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1 the thioester-containing alpha-macroglobulin protein superfamily.
2 tem is recruited to a member of the coupling protein superfamily.
3 functionally diverse germin/seed storage 7S protein superfamily.
4 to metalloenzymes within the amidohydrolase protein superfamily.
5 her members of the cyclic nucleotide-binding protein superfamily.
6 arrangement of transmembrane helices in this protein superfamily.
7 brane lipoprotein and member of the secretin protein superfamily.
8 -loop-helix-Per-ARNT-Sim homology (bHLH-PAS) protein superfamily.
9 spora, encodes a novel member of the PAS/LOV protein superfamily.
10 Fs (a minimum of 0.5%) to members of the ABC protein superfamily.
11 genes are demonstrated to belong to a novel protein superfamily.
12 rresponding polypeptide segments of the NtrC protein superfamily.
13 riant T cell epitopes encoded by the surface protein superfamily.
14 22 is a member of the plant small heat-shock protein superfamily.
15 tifs that describe possible subfamilies of a protein superfamily.
16 containing proteins) are members of the same protein superfamily.
17 roorotase, both members of an amidohydrolase protein superfamily.
18 ss multiple members of a polymorphic surface protein superfamily.
19 ongs to the ATP binding cassette transporter protein superfamily.
20 orted in p21ras, a distant relative in the G-protein superfamily.
21 genetically conserved EF-hand Ca(2+)-binding protein superfamily.
22 n for ral p24, a member of small GTP-binding protein superfamily.
23 ranscription factors of the nuclear receptor protein superfamily.
24 y, but is a member of the complement control protein superfamily.
25 nagement for a representative of the SWI/SNF protein superfamily.
26 nderstanding the evolution of this important protein superfamily.
27 ty for RapA, a representative of the SWI/SNF protein superfamily.
28 ly compromise mammalian members of the Sec14-protein superfamily.
29 ognition and binding by the small heat shock protein superfamily.
30 alcium signal modulators" within the EF-hand protein superfamily.
31 is the founding member of a large eukaryotic protein superfamily.
32 biogenesis that is a member of the secretin protein superfamily.
33 is probably common to all members of the ABC protein superfamily.
34 is distantly related to the odorant-binding protein superfamily.
35 calcium signal modulators within the EF-hand protein superfamily.
36 elongs to the l-2-haloacid dehalogenase-like protein superfamily.
37 ily branch of the aquaporin (major intrinsic protein) superfamily.
38 is a member of the CRP (cyclic AMP receptor protein) superfamily.
39 as revealed the functional diversity of many protein superfamilies.
40 encompassing a substantial fraction of both protein superfamilies.
41 or previously unrecognized families of large protein superfamilies.
42 re catalysts derived from invariant cores of protein superfamilies.
43 structural plasticity unparalleled in other protein superfamilies.
44 s that had been derived from a wide range of protein superfamilies.
45 in other proteins including members of the G-protein superfamily, a family that has structural homolo
46 nsus sequences from the major intrinsic lens protein superfamily; a "touchdown" PCR protocol accommod
47 Members of the ATP binding cassette (ABC) protein superfamily actively transport a wide range of s
49 ryotic FMNAT enzymes belong to two different protein superfamilies and apparently utilize different s
50 TNfn3 and TI I27 are members of different protein superfamilies and have no sequence identity but
51 ct of network construction used in analyzing protein superfamilies and present a heuristic approach f
52 dependent beta-ketoacyl reductase of the SDR protein superfamily and further suggest that the ACP of
53 protein 55 (ARA55/Hic-5) belongs to the LIM protein superfamily and is featured by three or four N-t
54 dered as the ancestor of the histidine triad protein superfamily and is highly conserved from bacteri
55 tion of events previously unknown in the GST protein superfamily and potentially explaining the disti
56 r kinase/heat shock protein 70/actin (ASKHA) protein superfamily and that they retain the highly cons
57 etory, antigen 5, and pathogenesis-related 1 protein) superfamily and has been shown to bind the inte
58 imum structural features of a member of this protein superfamily, and can be described as a "mini- zi
59 , the new protein itself is a member of this protein superfamily, and consequently we designated it H
60 lyases, DddY has not been classified into a protein superfamily, and its structure and catalytic mec
61 Both Mer and Ex are members of the Band 4.1 protein superfamily, and, based on analyses of mer ex do
62 e-dimensional structures of members of the G protein superfamily are considered in light of other bio
64 d Rh proteins, the only two members of their protein superfamily, are NH(3) and CO(2), respectively.
65 ransduction molecule in the heterotrimeric G protein superfamily, are thought to play a key role in t
66 members of the seven transmembrane domain G-protein superfamily as potential chemokine receptors.
67 APETALA2/ethylene responsive element binding protein superfamily, as a DELLA interactor with physiolo
68 entified activin A, a member of the TGF-beta protein superfamily, as a product of the murine fetal Le
69 on of DOCK7, a member of the DOCK180-related protein superfamily, as a Rac GTPase activator that is a
70 two members of the serine/arginine-rich (SR) protein superfamily (ASF/SF2 and SC35) act antagonistica
72 nodulin-like members of the major intrinsic protein superfamily branch of the aquaporin (major intri
73 of proteins, particularly enzymes, within a protein superfamily can be understood not only in terms
74 Rap proteins, members of the Ras small G protein superfamily, can inhibit Ras signaling through t
75 longation factor 2 (eEF2), a member of the G-protein superfamily, catalyzes the post-peptidyl transfe
76 , a member of doublecortin domain-containing protein superfamily, causes non-syndromic recessive deaf
78 guanine nucleotide-binding protein (small G protein) superfamily comprises 5 subfamilies (Ras, Rho,
81 Drosophila kelch gene encodes a member of a protein superfamily defined by the presence of kelch rep
82 re of an ammonia channel from the Amt/MEP/Rh protein superfamily, determined to 1.35 angstrom resolut
83 annotation of protein sequences, determining protein superfamily-domain relationships, and detecting
84 encode a new member of the small heat shock protein superfamily, DR1314 is predicted to encode a hyp
85 rs of the radical S-adenosylmethionine (SAM) protein superfamily; each has sequence motifs to ligate
87 brary-sequence length was evaluated using 54 protein superfamilies from the PIR39 database and 110 pr
88 ation data have been derived for a number of protein superfamilies from the Structural Classification
89 ion channels by members of the ABC transport protein superfamily has been implicated in hyperinsuline
90 nsus functional information for evolutionary protein superfamilies, has been updated to include annot
92 o belongs to the large winged helix/forkhead protein superfamily, HILS1 may also regulate gene transc
96 perfamily of unknown mode of action, the CAP protein superfamily [i.e. cysteine-rich secretory protei
97 ABC transporters form one of the largest protein superfamilies in all domains of life, catalyzing
98 ers a wealth of new interactions among three protein superfamilies in Drosophila and sets the stage f
99 Using known evolutionary relationships among protein superfamilies in SCOP database, support vector m
102 in-coupled receptors (GPCRs) are the largest protein superfamily in the human genome; they comprise 3
103 of Sec4, a member of the Rab family in the G protein superfamily, in two states: bound to GDP, and to
104 time the evolutionary tree of the ENase-like protein superfamily inferred from quantitative compariso
106 structure for the functionally diverse Nudix protein superfamily is nucleotide-diphosphate-X, where X
107 e results suggest that the expansion of this protein superfamily is one of the factors that have cont
108 YopM, a member of the leucine-rich repeat protein superfamily, is an effector produced by the bubo
109 RapA, a prokaryotic member of the SWI/SNF protein superfamily, is an integral part of the RNA poly
110 ucted from the structure-based alignments of protein superfamily members in the CAMPASS database.
112 (HA) receptor Lyve-1 is a member of the Link protein superfamily most similar to the leukocyte HA rec
114 The regulators of G protein signaling (RGS) protein superfamily negatively controls G protein-couple
115 Peroxiredoxins (Prxs or Prdxs) are a large protein superfamily of antioxidant enzymes that rapidly
117 ber of the DHH (Asp-His-His) phosphoesterase protein superfamily of molecules important for cell moti
119 most ancient members of the histidine triad protein superfamily of nucleotidyltransferases and hydro
124 in 1 (YB-1) belongs to the cold-shock domain protein superfamily, one of the most evolutionarily cons
125 the genera Anaplasma and Ehrlichia encode a protein superfamily, pfam01617, which includes the predo
126 diverse at the primary sequence level, this protein superfamily retains the same basic two-domain st
127 was shown to encode a member of the neurexin protein superfamily secreted by glia and subsequently lo
128 relationships between the evolution of this protein superfamily sequence and the acquisition of dist
130 bers of the scavenger receptor cysteine rich protein superfamily (SRCRSF) and the immunoglobulin supe
132 strong homology to the mitochondrial carrier protein superfamily, suggesting that LIP-36 is a chlorop
133 tural conservation across the ubiquitin-like protein superfamily suggests that the general principle
134 C) transporters belong to one of the largest protein superfamilies that expands from prokaryotes to m
135 plasmic binding proteins (PBPs) constitute a protein superfamily that binds a wide variety of ligands
136 s (ALDHs) are members of NAD(P)(+)-dependent protein superfamily that catalyze the oxidation of a wid
137 the GalT/Apa1 branch of the histidine triad protein superfamily that catalyzes the conversion of GDP
139 CheY is a member of the response regulator protein superfamily that controls the chemotactic swimmi
140 /3 activator of the Wiskott-Aldrich syndrome protein superfamily that functions during endosomal traf
141 the structures of the catalytic domains of a protein superfamily that includes other histone acetyltr
142 ns of sequence similarity and define a novel protein superfamily that is conserved in metazoans.
144 riplasmic binding proteins (PBPs) comprise a protein superfamily that is involved in prokaryotic solu
145 drial enzyme, therefore, represents a fourth protein superfamily that supports GSH transferase activi
146 s a member of the ATP Binding Cassette (ABC) protein superfamily, the members of which contain an imp
151 e multiple members of the parasite's surface protein superfamily; these extracellular proteins should
153 nd the ability of other members in the actin protein superfamily to efficiently use both ATP and GTP,
155 trinsic to the bacterial periplasmic binding protein superfamily, to establish allosterically control
156 ructure and function in the small heat-shock protein superfamily, was determined in the context of th
159 dedicator of cytokinesis (DOCK) 180-related protein superfamily were identified as targets of miR-21
160 be used to classify and analyse any diverse protein superfamily where sub-families have diverged ove
161 e-neighborhoods with genes for a plethora of protein superfamilies, which we predict to function as n
162 RPSs also code for a member of the MbtH-like protein superfamily, which are small proteins of unknown
163 nd YiiM are hypothetical members of the MOSC protein superfamily, which contain the C-terminal domain
164 ulatory factors belong to the helical repeat protein superfamily, which includes tetratricopeptide re
166 ures and biochemical data revealed a diverse protein superfamily with a common Greek-key beta sandwic
167 oughout phylogeny, yet there is a DNA-repair protein superfamily with a wide substrate specificity fo
168 and malate dehydrogenases comprise a complex protein superfamily with multiple enzyme homologues foun
170 er of the human cold shock domain-containing protein superfamily, with known functions in cell prolif
171 ember (1,604 residues, 182,187 Da) of the IF protein superfamily, with the majority of the molecule c
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