Phycocyanin-like phycobilisome proteins [46532] (26) oligomers of two different types of globin-like subunits containing two extra helices at the N-terminus binds a bilin chromophore
RPB6/omega subunit-like [63562] (2)
the bacterial omega and eukaryotic RPB6 subunits both function in polymerase assembly; the common core is involved in conserved interactions with other subunits uperfamily
Middle operon regulator, Mor [109659] (1) contains extra N-terminal dimerisation subdomain: alpha-hairpin (27-72) dimer is a four-helical bundle with right-handed twist
Alr1493-like [140216] (1) Pfam 04255; DUF433; contains extra C-terminal helix and N-terminal dimerisation interlock subdomain (scop_cf 47405)
Nanomeric phage protein-like [140219] (1) contains additional N and C-terminal helices and the C-terminal beta-strand forming an intersubunit beta-barrel with a channel
RpiR-like [158263] (1) Pfam 01418; contains two extra helices, one at each termini; overall arrangment of five helices is similar to the helical core of the lambda integrase-like catalytic domain (scop_fa 56350)
DNA-binding protein Mj223 [81690] (1) homologous to the MarR-like family in the DNA-binding region but dimerizes differently through the N- and C-terminal helical extensions to the common fold
Penicillinase repressor [101016] (4) homologous to the MarR-like family in the DNA-binding region but has a different dimerisation subdomain
Transcription factor MotA, activation domain [46813] (1) The N- and C-terminal helical extensions to the common fold form the dimer interface (distinct from that of ArsR-like family)
PF1790-like [140286] (1) sequence similarity to PH1932 in the N-terminal domain; the C-terminal domain provides new dimerisation interface made of a beta-hairpin and a coiled coil
HxlR-like [140304] (5) Pfam 01638; DUF24; the N- and C-terminal helical extensions to the common fold form the dimer interface similar to that of the ArsR-like family (scop_fa 46801)
STY4665 C-terminal domain-like [158308] (1) Pfam 07515; DUF1528; the "wing" hairpin, linker between helices 1 and 2 and the C-terminal tail together form an open beta-sheet barrel
PSPTO2686-like [158311] (1) Pfam 04337; DUF480; duplication: two "winged helix" domains are tightly packed "back-to-back" about pseudo twofold axis
YlxM/p13-like [109706] (2) Pfam 04297; UPF0122 structural and detectable sequence similarity to Sigma4 domain; contains extra C-terminal all-alpha oligomerization subdomain; forms different, helix-swapped dimers
KorB DNA-binding domain-like [109709] (1)
contains HTH motif in the common core; also contains extra N-terminal helix and C-terminal subdomain of 4 helices (left-handed superhelix) uperfamily
4-alpha-glucanotransferase, domain 2 [89013] (1) family 57 glycoside hydrolase; overall domain organization is similar to that of the alpha-mannosidase family
alpha-mannosidase, domain 2 [88693] (2) family 38 glycoside hydrolase; overall domain organization is similar to that of the 4-alpha-glucanotransferase family
Bacterial histone-fold protein [101318] (2) duplication: two repeats of histone fold are arranged as subunits in the archael histone dimer; new structure from Thermus thermophilus (1wws) comprised of dimers similar the to the H3-H4 tetramer
DNA polymerase III theta subunit-like [46576] (2) Pfam 06440 independent solution structure determinations of different members resulted in similar secondary structures but different folds
Apolipoprotein [47163] (3) Can exist in a coiled-coil oligomeric form, see PDB entry 1AV1 family may also include the five-helical bundle protein Apolipophorin-III
alpha-catenin/vinculin [47221] (4) possible duplication: contains several domains of this fold The listed PDB entries contain different large fragments but not the whole proteins
EsxAB dimer-like [140453] (1)
(hetero)dimer of alpha-hairpin subunits similar to that of the half-ferritin family; no bound metals uperfamily
ESAT-6 like [140454] (2) Pfam 06013; the conserwed WxG motif makes the turn at the alpha-hairpin tip
PE/PPE dimer-like [140459] (2)
(hetero)dimer of alpha-hairpin subunits similar to that of the half-ferritin family; no bound metals inside the bundle uperfamily
PE [140460] (1) Pfam 00934; pairs with with the N-terminal hairpin of PPE
PPE [140463] (1) Pfam 00823; contains extra C-terminal alpha-hairpin, unlike the PE family subunit
HP0062-like [158414] (1)
(homo)dimer of alpha-hairpin subunits similar to that of the half-ferritin family; no bound metals
4-helical cytokines [47266] (3)
there are two different topoisomers of this fold with different entanglements of the two crossover connections uperfamily
MAST3 pre-PK domain-like [140482] (1)
this domain precedes the Protein Kinase domain in Microtubule-associated serine/threonine-protein kinase 3 (MAST3) uperfamily
Bacillus cereus metalloprotein-like [158430] (1)
Duplication: tandem repeat of two domains of this fold with similar sequences; binds a dimetal ion cluster between the repeats
IVS-encoded protein-like [158446] (1)
IVS: Intervening sequence with conserved ORF in eubacterial 23S rRNA genes; forms a homopentamer with a toroid-shaped structure containing a tapered central channel
Bacteriophage CII protein [140520] (1) Pfam 05269; a compact helix-swapped dimer of the canonical fold; includes the extra C-terminal teramerisation region (alpha-helix); in the tetramer-DNA complex only two of the four HTH motifs interact with DNA
HAMP domain-like [158471] (1)
dimer of helix-loop-helix segments; distict from the HLH-like fold; parallel four-helical bundle with two overside connections
Pre-protein crosslinking domain of SecA [81766] (1)
core: 4 helices: bundle; flanked by two short beta-hairpins duplication: consists of two structural repeats
VCA0319-like [140553] (1) COG4453; extended and extra C-terminal helices; potential component of the bi-partite system also including an acetyltransferase
VirC2-like [158482] (1) Pfam 07181; duplicated ribbon-helix-helix motif; fold forms a trefoil knot
PutA pre-N-terminal region-like [158485] (1) in PutA it forms a separate ribbon-helix-helix domain connected to the N-terminal enzymatic domain by a flexible linker
MJ0366-like [158488] (1) PfamB 022101; duplicated ribbon-helix-helix motif; forms trefoil knot; predicted DNA binding
FlgN-like [140566] (1)
the last helix is shorter than the three others; a short extra helix between helices 2 an 3 fills the gap in the bundle uperfamily
DNA-binding domain (fragment?) of the TraM protein [63566] (1) old provisional classification awaiting the entire protein structure; structure of a different fragment of this protein (PDB 2g7o) is classified into a different superfamily
TraM-like [140580] (1)
multihelical oligomeric protein; structure of whole subunit is not known; the N-terminal part is implicated in DNA binding, the middle region forms tetrameric parallel coiled coil, surrounded by the C-terminal helices
LcrE-like [140598] (1) Duplication; contains two domains of this fold; Pfam 07201 (HrpJ-like) covers the first domain and the N-terminal half of the second domain
Hef domain-like [140629] (4) helicase/nuclease domain; forms homo and heterodimers; probably includes the Excinuclease UvrC C-terminal domain (scop_fa 81795, that contains a single NMR structure of a monomeric truncated domain, 1kft)
I/LWEQ domain [109886] (2) Pfam 01608 actin-binding motif that adopts different folds; possibly refolds upon binding
RNA-binding protein She2p [116941] (1)
5 helices; bundle, closed, left-handed twist; topological similarity to the middle domain of the L-aspartase-like fold (scop_cf 48556)
YoaC-like [140669] (1)
5 helices; bundle, one crossover connection, the arrangement of the first four helices is similar to the KaiA/RbsU domain fold (scop_cf 101214)
PF0609-like [140675] (1) specific to Thermococci; shares conserved carboxylic residues and similar dimerisation mode with the RNase III domain; contains integrated in the fold extra C-terminal helix, making it similar to the core fold of Ribosomal protein S7 (scop_cf 47972)
Ribosomal protein S7 [47972] (1)
core: 5 helices; contains one more helix and a beta-hairpin outside the core
RPA2825-like [158633] (1)
5 helices, array; long flexible loop between helices 1 and 2; the remaining helices are arranged similar to the PGBD-like fold (scop_cf 47089)
IpaD-like [140692] (1)
6 helices; bundle, up-and-down; can be divided into two four-helical bundles sharing two helices (3 and 6), which are twice longer than the rest
Mediator hinge subcomplex-like [140717] (1)
6 helices; heterodimer of structurally similar subunits; the N-terminal hairpins form a four-helical bundle, whereas the C-terminal helices form coiled coil structure
AF0941-like [140725] (1)
6 helices, arranged into two interconnected 3-helical bundles; can also be described as a 'kinked' four-helical bundle; right-handed superhelix
Rv1873-like [140737] (1) contains conserved motif HWuW at the beginning of the central helix
RUN domain-like [140740] (1)
multihelical; 3-helical bundle similar to one half of the DEATH domain fold is flanked by two alpha-hairpins forming a four-helical bundle; the axes of the three-helical and four-helical bundles are aproximately orthogonal to each other
TerB-like [158681] (1)
multihelical; contains two central helices; duplication: there are two three-helical repeats related by pseudo twofold symmetry
TerB-like [158682] (2)
members of this superfamily probably related to the tellurite resistance protein TerB (Pfam 05099) of yet undetermined structure
Regulator of G-protein signaling, RGS [48096] (1)
multihelical; consists of two all-alpha subdomains contains a 4-helical bundle with left-handed twist and up-and-down topology
Variable surface antigen VlsE [74747] (1)
multihelical; consists of two all-alpha subdomains; contains a 4-helical bundle with left-handed twist and up-and-down topology
PG0816-like [140752] (1)
multihelical; comprises two helical bundles, both are topologically similar to the RuvA C-terminal domain-like fold (scop_cf 46928)
YfbU-like [116959] (1)
multihelical; consist of two subdomains; forms 24-mer with the N-terminal sudbomains packing around the 4-fold axis and the C-terminal domains interacting at the 2-fold and 3-fold axes
MG296-like [158714] (1)
multihelical; in crystal forms helical polymers by swapping the two N-terminal helices to the next subunit in polymer; three subunits per turn of polymer helix
alpha/alpha toroid [48207] (6)
multihelical; up to seven alpha-hairpins are arranged in closed circular array; there may be sequence similarities between different superfamilies
SMc04008-like [158756] (1)
multihelcal; intertwined homodimer; there are 4 core helices in each subunits; contains putative metal ion-binding motif MxxxxxCxxC in the conserved surface site
H-NS histone-like proteins [81274] (1)
multihelical oligomeric protein; structure of whole subunit is not known yet but are probably composed of three different domains
H-NS histone-like proteins [81273] (1)
available NMR structures suggest two very different dimerisation modes of the N-terminal domain uperfamily
all-alpha NTP pyrophosphatases [101385] (1)
multihelical: dimeric 4-helical bundle surrounded by other helices; oligomerizes further in a tetramer
all-alpha NTP pyrophosphatases [101386] (4)
basic module consist of 5 active site-forming helices; four from one subunit/structural repeat; the fifth from the other subunit/repeat uperfamily
AF0060-like [140794] (1) consists of a single member with an orphan sequence; "circular permutation" of putative active site residues: the catalytic lysine resides in the N-terminal helix instead of the missing in this family C-terminal helix; probable biological unit is a tertramer, distinct from the MazG family tetramer
Type II deoxyuridine triphosphatase [101387] (2) one subunit comprises two degenerate structural repeats, organised into the "rigid" and "mobile" subdomains
MIF4G domain-like [100908] (5) duplication: family members contains 2 or more structurally similar domains of this fold connected by unstructured linkers
Pseudo ankyrin repeat [140861] (1) one repeat consist of 3 helices; there are similarities in the repeat sequence and assembly with the ankyrin repeat (scop_fa 48404)
PriB N-terminal domain-like [140913] (1)
multihelical bundle; contains buried central helix; also includes the PriA interface-forming insert subdomain (alpha+beta)
Triger factor/SurA peptide-binding domain-like [109998] (2)
there are sequence and functional similarities between the families, but their structural similarity is obscured by conformational flexibility (in the TF family) uperfamily
TF C-terminus [109999] (2) Pfam 05698; includes the upstream linker region not covered by the Pfam model
Terpenoid synthases [48575] (1)
multihelical; core: 8 helices (C-J) are arranged in 2 parallel layers
Terpenoid synthases [48576] (5)
duplication: two metal-binding sites are related by a pseudo dyad that also relates helices C-F to helices G-J uperfamily
GroEL equatorial domain-like [48592] (2)
duplication: two 4-helical subdomains are related by a pseudo dyad passing through the ATP-binding site uperfamily
Allosteric chorismate mutase [48604] (1) duplication: 2 weak structural repeats resembling subunits of E. coli protein
monomeric chorismate mutase [140942] (1) "un-swapped" four-helical relative of the homodimeric chorismate mutase domain
Secreted chorismate mutase-like [140945] (1) duplication; two structural repeats, like in the yeast enzyme, but with a different location of the remaining active site
AhpD [69119] (2) duplication: two-domain subunits form a helix-swapped trimer
Atu0492-like [140970] (5) duplication: similar subunit structure to the AhpD family, but the putative active site is conserved in different relative location; new hexameric architecture; similar dimeric interface to the CMD-like family
TTHA0727-like [140975] (2) similar to the CMD-like family by the subunit sequence and hexameric architecture; the segment-swapped subunit fold is similar to the AhpD domains
Topoisomerase V catalytic domain-like [140978] (1)
multihelical; irregular array; contains small amount of beta-structure and a 3-helical bundle with a variant homeofomain-like fold and HTH motif (scop_cf 46688)
PMT central region-like [158841] (1)
multihelical; comprises two four-helical bundles of different topologies and an irregular helical array packed against a small beta-sheet
Di-heme elbow motif [48711] (13) the main characteristic feature of this motif is the packing of its two hemes many members contains one or more complete motifs flanked by incomplete motifs and/or other domains