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1 chemokine receptors CCR5 and CCR2b share 89% amino acid homology.
2 ragments of collagens, they only share a 14% amino acid homology.
3 hly conserved structurally yet share limited amino acid homology.
4 roteins although they have only a very short amino acid homology.
5 d peptide, and the two peptides share an 87% amino acid homology.
6 trains, with 83% nucleotide homology and 86% amino acid homology.
7 re types 5 (AC5) and 6 (AC6), which have 65% amino acid homology.
8 n-coupled receptors having approximately 50% amino acid homology.
9 01 has a 77% (SARS-CoV-2) and 81% (SARS-CoV) amino acid homology.
10 canis gp19 has substantial carboxyl-terminal amino acid homology (59%) with E. chaffeensis VLPT and t
11  mouse GLC1A genes revealed a high degree of amino acid homology (82%) and the presence of several co
12                   Because the structural and amino acid homology among esterases of different classes
13 cated mycoplasma genes, their common DNA and amino acid homologies and structural and functional doma
14 nd its C-terminal phosphatase domain has 50% amino acid homology and 22% identity with the central po
15                                  Gab1 shares amino-acid homology and several structural features with
16 with G+C contents ranging from 40 to 70% and amino acid homologies as low as 20 to 25% for shared cor
17  two alphaviruses that have a high degree of amino acid homology, as well as a very broad host range.
18                                              Amino acid homology, as well as cysteine pairing similar
19                                 A search for amino acid homology based on the BLAST algorithm indicat
20 hat the vaccine-like isolate 98-38803 (99.5% amino acid homology based on the ORF5 gene) induces micr
21                                 Furthermore, amino acid homology between glutamate receptor M3 segmen
22                                              Amino acid homology between HCMVpp65(422-439) and TAF9(1
23                                  We observed amino acid homology between the cysteine-rich N terminus
24  homologous gene from the mouse revealed 93% amino acid homology between the human and mouse or rat (
25 topology; however, they contain little to no amino acid homology beyond the shared Ig loop region.
26 FHA secretion domain (Fha30) reveals limited amino acid homology but shared structural features, sugg
27 howed high (over 90%) nucleotide and deduced amino acid homologies, but lower homologies (48 to 61%)
28  Although ExoS and Exo53 possess 76% primary amino acid homology, Exo53 has been shown to express ADP
29 e human mitochondrial URFs 1 and 4, with 39% amino acid homology for URF1 and 26% for URF4.
30 n helicase motif III, a conserved segment of amino acid homology found in a superfamily of prokaryoti
31 een identified which have a highly conserved amino acid homology in all of the toxin families.
32     By comparison, mutations yielding a nine-amino acid homology in the M3 transmembrane segment, or
33                          Given the extensive amino acid homology in the MutS family our results with
34 ogy in the M3 transmembrane segment, or a 25-amino acid homology in the S4 stalk segment, do not affe
35 ing, we analyzed the phagotopes selected for amino acid homologies; in addition to the expected Env m
36       Rap and Ras share considerable primary amino acid homology, including Arg41.
37 d IGHJ genes generating stereotypes if HCDR3 amino acid homology is > 60%.
38 Ant4, of which gene configuration as well as amino acid homology is well conserved among mammals.
39 ariable, with nucleotide homology of 67% and amino acid homology of 65%.
40 f difference among protein-coding genes with amino acid homology of 91-97% among the seven mitochondr
41 ral novel genes and the previously described amino acid homology of HLA-H to MHC class 1 molecules pr
42                                          The amino acid homology of the E. canis P28 proteins ranged
43 FBPs that contains one or two copies of a 26 amino acid homology region that has been recently termed
44                                      DNA and amino acid homology search analysis revealed that JTAP-1
45                                      DNA and amino acid homology search analysis revealed this gene t
46                                              Amino acid homology searches of the human genome reveale
47                                              Amino acid homology searches using hypothetical translat
48 he Yersinia Yop virulon show a high level of amino acid homology, suggesting that P. aeruginosa may u
49 y 36 encodes for four lipoproteins with high amino acid homology that are expressed in vivo in humans
50 lphaherpesviruses and have 20 to 30% overall amino acid homology that is concentrated in the N-termin
51 ssified as a putative FEN-1 protein based on amino acid homology, there has been no biochemical evide
52               RAD9 and RAD9B share extensive amino acid homology throughout their entire sequences (3
53 he deduced protein (74.2 kD) exhibits strong amino acid homology to all known PC2s, including human,
54 , cps1B, and cps1C, were identified that had amino acid homology to bacterial carbohydrate biosynthes
55 cholera toxin, an oligomeric protein with no amino acid homology to ChiA.
56 rus (EBV) glycoprotein gp110 has substantial amino acid homology to gB of herpes simplex virus but lo
57  encoded by exl2 and exl3 had no significant amino acid homology to HmbR but contained six motifs tha
58 in revealed a novel protein with significant amino acid homology to orphan proteins identified in Sac
59                     RAFTK has an overall 48% amino acid homology to p125(FAK) and contains a kinase d
60                     In addition, hK2 has 78% amino acid homology to PSA.
61 y, encode inducer-repressors with sufficient amino acid homology to suggest that they could coregulat
62 s in GenBank, region 2 had approximately 25% amino acid homology to the COOH-terminal regions of huma
63                       Mouse B7-H1 shares 69% amino acid homology to the human counterpart.
64 t exhibits a 93% nucleotide homology and 99% amino acid homology to the human sequence.
65 morphic multicopy gene family with predicted amino acid homology to the major sheath protein of Trepo
66     The predicted AarC protein exhibited 88% amino acid homology to the previously identified GcpE pr
67  from mRNA isolated from VSMCs showed > 96 % amino acid homology to the rat and human P450 4A2 and 4A
68 NA library and was shown to have 85% and 87% amino acid homology to the rat and human proteins, respe
69 are two proteins with similar structure (64% amino acid homology), which are thought to act as "docki
70 mologies, SapD, SapE, and SapF had predicted amino acid homologies with type I protein secretion syst
71 equence level, there was a limited degree of amino acid homology with a domain of cyclin H that appea
72     The coding region of the gene shares 80% amino acid homology with Arabidopsis and 76% homology wi
73                        These results and the amino acid homology with beta-glycosyltransferases sugge
74                                       E1 has amino acid homology with eight regions of SV40 large tum
75                              GPD1-L has >80% amino acid homology with glycerol-3-phosphate dehydrogen
76 y open reading frame (ORF) 57 shares limited amino acid homology with HSV-1 ICP27 and Epstein-Barr vi
77 n of the active site residues and the 30-37% amino acid homology with known aspartic proteases, the d
78                Human CD1b shares significant amino acid homology with mouse CD1d1, which contains an
79                Human semaphorin A(V) has 86% amino acid homology with murine semaphorin A, whereas se
80                         NY-BR-1.1 shares 54% amino acid homology with NY-BR-1 and also shows tissue-r
81 housing with pet shop mice and shares 80-95% amino acid homology with previously characterized LCMV s
82  family and so named because it shares a 50% amino acid homology with receptors for the mammalian bom
83 ncodes a 95-amino acid protein having an 86% amino acid homology with SUMO-2.
84 onstructural protein that shares significant amino acid homology with the HCMV UL83-pp65 tegument pro
85 coded by bacteriophage T7 shares significant amino acid homology with the large fragment of Escherich
86 ing 5'-CAAT-3' tandem sequences revealed 48% amino acid homology with the lex-2B gene-encoded protein
87 ortantly, they also share gene structure and amino acid homology with the Plasmodium yoelii 235-kDa r
88  the secretin receptor despite their lack of amino acid homology with the secretin hormone.
89 ), 3,123 bp in length, whose product has 51% amino acid homology with the sequence encoded by the ORF
90  invertase from Moraxella lacunata, exhibits amino acid homology with the transposases of the IS110/I
91  of ExoS possessed considerably more primary amino acid homology with the vertebrate mono-ADP-ribosyl
92              This protein shares significant amino acid homology with the yeast protein SMT3, which f
93 -terminus of exoenzyme S has limited primary amino acid homology with the YopE cytotoxin of Yersinia,
94                                  HmuR shares amino acid homology with TonB-dependent outer membrane r
95 re observed at the nucleotide level; limited amino acid homology with two salivary gland-specific pro
96 ell receptor (BCR) share high structural and amino acid homology, yet interact with Ags in a distinct