ライフサイエンスコーパス: primary amino acid sequence

1 ring), located over 100 residues away in its primary amino acid sequence.

2 lationships between MAP1a's function and its primary amino acid sequence.

3 I kappaB zeta proteins are also conserved in primary amino acid sequence.

4 , which are similar in overall structure and primary amino acid sequence.

5 within a central domain including 25% of the primary amino acid sequence.

6 cal amino acid composition, but differing in primary amino acid sequence.

7 phorylation site near the middle of the Cdc6 primary amino acid sequence.

8 ucture, which is determined by the protein's primary amino acid sequence.

9 structure from positions 7.43 to 7.48 in the primary amino acid sequence.

10 ss of nucleolar phosphoproteins based on its primary amino acid sequence.

11 , with different enzyme kinetic profiles and primary amino acid sequences.

12 ld can be constructed from a wide variety of primary amino acid sequences.

13 o bands, which exhibited virtually identical primary amino acid sequences.

14 asymmetric protein composed of two identical primary amino acid sequences (66 kDa), of which one is c

15 However, there is little conservation in primary amino acid sequences across the cytoplasmic loop

16 lin-polyhedrin chimera demonstrates that the primary amino acid sequence affects occlusion body shape

17 The primary amino acid sequence alone is sufficient to accur

18 ed into two regions based on features of the primary amino acid sequence: an N-terminal nonrepeat reg

19 e pooled and subjected to CNBr digestion for primary amino acid sequence analysis.

20 otein is not known, but from analysis of the primary amino acid sequence and biochemical studies, it

21 The primary amino acid sequence and pattern of GCR expressio

22 de polypeptides (30 kD, 11.4 pI) with strong primary amino acid sequence and predicted secondary stru

23 s are commonly attributed to their impact on primary amino acid sequence and protein structure.

24 ist in bacteria and are largely unrelated in primary amino acid sequence and their modes of transcrip

25 Based on primary amino acid sequence and three-dimensional struct

26 Despite having similar primary amino acid sequences and predicted structures, t

27 based on all-atom 3D simulations of keratin primary amino acid sequences, and tyrosine phosphorylati

28 rogenases 1-3 and CRAD1), closely related in primary amino acid sequence (approximately 85%), that ar

29 Both are 46-kDa glycoproteins whose primary amino acid sequences are highly homologous.

30 a central domain of HgbA (in respect to the primary amino acid sequence) as important in Hb binding

31 These functions were related to the primary amino acid sequence by constructing and analysin

32 eta-helix supersecondary structural motif in primary amino acid sequences by using beta-strand intera

33 s encompassing a remarkably diverse range of primary amino acid sequences can provide E protein funct

34 GmGT-2 possesses various primary amino acid sequence characteristics common to al

35 letely specific for a peptide, including the primary amino acid sequence CNVKSDKSC, which contains a

36 Primary amino acid sequence comparisons demonstrate that

37 Primary amino acid sequence comparisons suggest that thi

38 may be higher than predicted on the basis of primary amino acid sequence comparisons.

39 m sequences that are subject to GC usage and primary amino acid sequence constraints.

40 nding the set of rules which dictate how the primary amino acid sequence determines tertiary structur

41 duct ion mass information readily identifies primary amino acid sequences differing by asparagine vs

42 deamidation, demonstrating the effect of the primary amino acid sequence, especially the -1 and +1 am

43 proteins are highly related throughout their primary amino acid sequence except for a hypervariable r

44 stone variants (e.g., H3.3), which differ in primary amino acid sequence from their canonical counter

45 ISG15, a 15-kDa protein of unique primary amino acid sequence, functions intracellularly a

46 The primary amino acid sequence has 26% identity with E. col

47 of cold adaptation involving changes in the primary amino acid sequence have not been documented yet

48 ctures of the two enzymes are identical, the primary amino acid sequences have diverged by 14 % in th

49 ein encoded by this gene, RteC, did not have primary amino acid sequence homology to any known protei

50 idopsis and soybean (Glycine max) based upon primary amino acid sequence homology to the rat PLMT, ph

51 izing enzymes in the human liver, share >85% primary amino acid sequence identity yet exhibit differe

52 MV and TSV coat proteins, which share little primary amino acid sequence identity, are functionally i

53 a series of decoy peptides derived from the primary amino acid sequence in the SOD2-binding site in

54 similarities to fungal kexins in the deduced primary amino acid sequence include a putative proenzyme

55 The salient features of the primary amino acid sequence include four putative transm

56 Their primary amino acid sequence indicates that these protein

57 8 by alpha2M* requires ligation of the GRP78 primary amino acid sequence (Leu(98)-Leu(115)).

58 in (AG alpha1), although the homology at the primary amino acid sequence level is limited to the firs

59 s UDG has a high degree of similarity at the primary amino acid sequence level to the enzyme found in

60 it, although not readily recognizable on the primary amino acid sequence level, is sufficiently high

61 dine kinases, although quite distinct at the primary amino acid sequence level, share a common struct

62 adopt the same fold but are unrelated at the primary amino acid sequence level.

63 ructural analysis suggested the linear GRP78 primary amino acid sequence LIGRTWNDPSVQQDIKFL (Leu(98)-

64 The primary amino acid sequence of 6Ckine is highly conserve

65 EFoldMine, a method that predicts, from the primary amino acid sequence of a protein, which amino ac

66 The primary amino acid sequence of BPV E5 is virtually unrec

67 telomeric DNA binding activity, although the primary amino acid sequence of Cdc13p has no previously

68 This finding demonstrates that the primary amino acid sequence of exon 7 of tTG confers som

69 r findings also establish a link between the primary amino acid sequence of helix alpha13 and the fun

70 ognition motif (DSGVVYS and DSGSIVVS) in the primary amino acid sequence of human, mouse, and rat FN.

71 The primary amino acid sequence of IRAK shares similarity wi

72 mary sequence of its gene; the change in the primary amino acid sequence of Mx8 integrase resulting f

73 Comparison of the primary amino acid sequence of phosphorelay proteins wit

74 Even though the primary amino acid sequence of PshA in Heliobacillus mob

75 Incidentally, by examining the primary amino acid sequence of rat, human, and chicken p

76 verse of 6 apoA-I (RO6 apoA-I), in which the primary amino acid sequence of repeat 6 (amino acids 143

77 The primary amino acid sequence of TgPNP is >40% identical t

78 Analyses of the primary amino acid sequence of the activation domain pre

79 In conclusion, exchanging the primary amino acid sequence of the active site exon of h

80 However, the primary amino acid sequence of the CaM-binding domain in

81 Computer analysis of the primary amino acid sequence of the CobB protein identifi

82 apabilities of FT-ICR, help to determine the primary amino acid sequence of the fragment ions beyond

83 The primary amino acid sequence of the N-terminal region of

84 thermoautotrophicum strain DeltaH showed the primary amino acid sequence of the proteins encoded by t

85 Our results suggest that the primary amino acid sequence of the T loop plays only a m

86 e have noted a hydrophobic region within the primary amino acid sequence of the terminase gpNu1 subun

87 Fc domain, stemming from differences in the primary amino acid sequence of the various subclasses, a

88 The primary amino acid sequence of wild-type GCAP1 was mutat

89 Comparison of the deduced primary amino acid sequences of plant, yeast, rat and hu

90 roteins could be deduced by alignment of the primary amino acid sequences of the antigens and cross-r

91 ontrast to the FPs of influenza and HIV, the primary amino acid sequences of the FPs of beta-CoVs in

92 Although the primary amino acid sequences of the Piv/MooV recombinase

93 Remarkably, the primary amino acid sequences of wheat-, rye-, and barley

94 burgdorferi to rifampicin may be due to the primary amino-acid sequence of its beta-subunit.

95 Analysis of the primary amino-acid sequences of PDK from various sources

96 nuclear localization signal (NLS) within its primary amino acid sequence or cotransport to the nucleu

97 tiple nuclear receptors, utilizing different primary amino acid sequences, repress transcription by i

98 ies, the truncation and fragmentation of the primary amino-acid sequence result in shorter or cleaved

99 otein, whose chromophore is derived from the primary amino-acid sequence, results in a red shift of t

100 rived from contiguous segments of lysozyme's primary amino acid sequence revealed subdomains within t

101 four well-known levels of protein structure: primary (amino acid sequence), secondary (helices, sheet

102 Amyloid fibers, independent of primary amino acid sequence, share a common cross-beta s

103 Analysis of the primary amino acid sequence shows that the AFXa gene pro

104 Analysis of the primary amino acid sequences shows that both genes are m

105 encodes a putative integrase protein with a primary amino acid sequence similar to that of the L5 in

106 pmental cycle and displays compositional and primary amino acid sequence similarities to eukaryotic h

107 cts of alcA, alcB, and alcC have significant primary amino acid sequence similarities with known micr

108 topology recognition even when no detectable primary amino acid sequence similarity is present.

109 tin-binding domain that bears structural and primary amino acid sequence similarity to WH2 domain fam

110 ly related to other CC and CXC chemokines in primary amino acid sequence structure.

111 ila cDNA for this ORF and examination of the primary amino acid sequence suggests that this cDNA enco

112 lysine residues by TG2 is not encoded in the primary amino acid sequence surrounding the target side

113 ncy of the enzyme, which is regulated by the primary amino acid sequences surrounding ORF1 cleavage s

114 ae pilin undergoes high-frequency changes in primary amino acid sequence that aid in the avoidance of

115 The 28-kDa protein had a primary amino acid sequence that was 43% similar to a pr

116 lthough these proteins share 58% identity in primary amino acid sequence, the local environment surro

117 NPAS2 is highly related in primary amino acid sequence to Clock, a transcription fa

118 ber of levels of protein structure, from the primary amino acid sequence to its three-dimensional fol

119 in the brain and the most similar in deduced primary amino acid sequence to the alpha 6 subunit.

120 How the primary amino acid sequence triggers misfolding and dete

121 unctional, and evolutionary information from primary amino acid sequences using phylogenetic profiles

122 e juxtamembrane secondary structure, not the primary amino acid sequence, was critical to the cleavag

123 n parsimony and neighbor-joining analyses of primary amino acid sequences, was supported by two addit

124 g that mutations other than those in the Us3 primary amino acid sequence were responsible for the fai

125 t of the pilus, can carry a wide spectrum of primary amino acid sequences which are generated by the

126 ISG15 is a 15-kDa protein of unique primary amino acid sequence, which is transcriptionally

127 highly related to other DUBs throughout the primary amino acid sequence, with a hypervariable region

128 To determine to what extent the primary amino acid sequence within exon 7 defines substr