#=GF ID CagD
#=GF AC PF16567.6
#=GF DE Pathogenicity island component CagD
#=GF AU Coggill P;0000-0001-5731-1588
#=GF SE pdb_3cwx
#=GF GA 25.00 25.00;
#=GF TC 462.50 462.30;
#=GF NC 23.10 21.90;
#=GF BM hmmbuild HMM.ann SEED.ann
#=GF SM hmmsearch -Z 47079205 -E 1000 --cpu 4 HMM pfamseq
#=GF TP Domain
#=GF RN [1]
#=GF RM 19109970
#=GF RT The Helicobacter pylori CagD (HP0545, Cag24) protein is
#=GF RT essential for CagA translocation and maximal induction of
#=GF RT interleukin-8 secretion.
#=GF RA Cendron L, Couturier M, Angelini A, Barison N, Stein M, Zanotti
#=GF RA G;
#=GF RL J Mol Biol. 2009;386:204-217.
#=GF DR INTERPRO; IPR032336;
#=GF DR SO; 0000417; polypeptide_domain;
#=GF CC CagD is a tightly conserved family of proteins found in the
#=GF CC pathogenic strains of Helicobacter species. It is one of some 30
#=GF CC proteins, produced from the genomic insert termed the
#=GF CC pathogenicity island, required for the type IV secretion system
#=GF CC - T4SS - that delivers CagA oncoprotein toxin into the host
#=GF CC cell. CagD is a covalent dimer in which each monomer folds as a
#=GF CC single domain composed of five beta-strands and three
#=GF CC alpha-helices. CagD partially associates with the inner
#=GF CC membrane, where it may be exposed to the periplasmic space; this
#=GF CC may indicate that CagD is released into the supernatant during
#=GF CC host cell infection in order then to bind to the host cell
#=GF CC surface, or to be incorporated into the pilus structure [1].
#=GF SQ 1
#=GS O25277_HELPY/3-207 AC O25277.1
O25277_HELPY/3-207 NNNSNKKLRGFFVKVLLSLVVFSSYGLANDDKEAKKEVLEKEKNTPNGLVYTNLDFDSFKATIKNLKDKKVTFKEVNPDIIKDEVFDFVIVNRVLKKIKDLKHYDPVIEKIFDEKGKEMGLNVELQINPEVKDFFTFKSISTTNKQRCFLSLRGETREILCDDKLYNVLLAVFNSYDPNDLLKHISTVESLKKIFYTITCEAVYL
#=GC seq_cons NNNSNKKLRGFFVKVLLSLVVFSSYGLANDDKEAKKEVLEKEKNTPNGLVYTNLDFDSFKATIKNLKDKKVTFKEVNPDIIKDEVFDFVIVNRVLKKIKDLKHYDPVIEKIFDEKGKEMGLNVELQINPEVKDFFTFKSISTTNKQRCFLSLRGETREILCDDKLYNVLLAVFNSYDPNDLLKHISTVESLKKIFYTITCEAVYL
//