LOCUS KHJ99694.1 863 aa PRT CON 15-DEC-2014
DEFINITION Oesophagostomum dentatum peptidase family M13 protein.
ACCESSION KN549208-10
PROTEIN_ID KHJ99694.1
SOURCE Oesophagostomum dentatum
ORGANISM Oesophagostomum dentatum
Eukaryota; Metazoa; Ecdysozoa; Nematoda; Chromadorea; Rhabditida;
Rhabditina; Rhabditomorpha; Strongyloidea; Strongylidae;
Oesophagostomum.
REFERENCE 1 (bases 1 to 574610)
AUTHORS Mitreva,M.
TITLE Draft genome of the hookworm Oesophagostomum dentatum
JOURNAL Unpublished
REFERENCE 2 (bases 1 to 574610)
AUTHORS Mitreva,M., Pepin,K.H., Abubucker,S., Martin,J., Minx,P.,
Warren,C., Palsikar,V.B., Zhang,X. and Wilson,R.K.
TITLE Direct Submission
JOURNAL Submitted (29-MAR-2014) The Genome Institute, Washington University
School of Medicine, 4444 Forest Park, St. Louis, MO 63108, USA
COMMENT Oesophagostomum dentatum, a Nodule worm, infects various livestock
species and can also be found in humans. The larval stages invade
the large intestinal wall and cause granulomatous inflammatory
reactions. O. dentatum infects pigs in all production systems
worldwide. Due to the lack of effective immune reactions worm
burdens can be high and the parasite is found in pigs of all age
groups. O. dentatum can be cultivated in vitro in all life cycle
stages and serves as a model for strongylid nematodes which
constitute a group of parasites most closely related to C. elegans.
The sequenced strain (OD-Hann) was collected in Lower Saxony,
Germany, around 1990 by Prof. Dr. Arwid Daugschies, and is since
maintained in pigs, currently at the Institute of Parasitology,
Vetmeduni Vienna, Austria. Material for sequencing was obtained
from Prof Dr Anja Joachim (Anja.Joachim@vetmeduni.ac.at) of the
Vetmeduni Vienna where it has been maintained since 2003. Worm
isolation and extraction of nucleic acids was done by Prof Joachim
and coworkers at the Institute of Parasitology, Vetmeduni Vienna,
or the Genome Institute production team.
This assembly consists of fragments, 3kb and 8kb insert whole
genome shotgun libraries. The sequences were generating on the
Roch/454 platform and assembled using Newbler. To improve
scaffolding, in house tools CIGA (Cdna tool for Improving Genome
Assembly) and Pygap (Gap closure tool) were used to map 454 cDNA
reads using blat to the genomic assembly to link genomic contigs
based on cDNA evidence. Only joins confirmed by additional
independent data typing were accepted and used to close gaps,
followed by the Pyramid assembler using Illumina paired reads to
close gaps and extending contigs.
The repeat library was generated using Repeatmodeler (A. Smit, R.
Hubley http://www.systemsbiology.org/). The Ribosomal RNA genes
were identified using RNAmmer
((http://www.cbs.dtu.dk/cgi-bin/nph-sw_request?rnammer ) and
transfer RNA's were identified with tRNAscan-SE (Lowe and Eddy,
1997). Non-coding RNAs, such as microRNAs, were identified by
sequence homology search of the Rfam database
(http://selab.janelia.org/software.html). Repeats and predicted
RNA's were then masked using RepeatMasker (A. Smit, R. Hubley & P.
Green http://repeatmasker.org). Protein-coding genes were predicted
using a combination of ab initio programs Snap (I. Korf, 2004),
Fgenesh (Softberry, Corp) and Augustus (M. Stanke, et. Al 2008) and
the annotation pipeline tool Maker (M. Yandell et. al., 2007) which
aligns mRNA, EST and protein information from same species or
cross-species to aid in gene structure determination and
modifications. A consensus gene set from the above prediction
algorithms was generated, using a logical, hierarchical approach
developed at the Genome institute. Gene product naming was
determined by BER (JCVI: http://ber.sourceforge.net).
Our goal is to explore this WGS draft sequence of Oesophagostomum
dentatum to better define proteins involved in nematode parasitism
that impact health and disease and are relevant to both
host-parasite relationships and basic biological processes.
For information regarding this assembly or project, or any other
GSC genome project, please visit our Genome Groups web page
(http://genome.wustl.edu/genome_group_index.cgi) and email the
designated contact person. For specific questions regarding the
Oesophagostomum dentatum genome project contact Makedonka Mitreva
(mmitreva@genome.wustl.edu) at Washington University School of
Medicine. The National Human Genome Research Institute (NHGRI) of
the National Institutes of Health (NIH) provided funds for this
project.
##Genome-Assembly-Data-START##
Finishing Goal :: High-Quality Draft
Current Finishing Status :: High-Quality Draft
Assembly Method :: Newbler v. MapAsmResearch-10/14/2011
Assembly Name :: O_dentatum_10.0.ec.cg.pg
Genome Coverage :: 15.0x
Sequencing Technology :: LaRoche 454
##Genome-Assembly-Data-END##
FEATURES Qualifiers
source /organism="Oesophagostomum dentatum"
/mol_type="genomic DNA"
/submitter_seqid="O_dentatum_1.0_Cont9"
/strain="OD-Hann"
/db_xref="taxon:61180"
/chromosome="Unknown"
/lab_host="pig"
/country="Germany: Lower Saxony"
/collection_date="1990"
/collected_by="Arwid Daugschies"
protein /locus_tag="OESDEN_00301"
/inference="protein motif:HMMPfam:IPR008753"
/inference="protein motif:HMMPfam:IPR018497"
/note="KEGG: cel:F18A12.8 1.5e-77 peptidase; hypothetical
protein; K01415 endothelin-converting enzyme"
/db_xref="InterPro:IPR008753"
/db_xref="InterPro:IPR018497"
intron_pos 12:1 (1/22)
intron_pos 124:0 (2/22)
intron_pos 151:0 (3/22)
intron_pos 203:0 (4/22)
intron_pos 230:2 (5/22)
intron_pos 285:0 (6/22)
intron_pos 335:0 (7/22)
intron_pos 357:2 (8/22)
intron_pos 402:0 (9/22)
intron_pos 438:0 (10/22)
intron_pos 469:2 (11/22)
intron_pos 503:1 (12/22)
intron_pos 533:0 (13/22)
intron_pos 553:1 (14/22)
intron_pos 582:0 (15/22)
intron_pos 617:2 (16/22)
intron_pos 663:2 (17/22)
intron_pos 691:1 (18/22)
intron_pos 731:2 (19/22)
intron_pos 760:1 (20/22)
intron_pos 781:2 (21/22)
intron_pos 815:0 (22/22)
BEGIN
1 MLQAKLLGAN TGLVGAICAL AIASLVFNIL IWNKVNKDDD VTKSAPIPVE PIPLEEVRIR
61 TDPVTTTKDK PRTIAFPMKT RLRTISSTFT AANPTNSKPL PVRVNDTIYC PSYGKPDTSD
121 AYKEAASYLL SGLDQSVDPC EDFYAFSCNT YVKNHNASEI GVSRVAAYDE AQQQVDVEIV
181 EALQAVDIGD SSQSLTERLT KAALLECVYH SRARTPVDNS KDVLIEMRDL FGGIPFLNHS
241 LKEGLDFFSV MGELEQNHAM GSLLHAAVSV DFKNVQQHTL FISQPILPIP RDYYVLPQHT
301 TVLEDRIKLV TKVLQSFAET VLDDASPYID LIKTSARDVV KLEMQIAMAS WPESAMRNYA
361 QQYNPYKLEQ LEKAYPSIKW KSYFNAMLST VSSTFDITKK NIIIAQPSYF GWLNALFTGE
421 TVDAKTIANY LLTHLIFEDA DFMGGNIKTH VMKSDYVRYA LRKGKGATRI GVQQFPRIFR
481 DSKDDPNIEC LNTIMVYMPF GPGYVYVKSK KNRDDVAKDI QHQTELVFKS FMKMIKELEW
541 MSTNAQKLAA EKATKMIRNY GWPKDLFGDF SNSQKVDAYH QTDYGDIINY YKTNSTHLYY
601 KIRKTMLKGY SNRESFRTVV SFLNRSFSRD QFLMSPAMVN AWYAPERNSI TFPYAIWNPP
661 YYNYGYPQAY NYGGQAGTGG HELVHGFDDQ GVQFGADGSL SGCTWIECGW MEPEVKASFN
721 NMAQCVVTQY STQCCPAKSG NIRCANGETT QGENIADIGG QLAAYYAYRE YVKELGKEEM
781 RLPGLEQYTP NQLFWISYGF TWCMSQTESK LISQLLTDLH APGSCRVNQV MQDIPEFAKD
841 FGCTIGQNMY PLPEQRCAVW VSE
//