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PHD finger Edit Wikipedia article
PHD zinc finger. Zinc atoms shown in grey
The PHD finger (Plant Homeo Domain) was discovered in 1993 as a Cys4-His-Cys3 motif in the homeodomain protein HAT3 in Arabidopsis thaliana. The PHD finger motif resembles the metal binding RING domain (Cys3-His-Cys4) and FYVE domain. It occurs as a single finger, but often in clusters of two or three, and it also occurs together with other domains, such as the chromodomain and the bromodomain.
The PHD finger, approximately 50-80 aminoacids in length, is found in more than 100 human proteins. Several of the proteins it occurs in are found in the nucleus, and are involved in chromatin-mediated gene regulation. The PHD finger occurs in proteins such as the transcriptional co-activators p300 and CBP, Polycomb-like protein (Pcl), Trithorax-group proteins like ASH1L, ASH2L and MLL, the autoimmune regulator (AIRE), Mi-2 complex (part of histone deacetylase complex), the co-repressor TIF1, the newly discovered JARID1-family of demethylases and many more.
 Structure data on the PHD finger
The NMR structure of the PHD finger from human WSTF (Williams Syndrome Transcription Factor) shows that the conserved cysteines and histidine coordinate two Zn2+ ions. In general, the PHD finger adopts a globular fold, consisting of a two-stranded beta-sheet and an alpha-helix. The region consisting of these secondary structures and the residues involved in coordinating the zinc-ions are very conserved among species. The loop regions I and II are variable and could contribute functional specificity to the different PHD fingers.
 Function of the PHD finger
Recently the PHD fingers of some proteins, including ING2, YNG1 and NURF, have been reported to bind to histone H3 tri-methylated on lysine 4 (H3K4me3), while other PHD fingers have tested negative in such assays. Interestingly, a protein called SMCX (or JARID1C) has a PHD finger, which has been reported to bind histone H3 tri-methylated lysine 9 (H3K9me3). Based on these recent publications, binding to tri-methylated lysines on histones may therefore be a property widespread among PHD fingers. Domains that bind to modified histones, are called epigenetic readers as they specifically recognize the modified version of the residue and binds to it. The modification H3K4me3 is associated with the transcription start site of active genes, while H3K9me3 is associated with inactive genes. The modifications of the histone lysines are dynamic, as there are methylases that add methyl groups to the lysines, and there are demethylases that remove methyl groups. The SMCX protein is actually a histone H3 lysine 4 demethylase, which means it is an enzyme that can remove the methyl groups of lysine 4 on histone 3 (making it H3K4me2 or H3K4me1). One can only speculate if the H3K9me3-binding of SMCX PHD domain provides a crosstalk between trimethylation of H3K9 and the demethylation of H3K4me3. Such crosstalks have been suggested earlier with other domains involved in chromatin regulation, and may provide a strictly coordinated regulation.
Another example is the PHD finger of the BHC80/PHF21A protein, which is a component of the LSD1 complex. In this complex, LSD1 specifically demethylates H3K4me2 to H3K4me0, and BHC80 binds H3K4me0 through its PHD finger to stabilize the complex at its target promoters, presumably to prevent further re-methylation. This is the first example of a PHD finger recognizing lysine methyl-zero status.
- Schindler U, Beckmann H et al. (1993) "HAT3-1, a novel Arabidopsis homeodomain protein containing a conserved cystein-rich region", Plant J, 4, 137-150
- Aasland R, Gibson T, Stewart AF (1995) "The PHD finger: implications for chromatin-mediated transcriptional regulation", TIBS, 20, 56-59
- Pascual J, Martinez-Yamout M et al. (2000)," Structure of the PHD Zinc Finger from Human Williams-Beuren Syndrome Transcription Factor", Journal of Molecular Biology, 304, 723-729
- PeÃ±a PV, Davrazou1 F, Shi X et al. (2006),"Molecular mechanism of histone H3K4me3 recognition by plant homeodomain of ING2", Nature, 442, 100 - 103
- Li H, Ilin S, Wang W et al. (2006),"Molecular basis for site-specific read-out of histone H3K4me3 by the BPTF PHD finger of NURF", Nature, 442, 91-95
- Iwase S, Lan F (2007),"The X-Linked Mental Retardation Gene SMCX/JARID1C Defines a Family of Histone H3 Lysine 4 Demethylases", Cell, 128, 1-12
- Lan F, Collins RE (2007), "Recognition of unmethylated histone H3 lysine 4 links BHC80 to LSD1-mediated gene repression." Nature, 448, 718-22
PHD-finger Provide feedback
PHD folds into an interleaved type of Zn-finger chelating 2 Zn ions in a similar manner to that of the RING and FYVE domains . Several PHD fingers have been identified as binding modules of methylated histone H3 .
Pascual J, Martinez-Yamout M, Dyson HJ, Wright PE; , J Mol Biol 2000;304:723-729.: Structure of the PHD zinc finger from human williams-beuren syndrome transcription factor PUBMED:11124022 EPMC:11124022
Shi X, Kachirskaia I, Walter KL, Kuo JH, Lake A, Davrazou F, Chan SM, Martin DG, Fingerman IM, Briggs SD, Howe L, Utz PJ, Kutateladze TG, Lugovskoy AA, Bedford MT, Gozani O; , J Biol Chem. 2006; [Epub ahead of print]: Proteome-wide analysis in S. cerevisiae identifies several PHD fingers as novel direct and selective binding modules of histone H3 methylated at either lysine 4 or lysine 36. PUBMED:17142463 EPMC:17142463
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|Number in seed:||28|
|Number in full:||1358|
|Average length of the domain:||35.50 aa|
|Average identity of full alignment:||47 %|
|Average coverage of the sequence by the domain:||3.52 %|
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search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
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For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the PHD_2 domain has been found. There are 2 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein seqence.
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