left).
(C) Ribbon representation of the complex (middle) highlights the secondary structural elements (protein, blue; peptide, yellow). Pink spheres represent Zn atoms. Only a single representation of Zn atoms of the lowest energy structure is shown in the ensemble for clarity.
(D) Electrostatic potential (isocontour value of ±70 kT/e) surface representation of the AIRE-PHD1 bound to the H3K4me0 peptide (yellow).
(E) Backbone protein-peptide interactions with inset showing the H3A1 interacting neighborhood. The peptide and protein residues are color coded by atom type with carbon atoms in yellow and green, respectively. The orientation of the peptide is the same as that in (C).
(F) Key protein-peptide side-chain interactions with insets respectively highlighting R2, K4, and T3 neighborhood and their surface grooves. The nonpolar nonbonded interacting atoms are labeled with ↔. The peptide orientation in the stick representation is depicted as in the ribbon diagram on left.

Figure 4.
Figure 4. Classification of the PHD Finger Family
Sequence features of structurally characterized three distinct subclasses of the PHD finger family with respect to ligand binding specificity, i.e., H3K4me0 (group I), H3K4me3 (group II), and nonhistone binding (group III). The recognition of H3K4me3 takes place by embracement of the trimethyl groups by characteristically positioned aromatic cage residues, whereas that of K4me0 is due to an ion pair formed with a distinct N-terminal Asp residue. The characteristic histone-peptide interacting positions are in red, and the Zn-chelating residues (the first and second tetrads are connected by regular and dotted lines, respectively) and conserved C-terminal aromatic residue characteristic of the entire PHD family are in green. In either of the H3 interacting PHD fingers, H3R2 often interacts with Asp/Glu (blue). These “red” and “blue” positions are absent in KAP1-PHD finger (bottom) indicated by ↑ that binds the adjacent bromodomain's Z[A] helix by patch of nonpolar residues (yellow). Topology diagrams (bottom; based on Aravind et al. [2006]), not drawn to scale, highlight these features for clarity. The domain boundaries and gi numbers are indicated in the alignments. The secondary structural elements of the AIRE-PHD1 are indicated above the sequence. The black ↑ indicates position where similar interactions involving protein side chain is observed in AIRE and BHC80 PHD fingers. The sequence of AIRE-PHD2 is shown below the alignment to show its grouping with group III as non-H3 binder.

The above figures are reprinted by permission from Cell Press: Structure (2009, 17, 670-679) copyright 2009.

Figures were selected by an automated process.