Common fold in helix-hairpin-helix proteins.
نویسندگان
چکیده
Helix-hairpin-helix (HhH) is a widespread motif involved in non-sequence-specific DNA binding. The majority of HhH motifs function as DNA-binding modules, however, some of them are used to mediate protein-protein interactions or have acquired enzymatic activity by incorporating catalytic residues (DNA glycosylases). From sequence and structural analysis of HhH-containing proteins we conclude that most HhH motifs are integrated as a part of a five-helical domain, termed (HhH)(2) domain here. It typically consists of two consecutive HhH motifs that are linked by a connector helix and displays pseudo-2-fold symmetry. (HhH)(2) domains show clear structural integrity and a conserved hydrophobic core composed of seven residues, one residue from each alpha-helix and each hairpin, and deserves recognition as a distinct protein fold. In addition to known HhH in the structures of RuvA, RadA, MutY and DNA-polymerases, we have detected new HhH motifs in sterile alpha motif and barrier-to-autointegration factor domains, the alpha-subunit of Escherichia coli RNA-polymerase, DNA-helicase PcrA and DNA glycosylases. Statistically significant sequence similarity of HhH motifs and pronounced structural conservation argue for homology between (HhH)(2) domains in different protein families. Our analysis helps to clarify how non-symmetric protein motifs bind to the double helix of DNA through the formation of a pseudo-2-fold symmetric (HhH)(2) functional unit.
منابع مشابه
Mechanism for the -Helix to -Hairpin Transition
The aggregation of -helix-rich proteins into -sheet-rich amyloid fibrils is associated with fatal diseases, such as Alzheimer’s disease and prion disease. During an aggregation process, protein secondary structure elements— -helices— undergo conformational changes to -sheets. The fact that proteins with different sequences and structures undergo a similar transition on aggregation suggests that...
متن کاملA MODEL FOR THE BASIC HELIX- LOOPHELIX MOTIF AND ITS SEQUENCE SPECIFIC RECOGNITION OF DNA
A three dimensional model of the basic Helix-Loop-Helix motif and its sequence specific recognition of DNA is described. The basic-helix I is modeled as a continuous ?-helix because no ?-helix breaking residue is found between the basic region and the first helix. When the basic region of the two peptide monomers are aligned in the successive major groove of the cognate DNA, the hydrophobi...
متن کاملNucleic Acid Helix-Coil Transitions Mediated by Helix-unwinding Proteins from Calf Thymus”
We have studied nucleic acid double helix destabilization mediated by purified calf helix-unwinding proteins, measuring ultraviolet hyperchromicity to detect helix melting. Both,calf unwinding protein 1 (UPl) and a high salt eluting protein fraction are found to depress strongly the helix melting temperature (T,) of the synthetic alternating copolymers poly[d(AT) ] and poly[r(AU)], indicating t...
متن کاملNucleic acid helix-coil transitions mediated by helix-unwinding proteins from calf thymus.
We have studied nucleic acid double helix destabilization mediated by purified calf helix-unwinding proteins, measuring ultraviolet hyperchromicity to detect helix melting. Both calf unwinding protein 1 (UP1) and a high salt eluting protein fraction are found to depress strongly the helix melting temperature (Tm) of the synthetic alternating copolymers poly[d(AT)] and poly[r(AU)], indicating th...
متن کاملNucleic Acid Helix-Coil Transitions Mediated by Helix-unwinding Proteins from Calf Thymus”
We have studied nucleic acid double helix destabilization mediated by purified calf helix-unwinding proteins, measuring ultraviolet hyperchromicity to detect helix melting. Both,calf unwinding protein 1 (UPl) and a high salt eluting protein fraction are found to depress strongly the helix melting temperature (T,) of the synthetic alternating copolymers poly[d(AT) ] and poly[r(AU)], indicating t...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Nucleic acids research
دوره 28 14 شماره
صفحات -
تاریخ انتشار 2000