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1 ansmitting the hormone binding signal to the catalytic domain.
2 bstrate and by an acidic patch in the kinase catalytic domain.
3 complexes that form over a large part of the catalytic domain.
4  cAMP, stimulates the activity of the PDE10A catalytic domain.
5 dopt a rigid structure, which stabilizes the catalytic domain.
6 nd a segment in the N-terminal region of the catalytic domain.
7  the available crystal structure of the GtfC catalytic domain.
8  by mitigating the global unfolding of LPL's catalytic domain.
9 targets as Ser33 and Ser34 in the N-terminal catalytic domain.
10 city to bind DNA and the processivity of the catalytic domain.
11 and a reporter of complementation within the catalytic domain.
12 lateral movements during the activity of the catalytic domain.
13 ), UCR1 and -2, which precede the C-terminal catalytic domain.
14 kely the pseudosymmetric site located in the catalytic domain.
15 ation and ROS production requiring the Sirt1 catalytic domain.
16 ET1ALT lacks the CXXC domain but retains the catalytic domain.
17 ertase Furin (RXXR) between the pro- and the catalytic domain.
18 -stranded RNA binding domains (dsRBDs) and a catalytic domain.
19 ukaryotic kingdoms and a conserved cytosolic catalytic domain.
20 al domain did not result in unmasking of the catalytic domain.
21 ite near Arg-106, which is distinct from the catalytic domain.
22 sts that this residue interacts with the MKK catalytic domain.
23 s at the junction of the propeptide with the catalytic domain.
24 giotensin converting enzyme 2, but without a catalytic domain.
25 ivity by directly binding to its ATP-binding catalytic domain.
26 l region and a carboxy-terminal caspase-like catalytic domain.
27 ce a detailed topological model of the CesA8 catalytic domain.
28 air in vivo by inactivating each of the four catalytic domains.
29 approximately 80% sequence identity in their catalytic domains.
30  regions that connect the protease-resistant catalytic domains.
31  in the N-terminal regulatory and C-terminal catalytic domains.
32  phospho-tail interacts with both the C2 and catalytic domains.
33 ry or the net homo-FRET between Venus-tagged catalytic domains.
34  switch to augment reductase activity in the catalytic domains.
35 induce an active dimeric conformation of the catalytic domains.
36 ted proteins, four of which were modified in catalytic domains.
37 catalytic site characteristic of minimal PLP catalytic domains.
38 tional units of CaMKII holoenzyme are paired catalytic-domains.
39 re, we present high-resolution structures of catalytic domain 2 from Danio rerio HDAC6 (henceforth si
40 as been proposed to bind, in addition to the catalytic domain, a site at the PAH N-terminal regulator
41  a large, multidomain protein containing two catalytic domains: a Ras of complex proteins (Roc) G-dom
42 delivery of its N-terminal adenylate cyclase catalytic domain (AC domain) into the cytosol, generates
43               We also observed that the DddY catalytic domain adopts a typical beta-barrel fold and c
44                In the complex structure, the catalytic domain adopts an open conformation, with the K
45                 On the anionic membrane, the catalytic domain adopts multiple orientations, including
46 ease and virulence, and glycosylation at the catalytic domain affects its thermostability; however, g
47 lated TrCel7A domains, we determine that the catalytic domain alone is sufficient for processive moti
48 AMTS structure comprises a metalloproteinase catalytic domain and a carboxy-terminal ancillary domain
49 es, we found that native HjLPMO9A contains a catalytic domain and a family-1 carbohydrate-binding mod
50                      RgNanH comprises a GH33 catalytic domain and a sialic acid-binding carbohydrate-
51      The C terminus of UBR5 harbors the HECT catalytic domain and an adjacent MLLE domain.
52       They consist of a separable C-terminal catalytic domain and an N-terminal transmembrane flippas
53                                    The VPS34 catalytic domain and BECN1:ATG14 subcomplex do not touch
54  extending from near the top of the enzyme's catalytic domain and crossing the membrane domain of the
55 ns, is composed of 747 amino acids forming a catalytic domain and extended N- and C-terminal regions.
56 rate-binding domain immediately precedes the catalytic domain and has tight associations with it.
57      We show that PolDIP2 binds to PrimPol's catalytic domain and identify potential binding sites.
58      By enhancing the linkage between ADAR's catalytic domain and the guide RNA, and by introducing a
59  sensitivity conferral protein (OSCP) to the catalytic domain and the membrane domain of subunit b to
60 ap, we explored the roles of residues of the catalytic domain and the regulatory subunit of human PI3
61                           In particular, the catalytic domain and the RNA-binding domain can move aro
62 s tight mechanochemical coupling between the catalytic domain and the rotating central shaft, as well
63 globular Sgf73 subunit lies between the Ubp8 catalytic domain and the ZnF-UBP domain and has been pro
64 ved by synergistic combination of E2-derived catalytic domain and tridomain.
65               They contain highly homologous catalytic domains and flexible C-terminal hypervariable
66 ng the regulatory domains docked against the catalytic domains and preventing substrate binding.
67  expressed, although some do not have active catalytic domains and their expression can be altered du
68 through association between the Rad50 ATPase catalytic domains and undergoes extensive conformational
69          The enzyme has a membrane extrinsic catalytic domain, and a membrane intrinsic domain where
70 fragment encompassing the propeptide and the catalytic domain, and found that the former runs across
71  near the junction between the prodomain and catalytic domain, and inhibits MMP9 by two mechanisms.
72 ts the dislodging and tethering of the VPS34 catalytic domain, and its regulation by VPS15, as a mast
73 of a C-terminal part of HUWE1, including the catalytic domain, and reveal an asymmetric auto-inhibite
74 on analyses and identified S1777, in TRPM7's catalytic domain, and S1565, in TRPM7's exchange domain
75  of Ubp10, USP36, also has IDRs flanking its catalytic domain, and these IDRs similarly contain bindi
76 t this fibrolytic bacterium uses diverse GH5 catalytic domains appended with different CBMs, includin
77 's disease (PD) have been identified in both catalytic domains, as well as in several of its multiple
78  organization or eventually consisted of one catalytic domain associated with a non-catalytic accesso
79 sphorylates UBE3A in a region outside of the catalytic domain at residue T485 and inhibits UBE3A acti
80 sertion, and orientation/localization of the catalytic domain at the membrane conjointly determine th
81 obe the functions of individual PKS and NRPS catalytic domains at the cellular metabolic level.
82 determined the crystal structure of the LuxO catalytic domain bound to a broad-spectrum inhibitor.
83 e report the crystal structures of the SETD2 catalytic domain bound to H3K36M or H3K36I peptides with
84 le, non-amphiphilic monomer with a canonical catalytic domain but a distinct C terminus compared with
85                         THEMIS lacks defined catalytic domains but contains two tandem repeats of a d
86 'large' SRs contain a compact amino-terminal catalytic domain, but differ conspicuously in their carb
87 istone deacetylase 1 (HDA-1), with an intact catalytic domain, but HDA-1 was not essential for de nov
88     We show that mutant ADAMTS-5 lacking the catalytic domain, but with a full suite of ancillary dom
89 udokinase domain regulates activation of the catalytic domain by forming receptor-regulated inhibitor
90 w that an N-terminal fragment comprising the catalytic domain can interact both with itself and with
91 t human RHOGAPs, from which 57 have a common catalytic domain capable of terminating RHO protein sign
92 odular architecture composed of a C-terminal catalytic domain (CAT), a central Trp-Gly-Arg (WGR) doma
93                        TrCel7A consists of a catalytic domain (CD) and a smaller carbohydrate-binding
94 eveloped an optogenetic toolbox fused to the catalytic domain (CD) of DNA-methyltransferase3A (DNMT3A
95 linker connected to an N- and O-glycosylated catalytic domain (CD)-a domain architecture common to ma
96 hermore, we investigated the binding of TET1-catalytic domain (CD)-GFP to DNA by Fluorescent Correlat
97                               Its C-terminal catalytic domain (CD2) alone is capable of binding singl
98 we present kinetic evidence showing that the catalytic domains (CDs) of TET2 and TET1 from mouse and
99  an alternative strategy that utilizes multi-catalytic domain cellulases.
100 e report a strong linear correlation between catalytic domain complementation and cyclase activity up
101                                          Its catalytic domain comprises the carboxy-terminal half (co
102            The crystal structure of LKA1gp49 catalytic domain consists of a beta-helix, an insertion
103                                          The catalytic domain consists of a central mixed beta-sandwi
104 lex that suggests that both the PNKP FHA and catalytic domains contact the XRCC4 coiled-coil and LigI
105  1-3 and helix 2 on the opposite face of the catalytic domain contribute to membrane binding.
106 presented of the 220 phosphodiesterase (PDE) catalytic domain crystal structures present in the Prote
107 inant MMP12 peptide fragments, including its catalytic domain, CTD, and a 20 amino acid peptide withi
108  increasing the expression of ATP synthase's catalytic domain, cytochrome c oxidase and its tyrosine
109 er, acquired resistance mutations within the catalytic domain decrease the efficacy of this strategy
110 mission, whereas overexpressing Tet3 or Tet1 catalytic domain decreased it.
111 g the crystal structure of the human nSMase2 catalytic domain determined at 1.85-A resolution.
112                                 We fused the catalytic domain (DHPH domain) of the RhoA activator ARH
113 affected by two LytM factors with degenerate catalytic domains, DipM and LdpF, which may serve as reg
114 or approximately 54% of the conformers whose catalytic domain directly interacts with the bilayer.
115  of K-Ras4B, thought to minimally impact the catalytic domain, directly interacts with the active sit
116  whereas mutation R360P in the N lobe of the catalytic domain disrupted an autoinhibitory mechanism,
117 i, which typically comprise multiple, single catalytic domain enzymes for biomass degradation, some b
118     An analog that docked poorly in the GtfC catalytic domain failed to inhibit the activity of Gtfs
119 composed of a pyridoxal 5'-phosphate-binding catalytic domain, flanked by the following two domains:
120 -anchored farnesyl and unrestrained HVR, the catalytic domain fluctuates reinlessly, exposing its eff
121          Residues Thr-123 and Phe-382 in the catalytic domain form a latch-like interaction with hydr
122 dy to the cysteine-rich domain liberates the catalytic domain from autoinhibition, enhancing enzymati
123      However, both the N- and C-terminal non-catalytic domains from all mammalian tolloids bind chord
124                                          The catalytic domain has a metallophosphatase fold, and two
125 nt and implications of the variations in the catalytic domain have not been described, and it is uncl
126 ependent conformational dynamics of the Cas9 catalytic domains (HNH and RuvC), responsible for concer
127  of Ca(2+)/CaM, elicited a large decrease in catalytic-domain homo-FRET, which was blocked by mutatin
128 3 to Val (E183V) mutation in the CaMKIIalpha catalytic domain, identified in a proband diagnosed with
129 nsient nature of ACP interactions with these catalytic domains imposes a major obstacle for investiga
130         Here we report structures of the A3B catalytic domain in a new crystal form that show alterna
131 rane binding involves helices 3 and 4 of the catalytic domain in addition to the farnesyl and polybas
132 deubiquitinating activity by maintaining the catalytic domain in an active conformation.
133 ggesting a role for Set1A independent of its catalytic domain in ESC self-renewal.
134 e governs the ability of K2 to bind the (pro)catalytic domain in favor of zymogen, thereby enforcing
135              Its crystal structure shows the catalytic domain in its active conformation with a short
136 e functional coupling between a reader and a catalytic domain in KDM5A--suggests a model for the spre
137  report the first structures of the APOBEC3B catalytic domain in multiple crystal forms.
138 he translocation domain interaction with the catalytic domain in serotype D.
139 y exposed protein surface extending from the catalytic domain in the C terminus of A3G to its N termi
140 rier domains and transported to neighbouring catalytic domains in an assembly line fashion.
141 this approach by constructing models for all catalytic domains in the human tyrosine kinase family, u
142 le of p58C in the coordinated actions of two catalytic domains in the primosome and ultimately could
143  of GlnRS, whereas missense mutations in the catalytic domain induce misfolding of the enzyme.
144 2) appears to strengthen the pseudosubstrate-catalytic domain interaction in a nucleotide-dependent m
145  spectrometric analyses showed that the UCR2-catalytic domain interaction occurs in trans, and establ
146                          We find the soluble catalytic domain interacts directly with the membrane-as
147  large conformational changes in the GRK5 RH/catalytic domain interface upon receptor binding.
148 into the Jumonji domain, which separates the catalytic domain into two fragments (JmjN and JmjC).
149 nomer form a tight hairpin, bringing the two catalytic domains into an active dimerized state.
150 he complex, including one in which the VPS34 catalytic domain is dislodged from the complex but remai
151             The structure of the alpha3beta3-catalytic domain is likewise closely similar to those of
152 owever, how the NTD activates the C-terminal catalytic domain is unclear.
153 membrane region, which links the NTD and the catalytic domain, is necessary and sufficient for activa
154 t on the structural organization of APOBEC3B catalytic domain, its substrate specificity and its poss
155 ficity are determined within the phosphatase catalytic domain itself.
156                          The kinase-like non-catalytic domain (KIND) of Spire directly interacts with
157 are dichain toxins, comprising an N-terminal catalytic domain (LC) disulfide bond linked to a C-termi
158 o 5 pc-9 molecules to the apoptosome and one catalytic domain may be parked on the hub, when an odd n
159                                     The Ubp8 catalytic domain mediates additional contacts with H2B,
160 sical interaction between the C-terminal and catalytic domains mediates ARTEMIS autoinhibition.
161  the PDE4B subtype, we generated mice with a catalytic domain mutant form of PDE4B (Y358C) that has d
162  is a zinc metalloprotease consisting of two catalytic domains (N- and C-).
163  the X-ray crystallographic structure of the catalytic domain of A-PGS from the opportunistic human p
164 veral drug-resistant mutations affecting the catalytic domain of Abl and other tyrosine kinases are n
165 ntration-dependent manner and the N-terminal catalytic domain of ACT (AC domain) is necessary and suf
166            To mediate repair, we exploit the catalytic domain of Adenosine Deaminase Acting on RNA (A
167 ion crystal structure of the Vif-binding and catalytic domain of APOBEC3F (A3F).
168                To study this phenomenon, the catalytic domain of APOBEC3G (A3G-CTD), an ssDNA-specifi
169 we identify a direct interaction between the catalytic domain of Aurora-A and a site flanking Myc Box
170 y occupies four distinct subsites within the catalytic domain of bacterial and human ThrRSs.
171 volving (i) the ubiquitin carboxyl hydrolase catalytic domain of BAP1, which interacts with the hydro
172 n efficient system for the production of the catalytic domain of CA IX in methylotrophic yeast Pichia
173 d to a p.Ser381Phe substitution in the CDC25 catalytic domain of CalDAG-GEFI.
174  through direct binding to the conserved HNH catalytic domain of Cas9.
175 rk reports a low resolution structure of the catalytic domain of CESA1 from Arabidopsis (Arabidopsis
176  Cre-mediated conditional elimination of the catalytic domain of CYLD induced dHSCs to exit quiescenc
177 ngineered zinc finger protein fused with the catalytic domain of dnmt3a.
178                         Here we targeted the catalytic domain of E3 ligase, CHIP, to YFP-tagged KCNQ1
179 er two histidines (H227 and H230) lie in the catalytic domain of eEF2K.
180  fused a catalytically inactive dCas9 to the catalytic domain of Gin recombinase using an optimized f
181 tructural studies showed that the C-terminal catalytic domain of human A3B has a tightly closed activ
182                 The crystal structure of the catalytic domain of KAT2A in complex with succinyl-CoA a
183  present the 1.05 A crystal structure of the catalytic domain of LytA in complex with a synthetic cel
184 oxide spin labels) in the active site of the catalytic domain of matrix metalloproteinase-12 (MMP-12
185         As a proof of principle, we used the catalytic domain of matrix metalloproteinase-14 (MMP-14)
186                             Mutations in the catalytic domain of Mps1 that give rise to inhibitor res
187                    NLRP3 associated with the catalytic domain of NEK7, but the catalytic activity of
188               Here, we identify the complete catalytic domain of nSMase2, which was misannotated beca
189 mpounds from this series in complex with the catalytic domain of PDE1B and PDE10A were determined, al
190 ramide was revealed to interact with the PIK-catalytic domain of PI3KC2beta and affect its compartmen
191  T590 and T597 in the variable insert of the catalytic domain of PIP5K6, and this modification inhibi
192 ion (P-CR), one of two unique domains in the catalytic domain of plant CesAs, was solved to 2.4 A res
193  a Cdc37 phosphomimetic peptide bound to the catalytic domain of PP5.
194 ally examining weak interactions between the catalytic domain of protein kinase Calpha and 14 substra
195                                          The catalytic domain of protein tyrosine kinases can interco
196 ecame spontaneously active when v-Src or the catalytic domain of Pyk2 was coexpressed with CFTR and w
197       Here we report that the N-terminal non-catalytic domain of separase binds to the C-terminal tai
198 ing of deactivated Cas9 (dCas9) nuclease and catalytic domain of the DNA methyltransferase DNMT3A tar
199 ing), a technique that couples an RBP to the catalytic domain of the Drosophila RNA-editing enzyme AD
200 ATP synthase, upon its dissociation from the catalytic domain of the enzyme.
201 stal structure has been determined of the F1-catalytic domain of the F-ATPase from Caldalkalibacillus
202 inal region of LifA shares homology with the catalytic domain of the large clostridial toxins, which
203 rporates two amino acid substitutions in the catalytic domain of the light chain (LC) metalloprotease
204 diate filaments identified a mutation in the catalytic domain of the MAP kinase 7 orthologue sma-5(kc
205 ction between CNNM2 and PRL-1 occurs via the catalytic domain of the phosphatase.
206 . monocytogenes strains and to determine the catalytic domain of the phosphodiesterase PdeA.
207 d zinc-associated Cys-X-X-Cys motif near the catalytic domain of the protein, decreases SIRT6 deacety
208 op interaction between the substrate and the catalytic domain of the ribozyme, resulting in a rearran
209 nformation of the substrate, docked into the catalytic domain of the ribozyme.
210                               By linking the catalytic domain of the RNA editing enzyme ADAR to an an
211 9 insert into hydrophobic pockets within the catalytic domain of the same subunit to stabilize the in
212 enzymatic function, a second mutation in the catalytic domain of this enzyme (R1625C) resulted in a c
213 eover, we show that active RasC binds to the catalytic domain of TOR, suggesting a mechanism of TORC2
214 igands that bind in the "palm" region of the catalytic domain of USP7 and inhibit its catalytic activ
215 cular dynamics simulations revealed that the catalytic domain of wild-type Cel7A and the FCA398 varia
216  Here we report the crystal structure of the catalytic domain of zebrafish PIP5K1A at 3.3 A resolutio
217              Gbetagamma also binds the C1/C2 catalytic domains of AC5 and AC6.
218 CAs (full-length CA I, II, VII, and XIII and catalytic domains of CA IX and XII) were characterized u
219 ocalized at the interface between the C2 and catalytic domains of cPKCs in an inactive kinase.
220 activity contributing to GEF activation, the catalytic domains of CYK-4 and ECT-2 directly interact.
221 ylation to specific gene loci by conjugating catalytic domains of DNA methyltransferases (DNMTs) to e
222 ed linker between the calmodulin-binding and catalytic domains of eEF2K.
223                                          The catalytic domains of most eukaryotic protein kinases are
224 In addition, using IAV without the stalk and catalytic domains of NA as a live attenuated vaccine was
225 ) found in the linker region between the two catalytic domains of the enzyme.
226   This structure is similar to those of core catalytic domains of the foot-and-mouth disease virus le
227             Point mutations in the predicted catalytic domains of the STELLO proteins indicate that t
228                       Superimposition of the catalytic domains of ThiC and glutamate mutase shows tha
229  Lyn was nullified by point mutations of Lyn catalytic domain or Src homology 2 (SH2) or SH3 domains
230 to their bacterial counterparts, yet several catalytic domains originated via horizontal gene transfe
231 mic volume without any appreciable change in catalytic-domain pair proximity or subunit stoichiometry
232    If correct, kinase-activity would require catalytic-domain pair separation.
233               The functional significance of catalytic-domain pairing is not known.
234 the autoinhibited holoenzyme is organized as catalytic-domain pairs distributed around a central olig
235                           In addition to its catalytic domain, PHD2 contains an evolutionarily conser
236                             Dehydratase (DH) catalytic domains play an important role during polyketi
237                            Furthermore, TET1 catalytic domain possessed demethylase activity in cance
238                                Revealed is a catalytic domain related in fold to Ulp family deubiquit
239  repeats, rather than the C-terminal oxidase catalytic domain, represent the major deacetylase/deacet
240                             In contrast, key catalytic domain residues and even a UDP-GlcNAc oxygen i
241   Here we present the first structure of the catalytic domain (residues 201-589) of the class I PhaC
242  and 3, which encode negative regulatory and catalytic domains, respectively.
243                TDP2 consists of a C-terminal catalytic domain responsible for its phosphodiesterase a
244 he conserved His residue in the hypothesized catalytic domain results in a complete loss of HHAT palm
245 1, which contains an Alu exon peptide in its catalytic domain, RNA sequencing analyses of A-to-I edit
246 s also expressed in cardiac muscle with high catalytic domain sequence similarity with other MLCKs bu
247 structural and sequence analysis of class II catalytic domains shows that bacterial GlyRS is closely
248 hat the linker forms an integral part of the catalytic domain structure, covering a hydrophobic patch
249 y of these mutants, we elucidated a new MLK4 catalytic domain structure.
250 ne kinase family, using all available kinase catalytic domain structures from any organism as structu
251                 ERManI and GMIA have similar catalytic domain structures, but each enzyme cleaves dis
252 roups that target the ATP-lid portion of the catalytic domain, such as a six-membered ring, confer se
253 ion of procaspase-8 filaments containing the catalytic domain, suggesting that procaspase-8 interacti
254                   Ectopic expression of TET1 catalytic domain suppressed colony formation and induced
255 l-1,6-deoxynojirimycin revealed a TIM barrel catalytic domain that contains a deep substrate-binding
256  member of the novel lyase family revealed a catalytic domain that displays an (alpha/alpha)6 barrel-
257 ses a major conformational transition in the catalytic domain that increases PAR production.
258 teins contain a bromodomain flanking the HAT catalytic domain that is important for the targeting of
259 ation of an alpha-helical region in the core catalytic domain that is juxtaposed to ssDNA, suggesting
260 ons that encode a transposase with a DD(E/D) catalytic domain that is topologically similar to RNase
261 l segments, within a construct of the myosin catalytic domain that lacks other reactive cysteines.
262 1 subunit N-terminal domain or in the CaMKII catalytic domain that largely prevent the in vitro inter
263 de RNA, and by introducing a mutation in the catalytic domain, the efficiency of converting a U A: G
264  the wild-type K-Ras4B (K-Ras4B(WT)-GTP/GDP) catalytic domain, the K-Ras4B(WT)-GTP-GAP complex, and t
265 erminal partner (VirA (C)DD) or a downstream catalytic domain, the N-terminal DD (VirFG (N)DD) exhibi
266 ichia pastoris, we also demonstrate that the catalytic domain, the N-terminus and the C- terminus of
267  including the papain-like protease 2 (PLP2) catalytic domain, the ubiquitin-like domain 2 (Ubl2), an
268 omains of individual subunits, including the catalytic domains, the interaction interfaces between su
269 thiolate subdomain away from the rest of the catalytic domain, thereby disrupting the NAD(+) and acet
270                Despite similarities in their catalytic domains, these ACs differ in regulation.
271 of NRPS catalysis is based around sequential catalytic domains: these are organized into modules, whe
272 etalloproteases (MMPs) with highly conserved catalytic domains, this strategy failed to identify inhi
273 bility of F12 to reversibly bind to the (pro)catalytic domain through K2 with high affinity and highl
274  structures revealing the MCR-1 periplasmic, catalytic domain to be a zinc metalloprotein with an alk
275 ctly binds Tip60 at a region adjacent to the catalytic domain to promote the protein acetyltransferas
276 inetic domain that transduces force from the catalytic domain to the lever arm to accomplish the powe
277 s of CesA, accessory proteins, or other CesA catalytic domains to control substrate delivery.
278 ane anchor that drives hexamerization of the catalytic domains to form the ATPase active sites.
279 furthermore, provides geometric access of L4 catalytic domains to the DNA ends during ligation and of
280  here and a globular-structured SUMO-binding catalytic domain, to stabilize p53.
281 el (MSM) to simulate the activation of c-Src catalytic domain, used as a prototypical tyrosine kinase
282 minal anticodon binding domains and that the catalytic domain uses a newly evolved group I intron bin
283 s and interacts with the minor groove of the catalytic domain V.
284 findings support the view that the karilysin catalytic domain was co-opted by competent bacteria thro
285           The X-ray crystal structure of the catalytic domain was determined at 2.1 A resolution and
286                                     The PLP2 catalytic domain was found to have both deubiquitinating
287 teraction of T3lec or T4lec with ppGalNAc-T2 catalytic domain was not mediated by carbohydrate.
288                                          The catalytic domain was overexpressed in Escherichia coli,
289  truncates comprising the disintegrin and/or catalytic domains were able to competitively block full-
290 res of the PRRSV nsp11 and coronavirus nsp15 catalytic domains were perfectly superimposed, especiall
291  to detect relative orientations of the Cas9 catalytic domains when associated with on- and off-targe
292 of resistant secondary mutations at the FLT3 catalytic domain, which is mainly on D835.
293 LOX or are located at a highly conserved LOX catalytic domain, which is relatively invariant in the p
294 nsists of tetratricopeptide repeat (TPR) and catalytic domains, which, together with UDP-GlcNAc, are
295 ion of individual structural elements in the catalytic domain while myosin is in complex with actin.
296 vealed that DddY contains a cap domain and a catalytic domain with a Zn(2+) bound at its active site.
297              It comprises a flat cylindrical catalytic domain with five-fold alpha/beta-propeller arc
298                    Thus, despite sharing the catalytic domain with ROCK2, ROCK1 appears to be the dom
299 resulted in an in-frame linkage of the PRKCA catalytic domain with the N-terminal of ATP2B4 and high
300                           We find that a non-catalytic domain within Cas9, REC3, recognizes target co

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