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Table 1 The gene prediction of N. lugens pattern recognition molecules

From: The genome- and transcriptome-wide analysis of innate immunity in the brown planthopper, Nilaparvata lugens

Predicted gene

GenBank ID

Locus

Size (aa)

Exon

Orientation

UTR

Best match

Similarity

Mw (KDa)

pI

PGRP-LB

KC355211

scaffold1556

216

3

-

no

D. melanogaster

58%

24.01

6.03

PGRP-LC

KC355212

scaffold1031

359

3

-

no

D. melanogaster

59%

39.51

7.12

GRP1

KC355197

scaffold991

550

10

+

no

L. migratoria

51%

62.34

5.44

GRP2

KC355198

scaffold5509

499

6

+

no

R. prolixus

57%

56.70

6.84

GRP3

KC355199

scaffold991

579

14

+

no

R. prolixus

60%

65.83

5.69

GRP4

KC355200

scaffold2822

362

11

-

no

L. migratoria

57%

41.89

5.97

GRP5

KC355201

scaffold1504

366

9

-

no

L. migratoria

57%

42.15

5.01

GRP6

KC355202

scaffold991

156

3

+

no

B.mori

64%

17.64

5.29

GRP7 (partial)

KC355203

scaffold412

455

16

+

no

R. prolixus

58%

51.44

6.42

  1. The genomic organization of exons and introns of the genes for pattern recognition proteins is predicted based on the mRNA-genome alignments at the NCBI spideyweb (http://www.ncbi.nlm.nih.gov/spidey/spideyweb.cgi). PGRP: Peptidoglycan recognition protein; GRP: β-glucan recognition protein. Locus, size and orientation indicate the location on scaffold, predicted amino acids (aa) and the transcription orientation of the genes. UTR: Untranslated regions. Molecular weight (Mw) and isoelectric point (pI) are analyzed using Compute pI/MW tool (http://web.expasy.org/compute_pi/). D. melanogaster, Drosophila melanogaster; L. migratoria, Locusta migratoria; R. prolixus, Rhodnius prolixus; B.mori, Bombyx mori.