ライフサイエンスコーパス: sequence homolog

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1 uence preference than Ets-1 and its proximal sequence homologs.

2 to improve accuracy on proteins without many sequence homologs.

3 ially for proteins without a large number of sequence homologs.

4 73, a p53 family protein, shares significant sequence homolog and functional similarity with p53.

5 covariation patterns in small sets of close sequence homologs and to translate them into functional

6 marks of both global homologies (full length sequence homologs) and local homologies (homologous subs

7 ing methods on proteins without thousands of sequence homologs, and that our method performs better o

8 d among F(420)-producing organisms, and weak sequence homologs are also found in non-F(420)-producing

9 ty contact prediction regardless of how many sequence homologs are available for proteins in question

10 currently popular methods no matter how many sequence homologs are available for the protein under co

11 in the multiple alignment as many confident sequence homologs as possible in order to produce the mo

12 The Arabidopsis genome encodes two IRE1 sequence homologs, AtIRE1A and AtIRE1B.

13 Moreover, the majority lack obvious sequence homologs between species, even when we restrict

14 mon comparative analysis methods that filter sequence homolog data based on alignment score cutoffs,

15 se methods demand for a very large number of sequence homologs for the protein under consideration an

16 eometrically match the 3D template and to be sequence homologs found by BLAST or PSI-BLAST, the annot

17 eference genome and efficiently retrieve the sequence homologs found in other bacterial genomes.

18 cDNAs for sequence homologs from Arabidopsis thaliana of these pro

19 Thirdly, the resulting sequence homologs from the structure alignment may be vi

20 The human thymine-DNA glycosylase has a sequence homolog in Escherichia coli that is described t

21 ed from multiple sequence alignment (MSA) of sequence homologs in a protein family.

22 a protein of 804 amino acids with no obvious sequence homologs in other organisms.

23 nnosidase, despite the identification of two sequence homologs in the bovine genome.

24 es in Caenorhabditis, we have identified med sequence homologs in the related nematodes C. briggsae a

25 with a new fold and only 0.3L-2.3L effective sequence homologs, including one beta protein of 182 res

26 predicted contacts for proteins without many sequence homologs is still of low quality and not very u

27 We show here that mouse Fgf15 is the sequence homolog of chick and human Fgf19/FGF19.

28 Recently, the first sequence homolog of T4 endonuclease V was identified fro

29 entified in the Escherichia coli genome as a sequence homolog of the human thymine DNA glycosylase wi

30 ligase, which was originally identified as a sequence homolog of Ubr1, the E3 component of the N-end

31 DmNopp140 (654 residues) is the sequence homolog of vertebrate Nopp140.

32 Documentation of sequence homologs of integral circadian and photorespons

33 Sequence homologs of IsdG and IsdI were identified in mu

34 the Myxococcus xanthus genes, identified 53 sequence homologs of sigma54-dependent enhancer binding

35 ccharomyces cerevisiae have been found to be sequence homologs of the exo1 gene from the fission yeas

36 egans cDNA libraries, a total of 11 distinct sequence homologs of the ppGaNTase gene family were clon

37 c22 (rsec22) and rat bet1 (rbet1), mammalian sequence homologs of yeast proteins identified as mediat

38 mbrane-associated protein that lacks obvious sequence homologs outside of nematodes.

39 ct prediction methods for the high volume of sequence homologs that are not available to most of the

40 oteins in a process analogous to that of its sequence homolog ubiquitin, a highly conserved 8.6-kDa p

41 No RyhB sequence homologs were found in Pseudomonas aeruginosa,

42 biquitous in eukaryotes, often with multiple sequence homologs within an organism.

43 ed from aligned families and sub-families of sequence homologs within and between species using combi

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