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1 F(2495), NPLY(2519), and DPF(2534) (315-HARE numbering).
2 serine protease domain (G216 in chymotrypsin numbering).
3 idues 184A, 185, 221A, and 224 (chymotrypsin numbering).
4 esidues 148, 348, 404, and 504 (ovine PGHS-1 numbering).
5 is located at position 290 (Escherichia coli numbering).
6 ), 226(M1), and 254(M2) (using alpha subunit numbering).
7 e Ile16-Asp194 salt bridge (chymotrypsinogen numbering).
8 n the loop at position 159 (Escherichia coli numbering).
9 pped by MCPF-CoA as Cys-114 (mature sequence numbering).
10 , 699, 703, and 710 (chicken skeletal myosin numbering).
11 thylation of residue G2470 (Escherichia coli numbering).
12 ally conserved "perturbing" Lys-194 (E. coli numbering).
13 S(1) pocket (position 189, chymotrypsinogen numbering).
14 ine of the TrkA domain (Y785 in TrkA residue numbering).
15 288L/F290V (all mutants given T. californica numbering).
16 3 and by the residue at position 119 (CYP4A3 numbering).
17 vative substitutions (N291G and P294K; human numbering).
18 enosine-1518 and -1519 (all Escherichia coli numbering).
19 he residue at position 192 (chymotrypsinogen numbering).
20 putative catalytic Glu-458 (Escherichia coli numbering).
21 on the 39-loop of the protease (chymotrypsin numbering).
22 igosaccharide side chain at position 146 (N2 numbering).
23 s at positions 27, 31, and 34 (based on ChTX numbering).
24 been deleted (TolR(62-133), Escherichia coli numbering).
25 mutated in silico to PVVV (P407V in the 2A79 numbering).
26 residues 81 to 83 and 117 to 122 of HA1 (H5 numbering).
27 with conserved Arg122 (PfDHFR-TS amino acid numbering).
28 d residue for ATP contact is Lys(6)(9) (P2X2 numbering).
29 (superscripts refer to Ballesteros-Weinstein numbering).
30 contributions at positions 37 and 69 (pcDHFR numbering).
31 the non-hydrogen-bonded Val 38 (eubacterial numbering).
32 e are straightforward based on the universal numbering.
33 STVs are associated with anomalous vertebral numbering.
34 om a population of citizens aged >/=50 years numbering 1.71 million in 2000 and 1.87 million in 2010
35 Roma (numbering 6 million) and the disabled (numbering 100 million) on a leading Hungarian carpooling
37 from four subjects showed additional phyla (numbering 2), genera (numbering 28), and SLOTUs (numberi
39 rRNA nucleotides 2618-2620 (Escherichia coli numbering 2583-2585) and 2541(2506), thereby reorienting
42 of G protein-coupled receptors, the Tas2rs, numbering 3 to approximately 66, depending on the specie
43 he superscripts denote Ballesteros-Weinstein numbering(3)) is experimentally observed and seems to be
44 rity groups in the European Union: the Roma (numbering 6 million) and the disabled (numbering 100 mil
49 terotrimer crystal structure, Glu153 (B'beta numbering) abuts the catalytic site on the C subunit, an
50 A single-site mutation of Pro(101) in EPSPS (numbering according to the enzyme from Escherichia coli)
51 ly identical, with the exception of Met-118 (numbering according to the mature BR sequence), which is
52 hose at positions 36 and 75 modulate fusion (numbering according to the Newcastle disease virus [NDV]
53 stal structures have suggested that Lys-110 (numbering according to the Sulfolobus solfataricus enzym
54 141 and Glu275 are in adenylosuccinate lyase numbering), acts as the general base in most fumarase cl
55 46/Val439 sequence differences (BRD4 BD1/BD2 numbering) allowed the identification of compound 27 dem
56 work reaches from betaL328 (Escherichia coli numbering) and betaQ441 via alphaQ399, betaR398, and alp
58 r (15)-NH2 (1) (a somatostatin agonist, SRIF numbering) and H-Cpa (2)-c[DCys (3)-Tyr (7)-DTrp (8)-Lys
59 otein surface (D132, Rhodobacter sphaeroides numbering) and leads to another acidic residue near the
60 superscripts refer to Ballesteros-Weinstein numbering) and non-polar interactions with residues in H
61 modified at the DPhe(7) position (alpha-MSH numbering) and pharmacologically characterized for agoni
62 n modified at the Trp(9) position (alpha-MSH numbering) and pharmacologically characterized for agoni
63 n modified at the His(6) position (alpha-MSH numbering) and pharmacologically characterized for agoni
64 ified the electrophilic cysteine as C759 (B1 numbering) and prepared a mixed disulfide between E. col
65 of both the Weinreb amide at C3 (beta-lactam numbering) and the amino acid side chain at C4 are well-
66 in KD1 interacts with Asp-189 (chymotrypsin numbering) and with the carbonyl oxygens of Gly-219 and
67 ct cells started at amino acid 4 (cystatin C numbering), and displayed reversible inhibition of papai
69 an intestine harbors a beneficial microbiota numbering approximately 10(12) organisms per gram of col
70 O-Alu is a representative of an Alu subclass numbering approximately 400,000 copies, suggesting many
71 , Asp114 (TM3), and Asp118 (TM3) (mouse MC4R numbering) are important for melanocortin-based peptide
72 amembrane residues, Lys-28 and Ser-26 (Abeta numbering), as the critical determinants for efficient i
73 )-Lys(9)-Thr(10)-Cys(11)]Thr(12)-NH(2) (SRIF numbering), at the five known human somatostatin recepto
75 erved serine residues, Ser(18) and Ser(20), (numbering based on isoform 1c) form at least one phospho
76 ked a threonine or arginine at position 319 (numbering based on the HXB2 genome) with AOP-RANTES resi
77 assignment of provisional subtypes, subtype numbering beyond "w," and the nomenclature of intergenot
78 drug-resistance (e.g., H275Y NA mutation [N1 numbering]) but revealed mutations outside the NA active
80 itions 163, 288, 289, 444, and 454 (PsAMADHs numbering) can, directly or not, significantly modulate
81 amino acid position 275 (H274Y, universal N2 numbering), conferring resistance against oseltamivir (T
82 esence of a tyrosine at position 249 (PpNRH1 numbering) confers high hydrolase activity for purine ri
83 There is currently no universally accepted numbering convention for the antiviral drug-related resi
85 ifications, an automated tool for HA subtype numbering conversion, linkouts to disease event data and
87 11 and alanine at positions 35 and 39 (hCRF numbering) decreases CRF1R activity and increases CRF2R
88 2, U2506, U2584, and A2602 (Escherichia coli numbering), demonstrating its potential for the analysis
89 utations at A2451, U2585, and C2063 (E. coli numbering) did not significantly affect either of the re
90 f the two conserved Met252 and Met428 (Kabat numbering) disrupted the interface interactions between
92 ues Asp-179(4.60) and Asp-275(6.58) (residue numbering follows the Ballesteros-Weinstein scheme), wit
93 APP that is phosphorylated at Thr668 (pAPP; numbering for APP695), we show that a phosphorylated, ca
98 idly survey a broad collection of compounds, numbering from tens of thousands to millions of members,
100 served Asn(633) of the PSI PsaB polypeptide (numbering from the Synechococcus elongatus crystal struc
101 ivation region (viz, A or C at position 1002 numbering from the translation start site of Ik-1) withi
102 residues 238-277 (58-97 in chymotrypsinogen numbering) from the protease domain of factor X bound on
103 single amino acid change at position 226 (H3 numbering), from glutamine (Q226) to leucine (L226), wit
104 t (position 5.38 using Ballesteros-Weinstein numbering) functions as a microswitch for regulating rec
106 nd slave oscillators, with groups of candles numbering greater than two, creating a synchronised moti
107 ssociated with drug resistance, NA-R292K (N2 numbering), has been found in some H7N9 clinical isolate
108 involving Glu235 (Glu70 in chymotrypsinogen numbering; hereafter, the numbers in brackets refer to t
109 R157K in the gene encoding hemagglutinin (H3 numbering), I109T in the gene encoding nucleoprotein, an
110 catalytic site (R152W, A246T, and D293N, N2 numbering), (ii) subtype-independent substitutions (E119
111 p(105), Val(120), and Leu(158), using OXA-48 numbering) impact on the relative levels of beta-lactone
112 regions (FIV numbering, with equivalent HIV numbering in superscript): I37(32)V in the active core r
114 nts in common eiders (Somateria mollissima), numbering in the hundreds to thousands of dead birds, ha
116 he7-d-Trp8-Lys9-Thr10-Phe11], L-363,301 (the numbering in the sequence refers to the position of the
119 rotein VP-1 region (positions 1740-1833, Dun numbering) in 49 biopsies obtained from 24 patients with
121 for one residue at the 101st position (Kabat numbering) in CDR3 of the variable heavy chain (V(H)), h
122 ue 399 in the B loop of HA2 (residue 72, HA2 numbering) in different monomers of the trimeric A(H1N1)
123 16S rRNA C1054 nucleobase (Escherichia coli numbering) in helix 34, and the carbamoylated gulosamine
124 Arg-15 (bovine pancreatic trypsin inhibitor numbering) in KD1 interacts with Asp-189 (chymotrypsin n
126 Site-directed mutation of Lys-1374 (human numbering) in RBF to Arg or Ile residues almost complete
127 16S rRNA at residues 1540 and 1541 (E. coli numbering) in the anti-Shine-Dalgarno mRNA binding seque
128 ferent residues, including Ser-675 (APP(695) numbering) in the APP cytoplasmic domain has been found
129 Arg(74), Arg(75), and Lys(78) (chymotrypsin numbering) in the catalytic function of activated protei
130 eration of a free radical at Tyr-385 (PGHS-1 numbering) in the cyclooxygenase active site; the Tyr-38
131 ition 292 (using the convention of rhodopsin numbering) in the dolphin LWS cone pigment results in a
132 acing the gatekeeper residue (Thr-338; c-Src numbering) in the inhibitor-binding site with a bulkier
133 on, lysine to glutamine, at position 166 (H3 numbering) in the major antigenic site of HA was reporte
134 ed a cysteine residue at position 442 (EU/OU numbering) in the third constant domain (C(H)3) of the h
135 o acid substitutions at PrP codon 164 (mouse numbering), in the beta2-alpha2 loop region of the prion
136 etion of a single residue, V(H)Ser113 (Kabat numbering), in the elbow region linking the V(H) and C(H
137 ifically at amino-acid residue T668 (APP-695 numbering) increases during staurosporine-induced apopto
138 leucine (L) residue at position HA1-226 (H3 numbering), indicative of human-like receptor binding po
141 e polymorphisms at -1082, -819, and -592 bp (numbering is relative to the transcription start site).
142 e c oxidase, Asp407 (Rhodobacter sphaeroides numbering) is at the interface of subunit I and subunit
145 ) (superscripts denote Ballesteros-Weinstein numbering) is experimentally observed and appears to be
146 (nucleotides 2042 to 2628; Escherichia coli numbering) is implicated in peptidyltransferase activity
148 1081 of large subunit rRNA (Escherichia coli numbering) is part of a domain targeted by antibiotics a
149 the conserved Trp256 (murine ferrochelatase numbering) is partially responsible for the observed por
150 erved AKR catalytic tetrad, His(120) (AKR1D1 numbering), is substituted by a glutamate in AKR1D1.
151 A2451 in 23S ribosomal RNA (Escherichia coli numbering) led to the proposal of a mechanism of rRNA ca
152 residues 263-271 (using the DENV serotype 3 numbering) located between the two globular domains of N
153 the single-amino acid R844H exchange (human numbering) located in the 310 helix of the C2A domain of
154 MCADH, while that in LCADH is Glu255 (MCADH numbering), located over 100 residues away in its primar
155 Our calculations show that adding CP-AMPARs numbering <5% of existing synaptic AMPARs is sufficient
156 proteases (residues 143-154 in chymotrypsin numbering) may be responsible for their differential rea
160 additional heteroatom at position 4 (oxazole numbering, N > O > CH) substantially increases activity
161 represent the Ballesteros-Weinstein residue numbering nomenclature(7)) and N86(2.50)D, obtained in c
162 a carboxylic acid, most likely E-242 (bovine numbering), occurred in P(M) and relaxed back in F.
163 (8)-Lys(9)-Thr(10)-Phe(11)-Cys(14)]-OH (SRIF numbering) (ODT-8) by one of the four conformationally b
164 (8)-Lys(9)-Thr(10)-Phe(11)-Cys(14)]-OH (SRIF numbering) (ODT-8) that is potent at all SRIF receptor s
166 rvey the entire spine and provide definitive numbering of disks and vertebrae was compared with neuro
167 ine or lysine at position 88 (using sequence numbering of E. coli RNHI), while the handle region popu
168 specially the Arg238-Glu459 salt bridge (the numbering of residues follows myosin II in Dictyostelium
169 ote: In the AOP version of this article, the numbering of the author affiliations was incorrect.
170 IDR, pcaReduce and mpath), as well as to the numbering of the bold-text annotations in the reference
172 ided with the original annotations and plate numbering of the paper atlas and enable viewing the mate
173 nd Arg134 constitute the catalytic site; the numbering of the residues includes the signal sequence.
174 ality was evaluated by using visual scoring, numbering of visible bronchi, and quantitative measureme
175 amino acids 326-336 (143-154 in chymotrypsin numbering) of factor X (fX) comprise a flexible surface
176 ent study indicated that Tyr99 (chymotrypsin numbering) of factor Xa and Thr99 of activated protein C
178 loops (amino acids 143-154, chymotrypsinogen numbering) of plasma serine proteases play key roles in
181 mediated by the residue at position 374 (HA0 numbering) of the HA2 subdomain as critical for HA trime
182 tions at either position 19, 79 or 81 (Kabat numbering) of the heavy chain strikingly converts h4A11.
183 structured portion (residues 7-29, glucagon numbering) of the micelle-bound 27-residue peptide is 1.
184 acids [aa] 61 to 87 using PB1-F2 amino acid numbering) of the PB1-F2-derived C-terminal peptides fro
185 le mutant (F86L/T93P/S118T; bovine rhodopsin numbering) of the tiger salamander UV cone pigment appea
187 -Phe-Trp(8)-Lys-Thr-Phe-Cys-OH (somatostatin numbering; OLT-8, 9) substituted by imBzl-l- or -d-His a
188 When attacking an Utetheisa egg cluster (numbering on average 20 eggs), the larva subjects it to
189 ve site of 23S rRNA, A2602 (Escherichia coli numbering), on the peptidyl transferase activity of the
190 ential RNA (RPR) and protein subunits (RPPs) numbering one in bacteria, and at least four in archaea
191 -I222T, rg-H274Y, rg-N294S, and rg-R371K, N2 numbering) or zanamivir (rg-E119A and rg-R371K) failed t
192 other Callophycus secondary metabolites, now numbering over 50, are tightly controlled by stereoelect
193 s loop (residues 143-154 in chymotrypsinogen numbering) plays a pivotal role in determining the macro
194 ates that amino acid residue 90 (B. fragilis numbering) plays an important role in conferring substra
195 n of APP, lysine 624, on the basis of APP695 numbering (position 28 relative to Abeta) that plays a c
196 An arginine (R481) (Rhodobacter sphaeroides numbering), positioned between the D-propionates of the
197 ution occurred at C(10) and C(9a) (mitomycin numbering) providing a CD(3) ether and a CD(3) hemiamina
198 4R, C725S, A728S, D730S, and C731S (Na(v)1.4 numbering) reduced block of Na(v)1.4 by 4-, 86-, 12-, 18
199 s3-Xxx7-DTrp8-Lys9-Thr10-Cys14]-Thr-NH2 (the numbering refers to the position in native SRIF), with X
200 y(8)-Lys(9)-Thr(10)-Zzz(11)-Cys(14)]-OH (the numbering refers to the position in native SRIF), with X
202 he other extends from positions -73 to -103 (numbering relative to the transcription start site of cf
203 ted at sites 1917 and 1951 (Escherichia coli numbering), respectively, in the 23S rRNA gene of C. bur
204 rt, and integrase), in which the amino acid numbering restarts at the first codon position of each d
205 yrosyl radical on R2 (Y122, Escherichia coli numbering) reversibly generates the transient thiyl radi
207 utein sequence begins with Gly121 (using the numbering scheme for the wild-type protein) and terminat
209 a conserved cysteine residue at position 83 (numbering scheme of the 140-residue form of FGF-1).
212 2 (TM7) equivalent to Lys(7.45) (Ballesteros numbering scheme) involved in covalently attaching retin
215 nnotate sequences with the five most popular numbering schemes: Kabat, Chothia, Enhanced Chothia, IMG
216 ressed by phosphorylation at Ser287 (Xenopus numbering; Ser216 of human Cdc25C) and subsequent bindin
218 saturated acyl chains at the stereospecific numbering (sn)-1 position from PC and likely a channelin
219 st that plant CPS prefers the stereospecific numbering (sn)-1 position whereas E. coli CPS acts on sn
221 d to Cys-305 (Cys-331 in human type II IMPDH numbering), suggesting that Cys-305 functions as a nucle
222 We establish a class D1 generic residue numbering system (CD1) to enable comparisons with orthol
223 achieved by the use of a computer encrypted numbering system at the National Cancer Institute) and b
227 (residue -34 to -15 and -11 to +6, using the numbering system in which the conserved histidine residu
229 Finally, a rule-base module based on a teeth numbering system is proposed to match labels of detected
231 otrypsin numbering system; for the urokinase numbering system it is Ile(159)-Lys(404)) and two point
234 at position +4 in the beta-polypeptide (the numbering system used assigns position 0 to the His whic
235 in lacking the N-terminal pyroglutamate (the numbering system used has Asp2 as the N-terminal residue
237 m label was located at positions (patchoulol numbering system) C5 (both isotopomers, ca. 100%) and C1
238 rg59+Asn108 mutants (using the P. falciparum numbering system) exhibit no significant fitness defects
239 H310A, H435Q, H435R, and H310A/H435Q, Kabat numbering system) expressed well in mammalian cell cultu
241 group of His157 (His159 in the yeast enolase numbering system) is in van der Waals contact (4.5 A) wi
242 acidic residue at position 144 (chymotrypsin numbering system) is the primary determinant of the dist
245 riants (I253A, H310A, and H310A/H435Q; Kabat numbering system) that exhibited differential serum pers
246 Lys65, His66, and Tyr71 (using the thrombin numbering system), that were resistant to HCII inhibitio
247 due that occupies position 192 (chymotrypsin numbering system), which plays a pivotal role in determi
248 man, were aligned, using the now-known Kabat numbering system, and a quantitative measure, variabilit
249 equences were also aligned using a different numbering system, since the locations of their CDRs (31-
250 framework to replace the inconsistent clade numbering system, using informal taxonomic names: Glugei
253 sidues Ile(16)-Lys(243) (in the chymotrypsin numbering system; for the urokinase numbering system it
256 erases of the exocyclic N6 of A2058 (E. coli numbering) that forms the macrolide binding site in the
257 e insertion loop at residue 60 (chymotrypsin numbering) that has been implicated in modeling studies
258 (NA)-like protein (NA-F144C and NA-T342A, N2 numbering) that increased the virus titers in three mamm
259 rm of the Abl tyrosine kinase (H396P; Abl-1a numbering) that is resistant to the Abl inhibitor imatin
260 fide bond (Cys(191)-Cys(220) in chymotrypsin numbering) that links two beta-loop structures that defi
261 g-73, Arg-75, and Arg-77 in chymotrypsinogen numbering) that play key roles in the function of thromb
262 erved tyrosine 837 (Saccharomyces cerevisiae numbering), that contacts the catalytic histidine of eIF
263 ines, R481 and R482 (Rhodobacter sphaeroides numbering), that interact directly with heme a and the h
264 D132(I) (subunit I; Rhodobacter sphaeroides numbering), the entrance of the K-channel has not been c
265 exchange or R915E, R916E substitutions (fly numbering) to effect local charge reversal at the 310 he
266 1) at Thr(697) and/or Thr(855) (rat sequence numbering) to inhibit phosphatase activity and increase
267 dine residue (His-287, murine ferrochelatase numbering) to leucine and reduced over 2 orders of magni
268 and that the NPXY tyrosine (Tyr743 by APP751 numbering, Tyr682 in APP695) is required for APP endocyt
269 hour) could be obtained via parallelization (numbering up) by simply wrapping several membrane tubing
270 ing of the base at position 1492 (by E. coli numbering) upon binding to the E. coli rRNA A site, but
272 ted that aspartate 143 (Escherichia coli TGT numbering) was involved in heterocyclic substrate recogn
273 eophilicity at the delta10 double bond (GGPP numbering) was synthesized and incubated with taxadiene
274 nizes MYPT1 phosphorylated at Thr(654) (M130 numbering), we determined that this calcium-independent
276 esidues (Tyr(677) and Tyr(701), using hFGFR1 numbering) were essential for bioactivity, but the remai
277 ovel NA-K432E and NA-T438I substitutions (N2 numbering) were identified at elevated frequencies (104/
278 Arg73, Arg75, and Arg77 in chymotrypsinogen numbering) were individually substituted with a Glu.
279 F linkage sites (using the original sequence numbering) were residue 39, which is at the beginning of
280 s(230), Arg(233), and Lys(239) (chymotrypsin numbering) were substituted with Ala in separate constru
281 teine at positions 3 and/or 14 (somatostatin numbering) were/was substituted with d-cysteine, norcyst
282 e chains of two residues, S353 and T354 (NIS numbering), were identified as the Na(+) ligands at Na2.
283 , Phe112Tyr, and Ala115Val (AgRP full-length numbering), were incorporated into the peptide macrocycl
284 tion, two substitutions, H274Y and R292K (N2 numbering), were introduced into each NA gene for compar
285 , or dual sulfation at both positions (Kabat numbering where H designates heavy chain) leads to an in
286 s Ser236 (Dictyostelium discoideum myosin II numbering) which was proposed to be involved in a hydrog
287 s (Gly22, His151, Lys243, and Glu321, atDGD2 numbering) which were entirely conserved between the str
288 ucleotide at position 1408 (Escherichia coli numbering), which is an adenosine in prokaryotic ribosom
289 This preference is linked to Phe902 (human numbering), which is responsible for low-affinity bindin
290 d, with the single exception of Glu-22 (IL-3 numbering), which is strictly conserved but nonetheless
291 ntains an aspartate residue [Asp157 (spinach numbering)], which is highly conserved in eukaryotic and
292 on, VRVIII (amino acids 586 to 591 [AAV8 VP1 numbering]), which lies on the surface of the protrusion
293 ernational ImMunoGeneTics information system numbering), whose presence rescued domain folding and st
294 Arg-173, Lys-175, and Lys-179; chymotrypsin numbering) with Ala, using an expression system that all
295 0d, K60f, E217, and R221 in chymotrypsinogen numbering) with alanine altered the substrate specificit
296 ite Ser-581 (full-length fatty acid synthase numbering) with alanine completely eliminated catalytic
297 His42, His124, and Glu126 (Aquifex aeolicus numbering), with particular attention paid to the effect
298 combinations of three critical regions (FIV numbering, with equivalent HIV numbering in superscript)
299 itions 1345-1350/1372-1376 (Escherichia coli numbering), within the three-way junction loop, which bi
300 rporation of a quaternary center at C-6 (THP numbering) would restore the facial selectivity with mor