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1 is distantly related to the odorant-binding protein superfamily.
2 calcium signal modulators within the EF-hand protein superfamily.
3 elongs to the l-2-haloacid dehalogenase-like protein superfamily.
4 the thioester-containing alpha-macroglobulin protein superfamily.
5 tem is recruited to a member of the coupling protein superfamily.
6 functionally diverse germin/seed storage 7S protein superfamily.
7 to metalloenzymes within the amidohydrolase protein superfamily.
8 her members of the cyclic nucleotide-binding protein superfamily.
9 arrangement of transmembrane helices in this protein superfamily.
10 brane lipoprotein and member of the secretin protein superfamily.
11 -loop-helix-Per-ARNT-Sim homology (bHLH-PAS) protein superfamily.
12 spora, encodes a novel member of the PAS/LOV protein superfamily.
13 Fs (a minimum of 0.5%) to members of the ABC protein superfamily.
14 genes are demonstrated to belong to a novel protein superfamily.
15 rresponding polypeptide segments of the NtrC protein superfamily.
16 riant T cell epitopes encoded by the surface protein superfamily.
17 22 is a member of the plant small heat-shock protein superfamily.
18 tifs that describe possible subfamilies of a protein superfamily.
19 containing proteins) are members of the same protein superfamily.
20 roorotase, both members of an amidohydrolase protein superfamily.
21 ss multiple members of a polymorphic surface protein superfamily.
22 ongs to the ATP binding cassette transporter protein superfamily.
23 y, but is a member of the complement control protein superfamily.
24 orted in p21ras, a distant relative in the G-protein superfamily.
25 n for ral p24, a member of small GTP-binding protein superfamily.
26 medium-length dehydrogenase/reductase (MDR) protein superfamily.
27 oposed Transmembrane Acyl Transferase (TmAT) protein superfamily.
28 open reading frames encoding a novel "Oblin" protein superfamily.
29 reaction mechanism in a seemingly well-known protein superfamily.
30 ifier (SUMO) is a member of a ubiquitin-like protein superfamily.
31 lipid transfer proteins as members of an RBG protein superfamily.
32 genetically conserved EF-hand Ca(2+)-binding protein superfamily.
33 ranscription factors of the nuclear receptor protein superfamily.
34 nagement for a representative of the SWI/SNF protein superfamily.
35 nderstanding the evolution of this important protein superfamily.
36 some biogenesis proteins that belong to WD40 protein superfamily.
37 ty for RapA, a representative of the SWI/SNF protein superfamily.
38 ly compromise mammalian members of the Sec14-protein superfamily.
39 ognition and binding by the small heat shock protein superfamily.
40 alcium signal modulators" within the EF-hand protein superfamily.
41 is the founding member of a large eukaryotic protein superfamily.
42 biogenesis that is a member of the secretin protein superfamily.
43 is probably common to all members of the ABC protein superfamily.
44 ily branch of the aquaporin (major intrinsic protein) superfamily.
45 is a member of the CRP (cyclic AMP receptor protein) superfamily.
46 s bacterial DNA gyrase, a member of the GHKL proteins superfamily.
47 as revealed the functional diversity of many protein superfamilies.
48 encompassing a substantial fraction of both protein superfamilies.
49 or previously unrecognized families of large protein superfamilies.
50 re catalysts derived from invariant cores of protein superfamilies.
51 structural plasticity unparalleled in other protein superfamilies.
52 s that had been derived from a wide range of protein superfamilies.
53 in other proteins including members of the G-protein superfamily, a family that has structural homolo
54 nsus sequences from the major intrinsic lens protein superfamily; a "touchdown" PCR protocol accommod
55 Members of the ATP binding cassette (ABC) protein superfamily actively transport a wide range of s
58 ryotic FMNAT enzymes belong to two different protein superfamilies and apparently utilize different s
59 TNfn3 and TI I27 are members of different protein superfamilies and have no sequence identity but
60 ct of network construction used in analyzing protein superfamilies and present a heuristic approach f
61 dependent beta-ketoacyl reductase of the SDR protein superfamily and further suggest that the ACP of
62 protein 55 (ARA55/Hic-5) belongs to the LIM protein superfamily and is featured by three or four N-t
63 dered as the ancestor of the histidine triad protein superfamily and is highly conserved from bacteri
65 tion of events previously unknown in the GST protein superfamily and potentially explaining the disti
66 r kinase/heat shock protein 70/actin (ASKHA) protein superfamily and that they retain the highly cons
67 PSI but which belong to the Chl a/b-binding protein superfamily and which are unrelated to the CBP o
68 etory, antigen 5, and pathogenesis-related 1 protein) superfamily and has been shown to bind the inte
69 imum structural features of a member of this protein superfamily, and can be described as a "mini- zi
70 , the new protein itself is a member of this protein superfamily, and consequently we designated it H
71 lyases, DddY has not been classified into a protein superfamily, and its structure and catalytic mec
72 Both Mer and Ex are members of the Band 4.1 protein superfamily, and, based on analyses of mer ex do
74 onse, members of the RelA/SpoT homolog (RSH) protein superfamily are activated by specific stress sti
75 e-dimensional structures of members of the G protein superfamily are considered in light of other bio
78 d Rh proteins, the only two members of their protein superfamily, are NH(3) and CO(2), respectively.
79 ransduction molecule in the heterotrimeric G protein superfamily, are thought to play a key role in t
80 members of the seven transmembrane domain G-protein superfamily as potential chemokine receptors.
81 APETALA2/ethylene responsive element binding protein superfamily, as a DELLA interactor with physiolo
82 entified activin A, a member of the TGF-beta protein superfamily, as a product of the murine fetal Le
83 on of DOCK7, a member of the DOCK180-related protein superfamily, as a Rac GTPase activator that is a
84 two members of the serine/arginine-rich (SR) protein superfamily (ASF/SF2 and SC35) act antagonistica
86 nodulin-like members of the major intrinsic protein superfamily branch of the aquaporin (major intri
87 clade within the large HD-domain/PDEase-like protein superfamily, but no eukaryotic members of this s
88 of proteins, particularly enzymes, within a protein superfamily can be understood not only in terms
89 Rap proteins, members of the Ras small G protein superfamily, can inhibit Ras signaling through t
90 -adenosylmethionine (RaS) enzymes, a diverse protein superfamily capable of catalyzing chemically dif
91 longation factor 2 (eEF2), a member of the G-protein superfamily, catalyzes the post-peptidyl transfe
92 , a member of doublecortin domain-containing protein superfamily, causes non-syndromic recessive deaf
94 ncement (ACE), to search both highly diverse protein superfamilies-composed of single-fold and fold-s
95 guanine nucleotide-binding protein (small G protein) superfamily comprises 5 subfamilies (Ras, Rho,
99 Drosophila kelch gene encodes a member of a protein superfamily defined by the presence of kelch rep
100 re of an ammonia channel from the Amt/MEP/Rh protein superfamily, determined to 1.35 angstrom resolut
101 ase (HO)-like metalloenzymes are an emerging protein superfamily diverse in reaction outcome and mech
102 annotation of protein sequences, determining protein superfamily-domain relationships, and detecting
103 encode a new member of the small heat shock protein superfamily, DR1314 is predicted to encode a hyp
104 rs of the radical S-adenosylmethionine (SAM) protein superfamily; each has sequence motifs to ligate
106 nstitute one of the largest and most ancient protein superfamilies found in all living organisms.
107 brary-sequence length was evaluated using 54 protein superfamilies from the PIR39 database and 110 pr
108 ation data have been derived for a number of protein superfamilies from the Structural Classification
109 ion channels by members of the ABC transport protein superfamily has been implicated in hyperinsuline
110 nsus functional information for evolutionary protein superfamilies, has been updated to include annot
112 o belongs to the large winged helix/forkhead protein superfamily, HILS1 may also regulate gene transc
116 perfamily of unknown mode of action, the CAP protein superfamily [i.e. cysteine-rich secretory protei
117 ABC transporters form one of the largest protein superfamilies in all domains of life, catalyzing
118 ers a wealth of new interactions among three protein superfamilies in Drosophila and sets the stage f
119 Using known evolutionary relationships among protein superfamilies in SCOP database, support vector m
122 from the luciferase-like hydride transferase protein superfamily in the biosynthesis of bioactive mol
123 in-coupled receptors (GPCRs) are the largest protein superfamily in the human genome; they comprise 3
124 ther, our analyses suggest an origin of this protein superfamily in the last common eukaryotic ancest
125 of Sec4, a member of the Rab family in the G protein superfamily, in two states: bound to GDP, and to
127 time the evolutionary tree of the ENase-like protein superfamily inferred from quantitative compariso
130 structure for the functionally diverse Nudix protein superfamily is nucleotide-diphosphate-X, where X
131 e results suggest that the expansion of this protein superfamily is one of the factors that have cont
132 YopM, a member of the leucine-rich repeat protein superfamily, is an effector produced by the bubo
133 RapA, a prokaryotic member of the SWI/SNF protein superfamily, is an integral part of the RNA poly
134 ucted from the structure-based alignments of protein superfamily members in the CAMPASS database.
136 (HA) receptor Lyve-1 is a member of the Link protein superfamily most similar to the leukocyte HA rec
138 The regulators of G protein signaling (RGS) protein superfamily negatively controls G protein-couple
139 Peroxiredoxins (Prxs or Prdxs) are a large protein superfamily of antioxidant enzymes that rapidly
142 ber of the DHH (Asp-His-His) phosphoesterase protein superfamily of molecules important for cell moti
144 most ancient members of the histidine triad protein superfamily of nucleotidyltransferases and hydro
149 in 1 (YB-1) belongs to the cold-shock domain protein superfamily, one of the most evolutionarily cons
150 the genera Anaplasma and Ehrlichia encode a protein superfamily, pfam01617, which includes the predo
151 diverse at the primary sequence level, this protein superfamily retains the same basic two-domain st
152 was shown to encode a member of the neurexin protein superfamily secreted by glia and subsequently lo
153 relationships between the evolution of this protein superfamily sequence and the acquisition of dist
155 bers of the scavenger receptor cysteine rich protein superfamily (SRCRSF) and the immunoglobulin supe
157 strong homology to the mitochondrial carrier protein superfamily, suggesting that LIP-36 is a chlorop
158 tural conservation across the ubiquitin-like protein superfamily suggests that the general principle
159 synthesized by a previously uncharacterized protein superfamily, termed DUF5825, in conjunction with
160 C) transporters belong to one of the largest protein superfamilies that expands from prokaryotes to m
161 plasmic binding proteins (PBPs) constitute a protein superfamily that binds a wide variety of ligands
162 s (ALDHs) are members of NAD(P)(+)-dependent protein superfamily that catalyze the oxidation of a wid
163 the GalT/Apa1 branch of the histidine triad protein superfamily that catalyzes the conversion of GDP
165 CheY is a member of the response regulator protein superfamily that controls the chemotactic swimmi
166 /3 activator of the Wiskott-Aldrich syndrome protein superfamily that functions during endosomal traf
167 the structures of the catalytic domains of a protein superfamily that includes other histone acetyltr
168 ns of sequence similarity and define a novel protein superfamily that is conserved in metazoans.
170 riplasmic binding proteins (PBPs) comprise a protein superfamily that is involved in prokaryotic solu
171 in belonging to the Wiskott-Aldrich syndrome protein superfamily that participates in endosomal recep
172 drial enzyme, therefore, represents a fourth protein superfamily that supports GSH transferase activi
173 s a member of the ATP Binding Cassette (ABC) protein superfamily, the members of which contain an imp
178 e multiple members of the parasite's surface protein superfamily; these extracellular proteins should
179 es with 5-ASA inactivation, belonging to two protein superfamilies: thiolases and acyl-CoA N-acyltran
181 nd the ability of other members in the actin protein superfamily to efficiently use both ATP and GTP,
183 trinsic to the bacterial periplasmic binding protein superfamily, to establish allosterically control
185 ructure and function in the small heat-shock protein superfamily, was determined in the context of th
187 r understand the evolution of this PCAD-Memo protein superfamily, we explored their structural and fu
189 dedicator of cytokinesis (DOCK) 180-related protein superfamily were identified as targets of miR-21
190 be used to classify and analyse any diverse protein superfamily where sub-families have diverged ove
191 e-neighborhoods with genes for a plethora of protein superfamilies, which we predict to function as n
192 RPSs also code for a member of the MbtH-like protein superfamily, which are small proteins of unknown
193 nd YiiM are hypothetical members of the MOSC protein superfamily, which contain the C-terminal domain
194 ulatory factors belong to the helical repeat protein superfamily, which includes tetratricopeptide re
195 this, cellular life has evolved the ferritin protein superfamily, which includes the 24 subunit ferri
196 sin is part of the microtubule-binding motor protein superfamily, which serves important roles in cel
197 other species as well as members of the same protein superfamily, which share the same structural ele
199 ures and biochemical data revealed a diverse protein superfamily with a common Greek-key beta sandwic
200 oughout phylogeny, yet there is a DNA-repair protein superfamily with a wide substrate specificity fo
201 (MfmAB) and are members of the ureohydrolase protein superfamily with binuclear metal-dependent activ
202 and malate dehydrogenases comprise a complex protein superfamily with multiple enzyme homologues foun
204 er of the human cold shock domain-containing protein superfamily, with known functions in cell prolif
205 ember (1,604 residues, 182,187 Da) of the IF protein superfamily, with the majority of the molecule c