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P4

Gene Name P4
Sequence Strain (Species/Organism) Leishmania amazonensis
VO ID VO_0011288
NCBI Nucleotide GI 29165286
NCBI Protein GI 29165287
Protein Accession AAO65599.1
Other Database IDs CDD:280435
CDD:211382
Taxonomy ID 5659
Gene Strand (Orientation) ?
Protein Name P4 nuclease
Protein pI 7.27
Protein Weight 32555.78
Protein Length 371
Protein Note S1/P1 Nuclease; pfam02265
DNA Sequence
>gi|29165286|gb|AY219923.1| Leishmania amazonensis P4 nuclease mRNA, complete cds
ATGCCTGCGCCTGTCAGTCTCCGTCTGCCTCTCACAGCGCTGTGCCTCCTGGTGCTCAGCTCTGCGCTGT
GCGTGACTGAGGTGCTCGGATGGGGCTGCGTGGGCCACATGCTCCTCGCCGAGATCGCGCGGCGCCAGCT
GGACTTAGAGAATGAGGAAAAGATCGAGCTGATGGCGGCAGTATTTTCGGGCAGCGGTCCGTTCCCGATG
TCTCCGAGCATGGTGCAAGCGGCATGCTGGGCGGATGACGTGAAGCTTTGGCGTCAGTACGCCATGAGCA
CGTGGCACTTCTACGCCATGCCATATAACCCCGGAAACATCAATATCACCGATCCGGTCAATACAGTGAA
CGCCGTCACTGTGTGCCTTGATATGGTGACCTCGCTTAAGAACTCGAAAGCGCCGCTGTACTTGTTGAAC
TTTGCTTGGGTGAACCTGGTGCACATCTTTGGCGATCTGCATCAGCCCCTGCACACGATATCTAGGTACA
CTACCGCCTACCCGCACGGAGATCAAGGAGGCAACGCGATTTCGGTTCGTGTAGGCGGAAAAAAGGTGAA
GCTGCATGCCCTCTGGGATAATATTTGCAGTGCTACGCCACCACGCTACCAGCGGCCCCTCTCCCACACC
GACCTCTTCGCCCTCTCTGCGACAGCGGACGGGCTGGTGGAAACTTACACGTTTTCAGAGGCGTTGGAGA
CACTCGTGGACGTGATGGCGATTCATGAGGAGAGCTACATGTTTGCGGTAAACACCAGCTACCCCGGCGT
CACACCAGGTGGGACTCTCAGTCGTGCCTACCTTGATAAATGCAAGCGTGTCGCTGAGGCTCGACTGACG
CTTGGCGGCTACCGCCTCGGTTACCTTCTGAATCAGCTGCTGTCGGGCATCACTGTGGACAAGGCCGCAC
TGGAGGCGCACCGCGCTGCGCGTCCGAAGTGGAGCGCGTAA
Protein Sequence
>AAO65599.1 P4 nuclease [Leishmania amazonensis]
MPAPVSLRLPLTALCLLVLSSALCVTEVLGWGCVGHMLLAEIARRQLDLENEEKIELMAAVFSGSGPFPM
SPSMVQAACWADDVKLWRQYAMSTWHFYAMPYNPGNINITDPVNTVNAVTVCLDMVTSLKNSKAPLYLLN
FAWVNLVHIFGDLHQPLHTISRYTTAYPHGDQGGNAISVRVGGKKVKLHALWDNICSATPPRYQRPLSHT
DLFALSATADGLVETYTFSEALETLVDVMAIHEESYMFAVNTSYPGVTPGGTLSRAYLDKCKRVAEARLT
LGGYRLGYLLNQLLSGITVDKAALEAHRAARPKWSA

Molecule Role Protective antigen
Molecule Role Annotation Susceptible BALB/c mice were immunized with the DNA encoding P4 alone, P4/IL-12, or P4/HSP70 prior to challenge with L. amazonensis promastigotes. Mice immunized with P4 alone had a delayed onset of lesion development and significantly smaller lesions than the infection control group at 11 weeks postinfection (P < 0.05). P4/IL-12 immunized animals showed no sign of lesion development in three independent experiments (P < 0.01). Our results indicate that different vaccine combinations, including DNA encoding P4, HSP70, or IL-12, can provide significant protection against both Old World and New World cutaneous leishmaniasis (Campbell et al., 2003).
References