ライフサイエンスコーパス: opposite face

1 ydrophobic cystine pairs plus two Ala on the opposite face.

2 rily conserved amino acids in Prp18 form the opposite face.

3 he glutamine side chains were arrayed on the opposite face.

4 t with departure of a leaving group from the opposite face.

5 esponsive ones (A300, I302, E303) lie on the opposite face.

6 merization followed by re-protonation on the opposite face.

7 ce while the polar residues aggregate on the opposite face.

8 wo sites to be at one end of the molecule on opposite faces.

9 as polar/apolar residue pairs tend to occupy opposite faces.

10 On the opposite face, aligned along one helix, are exposed resi

11 Cell migration has two opposite faces: although necessary for physiological pro

12 of the helix, hydrophilic amino acids on the opposite face, and a number of basic amino acids surroun

13 e face is concomitant with delivery from the opposite face by the conjugate acid of the second enzymi

14 s of lipophilic ligand atoms are enclosed on opposite faces by lipophilic protein atoms, (2) neutral-

15 oss-strand cysteine residues that project on opposite faces close to the termini of the hairpin can s

16 matic and hydrophobic side-chains, while the opposite face contains a series of conserved charged or

17 splays hydrophobic leucine residues, and the opposite face displays hydrophilic lysine residues.

18 ctrostatic repulsion among phosphates on the opposite face drives bending toward the less negative su

19 the sites of Ig5 polysialylation are on the opposite face from the FN1 residues previously found to

20 of the molecule is strongly negative and the opposite face has a strong positive electrostatic field.

21 They are strikingly absent from the opposite face, implying that it is likely to face inward

22 p/bulge segment of the RNA aptamer while the opposite face is capped by a stacked alignment of the A1

23 f the trimer is strikingly acidic, while the opposite face is more neutral.

24 N-terminal arm with the minor groove on the opposite face of DNA relative to the major groove that i

25 The other region, located on the opposite face of Doc1, is required for Doc1 to enhance s

26 Cys residue at position 27, which is on the opposite face of helix I, thereby indicating that the fa

27 ll likelihood because position 226 is on the opposite face of helix VII from position 228.

28 fication of Cys148, a residue located on the opposite face of RGS4, can disrupt RGS/Galpha interactio

29 is 19 of MGS and Lys 13 of TIM appear on the opposite face of the 2PG carboxylate plane, their relati

30 e catalytic base Asp 71 is positioned on the opposite face of the 2PG-carboxylate plane as Glu 165 of

31 e compounds likely bind within a site on the opposite face of the active site, and function as allost

32 s of nucleophilic attack by the amine on the opposite face of the alkene radical cation to the one sh

33 forms dimers through the AXXXG motif on the opposite face of the alpha-helix.

34 o other binding sites and that a loop on the opposite face of the ATPase rings stabilizes interaction

35 The best predicted site was on the opposite face of the beta sheet from the pan-HSP90 radic

36 s orients the four phthalimido groups on the opposite face of the catalyst.

37 ntation, beta-strands 1-3 and helix 2 on the opposite face of the catalytic domain contribute to memb

38 sepair with the internal C and stacks on the opposite face of the chromophore.

39 Val-203 interacts with the opposite face of the cofactor NAD+ from the alcohol subs

40 nd the C termini are located together on the opposite face of the dimer to facilitate membrane intera

41 DNA looping, movement of the operator to the opposite face of the DNA helix from the natural binding

42 ipulation places the IHF binding site on the opposite face of the DNA helix, directs the IHF-induced

43 A secondary surface resides on the opposite face of the domain and involves residues in hel

44 both cases, the catalytic domain lies on the opposite face of the enzyme from the SH2 and SH3 domains

45 ODH (e.g., A77 1726) bind to a pocket on the opposite face of the flavin cofactor from dihydroorotate

46 Another ion-binding site on the opposite face of the G domain has been recently observed

47 acing the RcNtrC tandem binding sites on the opposite face of the helix (-113 bp) completely abolishe

48 e also identified a patch of residues on the opposite face of the helix and residues near both ends o

49 pid acyl chains and cationic residues on the opposite face of the helix interacting with the head gro

50 A residue on the opposite face of the helix only reacted with MTS reagent

51 e, and allow the nonpolar residues along the opposite face of the helix to remain immersed in the hyd

52 d exposes the hydrophobic amino acids on the opposite face of the helix.

53 cyclopropanation reaction takes place on the opposite face of the heterocycle, and the opposite enant

54 tes with the nucleophilic substituent on the opposite face of the ligand to the iron.

55 omain (cytodomain) regulates fusion from the opposite face of the membrane by an unknown mechanism.

56 Intercalation is on the opposite face of the modified S,R,S,RA6.T17 base pair as

57 Two arginine residues on the opposite face of the molecule (Arg-13 and Arg-32) and un

58 e ifnar1 binding site, was identified on the opposite face of the molecule.

59 e formed by the PGRP-specific segment on the opposite face of the molecule.

60 related by 2-fold symmetry, are found on the opposite face of the molecule.

61 loops and sites of glycosylation are on the opposite face of the NEC4 molecule from the site that in

62 F-AC is involved in RNA binding, whereas the opposite face of the NELF-AC subcomplex binds NELF-B.

63 in the opposite direction, and presents the opposite face of the nonsymmetrical, heterodimeric, IHF

64 hin the third helix of the EH domain, on the opposite face of the NPF-binding pocket, as being critic

65 ) results in preferential epoxidation of the opposite face of the olefin, which is followed by regios

66 n be explained by preferential attack on the opposite face of the oxocarbenium to the C2-H2 bond and

67 s pore, loop L3 was found to move toward the opposite face of the pore, resulting in decreasing the c

68 d phospholipid headgroup binding site on the opposite face of the PT1-Ca2+ complex as suggested by Ma

69 C lacking bound substrate, donates H* to the opposite face of the resultant radical.

70 ly small chemical shift perturbations on the opposite face of the SH3 domain.

71 The opposite face of the somatomedin B-like domain interacts

72 FIIB or TFIIA suggests that BRF binds on the opposite face of the TBP-DNA complex from TFIIB and that

73 r with a large loop from each monomer on the opposite face of the tetramer (the alpha-face), which is

74 acent to the orthosteric binding site at the opposite face of Trp101.

75 egation of polar and hydrophobic residues to opposite faces of a predicted alpha-helical transmembran

76 with the two ATPases bound simultaneously to opposite faces of a single ClpP molecule were seen by el

77 nd a stem-loop binding protein (SLBP) target opposite faces of a unique highly conserved stem-loop RN

78 The two DAT epitopes were found on opposite faces of cellular and intracellular membranes,

79 derived from attack of the aza-anion on the opposite faces of conjugate system was obtained, startin

80 pushing out the T-bases of GTC's so that the opposite faces of each phenoxazone are stacked by the 3'

81 ubunit interface contains contributions from opposite faces of each subunit, designated + and -.

82 this study, we identify two basic patches on opposite faces of Ig3 that are critical for actin bindin

83 ly interact with RFXANK in vivo, bind to two opposite faces of its ankyrin repeats.

84 the 3'-sides of both G bases stacking on the opposite faces of its planar phenoxazone chromophore, a

85 bind to two distinct hydrophobic grooves on opposite faces of KIX.

86 e C1-C14 and C15-C10 bonds are formed on the opposite faces of the 14,15 double bond of the substrate

87 unusual interface, with Tfb3 binding on two opposite faces of the Arch.

88 hairpin, with the side chains projecting on opposite faces of the beta-sheet.

89 and two short alpha-helices which pack onto opposite faces of the beta-sheet.

90 es the addition of a hydride and a proton to opposite faces of the C horizontal lineC bond, has been

91 ently, the bound BMP and PGD(2) direct their opposite faces of the cyclopentane moieties toward the n

92 ow the 2 S-domains to bind to these sites on opposite faces of the dimer.

93 perpendicular faces of the DNA, rather than opposite faces of the DNA as in Oct-1.

94 exclusive even though the two ligands occupy opposite faces of the DNA double helix.

95 ecognition sites for two Fur dimers bound to opposite faces of the DNA helix.

96 domain subunits bind nearly symmetrically to opposite faces of the DNA in a head-to-head fashion with

97 the SAP-1 monomer and SRF dimer are bound on opposite faces of the DNA, and that the DNA recognition

98 bithorax and Extradenticle homeodomains bind opposite faces of the DNA, with their DNA-recognition he

99 approximately 4/5 bp, placing nucleosomes on opposite faces of the DNA.

100 The two dimers clamp DNA from opposite faces of the double helix and form a topologica

101 two operator sequences overlap and occur on opposite faces of the double helix.

102 ng repeats to which PecS binds as a dimer on opposite faces of the duplex.

103 ely charged amino and guanidino groups along opposite faces of the elongated molecule, facilitating i

104 cture, pairs of inhibitory molecules bind to opposite faces of the enzyme tetramer.

105 f two distinct paxillin-binding sites on the opposite faces of the FAT domain.

106 tryptophan oxidation and oxygen reduction on opposite faces of the flavin ring.

107 xidation and oxygen reduction are located on opposite faces of the flavin ring.

108 ablish the localization of Ypt1 and Ypt31 to opposite faces of the Golgi: early and late, respectivel

109 ide chains of Lys331 and Pro417 pack against opposite faces of the guanine nucleotide base.

110 tative DNA-binding sites (sites I and II) on opposite faces of the H5 globular domain.

111 abilization from side-chain substitutions on opposite faces of the hairpin.

112 ur dimers interact with these sequences from opposite faces of the helix.

113 other basic) located near the C terminus on opposite faces of the helix.

114 the upstream and downstream contacts are on opposite faces of the helix.

115 ntacts with all of the above residues on the opposite faces of the IIIS6 helix, except for the putati

116 targeting and transforming activities lie on opposite faces of the MCV sT molecule and can be genetic

117 BlaI and, probably, MecI dimers bind to opposite faces of the mec DNA double helix in an up-and-

118 r contains two ubiquitin binding surfaces on opposite faces of the molecule that cannot bind simultan

119 unction, important 2'-hydroxyl groups lie on opposite faces of the molecule, defining distinct loci f

120 ement regulatory activities of CD55 occur on opposite faces of the molecule.

121 d the carbohydrate-binding sites situated on opposite faces of the molecule.

122 een 1.8 and 1.9 A normal to the centroids of opposite faces of the near coplanar of the 2-butene comp

123 nomers bind to two identical surfaces on the opposite faces of the neuroligin-1 dimer to form a heter

124 es the geometry of key catalytic residues on opposite faces of the NNIBP.

125 produces two sites of increased digestion on opposite faces of the nucleosome and decreased digestion

126 he imidazoline substituents R(1) and R(2) on opposite faces of the palladium square plane.

127 at the 3'-sides of both G-bases stack on the opposite faces of the phenoxazone plane.

128 red residues map to two different regions on opposite faces of the protein, suggesting that the inter

129 ignals on mu2 and mu4, which were located on opposite faces of the proteins.

130 s the same face of the proximal double bond, opposite faces of the resulting enolate anion intermedia

131 ine distinct protein interaction surfaces on opposite faces of the RHD.

132 directing groups can promote epoxidation on opposite faces of the ring scaffold, evidence of competi

133 stinct groups that form discrete clusters on opposite faces of the S1 domain.

134 he pairs form an ordered monolayer, exposing opposite faces of the same molecule.

135 served aspartate residue that are located on opposite faces of the sugar ring.

136 The K2hPg residues occupied opposite faces of this helix, an arrangement that minimi

137 l phosphonates: reduction proceeded from the opposite face relative to that observed in the analogous

138 ive partners, Bag6 wraps around TRC35 on the opposite face relative to the Get4-5 interface.

139 genesis analysis revealed that there are two opposite faces that are involved in self-association and

140 On the opposite face, the N-terminal gamma chains fold into a s

141 uding a potential new regulatory site on the opposite face to that involved in the binding of rapamyc

142 ly with CRP, and is distinct from and on the opposite face to the proposed determinant for alphaCTD-C

143 principle of phenoxazone ring requiring its opposite faces to be stacked by the 3'-sides of two G ba

144 en" conformer (where the two guanines are on opposite faces) to the "closed" conformer (where the two

145 In contrast, the opposite face tolerated virtually all possible substitut

146 the active site of the molecule, whereas the opposite face was predominantly affected by the mutation

147 and MPB83 contain two functional surfaces on opposite faces, which are probably involved in binding t

148 ha(3)) on one face and helix alpha(2) on the opposite face with a characteristic Rossmann fold compri