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The members of this protein family are characterized by the presence of
two transmembrane regions (TM1 and TM2) flanking a large hydrophilic
loop located in the periplasmatic side of the plasma membrane ( Cuth-
bertson et al., 2009 ; Morona et al., 2000 ). In addition, they also contain
a proline- and glycine-rich domain preceding and overlapping the TM2
( Cuthbertson et al., 2009 ; Morona, Purins, Tocilj, Matte, & Cygler, 2009 ).
The PCP proteins can be distinguished according to the type of poly-
saccharide, association with the Wzy or ABC-dependent assembly and
export pathways, coiled-coil prediction profile and presence of charac-
teristic domains ( Fig. 7.2 ) ( Morona et al., 2009 , 2000 ). The PCP-1 family
comprises the Wzz proteins, which participate in the biosynthesis of the
O-antigen of LPS and the enterobacterial common antigen by the Wzy-
dependent pathway ( Morona et al., 2009 , 2000 ; Whitfield, 2010 ). The
PCP-2 refers to the proteins involved in the polymerization and export
of high molecular polysaccharides, including the EPS, also following the
Wzy-dependent pathway. The PCP-2 of Gram-negative bacteria, includ-
ing Wzc, is designated as PCP-2a ( Morona et al., 2000 ). The members of
this group possess an additional carboxy-terminal cytoplasmic domain,
which contains the Walker Box A and B motifs that are found in a vari-
ety of ATP- and GTP-hydrolysing proteins ( Cuthbertson et al., 2010 ;
Figure 7.2 General characteristics of the polysaccharide copolymerase (PCP) family
proteins. The members of this family possess two transmembrane regions (TM1 and
TM2) flanking a large periplasmatic loop and a proline- and glycine-rich domain that
precedes and overlaps the TM2 (depicted in grey). PCP-1 proteins participate in the bio-
synthesis of the O-antigen of LPS following the Wzy-dependent pathway. The PCP-2a
are involved in EPS assembly and export in Gram-negative bacteria, also following the
Wzy-dependent pathway. The members of this group possess an additional carboxy-
terminal cytoplasmic domain, containing the Walker Box A and B motifs, a DXD sig-
nature, and a carboxy-terminal tyrosine rich region. PCP-3 proteins participate in the
ABC-dependent EPS assembly and export systems. The PCP-1 and PCP-3 proteins are
smaller than the PCP-2a, lacking the additional carboxy-terminal cytoplasmic region
( Cuthbertson et al., 2009 ; Morona et al., 2000 , 2009 ; Whitfield, 2010 ).
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