Table 2.
LCR Data Summary.
| PlasmoDB ID | Gene Annotation (Abbreviation) | Heterozygosity | Plasmodium reichenowi Divergencea | LCR Family | AT-content (%) |
| PFE0305w | Transcription initiation factor Tfiid, TATA-binding protein (PfTfiid) | 0 | Deletion | Heterogeneous | 76.1 |
| MAL7P1.91 | Exported serine/threonine protein kinase (PfSTPK) | 0 | Deletion | Heterogeneous | 74.5 |
| PFL0950c | P-type ATPase2 (PfATPase2) | 0 | Deletion | Heterogeneous | 81.7 |
| MAL13P1.148 | Myosin II (PfMyo) | 0 | Deletion | Heterogeneous | 84.1 |
| PFB0500c | Rab5.1 protein, putative (PfRab5) | 0 | Insertion | Heterogeneous | 88.9 |
| PFD0950w | Ran-binding protein 1 (PfRanB1) | 0 | Insertion | Heterogeneous | 70.5 |
| PFE0120c | Merozoite surface protein 8.I (PfMSP8) | 0 | None | Heterogeneous | 86.9 |
| PFE0805w | Cation-transporting ATPase 1.I (PfCTA) | 0 | None | Heterogeneous | 80.9 |
| PFE0805w | Cation-transporting ATPase 1.II (PfCTA) | 0 | None | Heterogeneous | 94.8 |
| MAL7P1.91 | Exported serine/threonine protein kinase (PfSTPK) | 0 | None | Heterogeneous | 73.3 |
| PF10_0345 | Merozoite surface protein 3 (PfMSP3) | 0 | None | Heterogeneous | 64.9 |
| PFL2140c | ADP-ribosylation factor GTPase-activating protein (PfARF) | 0 | None | Heterogeneous | 83.2 |
| MAL13P1.148 | Myosin I (PfMyo) | 0 | None | Heterogeneous | 83.7 |
| MAL13P1.301 | Guanylyl cyclase II (PfGCyII) | 0 | None | Heterogeneous | 68.3 |
| PFD0590c | DNA polymerase alpha (PfPolA) | 0 | Not found | Heterogeneous | 79.8 |
| PFL1700c | Vacuolar-type H+-translocating inorganic pyrophosphatase (PfTIPP) | 0 | Not found | Heterogeneous | 82.5 |
| PF13_0257 | Glutamate-tRNA ligase (PftRNAlig) | 0 | Unknown | Heterogeneous | 86.9 |
| PFB0685c | Acyl CoA synthetase (PfACS9) | 0.734 | Deletion | HighGC | 61.9 |
| PFD0085c | Acyl-CoA synthetase, putative (PfACS6) | 0.648 | Deletion | HighGC | 73.6 |
| PFD0865c | Cdc2-related protein kinase 1 (Pfcdc2) | 0.8 | Deletion | HighGC | 72.6 |
| PF07_0030 | Heat shock protein 86 family protein (PfHSP86) | 0.56 | Deletion | HighGC | 72.3 |
| MAL13P1.176 | Reticulocyte-binding protein 2 homolog B (PfRBP2b) | 0.633 | Insertion | HighGC | 70.9 |
| PF13_0198 | Reticulocyte-binding protein 2 homolog A (PfRBP2a) | 0.695 | NA | HighGC | 70.8 |
| PFA0675w | RESA-like protein with DNAJ domain (PfRLP) | 0.764 | Not found | HighGC | 68.5 |
| PFE0120c | Merozoite surface protein 8.III (PfMSP8) | 0.716 | Not found | HighGC | 73.9 |
| PFL1370w | NIMA-related protein kinase (Pfnek-1) | 0.914 | Not found | HighGC | 61.8 |
| PFI0925w | Gamma-glutamylcysteine synthetase (PfGGS) | 0.833 | Unknown | HighGC | 65.5 |
| PF10_0071 | RhoGAP protein (PfrhoGap) | 0.75 | Unknown | HighGC | 71.2 |
| PFL1880w | Acyl CoA synthetase (PfACS11) | 0.719 | Deletion | PolyN | 89.3 |
| PFE0120c | Merozoite surface protein 8.II (PfMSP8) | 0.531 | Insertion/deletion | PolyN | 88.3 |
| PF11_0395 | Guanylyl cyclase 1.I (PfGCy1) | 0.806 | Not found | PolyN | 83.8 |
| PF11_0395 | Guanylyl cyclase 1.II (PfGCy1) | 0.72 | Not found | PolyN | 82.1 |
| PF13_0150 | DNA-directed RNA polymerase 3 largest subunit (RNApol3) | 0.8 | Not found | PolyN | 90.5 |
| PFL0465c | Zinc finger transcription factor (Pfkrox1) | 0.72 | Unknown | PolyN | 80.3 |
NOTE.—Sixteen loci used in the first portion of the study comparing 16 different isolates are given in bold and loci used in the second part of the study comparing sequence from 5 isolates are not in bold. “None” indicates no size difference and no divergence. “Insertion” or “deletion” represents the P. reichenowi sequence size difference, for example, “deletion” indicating a shorter sequence in P. reichenowi than that of P. falciparum or any of its alleles (the one “insertion/deletion” represents a single instance in which the P. reichenowi sequence was an intermediate size compared with P. falciparum alleles). “Unknown” indicated that only part of the P. reichenowi sequence was found and “not found” indicates unsuccessful searches for a P. reichenowi ortholog for this gene. Unsuccessful searches likely result from the incomplete nature of P. reichenowi genome data (rather than the absence of the locus in the P. reichenowi genome) because in all cases sequence data were successfully found from regions up- and downstream and/or from known orthologs from multiple, more divergent, Plasmodium species.
Divergence as measured by size difference of P. falciparum loci with orthologous P. reichenowi sequence.