- Research article
- Open Access
Classification of the human THAP protein family identifies an evolutionarily conserved coiled coil region
BMC Structural Biology volume 19, Article number: 4 (2019)
The Correction to this article has been published in BMC Structural Biology 2019 19:7
The THAP (Thanatos Associated Proteins) protein family in humans is implicated in various important cellular processes like epigenetic regulation, maintenance of pluripotency, transposition and disorders like cancers and hemophilia. The human THAP protein family which consists of twelve members of different lengths has a well characterized amino terminal, zinc-coordinating, DNA-binding domain called the THAP domain. However, the carboxy terminus of most THAP proteins is yet to be structurally characterized. A coiled coil region is known to help in protein oligomerization in THAP1 and THAP11. It is not known if other human THAP proteins oligomerize. We have used bioinformatic tools to explore the possibility of dimerization of THAP proteins via a coiled coil region.
Classification of human THAP protein into three size based groups led to the identification of an evolutionarily conserved alpha helical region, downstream of the amino terminal THAP domain. Secondary structure predictions, alpha helical wheel plots and protein models demonstrated the strong possibility of coiled coil formation in this conserved, leucine rich region of all THAP proteins except THAP10.
The identification of a predicted oligomerization region in the human THAP protein family opens new directions to investigate the members of this protein family.
The THAP (Thanatos Associated Proteins) protein family is characterized by a conserved amino-terminal zinc-coordinating DNA-binding domain . The THAP protein family in humans consists of twelve members that vary in size from 200 to 900 amino acid residues. THAP7 and THAP11 have been characterized as transcription factors [2, 3]. Other THAP proteins have been implicated in diverse cellular responses; THAP0 is a member of the apoptotic cascade induced by IFN-γ , THAP1, with RRM1, regulates cell proliferation , THAP5 is a cell cycle inhibitor , and THAP9 is an active transposase in humans . The THAP11 homologue in mice is essential for pluripotency in mice . THAP proteins have also been linked to various diseases: THAP1 is implicated in torsional dystonia and hemophilia , THAP5 is implicated in several heart diseases [9, 10] and THAP2, 10 and 11 are implicated in various cancers .
Coiled coils are structural features in proteins that mediate protein oligomerization and are characterized by amphipathic alpha helices of each monomer twisting around each other. They are often made of a repeated pattern of seven amino acids called a “heptad repeat” which fold into amphipathic alpha helices . If the amino acids in each heptad are labelled from a to g, non-polar/hydrophobic residues usually occur at every a and d position and charged amino acids at every e and g position (Additional file 1: Figure S1a). Leucine zippers are coiled coil regions which predominantly have leucine in the d position of the heptad repeat. The side chains of the hydrophobic residues at a and d on each monomer strand undergo ‘knobs-into-holes’ packing  by interlocking with a similar pattern on another monomer strand to form a hydrophobic core. Helical regions of proteins can be visually represented by a helical wheel plot (Additional file 1: Figure S1b) wherein the amino acid sequence of the protein is plotted in a rotating manner around a central axis .
Coiled coils enable oligomerization of various proteins like signal transducers, transcription factors, actin and many more [14,15,16]. Protein oligomerization is observed in most cellular processes like formation of cytoskeleton, cell signal transduction, regulation of gene expression, transposition [16, 17]. Proteins can undergo homo-oligomerization (binding itself) or hetero-oligomerization (binding other protein interaction partners).
Formation of homo-oligomers is commonly seen in transcription factors . Biochemical evidence suggests that THAP proteins may undergo homo dimerization. THAP0, also known as PRKRIR and Death Associated Protein 4, forms a homodimer using amino acid residues 1–488 [4, 18]. However, there are no structural studies which report the formation of coiled coils in THAP0. Mutation studies on THAP1 demonstrate the formation of a coiled coil region (residues 139–190) which is indispensable for THAP1 homo dimerization . The recently reported carboxy terminal coiled coil region of human THAP11 (residues 254–306, PDB id: 5AJS) has been shown to form parallel homo dimers .
Hetero-dimerization of proteins also has important functional consequences as seen in cell shape determining proteins of H. pylori  and SNARE (soluble NSF Attachment Receptors) in yeast and mammals . Some human THAP proteins are reported to form heterodimers with HCF-1 . THAP0 binds MST1 , THAP3 shares sequence similarity and protein interaction partners with THAP1 . THAP7 binds to hypo-acetylated histone H4 tails via its carboxy terminal 77 amino acid residues (residues 232–309). The THAP domain and the Histone interacting domain (HID, a predicted coiled coil region of THAP7) play key roles in binding TAF- 1β and transcriptional repression .
The carboxy terminal portions of most THAP proteins, except for THAP1 and THAP11, are yet to be structurally and functionally characterized [8, 19]. In this study, we explore the possibility of oligomerization of THAP proteins by predicting a coiled coil region in a ~ 40 amino acid leucine rich region that is located downstream of the highly conserved DNA-binding THAP domain.
Secondary structure prediction
Secondary structures of THAP proteins were predicted using JPRED , PSIPRED  and Phyre2 . Briefly, JPRED constructs a Multiple Sequence Alignment using PSI-BLAST  for individual input sequences and uses it to predict local secondary structure using Jnet . PSIPRED generates a sequence similarity search using PSI-BLAST  and then predicts the secondary structure using artificial neural network machine learning approach, followed by filtering the predicted secondary structures using two separate neural networks followed by actual structure prediction. Phyre2 scans the sequence using PSI-BLAST , followed by secondary structure prediction using the neural network secondary structure prediction.
Multiple sequence alignment of the THAP proteins
Amino acid sequences of the twelve THAP proteins were downloaded from NCBI (NP_004696.2, CAG33537.1, AAH08358.1, AAH92427.1, AAH69235.1, Q7Z6K1.2, AAH22989.1, NP_001008695.1, Q8NA92.1, NP_078948.3, NP_064532, NP_065190.2 and aligned using Clustal Omega . Clustal Omega allows identification of conserved and similar amino acids among the input sequences based on HMM models.
Sequence conservation score analysis of THAP proteins
Sequence conservation score for each position of the predicted coiled coil region of THAP proteins were generated using “Protein Residue conservation Prediction” . Briefly, the conservation of an amino acid at a position when aligned with similar protein sequences indicates significant evolutionary pressure at that position. This is quantified using Jensen-Shannon divergence (JSD) and is combined with a window based extension method to take into account the conservation of sequentially adjacent residues.
Generation of protein models
Protein models were generated by I TASSER , RaptorX  and LOMETS . Briefly, the amino acid sequences of the THAP proteins were submitted to the I TASSER server, RaptorX server and LOMETS server with no specified template. Suitable templates depending on sequence similarity searches were identified from the PDB database. Monte Carlo simulations were used to assemble the full- length conformations of identified templates and models were generated for the sequence of interest. Lastly, all the conformations were confirmed and cluster centroids were identified which were then used to build the final models after refinement of cluster centroids.
Helical wheel plot analysis
Helical wheel plots of the selected residues of THAP proteins were generated using ‘DRAW COIL’ . Briefly, a helical wheel plot visualizes the arrangement of amino acids in a helical wheel pattern i.e. if a protein has strong probability of forming a coiled coil, hydrophobic amino acids cluster to one side of the helical wheel plot and hydrophilic amino acids cluster on the opposite side (amphipathic pattern), which is common for proteins forming leucine zippers. In addition to predicting amphipathic pattern, DRAW COIL also predicts probable hydrophobic and electrostatic interactions between the amino acid residues of a homodimer.
Higher order oligomeric structure prediction
The possibility of forming higher order oligomeric structures by the predicted alpha helical regions of THAP proteins (except THAP10) and their respective interacting partners indicated by STRING database  was predicted by Multicoil  and LOGICOIL . Briefly, Multicoil predicts a probable dimer or a trimer by calculating the pairwise frequency values of a given amino acid residue pair in the input peptide or protein sequence and comparing it to the pairwise frequency values available from the established coiled coil data. LOGICOIL use Bayesian variable selection along with multinomial probit regression method to predict the formation of a higher order oligomeric structure like parallel or anti-parallel dimer, trimer or a tetramer of a given protein/peptide sequence.
Prediction of leucine-rich alpha helical regions in THAP proteins by secondary structure analysis and multiple sequence alignment
The probability of secondary structure formation of human THAP proteins was predicted by JPRED, PSIPRED and Phyre2. Analysis of results from all three secondary structure prediction tools identifies a region spanning around 40 amino acid residues downstream of the THAP domain in each THAP protein (except THAP10), that has a high probability of forming alpha helices, as shown in Table 1.
The predicted alpha helical regions correspond to residues 150–180 in THAP0, which is a part of the biochemically studied larger region spanning residues 1–488 [4, 18], residues 143–188 in THAP1 which overlaps with the experimentally verified coiled coil region (residues 139–190) , residues 135–178 in THAP2, residues 189–224 in THAP3, residues 362–398 in THAP4, residues 331–372 in THAP5, residues 148–193 in THAP6, residues 237–281 in THAP7, which overlaps with the predicted HID  in THAP7, residues 180–209 in THAP8, residues 145–182 in THAP9 and residues 254–310 in THAP11, which is a part of the previously reported X ray crystal structure of the coiled coil region (residues 247–314) of THAP11 .
The predicted alpha helical region in THAP0, THAP3 THAP4, THAP5, THAP6, THAP7, THAP8, THAP9 and THAP11 are rich in leucine (Additional file 1: Table S1) and hydrophobic residues as seen in the characteristic heptad repeats of coiled coils. However, THAP11 is an exception to the general rule since it does not have a leucine at every d position but still forms a coiled coil region (residues 254–306) . The corresponding regions in THAP1 and THAP2 are leucine poor (Additional file 1: Table S1).
The human THAP protein family was divided into three groups based on conservation in predicted alpha helical regions
Multiple sequence alignment of the predicted alpha helical regions of all the THAP proteins (except THAP10) did not show any conservation of specific amino acid residues as shown in Additional file 1: Figure S2. However, multiple sequence alignment of THAP1, THAP2, THAP3 and THAP6 revealed strong conservation of basic amino acid residues (Fig. 1a). Similarly, multiple sequence alignment of THAP7, THAP8 and THAP11 proteins identified two conserved Leu residues and basic amino acid residues (Fig. 1b). Leu and Ser were found to be conserved upon multiple sequence alignment of THAP0, THAP4, THAP5 and THAP9 (Fig. 1c).
To obtain a more conserved picture over the entire THAP family, we classified the THAP proteins into three groups, based on the conservation found among the predicted alpha helical regions (1) Short THAP proteins (sTHAP): which include THAP1, THAP2, THAP3 and THAP6. (2) Medium sized THAP proteins (mTHAP): which include THAP7, THAP8, THAP10 and THAP11. (3) Long THAP proteins (lTHAP): which include THAP0, THAP4, THAP5 and THAP9 as shown in Fig. 2. Interestingly, the above classification also followed a length wise classification of all the THAP proteins i.e. Short THAP proteins (sTHAP): which have a length of less than 250 amino acid residues a (2) Medium sized THAP proteins (mTHAP): which have a length of less than 350 amino acid residues (3) Long THAP proteins (lTHAP): which have a length of more than 350 amino acid residues as shown in Fig. 2.
It is to be noted that the sequence conservation within the predicted alpha helical regions is only observed on classification of the THAP protein family. Multiple sequence alignment of all twelve full length THAP proteins did not yield any significant similarity downstream of the AVPTIF motif, which is speculated to be the carboxy- terminal boundary of the THAP domain, as shown in Additional file 1: Figure S3a. Moreover, inter-group multiple sequence alignment of the predicted alpha helical regions of sTHAP with mTHAP protein groups (Additional file 1: Figure S3b, sTHAP with lTHAP protein groups (Additional file 1: Figure S3c, and mTHAP with lTHAP protein groups (Additional file 1: Figure S3d) did not show any conservation of specific amino acid residues.
The conserved amino acid sequences of the predicted alpha helical regions of the sTHAP protein group (Fig. 3a), mTHAP protein group (Fig. 3b) and lTHAP protein group (Fig. 3c) when aligned independent of the flanking regions of the proteins, demonstrated the heptad pattern that characterise coiled coil regions . The high sequence conservation score (above 0.4) of the entire predicted alpha helical region of sTHAP group proteins (Fig. 4a) and mTHAP group proteins (Fig. 4b) indicate strong evolutionary conservation pressure in this region. The sequence conservation score is high (above 0.4) in the center of the predicted alpha helical region of lTHAP group proteins. This indicates a strong evolutionary conservation pressure within the predicted alpha helical region of lTHAP group proteins (Fig. 4c).
Prediction of alpha helical regions in THAP protein models generated by threading-based models
The structures of the human THAP proteins (except THAP10) were predicted using I TASSER, RaptorX and LOMETS (Additional file 1: Figure S4 Panel A. However, the threading-based models generated by LOMETS and I TASSER are more compact than the ones predicted by RaptorX and thus we use the I TASSER predicted protein models to visualize the predicted alpha helical secondary structures (Additional file 1: Figure S4 Panel B). It was interesting to note that the alpha helical regions predicted by I TASSER in each THAP protein (Additional file 1: Figure S4, Panel B), overlapped with the alpha helical region predicted by secondary structure prediction tools (Table 1, Fig. 3) and the region of amino acid similarity predicted by multiple sequence alignment (Fig. 1). The structural superposition of the predicted alpha helical regions of the sTHAP (Fig. 5) and mTHAP protein (Additional file 1: Figure S5) groups indicate structural similarity. The structure predictions for longer proteins are rather poor and less reliable. Thus, we do not attempt to superpose the predicted alpha helical regions of the lTHAP group.
This suggests that the potential to form alpha helices in these ~ 40 amino acid spanning regions may be independent of the folding of the flanking regions of the THAP proteins. Furthermore, the predicted helical region in THAP11 (residues 254–310; Table 1, Additional file 1: Figure S4, Panel B) is a part of the previously reported X ray crystal structure of the coiled coil region (residues 247–314) of THAP11  (Additional file 1: Figure S6).
Predicted alpha helical regions of THAP proteins arranged in an amphipathic pattern in helical wheel plots
Coiled coil regions mediate protein oligomerization wherein amphipathic alpha helices of each monomer twist around each other. DRAW COIL was used to investigate the presence of amphipathic pattern (arrangement of hydrophobic amino acid residues on one side of the alpha helical region and polar amino acid residues on the other side of the helix, when viewing the helix from the top) of amino acid residues and electrostatic interactions between charged amino acid residues within the predicted alpha helical regions in all THAP proteins, except for THAP10.
In the sTHAP protein group, the predicted alpha helical regions of THAP1 show a very strong amphipathic arrangement by clustering of non-polar amino acid residues (depicted by grey) on the top of the helical wheel and clustering of polar, acidic and basic amino acids residues (depicted by yellow, red and blue respectively) on the bottom of the helical wheel as seen in Fig. 6a. However, the predicted alpha helical regions of THAP2 and THAP3 of the sTHAP group (Fig. 6a), THAP8 of the mTHAP protein group (Fig. 6b) and THAP0 and THAP9 of the lTHAP group (Fig. 6c) show moderate amphipathic arrangement, whereas the predicted alpha helical regions of THAP4, THAP 5, THAP6, THAP7 and THAP11 (Fig. 6a, b,c) show very little amphipathic arrangement.
Within the predicted alpha helical region of the sTHAP protein group, interactions were predicted between Glu174 and Arg175 and Lys181 and Glu182 in THAP1, Glu158 and Arg159 in THAP2 and between Arg161 and Lys166 and Arg175 and Glu176 in THAP6, as shown in Fig. 6a. Similarly, within the mTHAP proteins group, interactions were predicted between Arg 264 and Glu 265 and Glu 279 and Lys 280 in THAP7 and Lys299 and Asp300 in THAP11 as shown in Fig. 6b. The interaction between Lys299K and Glu300 is reported to be very important for THAP11 dimerization as reported earlier . In the lTHAP protein group, interactions were predicted between Lys 160 and Glu 161 and Lys163 and Glu164 in THAP0, between Lys344 and Glu349, Lys351 and Glu 352, Arg358 and Glu363 in THAP5 as shown in Fig. 6c. No electrostatic attractive interactions were predicted in the predicted alpha helical regions of THAP 3,4, 8, 9 (Fig. 6a, b, c).
Predicted alpha helical regions are highly likely to form higher order oligomeric structures
The predicted alpha helical regions of all the THAP proteins except for THAP10 have a high probability to form higher order oligomeric structures as predicted by LOGICOIL and Multicoil. Interestingly, most of the interacting partners of THAP proteins (except THAP10) as predicted by STRING database also have a high probability of forming higher order oligomeric structures (Additional file 1: Table S2). This indicates that THAP proteins could form both homo- as well as hetero-oligomers.
We classify the human THAP protein family into three size based groups. Classification of proteins into families is used as a starting tool to get better insights into protein structure, function and evolutionary significance. CATH (class, architecture, topology, homologous superfamily)  and SCOP (Structural Classification of Proteins)  databases classify protein families based on fold domain recognition approach whereas Pfam  is a database based on amino acid sequence based classification. The fold domain approach gives a global view of protein structure while the sequence based classification gives insights into the evolutionary relationship (convergent or divergent) amongst proteins of the family. Based on inter- and intra-group multiple sequence alignments, we suggest that the three groups of human THAP protein family have become evolutionary divergent.
We report putative coiled-coil forming regions in all the human THAP proteins except THAP10. Since the discovery of the human THAP protein family , experimental studies describe cellular functions of several THAP proteins [1,2,3,4,5], structures of their DNA binding domains (THAP1)  and coiled coil regions (THAP11) .
Although the members of the human THAP protein family differ in their overall structures and cellular functions, they appear to have evolutionarily conserved domains like the well characterized amino-terminal DNA-binding THAP domain. This is the first extensive computational study conducted on the entire human THAP protein family which identifies a second conserved alpha helical region downstream of the THAP domain that is predicted to form coiled coils in all THAP proteins except for THAP10.
It is to be noted that the coiled coil regions predicted in this study have been biochemically and structurally characterized to be important for the homo-dimerization of THAP0 [4, 18], THAP1  and THAP11 .
Coiled coil regions are known to mediate oligomerization of proteins . Protein oligomerization is important in many cellular functions like change in cell shape and cell movement by actin , endocytosis mediated membrane fission by dynamin dimers , signal transduction via membrane receptors by receptor dimerization upon ligand binding, entry and exit from the cell cycle by stable p53 oligomers .
Transcription factors are characterized by the presence of DNA binding domains and coiled coil regions [41, 43]. bHLH (basic Helix-Loop-Helix) leucine zippers, one of the most extensively studied family of transcription factors, have a coiled coil region, downstream of a DNA binding domain, which aids in the formation of homotypic dimers. Dimerization of bHLH regulates its functions by enhancing its DNA binding specificity and allowing it to bind two distantly spaced DNA elements .
THAP1 , THAP5 , THAP7  and THAP11  proteins of the human THAP protein family function as transcription regulators. With the identification of the predicted coiled coil region downstream of the conserved DNA binding domain in most THAP proteins and the predicted Nuclear Localization Signal (NLS)  in some THAP proteins (Additional file 1: Table S3), we speculate that many other members of the human THAP protein family may be transcription regulators.
The prediction of evolutionarily conserved coiled coil regions, in all human THAP proteins except THAP10, (upon classification of the THAP protein family into three groups), opens new directions to experimentally explore the cellular functions of THAP proteins. Since coiled coils enable protein oligomerization, this study suggests the possibility of higher order homo- and hetero-oligomer formation by THAP proteins. For example, the presence of a coiled coil region in THAP3 hints at possible interactions with THAP1 . THAP5, a cell cycle inhibitor, may form oligomers via its coiled coil region and act as a decision maker for the cell to continue with the cell cycle or undergo apoptosis similar to p53 . THAP6, which is speculated to function as a transcription factor, may use its predicted coiled coil region to form a leucine zipper. This study may direct further investigations to understand the structure and function of less understood THAP proteins like THAP8 and THAP9. Also, it would be interesting to study the role of THAP10, which is the only THAP family member that does not have a predicted coiled coil region.
basic Helix Loop Helix
protein-kinase, IFN-inducible double-stranded RNA dependent inhibitor, and repressor of P58 repressor
Thanatos Associated Proteins
Roussigne M, Kossida S, Lavigne A-C, Clouaire T, Ecochard V, Glories A, Amalric F, Girard J-P. The THAP domain: a novel protein motif with similarity to the DNA-binding domain of P element transposase. Trends Biochem Sci. 2003;28:66–9.
Macfarlan T, Kutney S, Altman B, Montross R, Yu J, Chakravarti D. Human THAP7 Is a Chromatin-associated, Histone Tail-binding Protein That Represses Transcription via Recruitment of HDAC3 and Nuclear Hormone Receptor Corepressor. J Biol Chem. 2004;280:7346–58.
Dejosez M, Krumenacker JS, Zitur LJ, Passeri M, Chu L-F, Songyang Z, Thomson JA, Zwaka TP. Ronin is essential for embryogenesis and the pluripotency of mouse embryonic stem cells. Cell. 2008;133:1162–74.
Lin Y, Khokhlatchev A, Figeys D, Avruch J. Death-associated protein 4 binds MST1 and augments MST1-induced apoptosis. J Biol Chem. 2002;277:47991–8001.
Cayrol C, Lacroix C, Mathe C, Ecochard V, Ceribelli M, Loreau E, Lazar V, Dessen P, Mantovani R, Aguilar L, Girard J-P. The THAP-zinc finger protein THAP1 regulates endothelial cell proliferation through modulation of pRB/E2F cell-cycle target genes. Blood. 2007;109:584–94.
Balakrishnan MP, Cilenti L, Mashak Z, Popat P, Alnemri ES, Zervos AS. THAP5 is a human cardiac-specific inhibitor of cell cycle that is cleaved by the proapoptotic Omi/HtrA2 protease during cell death. Am J Physiol Heart Circ Physiol. 2009;297:H643–53.
Majumdar S, Singh A, Rio DC. The human THAP9 gene encodes an active P-element DNA transposase. Science. 2013;339:446–8.
Richter A, Hollstein R, Hebert E, Vulinovic F, Eckhold J, Osmanovic A, Depping R, Kaiser FJ, Lohmann K. In-depth Characterization of the Homodimerization Domain of the Transcription Factor THAP1 and Dystonia-Causing Mutations Therein. J Mol Neurosci. 2017;62:11–6.
Gervais V, Campagne S, Durand J, Muller I, Milon A. NMR studies of a new family of DNA binding proteins: the THAP proteins. J Biomol NMR. 2013;56:3–15.
Leite KRM, Morais DR, Reis ST, Viana N, Moura C, Florez MG, Silva IA, Dip N, Srougi M. MicroRNA 100: a context dependent miRNA in prostate cancer. Clinics. 2013;68:797–802.
Burkhard P, Stetefeld J, Strelkov SV. Coiled coils: a highly versatile protein folding motif. Trends Cell Biol. 2001;11:82–8.
Lupas AN, Bassler J. Coiled Coils - A Model System for the 21st Century. Trends Biochem Sci. 2017;42:130–40.
Schiffer M, Edmundson AB. Use of Helical Wheels to Represent the Structures of Proteins and to Identify Segments with Helical Potential. Biophys J. 1967;7:121–35.
Fischer NW, Prodeus A, Malkin D, Gariépy J. p53 oligomerization status modulates cell fate decisions between growth, arrest and apoptosis. Cell Cycle. 2016;15:3210–9.
O’Shea E, Klemm J, Kim P, Alber T. X-ray structure of the GCN4 leucine zipper, a two-stranded, parallel coiled coil. Science. 1991;254:539–44.
Clarke M, Spudich JA. Nonmuscle Contractile Proteins: The Role of Actin and Myosin in Cell Motility and Shape Determination. Annu Rev Biochem. 1977;46:797–822.
Michel K, O’Brochta DA, Atkinson PW. The C-terminus of the Hermes transposase contains a protein multimerization domain. Insect Biochem Mol Biol. 2003;33:959–70.
Gale M Jr, Blakely CM, Hopkins DA, Melville MW, Wambach M, Romano PR, Katze MG. Regulation of interferon-induced protein kinase PKR: modulation of P58IPK inhibitory function by a novel protein, P52rIPK. Mol Cell Biol. 1998;18:859–71.
Cukier CD, Maveyraud L, Saurel O, Guillet V, Milon A, Gervais V. The C-terminal region of the transcriptional regulator THAP11 forms a parallel coiled-coil domain involved in protein dimerization. J Struct Biol. 2016;194:337–46.
An DR, Im HN, Jang JY, Kim HS, Kim J, Yoon HJ, Hesek D, Lee M, Mobashery S, Kim SJ, Suh SW. Structural Basis of the Heterodimer Formation between Cell Shape-Determining Proteins Csd1 and Csd2 from Helicobacter pylori. PLoS One. 2016;11(10):e0164243.
Parry DAD, Fraser RDB, Squire JM. Fifty years of coiled-coils and alpha-helical bundles: a close relationship between sequence and structure. J Struct Biol. 2008;163:258–69.
Mazars R, Gonzalez-de-Peredo A, Cayrol C, Lavigne A-C, Vogel JL, Ortega N, Lacroix C, Gautier V, Huet G, Ray A, Monsarrat B, Kristie TM, Girard J-P. The THAP-zinc finger protein THAP1 associates with coactivator HCF-1 and O-GlcNAc transferase: a link between DYT6 and DYT3 dystonias. J Biol Chem. 2010;285:13364–71.
Drozdetskiy A, Cole C, Procter J, Barton GJ. JPred4: a protein secondary structure prediction server. Nucleic Acids Res. 2015;43:W389–94.
Jones DT. Protein secondary structure prediction based on position-specific scoring matrices. J Mol Biol. 1999;292:195–202.
Kelley LA, Mezulis S, Yates CM, Wass MN, Sternberg MJE. The Phyre2 web portal for protein modeling, prediction and analysis. Nat Protoc. 2015;10:845–58.
Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ, Gapped BLAST. PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997;25:3389–402.
Cuff JA, Barton GJ. Application of multiple sequence alignment profiles to improve protein secondary structure prediction. Proteins. 2000;40:502–11.
Sievers F, Wilm A, Dineen D, Gibson TJ, Karplus K, Li W, Lopez R, McWilliam H, Remmert M, Söding J, Thompson JD, Higgins DG. Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega. Mol Syst Biol. 2011;7:539.
Capra JA, Singh M. Predicting functionally important residues from sequence conservation. Bioinformatics. 2007;23:1875–82.
Yang J, Zhang Y. I-TASSER server: new development for protein structure and function predictions. Nucleic Acids Res. 2015;43:W174–81.
Peng J, Xu J. RaptorX: exploiting structure information for protein alignment by statistical inference. Proteins. 2011;79(Suppl 10):161–71.
Wu S, Zhang Y. LOMETS: A local meta-threading-server for protein structure prediction. Nucleic Acids Res. 2007;35(10):3375–82.
DrawCoil 1.0 https://grigoryanlab.org/drawcoil/. Accessed 10 June 2017.
Szklarczyk D, Franceschini A, Wyder S, et al. STRING v10: protein–protein interaction networks, integrated over the tree of life. Nucleic Acids Res. 2015;43(Database issue):D447–52.
Wolf E, Kim PS, Berger B. MultiCoil: A Program for Predicting Two- and Three-Stranded Coiled Coils. Protein Sci. 1997;6:1179–89.
Vincent TL, Green PJ, Woolfson DN. LOGICOIL: Multi-state classification of coiled-coil oligomeric state. Bioinformatics. 2013;29(1):69–76.
Sillitoe I, Lewis TE, Cuff A, Das S, Ashford P, Dawson NL, Furnham N, Laskowski RA, Lee D, Lees JG, Lehtinen S, Studer RA, Thornton J, Orengo CA. CATH: comprehensive structural and functional annotations for genome sequences. Nucleic Acids Res. 2015;43:D376–81.
Murzin AG, Brenner SE, Hubbard T, Chothia C. SCOP: a structural classification of proteins database for the investigation of sequences and structures. J Mol Biol. 1995;247:536–40.
Bateman A, Coin L, Durbin R, Finn RD, Hollich V, Griffiths-Jones S, Khanna A, Marshall M, Moxon S, Sonnhammer ELL, Studholme DJ, Yeats C, Eddy SR. The Pfam protein families database. Nucleic Acids Res. 2004;32:D138–41.
Campagne S, Saurel O, Gervais V, Milon A. Structural determinants of specific DNA-recognition by the THAP zinc finger. Nucleic Acids Res. 2010;38:3466–76.
Vinson C, Myakishev M, Acharya A, Mir AA, Moll JR, Bonovich M. Classification of Human B-ZIP Proteins Based on Dimerization Properties. Mol Cell Biol. 2002;22:6321–35.
Ferguson SM, De Camilli P. Dynamin, a membrane-remodelling GTPase. Nat Rev Mol Cell Biol. 2012;13:75–88.
Amoutzias GD, Robertson DL, Van de Peer Y, Oliver SG. Choose your partners: dimerization in eukaryotic transcription factors. Trends Biochem Sci. 2008;33:220–9.
Balakrishnan MP, Cilenti L, Ambivero C, Goto Y, Takata M, Turkson J, Li XS, Zervos AS. THAP5 is a DNA-binding transcriptional repressor that is regulated in melanoma cells during DNA damage-induced cell death. Biochem Biophys Res Commun. 2011;404:195–200.
Parker JB, Palchaudhuri S, Yin H, Wei J, Chakravarti D. A Transcriptional Regulatory Role of the THAP11-HCF-1 Complex in Colon Cancer Cell Function. Mol Cell Biol. 2012;32:1654–70.
Kosugi S, Hasebe M, Matsumura N, Takashima H, Miyamoto-Sato E, Tomita M, Yanagawa H. Six classes of nuclear localization signals specific to different binding grooves of importin alpha. J Biol Chem. 2009;284:478–85.
Clamp M, et al. The Jalview Java alignment editor. Bioinformatics. 2004;20:426–7.
We acknowledge Dr. Umashankar Singh for providing reviews about the study and manuscript. We also thank Lata Rani, Poonam Pandey and Althaf Shaik for their help with ITASSER and VMD and Sudipta Das for his help with Photoshop.
This research was funded by IIT Gandhinagar (computers and network access required for collection, analysis and interpretation of data and in writing the manuscript; HMS stipend), SERB (ECR/2016/000479) and DBT Ramalingaswami Fellowship (BT/RLF/Re-entry/ 43/2013) (Awarded to SM).
Availability of data and materials
All data generated or analyzed during this study, including raw sequence files, are included in this article and its Additional files.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
There is an error for one of the contributing authors. This has now been updated in the original article.
Figure S1. Amino acids are represented as (a) a, d (hydrophobic); e, g (charged); b, c, f (polar) (b) Hydrophobic (Grey circles), Charged (textured circles), Polar (white circles). Figure S2. The color coding in Jalview  is described in the legend for Fig. 1. Figure S3. (a) The Multiple Sequence alignment was generated using CLUSTAL OMEGA, which represents conserved amino acid residues by an asterisk (*) mark and similarly charged amino acid residues by a colon (:). The most conserved region in all twelve THAP proteins is the amino terminal THAP domain, highlighted in grey. No conservation is found when the predicted alpha helical regions of (b) sTHAP with mTHAP (c) sTHAP with lTHAP (d) mTHAP with lTHAP protein groups are aligned with each other. The Multiple Sequence Alignments for Figures S3b, c and d were generated using CLUSTAL OMEGA and visualized using Jalview. The color coding in Jalview is described in the legend for Fig. 1. Figure S4. Protein models generated for (a) Full length THAP protein (b) Corresponding predicted alpha helical region. I TASSER results were viewed using VMD, selecting Ribbon model for secondary structure of proteins with alpha helix (purple), 310 helix (blue), Π- helix (red), beta sheet (yellow), turn (cyan) and coils (white). Figure S5. Superposition of THAP7 (green), THAP8 (blue), THAP11 (red). Figure S6. The reported crystal structure of THAP11 (yellow) is overlapped (using PyMOL) with the structure of the helical region of THAP11 (cyan) predicted using I TASSER. Table S1. Leucine content in THAP proteins and their predicted alpha helical regions. Table S2. LOGICOIL and Multicoil predicts higher order oligomer formation. Table S3. NLSmapper predicts NLS in THAP0, THAP1, THAP2, THAP4, THAP5, THAP9. The predicted NLS regions in THAP1 and THAP9 overlap with the predicted coiled coil regions of the respective proteins. (DOCX 2200 kb)