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1 g increased complementarity with the primary hydrophobic pocket.
2 e dihydroisoquinoline to bind in an adjacent hydrophobic pocket.
3 in but with distinct interactions within the hydrophobic pocket.
4 inal chemical investigation of the conserved hydrophobic pocket.
5 conformation, allowing access to an extended hydrophobic pocket.
6 ospholipid-cycling into and out of the Sfh1* hydrophobic pocket.
7 teraction site was identified in a conserved hydrophobic pocket.
8 of the penetration protein and embedded in a hydrophobic pocket.
9 ormation of the ferric protein with a closed hydrophobic pocket.
10 1, spanned from the active site pocket to a hydrophobic pocket.
11 l vicinal disulfide bond that is buried in a hydrophobic pocket.
12 were changed to match those of CatM in this hydrophobic pocket.
13 cacy of anticancer drugs directed toward its hydrophobic pocket.
14 isting of a shallow groove linked to a small hydrophobic pocket.
15 d, ordered beta1-alpha1 loop and an adjacent hydrophobic pocket.
16 D630N on an increased affinity of O2 for its hydrophobic pocket.
17 ense quite different environments within the hydrophobic pocket.
18 teraction between the N-terminal helix and a hydrophobic pocket.
19 smembrane receptor that contains a conserved hydrophobic pocket.
20 protein and the methyl group inserted into a hydrophobic pocket.
21 her with Trp(803) and Phe(804), form a large hydrophobic pocket.
22 ciation of the RS20 domain from calmodulin's hydrophobic pocket.
23 istinct nonpolar side chains that fill three hydrophobic pockets.
24 nd-gated ion channels, and ligand binding to hydrophobic pockets.
25 through a complex network of interconnected hydrophobic pockets.
26 Spa15 where labels are seen to be buried in hydrophobic pockets.
27 th scales that accompany exposure of protein hydrophobic pockets.
30 active, so-called DFG-out state, occupying a hydrophobic pocket adjacent to the ATP binding site.
31 ng decreases the size and accessibility of a hydrophobic pocket, adjacent to the ATP site, to inhibit
32 troduction of a single substitution into the hydrophobic pocket affected entry through both nectin-4
34 erated tyrosine then collapses into a nearby hydrophobic pocket, anchoring a modified conformational
35 We hypothesize that compound 7 binds to this hydrophobic pocket and as a consequence inhibits EBOV in
37 d a novel binding mode with occupancy of the hydrophobic pocket and channel of ATX but no interaction
39 atalytic chamber pointing toward an extended hydrophobic pocket and is critical for the inactivation.
40 The D ring of the chromophore sits within a hydrophobic pocket and is tilted by approximately 80 deg
41 nd that the myristoyl group inserts into the hydrophobic pocket and leads to a tighter packing of the
42 d on the surface of MDM2 and will "open" the hydrophobic pocket and stabilize the MDM2-p53 complex, w
43 te determinant NUMB with both the N-terminal hydrophobic pocket and the acidic domain of MDM2 also in
46 x to the CP where it enters and exits the CP hydrophobic pocket and then folds back to contact the vi
48 nalyses suggest that these mutations distort hydrophobic pockets and affect residues in the NA active
50 evel scale rationalizes the hydration of two hydrophobic pockets and the presence of a void in a thir
51 rings bind into distinct relatively narrow, hydrophobic pockets, and both are required for biochemic
52 ocated in the alpha5-beta3 loop, buried in a hydrophobic pocket approximately 16 A from the SAM-bindi
54 gs with modifications that interact with the hydrophobic pocket are potential specific inhibitors of
55 P binding pocket not only contributes to the hydrophobic pocket, as previously thought, but also recr
56 ive-helix bundle; Tyr-377 of F3 docks into a hydrophobic pocket at one end of the bundle, whereas a b
58 e in its prefusion conformation, suggested a hydrophobic pocket at or near the GP1 and GP2 interface
59 the long hypothesized binding of CO(2) in a hydrophobic pocket at the active site and demonstrate th
60 bl tyrosine kinase, myristate binds within a hydrophobic pocket at the base of the kinase domain and
61 on-induced dimerization that features a deep hydrophobic pocket at the center of the receiver domain
63 ral model, showed that Tyr(981) may lie in a hydrophobic pocket at the end of the S6 transmembrane se
64 and marine toxins target this cleft and the hydrophobic pocket at the front end of the cleft (viewin
68 e molecule is characterized by two prominent hydrophobic pockets at either end of the peptide binding
69 could spontaneously release from its initial hydrophobic pocket before MA protein interacts with the
73 I relative to TM-III by sliding into a tight hydrophobic pocket between TM-III and TM-V and that the
74 ubstitution of the residues constituting the hydrophobic pocket between TM-III and TM-V in the ghreli
75 channel-drug complex revealed six equivalent hydrophobic pockets between the peripheral and pore-form
77 binds in a channel-specific orientation to a hydrophobic pocket bounded by the S5/pore helix/S6 of on
78 nding kinetics of a ligand to a prototypical hydrophobic pocket by explicit-water molecular dynamics
80 e we show that the binding affinity of MDM2s hydrophobic pocket can be regulated through the RING fin
82 ide chain of alanine binds in a well defined hydrophobic pocket characterized by conserved residues I
83 structure allows the definition of conserved hydrophobic pockets comparable with those of ClpS or Bam
84 the ATG3 binding surface on ATG12 contains a hydrophobic pocket corresponding to the binding pocket o
85 eptides and small molecules that bind in the hydrophobic pocket could be selectively detected, provid
86 acids in the G domain demonstrated that the hydrophobic pocket created by these amino acids is neces
87 dies suggest that the 4'-ethynyl fits into a hydrophobic pocket defined by RT residues Ala-114, Tyr-1
90 igopyridines potentially targeting the Mcl-1 hydrophobic pocket, evaluated their capacity to inhibit
91 ling structure shows that ZAA binds the MD-2 hydrophobic pocket exclusively via specific molecular re
94 gages the receptor by binding to an extended hydrophobic pocket facilitated by the large outward move
95 Tyr residue that provides the bottom of the hydrophobic pocket for ATP yielded a PI4KIIIbeta enzyme
96 structures reveal that PylRS utilizes a deep hydrophobic pocket for recognition of the Pyl side chain
100 nding pockets at the BSSalpha active site: a hydrophobic pocket for toluene binding and a polar pocke
103 (TBHQ), shows that the inhibitor binds in a hydrophobic pocket formed at an interface between HA mon
105 be rotated away from the metal center, to a hydrophobic pocket formed by Ala212, Val293 and Phe295.
106 modeling indicates that PD-118057 binds to a hydrophobic pocket formed by L646 of one hERG1 subunit a
109 XLF Leu-115 ("Leu-lock") inserts into a hydrophobic pocket formed by XRCC4 Met-59, Met-61, Lys-6
110 gatively charged glutamate residues within a hydrophobic pocket formed from six of the alpha-helices,
112 rm IgE-Fc structures and that it retains the hydrophobic pocket found in the hinge region of the clos
113 that mutation of a highly conserved FAK-like hydrophobic pocket (HP1) abrogates CCM3-CCM2 interaction
114 receptor, including the highly sought after hydrophobic pocket important for the binding of the C3 a
115 ined that the binding site for Taxol is in a hydrophobic pocket in beta-tubulin, little was known abo
118 f some of the residues in the GAF domain and hydrophobic pocket in interaction with isoleucine and GT
119 eling studies demonstrate the existence of a hydrophobic pocket in pol eta that participates in the i
123 yl or even cyclododecyl groups, fit into the hydrophobic pocket in the active site of CA IX but not C
124 y inhibited by zanamivir owing to an altered hydrophobic pocket in the active site of the enzyme requ
125 henylalanine side-chain inserts into a major hydrophobic pocket in the apple 2 domain and the isoleuc
126 lecules reveals that the compounds bind in a hydrophobic pocket in the CDC25 domain of SOS adjacent t
127 f ADAMTS13 that appears to interact with the hydrophobic pocket in the central A2 domain of von Wille
129 is issue of Blood, de Groot et al identify a hydrophobic pocket in the Cys-rich domain of ADAMTS13 th
130 e burial of Ubc12's N-acetyl-methionine in a hydrophobic pocket in the E3, Dcn1, promotes cullin nedd
133 idated by the docking simulation: one at the hydrophobic pocket in the ICAM-1 binding domain (the alp
134 d a high-affinity propofol binding site in a hydrophobic pocket in the middle of a triangular cleft l
135 are noncompetitive inhibitors that bind in a hydrophobic pocket in the p66 subunit of reverse transcr
138 tors are designed to effectively fill in the hydrophobic pocket in the S1'-S2' subsites and retain al
139 EX5 structures reported here reveal a unique hydrophobic pocket in the subdomain interface that might
140 psid-binding antiviral compounds because the hydrophobic pocket in VP1 is filled with multiple bulky
141 n a catalytic pocket, (ii) the creation of a hydrophobic pocket in water, (iii) self-replication prop
142 tains six antiapoptotic members, each with a hydrophobic pocket in which Bcl-2 homology region 3 (BH3
143 r CO2 binding site for CAIR and N5-CAIR in a hydrophobic pocket in which the carboxylate or CO2 inter
146 their phenolic moieties occupying equivalent hydrophobic pockets in each protomer and their CoA moiet
150 binaphthyl-5,5'-disulfonic acid (bis-ANS) to hydrophobic pockets in the blood protein von Willebrand
151 a ligand side chain that binds in a shallow hydrophobic pocket, in the presence and absence of a nei
152 through a local conformational change and a hydrophobic pocket interaction, whereas the S443 destabi
154 omplementary surface on Rae1 displays a deep hydrophobic pocket, into which Met51 fastens like a bolt
155 orresponding regions in ADAMTS1 identified a hydrophobic pocket involving residues Gly471-Val474 as b
156 pite the small size of the protein domain, a hydrophobic pocket is formed by the side chains of nonpo
157 An allosteric model for regulation of the hydrophobic pocket is supported by differences in protei
159 ing to a 156 +/- 18 microM Kd interaction: a hydrophobic pocket lined by 4 critical residues (L173, N
161 binding site for RPR, previously mapped to a hydrophobic pocket located between two adjacent subunits
162 A resolution revealed a flavivirus-conserved hydrophobic pocket located next to the AdoMet-binding si
163 The docking of the farnesyl group to the hydrophobic pockets located at both CaM lobes further en
164 three structural elements contributing to a hydrophobic pocket, namely, the hydrophobic loop, the DN
165 ent-copalyl diphosphate substrate binds to a hydrophobic pocket near a cluster of Asp and Arg residue
166 actions of the amino acid side chains with a hydrophobic pocket near R47, as revealed by our crystal
168 that serves as the gatekeeper to the buried hydrophobic pocket occupied by 2,4-difluorophenyl of PH-
169 Using antibodies (Abs) that bind near the hydrophobic pocket of AMA1 and AMA1 mutated in the pocke
170 results identify the binding of RON2 to the hydrophobic pocket of AMA1 as the step that commits Plas
171 2), which is thought to insert itself into a hydrophobic pocket of another cadherin molecule (thereby
172 esults identify the molecular surface of the hydrophobic pocket of ATX as a target-binding site for i
173 compete with one another for binding at the hydrophobic pocket of BTD using overlapping but specific
177 We then mutated residues that reside in the hydrophobic pocket of CypA where proline-containing pept
178 h this mechanism, where 4EGI-1 attaches to a hydrophobic pocket of eIF4E between beta-sheet2 (L60-T68
180 information on small molecules bound in the hydrophobic pocket of gp41, using a paramagnetic probe p
181 of Glu37, a glutamate residue embedded in a hydrophobic pocket of HdeA, is important in controlling
182 , these results indicate that the C-terminal hydrophobic pocket of MA, which encompasses both residue
183 protrusion of that fatty acyl chain from the hydrophobic pocket of MD-2, independent of association w
184 -3 binds as an asymmetrical dimer within the hydrophobic pocket of MD-2, inducing an active receptor
185 in interaction occurs between the N-terminal hydrophobic pocket of MDM2 and the transactivation motif
188 ubstrate or "lid" adjacent to the N-terminal hydrophobic pocket of MDM2 has a phosphorylation site, a
189 results demonstrate the crucial roles of the hydrophobic pocket of Munc18 in mast cell degranulation,
190 (D3R, L8A) that perturb interaction with the hydrophobic pocket of Munc18-1 rescues impaired secretio
191 e 5 has identified the E132A mutation in the hydrophobic pocket of Munc18-2, prompting us to examine
193 The cyclohexyl group of Ches binds in the hydrophobic pocket of NanB occupied by the acetamidometh
194 E6A Pisoform 1 (Ki22M) reported to bind the hydrophobic pocket of other Hect ligases, presumably blo
196 The PLD2-GEF catalytic site is formed by a hydrophobic pocket of residues Phe-107, Phe-129, Leu-166
199 ecule, termed deep water, Dw, and bound in a hydrophobic pocket of the active site forms a short, str
200 at the leucine side chain protrudes into the hydrophobic pocket of the active site that accommodates
202 models places the P-CR connector loop into a hydrophobic pocket of the catalytic core, with the coile
203 r fitting of the 6-benzylthio group into the hydrophobic pocket of the enzyme at the 6-position.
204 petitive binding of the co-salt anion to the hydrophobic pocket of the host and counterion binding to
205 (NTA) is held in the helix alpha1 and loop 5 hydrophobic pocket of the human eIF3b RNA recognition mo
206 The lipid chain of the cysLT binds in a hydrophobic pocket of the N-terminal domain, whereas bin
210 the peptide (F263) anchors into a transient hydrophobic pocket of the receptor to facilitate the for
211 ial to inhibit HIV-1 fusion by targeting the hydrophobic pocket of transmembrane glycoprotein gp41.
212 hat overexpressed spartin binds to the Ile44 hydrophobic pocket of ubiquitin, suggesting spartin migh
213 tyl)-cognitin presumably interacted with the hydrophobic pockets of Abeta, which confers stabilizing
215 D)-helix with its anchors buried in the main hydrophobic pockets of the two CaM lobes establishes tha
216 er and the (2)beta(2)85 Phe-(2)beta(2)88 Leu hydrophobic pocket on a different tetramer is observed b
218 easing when Pro-139 (IC-2 loop) anchors in a hydrophobic pocket on Galphai1 (Val-34, Leu-194, Phe-196
219 teracting region (RIR) motifs that bind in a hydrophobic pocket on the C-terminal domain of Rev1.
221 eracting protein (PIP) motifs that bind in a hydrophobic pocket on the front side of PCNA as well as
225 YPX(n)L late domains bind in a conserved hydrophobic pocket on the second arm near the apex of th
226 a mutagenesis approach, we have identified a hydrophobic pocket on the Spt5 NGN domain as binding sit
227 orms a striking hook that binds to a shallow hydrophobic pocket on the surface of each She2p subunit
228 insertion (residues 98-151) forming a unique hydrophobic pocket on the surface that likely accommodat
229 that a loop from TBC1d5 binds to a conserved hydrophobic pocket on VPS29 opposite the VPS29-VPS35 int
230 ementarity of the molecules that include two hydrophobic pockets on IL-13 that accommodate Phe32 [com
234 hor of MT-WQ-IDL also binds with the shallow hydrophobic pocket outside the groove of the NHR trimer,
236 conserved interaction between Phe(727) and a hydrophobic pocket present on the adjacent subunit is cr
237 e 3-phenoxyphenyl side chain is located in a hydrophobic pocket previously reported to bind farnesyl
240 tructural event - a closure of the A/B helix hydrophobic pocket results from the integrated effect of
241 ClpAP, demonstrate that modification of the hydrophobic pocket results in altered N-end rule specifi
242 cture of apoNPC2, the sterol binds in a deep hydrophobic pocket sandwiched between the two beta-sheet
243 to levels of full efficacy in vivo through a hydrophobic pocket separate from the orthosteric site of
245 roduct to 5hmC, probably because the reduced hydrophobic pocket size restricts the binding of 5hmC as
246 ester the Trp residue of the ULM ligand in a hydrophobic pocket, Snu17p and Bud13p utilize a large in
247 site with concomitant formation of a highly hydrophobic pocket spatially suited to accommodate SL010
248 f the Ile(181) (P1') main chain, whereas the hydrophobic pockets stabilize the side chains of Ile(181
249 section of the gp41 coiled coil containing a hydrophobic pocket suitable for small molecule binding.
250 e four leucine residues in Ca(V)beta3 form a hydrophobic pocket surrounding key residues in the alpha
252 y-Pro analog revealed that ARM1 binds in the hydrophobic pocket that accommodates the omega-end of LT
253 recognition centre connected to an interior hydrophobic pocket that adaptively expands to ensheath d
254 dicate that loop 2 constitutes the predicted hydrophobic pocket that binds the AIP thiolactone ring w
255 e crystal structure of SIRT6 reveals a large hydrophobic pocket that can accommodate long-chain fatty
256 peptide reveals that SIRT2 possesses a large hydrophobic pocket that can accommodate the myristoyl gr
257 of the passenger, at the entrance of a large hydrophobic pocket that contains a bound detergent molec
259 receiver domain, promoting the opening of a hydrophobic pocket that is essential for homodimer forma
261 he chlorine substituent is accommodated by a hydrophobic pocket that is larger than the homologous si
262 rtially buries protoporphyrin within a large hydrophobic pocket that is located at the end of its bet
263 odes of these hits and revealed an auxiliary hydrophobic pocket that is positioned adjacent to the ph
264 ter of 10'-demethoxystreptonigrin binds in a hydrophobic pocket that mainly consists of cap domain re
266 ase protein family and contains a novel core hydrophobic pocket that may be responsible for binding a
267 The Arc N-terminal lobe evolved a unique hydrophobic pocket that mediates intermolecular binding
268 re, with the acyl chain deeply buried into a hydrophobic pocket that runs perpendicular to a long gro
269 s is due, in part, to a phenylalanine in the hydrophobic pocket that selects for the alternative ster
270 ATP-binding site of Grp94 possesses a unique hydrophobic pocket that was used to design isoform-selec
271 e body of the Tim8-Tim13 complex contain six hydrophobic pockets that likely interact with specific s
272 n formed a stable dimer, which contained two hydrophobic pockets that provide a molecular interface f
273 tures, including a central basic patch and a hydrophobic pocket, that are important for dsRNA binding
274 In crystal structures, AurkinA binds to a hydrophobic pocket (the 'Y pocket') that normally accomm
275 uilibrium between the destabilization of the hydrophobic pocket, the overall folding energy, the acti
277 suggested that compounds 1 and 2 target the hydrophobic pocket, thereby blocking access to the activ
278 action site on MAPKs, the common docking and hydrophobic pocket, they use distinct kinase interaction
279 95.5-8 is able to use a reactive lysine in a hydrophobic pocket to accelerate promiscuous Knoevenagel
280 to the formation of a previously undisclosed hydrophobic pocket to accommodate the alpha-phenyl ring
281 s is necessary to complete a solvent-exposed hydrophobic pocket to form the catalytically competent a
282 at these type II inhibitors utilize the same hydrophobic pocket to gain strong inhibitory potency (13
283 agates conformational energy from within the hydrophobic pocket to the helical unit that gates pocket
284 s that Phe19 and Leu53 of IGF-II lock into a hydrophobic pocket unique to domain 11 of mammalian IGF2
285 hain of PS, PE, and PC lipids is buried in a hydrophobic pocket whereas the 1'-acyl chain is exposed.
286 ety of 2 which is favorably located within a hydrophobic pocket, whereas in NTPDase1 it is exposed to
287 ed end of the fatty acid chain buried in the hydrophobic pocket, whereas the carboxylate end of the l
289 small central volume surrounded by four deep hydrophobic pockets, which may explain hERG's unusual se
290 the tetramer, the "inner" beta-sheet forms a hydrophobic pocket while the helix and loop are solvent-
292 Small molecule inhibitors binding into a hydrophobic pocket within capsid viral protein 1 were pr
295 otinic, and 5-HT3A receptors suggests that a hydrophobic pocket within the Cys-loop and the M4 segmen
296 system, we selected mimetics of a conserved hydrophobic pocket within the N-heptad repeat region of
297 y to be nonspecific and does not involve the hydrophobic pocket within the PER2 PAS domains that in o
299 rotein includes a GAF domain that contains a hydrophobic pocket within which isoleucine and valine bi
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