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1 chemokine receptors CCR5 and CCR2b share 89% amino acid homology.
2 hly conserved structurally yet share limited amino acid homology.
3 ragments of collagens, they only share a 14% 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 canis gp19 has substantial carboxyl-terminal amino acid homology (59%) with E. chaffeensis VLPT and t
10 mouse GLC1A genes revealed a high degree of amino acid homology (82%) and the presence of several co
12 cated mycoplasma genes, their common DNA and amino acid homologies and structural and functional doma
13 nd its C-terminal phosphatase domain has 50% amino acid homology and 22% identity with the central po
15 with G+C contents ranging from 40 to 70% and amino acid homologies as low as 20 to 25% for shared cor
16 two alphaviruses that have a high degree of amino acid homology, as well as a very broad host range.
19 hat the vaccine-like isolate 98-38803 (99.5% amino acid homology based on the ORF5 gene) induces micr
22 homologous gene from the mouse revealed 93% amino acid homology between the human and mouse or rat (
23 topology; however, they contain little to no amino acid homology beyond the shared Ig loop region.
24 FHA secretion domain (Fha30) reveals limited amino acid homology but shared structural features, sugg
25 howed high (over 90%) nucleotide and deduced amino acid homologies, but lower homologies (48 to 61%)
26 Although ExoS and Exo53 possess 76% primary amino acid homology, Exo53 has been shown to express ADP
28 n helicase motif III, a conserved segment of amino acid homology found in a superfamily of prokaryoti
32 ogy in the M3 transmembrane segment, or a 25-amino acid homology in the S4 stalk segment, do not affe
33 ing, we analyzed the phagotopes selected for amino acid homologies; in addition to the expected Env m
36 Ant4, of which gene configuration as well as amino acid homology is well conserved among mammals.
38 f difference among protein-coding genes with amino acid homology of 91-97% among the seven mitochondr
39 ral novel genes and the previously described amino acid homology of HLA-H to MHC class 1 molecules pr
41 FBPs that contains one or two copies of a 26 amino acid homology region that has been recently termed
46 he Yersinia Yop virulon show a high level of amino acid homology, suggesting that P. aeruginosa may u
47 y 36 encodes for four lipoproteins with high amino acid homology that are expressed in vivo in humans
48 lphaherpesviruses and have 20 to 30% overall amino acid homology that is concentrated in the N-termin
49 ssified as a putative FEN-1 protein based on amino acid homology, there has been no biochemical evide
51 he deduced protein (74.2 kD) exhibits strong amino acid homology to all known PC2s, including human,
52 , cps1B, and cps1C, were identified that had amino acid homology to bacterial carbohydrate biosynthes
54 rus (EBV) glycoprotein gp110 has substantial amino acid homology to gB of herpes simplex virus but lo
55 encoded by exl2 and exl3 had no significant amino acid homology to HmbR but contained six motifs tha
56 in revealed a novel protein with significant amino acid homology to orphan proteins identified in Sac
59 y, encode inducer-repressors with sufficient amino acid homology to suggest that they could coregulat
60 s in GenBank, region 2 had approximately 25% amino acid homology to the COOH-terminal regions of huma
63 morphic multicopy gene family with predicted amino acid homology to the major sheath protein of Trepo
64 The predicted AarC protein exhibited 88% amino acid homology to the previously identified GcpE pr
65 from mRNA isolated from VSMCs showed > 96 % amino acid homology to the rat and human P450 4A2 and 4A
66 NA library and was shown to have 85% and 87% amino acid homology to the rat and human proteins, respe
67 are two proteins with similar structure (64% amino acid homology), which are thought to act as "docki
68 mologies, SapD, SapE, and SapF had predicted amino acid homologies with type I protein secretion syst
69 equence level, there was a limited degree of amino acid homology with a domain of cyclin H that appea
70 The coding region of the gene shares 80% amino acid homology with Arabidopsis and 76% homology wi
74 y open reading frame (ORF) 57 shares limited amino acid homology with HSV-1 ICP27 and Epstein-Barr vi
75 n of the active site residues and the 30-37% amino acid homology with known aspartic proteases, the d
79 family and so named because it shares a 50% amino acid homology with receptors for the mammalian bom
81 onstructural protein that shares significant amino acid homology with the HCMV UL83-pp65 tegument pro
82 coded by bacteriophage T7 shares significant amino acid homology with the large fragment of Escherich
83 ing 5'-CAAT-3' tandem sequences revealed 48% amino acid homology with the lex-2B gene-encoded protein
84 ortantly, they also share gene structure and amino acid homology with the Plasmodium yoelii 235-kDa r
86 ), 3,123 bp in length, whose product has 51% amino acid homology with the sequence encoded by the ORF
87 invertase from Moraxella lacunata, exhibits amino acid homology with the transposases of the IS110/I
88 of ExoS possessed considerably more primary amino acid homology with the vertebrate mono-ADP-ribosyl
90 -terminus of exoenzyme S has limited primary amino acid homology with the YopE cytotoxin of Yersinia,
92 re observed at the nucleotide level; limited amino acid homology with two salivary gland-specific pro
93 ell receptor (BCR) share high structural and amino acid homology, yet interact with Ags in a distinct
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