Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 1998 Sep 21;188(6):1063–1074. doi: 10.1084/jem.188.6.1063

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).

PMC Copyright notice

Nucleotide and amino acid sequence of mBLTR cDNA. (A) Nucleotide sequence is numbered on the left and the deduced amino acid sequence is numbered beginning with the predicated initiating methionine on the right. 20 nucleotides obtained from 5′ RACE are underlined and the polyadenylation signal sequence is double underlined. Two putative N-linked glycosylation sites are indicated in bold. These data are available from GenBank/EMBL/DDBJ under accession number AF044030. (B) Amino acid sequence alignment of the mBLTR open reading frame with the chemoattractant receptors: human LTB₄ receptor (hBLTR), murine lipoxin A₄ receptor (mLXAR), murine formyl-Met-Leu-Phe receptor (mFMLPR), murine C5a receptor (mC5aR), and murine CXCR2. The transmembrane domains predicted from a Kyte-Doolittle hydrophobicity analysis are overlined and labeled as I-VII. The shaded area indicates ≥90% sequence homology and the boxed area indicates regions of identity.

Nucleotide and amino acid sequence of mBLTR cDNA. (A) Nucleotide sequence is numbered on the left and the deduced amino acid sequence is numbered beginning with the predicated initiating methionine on the right. 20 nucleotides obtained from 5′ RACE are underlined and the polyadenylation signal sequence is double underlined. Two putative N-linked glycosylation sites are indicated in bold. These data are available from GenBank/EMBL/DDBJ under accession number AF044030. (B) Amino acid sequence alignment of the mBLTR open reading frame with the chemoattractant receptors: human LTB₄ receptor (hBLTR), murine lipoxin A₄ receptor (mLXAR), murine formyl-Met-Leu-Phe receptor (mFMLPR), murine C5a receptor (mC5aR), and murine CXCR2. The transmembrane domains predicted from a Kyte-Doolittle hydrophobicity analysis are overlined and labeled as I-VII. The shaded area indicates ≥90% sequence homology and the boxed area indicates regions of identity.