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1                                Asp142 in the homotetrameric ADP-glucose pyrophosphorylase (ADP-Glc PP
2                      Lysine (Lys)-195 in the homotetrameric ADP-glucose pyrophosphorylase (ADPGlc PPa
3 omologous to those of bacterial and archaeal homotetrameric alcohol dehydrogenases (ADHs) and also to
4 e (Zea mays) rf2a and rf2b genes both encode homotetrameric aldehyde dehydrogenases (ALDHs).
5 esence of secretable and functionally active homotetrameric alpha- and beta-tryptases in transfected
6                 The four active sites of the homotetrameric apoenzyme appear to divide into two numer
7 herichia coli MgsA is described, revealing a homotetrameric arrangement for the protein that distingu
8 ined by both the direct DNA contacts and the homotetrameric arrangement of the Cre monomers.
9  functional CRAC channel pore is formed by a homotetrameric assembly of Orai1 subunits.
10 rate that Kir 2.2 channels are formed by the homotetrameric association of Kir 2.2 subunits and do no
11 alcium selectivity filter constructed in the homotetrameric bacterial NaV channel NaVAb.
12 t differences between D. radiodurans SSB and homotetrameric bacterial SSB proteins may confer a selec
13 ly showed that Escherichia coli (Eco) SSB, a homotetrameric bacterial SSB, undergoes not only rapid s
14 biochemical analyses, we identified a single homotetrameric bifunctional ammonia-lyase (PTAL) among e
15                Here we report that KRP130, a homotetrameric BimC-related kinesin purified from Drosop
16       Each pore-forming alpha subunit of the homotetrameric BK(Ca) channel is expected to contain two
17 dimeric by gel filtration chromatography and homotetrameric by dynamic light scattering and to contai
18  the cold receptor that forms a nonselective homotetrameric cation channel.
19 n two adjacent hERG1 subunits, and, hence, a homotetrameric channel has four identical RPR binding si
20 in the fully assembled, membrane-associated, homotetrameric channel protein.
21  of the influenza virus M(2) protein forms a homotetrameric channel that transports protons.
22 e of the complex shows the drug bound in the homotetrameric channel, threaded between the side chains
23 er) and increase the open probability of the homotetrameric channel.
24 ind that each of hBest1, 2, 3, and 4 forms a homotetrameric channel.
25  module between two adjacent subunits of the homotetrameric channel.
26 in tobacco mesophyll protoplasts: KAT2 forms homotetrameric channels active at the plasma membrane, w
27 gion, preventing surface expression of Kv1.1 homotetrameric channels and of heteromeric Kv1 channels
28 eases surface expression of functional Kv1.1 homotetrameric channels and support a model whereby a DT
29 mutation is permissive for the expression of homotetrameric channels that are nonselective for cation
30 e compared this pH-dependence with that from homotetrameric channels with four copies of the mutation
31   However, L18A/L25A channels failed to form homotetrameric channels, as assessed by Co-IP, suggestin
32 inity (K(d) values 7-21 nM) to each of these homotetrameric channels.
33 yl-tRNA synthetase, operates as well in this homotetrameric class II tRNA synthetase.
34 ess at least two distinct PEPC enzyme-forms, homotetrameric Class-1 and heteromeric Class-2, that dif
35 he Kv1.1 outward current when expressed as a homotetrameric complex (EC(50) = 0.34 nM).
36 at RECQ1 can form what appears to be a flat, homotetrameric complex and propose that RECQ1 tetramers
37 l muscle (RyR1) receptor isoforms, RyR3 is a homotetrameric complex comprising two main components, a
38 mass of 270 kDa, compatible with its being a homotetrameric complex of the approximately 64-kDa subun
39  pure SNAP-23N crystallizes as a coiled-coil homotetrameric complex.
40 tracellular superoxide dismutase (SOD3) is a homotetrameric copper- and zinc-containing glycoprotein
41 nformational ensembles of the D2 -symmetric, homotetrameric copper-sensitive operon repressor (CsoR)
42  Cys-504-Cys-504 dithiol-disulfide switch in homotetrameric CRMP2.
43                                              Homotetrameric Cys10 TTR variants, including TTR-Cys, TT
44 otubule gliding at a rate similar to that of homotetrameric Eg5 in vitro.
45 onucleases, thought to have evolved from the homotetrameric endonucleases.
46 +)-dependent enzyme, GCYH-IB is a bimodular, homotetrameric enzyme activated by a variety of divalent
47 of ATP binds at the subunit interface of the homotetrameric enzyme and that the majority of the ATP-e
48                           Each chain of this homotetrameric enzyme consists of 330 residues.
49 a reduction in the overall dimensions of the homotetrameric enzyme following substrate binding and ox
50 e synthase revealed four active sites of the homotetrameric enzyme located within deep tunnels.
51 tes reside in different subunits of a single homotetrameric enzyme molecule.
52                                         This homotetrameric enzyme possesses 222 symmetry, which impo
53                                          The homotetrameric enzyme provides a unique environment for
54                                          The homotetrameric enzyme required NADPH, flavin mononucleot
55                          PAAS is a cytosolic homotetrameric enzyme that belongs to group II pyridoxal
56 yl-acyl carrier protein (ACP) reductase is a homotetrameric enzyme that catalyzes the last reductive
57                  Pyruvate decarboxylase is a homotetrameric enzyme which crystallizes with two subuni
58 ate dehydrogenase from Escherichia coli is a homotetrameric enzyme which is allosterically regulated
59  manganese superoxide dismutase (MnSOD) is a homotetrameric enzyme which protects mitochondria agains
60 i pyruvate oxidase (PoxB), a lipid-activated homotetrameric enzyme, upon substrate binding.
61 utamate at residue 487 in the 500 amino acid homotetrameric enzyme.
62 , supporting the conclusion that ACAT-1 is a homotetrameric enzyme.
63 sessed just 16-18% activity of the glutamate homotetrameric enzyme.
64                                          The homotetrameric enzymes belong to the type I family of ex
65                                          The homotetrameric Escherichia coli single-stranded DNA bind
66                                          The homotetrameric Escherichia coli single-stranded DNA-bind
67     The kinetic mechanism of transfer of the homotetrameric Escherichia coli SSB protein between ssDN
68 or DrSSB that strongly resemble those of the homotetrameric Escherichia coli SSB, further supporting
69 ned the kinetic mechanism for binding of the homotetrameric Escherichia coliSSB protein to single-str
70     We demonstrate our approach on the yeast homotetrameric FBP1 complex, the rate-limiting enzyme in
71 dehydrogenase (IVD) is an intramitochondrial homotetrameric flavoenzyme that catalyzes the conversion
72 ort chain acyl-CoA dehydrogenase (SCAD) is a homotetrameric flavoenzyme that catalyzes the first intr
73  7.3 +/- 1.1 mum(2).s(-1), consistent with a homotetrameric form of Kaede.
74 ition, it has not been demonstrated that the homotetrameric form of these proteins is essential for t
75 ntisense response, due to the formation of a homotetrameric G quartet structure.
76                    In fluorescently labelled homotetrameric GIRK1 channels and in the heterotetrameri
77  similar to the distal (B/D) subunits in the homotetrameric GluA2 alpha-amino-3-hydroxy-5-methyl-4-is
78                  In this study, we expressed homotetrameric HCN2 channels in Xenopus oocytes and perf
79 x cooperative interaction of the subunits in homotetrameric HCN2 pacemaker channels.
80 hese studies to investigate formation of the homotetrameric hemoglobin H, whose formation in vivo is
81 onding enzyme from Saccharomyces uvarum, the homotetrameric holoenzyme assembly has approximate 222 s
82 on equilibrium analysis indicates an alpha 4 homotetrameric holoenzyme structure (4 x 38,861 Da).
83                             The structure of homotetrameric htADH is highly homologous to those of ba
84  the same family, kappaM-RIIIK, inhibits the homotetrameric human Kv1.2 channels.
85                                    Glu162 in homotetrameric human MnSOD spans a dimeric interface and
86                                          The homotetrameric influenza A M2 channel (AM2) is an acid-a
87                      Ryanodine receptors are homotetrameric intracellular calcium release channels.
88 .0 A resolution, which establishes PKD2 as a homotetrameric ion channel and provides insight into pot
89 Nematostella Shaker genes express functional homotetrameric K(+) channels in vitro.
90 s with high affinity to membranes expressing homotetrameric K(v)1.3 channels, and high affinity diTC
91                      The dynamic behavior of homotetrameric kinesin-5 during mitosis is poorly unders
92                              Eg5 or KSP is a homotetrameric Kinesin-5 involved in centrosome separati
93                                     Eg5 is a homotetrameric kinesin-5 motor protein that generates ou
94                                              Homotetrameric kinesin-5 motors are essential for chromo
95 ulations to dissect the various roles of the homotetrameric kinesin-5, KLP61F, in astral, centrosome-
96                                 Eg5/KSP is a homotetrameric, Kinesin-5 family member whose ability to
97                                              Homotetrameric Kv1.1 channels were localized to endoplas
98 y of tRNA(Met)i The crystal structure of the homotetrameric m1A58 tRNA Mtase from Mycobacterium tuber
99 heart of the H+ conductance mechanism in the homotetrameric M2 H+ channel from influenza A is a set o
100                                          The homotetrameric M2 integral membrane protein of influenza
101                                          The homotetrameric M2 proton channel of influenza A plays a
102             The system for this study is the homotetrameric M2 proton channel protein from the influe
103 removed by the product of the SOD2 gene, the homotetrameric manganese superoxide dismutase (MnSOD).
104 otein from influenza A virus is a 97-residue homotetrameric membrane protein that functions as a prot
105      Isovaleryl-CoA dehydrogenase (IVD) is a homotetrameric mitochondrial flavoenzyme which catalyzes
106 -CoA dehydrogenase (IVD), a nucleus-encoded, homotetrameric, mitochondrial flavoenzyme that catalyzes
107 al analyses of drug binding to the bacterial homotetrameric model CaV channel CaVAb, which is inhibit
108                                              Homotetrameric models of three mammalian Kir channels (K
109                          Kinesin-5 is a slow homotetrameric motor protein best known for its essentia
110    Kinesin-5 (also called Eg5 or kif11) is a homotetrameric motor protein that functions by modulatin
111                               Kinesin-5 is a homotetrameric motor protein that interacts with adjacen
112                 The crystal structure of the homotetrameric MtbThyX was determined in the presence of
113  a concatenated channel as that observed for homotetrameric mutant channels.
114 quaternary structure, a potato small subunit homotetrameric mutant, TG-15, was subjected to iteration
115                   Escherichia coli NikR is a homotetrameric Ni(2+)- and DNA-binding protein that func
116                                    NikR is a homotetrameric nickel regulatory protein whose binding t
117 ent, an intrinsic RNA kinase activity, and a homotetrameric or homodimeric quaternary structure, that
118 s are the largest known ion channels, with a homotetrameric organization and approximately 5,000 resi
119 5 motors, which display a conserved, bipolar homotetrameric organization consisting of two motor dime
120                                              Homotetrameric P. falciparum aldolase (PfALDO) crystalli
121 The influenza A virus M2 protein (A/M2) is a homotetrameric pH-activated proton transporter/channel t
122 His-37 from symmetry-related monomers of the homotetrameric pore converge to form a coordination site
123 ed that the principal functional unit of the homotetrameric PPK is a dimer.
124 at the MGAT2 enzyme primarily functions as a homotetrameric protein and as a tetrameric protein.
125                                   ACAT1 is a homotetrameric protein and contains nine transmembrane d
126  to cobalt and nickel regulator) is a 40-kDa homotetrameric protein and metalloregulator that control
127 igand interaction between biotin (B) and the homotetrameric protein complex streptavidin (S(4)) in th
128 In the crystal structure each subunit of the homotetrameric protein contains one substrate-binding si
129                  Aldolase (E.C. 4.1.2.13), a homotetrameric protein encoded by the ALDOA gene, conver
130              Transthyretin (TTR) is a plasma homotetrameric protein implicated in fatal systemic amyl
131  of the transmembrane-spanning region of the homotetrameric protein in the presence and absence of th
132 transthyretin (TTR), a human beta-sheet-rich homotetrameric protein that must undergo rate-limiting t
133 67 dihydrofolate reductase (DHFR) is a novel homotetrameric protein that possesses 222 symmetry and a
134                                      It is a homotetrameric protein that spans the membrane multiple
135                                          The homotetrameric protein transthyretin (TTR) must undergo
136                            The amyloidogenic homotetrameric protein transthyretin (TTR) must undergo
137                     The subunit size of this homotetrameric protein was 55 kDa, which is about half t
138   This is the case of transthyretin (TTR), a homotetrameric protein whose dissociation into its monom
139      The ryanodine receptor (RyR) is a large homotetrameric protein with a hydrophobic domain at the
140                              Streptavidin, a homotetrameric protein with extremely tight biotin bindi
141             This study shows that MHPCO is a homotetrameric protein with one flavin adenine dinucleot
142                                         This homotetrameric protein wraps ssDNA in multiple distinct
143 chondrial ssDNA-binding protein (mtSSB) is a homotetrameric protein, involved in mtDNA replication an
144  of symmetry at the dimer interfaces in this homotetrameric protein, suggesting that the quaternary s
145                     Transthyretin (TTR) is a homotetrameric protein.
146 a dimer of dimer quaternary structure of the homotetrameric protein.
147                                              Homotetrameric proteins can assemble by several differen
148  and that selective pressure may have caused homotetrameric proteins to evolve to assemble by a singl
149 ent members of the AQP family, the signature homotetrameric quaternary structure is conserved.
150        A recent crystal structure of active, homotetrameric R67 DHFR indicates that a single active s
151 olate and NADPH by approximately 100-fold in homotetrameric R67 DHFR.
152 wild-type and Lys --> Gln or Glu site mutant homotetrameric rabbit cytosolic SHMTs identified lysine
153             Here, we report a structure of a homotetrameric rat GluA2 receptor in complex with partia
154 4-isoxazole propionic acid (AMPA)-sensitive, homotetrameric, rat GluA2 receptor at 3.6 A resolution i
155                                   Unlike the homotetrameric recombinant GluR2, the native heterotetra
156 -contraction coupling involves activation of homotetrameric ryanodine receptor ion channels (RyR1s),
157 s of the square-shaped cytoplasmic region of homotetrameric RyR3.
158                       Human lung tryptase, a homotetrameric serine protease unique to mast cell secre
159 in the last transmembrane region (S6) of the homotetrameric Shaker K+ channel creates metal binding s
160                           We showed that the homotetrameric species exchanged dimers, because when th
161 tein is the adduct of the G26C mutant of the homotetrameric SSB from Escherichia coli and a diethylam
162  many of the same reactions catalyzed by the homotetrameric SSB of bacteria, but its origin, subunit
163 ing properties of these two highly conserved homotetrameric SSB proteins, and these differences might
164                               In contrast to homotetrameric SSB proteins, asymmetry exists between th
165       Escherichia coli SSB, a representative homotetrameric SSB, binds to ssDNA by wrapping the DNA u
166  results extend our previous observations on homotetrameric SSBs to homodimeric SSBs, indicating that
167  DrSSB that are analogous to those mapped in homotetrameric SSBs, although there are distinct contact
168 nylated Cp*Ir moiety (Cp* = C5Me5(-)) within homotetrameric streptavidin (Sav) (referred to as Cp*Ir(
169        The purified DAHP synthase displays a homotetrameric structure and exhibits maximal activity a
170 ar mass of 185 +/- 35 kDa, consistent with a homotetrameric structure for the native enzyme.
171                                          The homotetrameric structure of ES* was solved by MAD phasin
172                                          The homotetrameric structure of the ryanodine-sensitive intr
173                                         This homotetrameric structure reveals a novel KaiB interface
174 tes at each protein-protein interface in the homotetrameric structure with binding constants relative
175  Previous studies demonstrated a specialized homotetrameric structure with two pairs of catalytic dom
176 ristics of mammalian class 1 ALDHs include a homotetrameric structure, high expression in liver, sens
177 se product of ca. 50,000 Da assembles into a homotetrameric structure.
178 tuber LS and, in turn, enabling it to form a homotetrameric structure.
179   The building block structure consists of a homotetrameric subunit complex with three unique supramo
180                          The pseudo-fourfold homotetrameric synapse formed by Cre protein and target
181 thods to dissect the domain structure of the homotetrameric T4 Pnk protein and to localize essential
182 te editing status, in an otherwise identical homotetrameric TMD.
183      The p53 tumor suppressor gene encodes a homotetrameric transcription factor which is activated i
184  Common to both viruses is the M2 protein, a homotetrameric transmembrane proton channel that acidifi
185                     Transthyretin (TTR) is a homotetrameric transport protein, assembled from monomer
186  single subunit of the previously determined homotetrameric tRNA splicing endonuclease from Methanoco
187                                     p53 is a homotetrameric tumor suppressor protein that is found to
188  scorpion toxin, Charybdotoxin (CTX), blocks homotetrameric, voltage-gated K(+) channels by binding n
189                    Thus eubacterial SSBs are homotetrameric whilst the eucaryal RPA protein is a hete

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