Tag Content
SG ID
SG00000054 
UniProt Accession
Theoretical PI
8.99  
Molecular Weight
57802 Da  
Genbank Nucleotide ID
Genbank Protein ID
Gene Name
spe-8 
Gene Synonyms/Alias
 
Protein Name
 
Protein Synonyms/Alias
SubName: Protein SPE-8 
Organism
Caenorhabditis elegans 
NCBI Taxonomy ID
6239 
Chromosome Location
chr:I;118104-120870;1
View in Ensembl genome browser  
Function in Stage
Function in Cell Type
Description
Temporarily unavailable 
The information of related literatures
1. S. W. L'Hernault, D. C. Shakes and S. Ward (1988) Developmental genetics of chromosome I spermatogenesis-defective mutants in the nematode Caenorhabditis elegans. Genetics 120(2): 435-52. 

Abstract
Mutations affecting Caenorhabditis elegans spermatogenesis can be used to dissect the processes of meiosis and spermatozoan morphological maturation. We have obtained 23 new chromosome I mutations that affect spermatogenesis (spe mutations). These mutations, together with six previously described mutations, identify 11 complementation groups, of which six are defined by multiple alleles. These spe mutations are all recessive and cause normally self-fertile hermaphrodites to produce unfertilized oocytes that can be fertilized by wild-type male sperm. Five chromosome I mutation/deficiency heterozygotes have similar phenotypes to the homozygote showing that the probable null phenotype of these genes is defective sperm. Spermatogenesis is disrupted at different steps by mutations in these genes. The maturation of 1 degree spermatocytes is disrupted by mutations in spe-4 and spe-5. Spermatids from spe-8 and spe-12 mutants develop into normal spermatozoa in males, but not in hermaphrodites. fer-6 spermatids are abnormal, and fer-1 spermatids look normal but subsequently become abnormal spermatozoa. Mutations in five genes (fer-7, spe-9, spe-11, spe-13 and spe-15) allow formation of normal looking motile spermatozoa that appear to be defective in either sperm-spermathecal or sperm-oocyte interactions. PMID: [3197956] 

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Figures for illustrating the function of this protein/gene
Ref: S. W. L'Hernault, D. C. Shakes and S. Ward (1988) Developmental genetics of chromosome I spermatogenesis-defective mutants in the nematode Caenorhabditis elegans. Genetics 120(2): 435-52. PMID: [3197956]
Ref: S. W. L'Hernault, D. C. Shakes and S. Ward (1988) Developmental genetics of chromosome I spermatogenesis-defective mutants in the nematode Caenorhabditis elegans. Genetics 120(2): 435-52. PMID: [3197956]
Ref: S. W. L'Hernault, D. C. Shakes and S. Ward (1988) Developmental genetics of chromosome I spermatogenesis-defective mutants in the nematode Caenorhabditis elegans. Genetics 120(2): 435-52. PMID: [3197956]
Function
 
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Subcellular Location
 
Tissue Specificity
 
Gene Ontology
GO IDGO termEvidence
GO:0005524 F:ATP binding IEA:UniProtKB-KW.
GO:0004713 F:protein tyrosine kinase activity IEA:UniProtKB-KW.
GO:0007286 P:spermatid development IMP:WormBase.
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Interpro
IPR011009;    Kinase-like_dom.
IPR000719;    Prot_kinase_cat_dom.
IPR017441;    Protein_kinase_ATP_BS.
IPR001245;    Ser-Thr/Tyr_kinase_cat_dom.
IPR000980;    SH2.
IPR008266;    Tyr_kinase_AS.
IPR020635;    Tyr_kinase_cat_dom.
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Pfam
PF07714;    Pkinase_Tyr;    1.
PF00017;    SH2;    1.
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SMART
SM00252;    SH2;    1.
SM00219;    TyrKc;    1.
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PROSITE
PS00107;    PROTEIN_KINASE_ATP;    1.
PS50011;    PROTEIN_KINASE_DOM;    1.
PS00109;    PROTEIN_KINASE_TYR;    1.
PS50001;    SH2;    1.
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PRINTS
PR00109;    TYRKINASE.;   
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Created Date
18-Oct-2012 
Record Type
Experiment identified 
Protein sequence Annotation
Nucleotide Sequence
Length: bp   Go to nucleotide: FASTA
Protein Sequence
Length: 512 bp   Go to amino acid: FASTA
The verified Protein-Protein interaction information
UniProt
Gene Symbol Ref Databases
Other Protein-Protein interaction resources
String database  
View Microarray data
Temporarily unavailable 
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