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

1 d from the primary antigen by 11 to 13% (HA1 amino acid sequence homology).

2 PleC-PleD, NtrY-NtrX, and CckA-CtrA based on amino acid sequence homology.

3 ryotic GS form two distinct families lacking amino acid sequence homology.

4 s of LP2086 were identified based on deduced amino acid sequence homology.

5 human Smac binding to XIAP, based largely on amino acid sequence homology.

6 ent protein despite low ( approximately 23%) amino acid sequence homology.

7 r known plant beta-galactosidase showed high amino acid sequence homology.

8 uses do not have a significant percentage of amino acid sequence homology.

9 tion and the two proteins also share limited amino acid sequence homology.

10 element, IS994, has a significant predicted amino acid sequence homology (64.8 and 71.9%) to the two

11 LlaBIII shares >95% amino acid sequence homology across its first three prot

12 HMW-MAA mimicry, since they display partial amino acid sequence homology along with a similar struct

13 otic and eukaryotic kingdoms.Despite limited amino acid sequence homology among HPt domains, our anal

14 1L1 derived from multiple species and assess amino acid sequence homology among human, monkey, dog, h

15 ings involving these proteins, which display amino acid sequence homology and biochemical binding pro

16 ecause the 2 cytotoxic factors exhibited 50% amino acid sequence homology and bound to the same recep

17 n (PyST), which shares with MTA both partial amino acid sequence homology and cellular location, also

18 EptC shares significant amino acid sequence homology and domain structure with t

19 ily of G protein-coupled receptors, share no amino acid sequence homology and selectively activate ei

20 Both proteins share amino acid sequence homology and structural organization

21 BPA), glycolytic pathway enzymes, exhibit no amino acid sequence homology and utilize two different c

22 deled Chlamydomonas PetF1 and HydA2 based on amino-acid sequence homology, and produced two promising

23 The GmSBP proteins share amino acid sequence homology as well as putative structu

24 ict the substrate of a SCADH on the basis of amino acid sequence homology, as the substrates are not

25 The low levels of amino acid sequence homology between E3-19K proteins sug

26 In light of the absence of amino acid sequence homology between EIAV p9 and the fun

27 Given the high amino acid sequence homology between fish enzymes, a 3-D

28 Amino acid sequence homology between PrP-res and PrP-sen

29 Amino acid sequence homology between the envelope protei

30 The highly conserved amino acid sequence homology between the human, mouse, a

31 Interestingly, and despite 66% amino acid sequence homology between the two proteins, p

32 h predicts regions displaying high levels of amino-acid sequence homology between the predicted gene

33 A region of amino acid sequence homology, containing residues that a

34 e been classified into three groups based on amino acid sequence homology, effector systems, and phar

35 Thus, in addition to amino acid sequence homology, endo VIII shares a number

36 The amino acid sequence homologies exhibited by the P30 adhe

37 eraction with EF2 despite the high degree of amino acid sequence homology exhibited by EF2s from vari

38 uter-assisted analyses indicated that subtle amino acid sequence homology exists between BARF1 and c-

39 han HCF-1 but shares three regions of strong amino acid sequence homology, including the beta-propell

40 Amino acid sequence homology indicates that ARID DNA bin

41 is also the defining residue of a region of amino acid sequence homology known as the N-box that is

42 s-1), which contains a gene that predicts an amino acid sequence homology of 41% with T4-pdg.

43 The amino acid sequence homology of CEBP-1 with other plant

44 Based on amino acid sequence homology of the Bacillus subtilis ve

45 rom label incorporation, despite the greater amino acid sequence homology of the LMP7 subunit to that

46 The amino acid sequence homology of these cDNAs compared to

47 Amino acid sequence homology predicts this transporter (

48 As predicted from the amino acid sequence homology, recombinant DiTG catalyzed

49 ithecidae shared 87, 91 to 92, and 96 to 99% amino acid sequence homology, respectively.

50 An amino acid sequence homology search of the GenBank and E

51 ase A gene family could not be determined by amino acid sequence homology, suggesting the possibility

52 Amino acid sequence homology suggests that they may comp

53 Despite limited amino acid sequence homology, the conformations of the c

54 Despite sharing significant amino acid sequence homology, the RAD2 proteins exhibit

55 B. anthracis, produce CDCs with significant amino acid sequence homology to ALO.

56 ded by this gene, RteC, did not have primary amino acid sequence homology to any known proteins in th

57 code small proteins (LipA and LipB) that had amino acid sequence homology to bacterial adhesins and s

58 Bimgamma shares the highest amino acid sequence homology to BimEL and BimL, two proa

59 egions (amino acids 289-294 and 295-300) had amino acid sequence homology to both tyrosinase-related

60 Each of these proteins has significant amino acid sequence homology to capsid proteins in alpha

61 hose secretion machinery components share an amino acid sequence homology to components of the flagel

62 pical activator of Cdk1 and Cdk2 that has no amino acid sequence homology to cyclins, are sterile and

63 n was identified, DEDD2, which is closest in amino acid sequence homology to death effector domain-co

64 onal co-repressor, HDAC2 possesses extensive amino acid sequence homology to HDAC1 (the founding memb

65 e deduced mouse Abca13 protein shows highest amino acid sequence homology to human ABCA1 (50%), ABCA4

66 66-amino-acid protein which shows 56 and 41% amino acid sequence homology to human and mouse IFN-gamm

67 alculated molecular mass of 45.2 kDa and 72% amino acid sequence homology to human bomapin; however,

68 , the extracellular domain of which shows no amino acid sequence homology to LST1/C exerted a weaker

69 Among the receptors with the highest amino acid sequence homology to NPFF1 and NPFF2 are memb

70 protein coupled receptor that bears striking amino acid sequence homology to opiate receptors.

71 EngF does not have amino acid sequence homology to previously isolated EngB

72 Methanocaldococcus jannaschii, which has no amino acid sequence homology to SCO 6655.

73 n-sulfur (Fe-S) protein, consistent with its amino acid sequence homology to the 4Fe-4S clusters in a

74 tubulin signature motif and contains limited amino acid sequence homology to the bacterial cell divis

75 y was identified, Bcl-B, which is closest in amino acid sequence homology to the Boo (Diva) protein.

76 and soybean (Glycine max) based upon primary amino acid sequence homology to the rat PLMT, phosphatid

77 transferase, despite the lack of significant amino acid sequence homology to these enzymes.

78 This paper describes a protein with amino acid sequence homology to TLS that was isolated fr

79 II transmembrane protein with 15-20% overall amino acid sequence homology to TNF, LT-alpha, FasL, and

80 0, encodes an open reading frame that shares amino acid sequence homology to transcriptional regulato

81 sequenced and shown to encode a protein with amino acid sequence homology to type II thiolases.

82 sequencing of the murine San5 cDNA revealed amino acid sequence homology to yeast Nop5p, a nucleolar

83 , and its predicted gene product showed high amino-acid sequence homology to GMPPs from other species

84 grouped into six subfamilies on the basis of amino acid sequence homology (TRPC, TRPV, TRPM, TRPA, TR

85 philus ducreyi (Hd-CDT), which share limited amino acid sequence homology, were directly compared.

86 e N-glycosylation site) with 74% DNA and 66% amino acid sequence homologies with the mouse cDNA count

87 its deduced product (PikD) was found to have amino acid sequence homology with a small family of bact

88 From its amino acid sequence homology with AmpD, we recognized Yb

89 The chicken ecto-ATPase showed considerable amino acid sequence homology with CD39 over the entire l

90 -related proteins (ARPs) share less than 60% amino acid sequence homology with conventional actins an

91 related receptor (ERR) alpha-1 shares a high amino acid sequence homology with estrogen receptor alph

92 tensin II AT(1) receptors have more than 90% amino acid sequence homology with human AT(1) receptors

93 This DNA ligase shares significant amino acid sequence homology with human DNA ligase IV; a

94 usly sequenced mouse genomic DNA showing 67% amino acid sequence homology with human PB39.

95 IL-22RA2 shares amino acid sequence homology with IL-22RA1 (also known a

96 Although it has low amino acid sequence homology with known 2-oxoglutarate-d

97 NanH revealed that it exhibited significant amino acid sequence homology with many microbial sialida

98 FLVCR has significant amino acid sequence homology with members of the major f

99 uble fraction of MR-1, and it shares partial amino acid sequence homology with multiheme c-type cytoc

100 ts an 89.3-kDa polypeptide sharing extensive amino acid sequence homology with MutS homologs from bot

101 dehydrogenase (AlaDH) showing no significant amino acid sequence homology with previously known bacte

102 cDNA library and identified on the basis of amino acid sequence homology with prohibitin from mammal

103 This protein shares approximately 50% amino acid sequence homology with the amino acid transpo

104 se was identified in Escherichia coli by its amino acid sequence homology with the ENP1 endopeptidase

105 PEG-3 shares significant nucleotide and amino acid sequence homology with the hamster growth arr

106 ein-coupled receptors (GPCRs) sharing little amino acid sequence homology with the larger rhodopsin-l

107 gion showed 87% nucleotide homology, and 89% amino acid sequence homology, with human HSS.