Updated annotation (from data): Formiminoglutamic iminohydrolase (EC 3.5.3.13) Rationale: Specifically important for utilizing L-Histidine. Automated validation from mutant phenotype: the predicted function (FORMIMINOGLUTAMATE-DEIMINASE-RXN) was linked to the condition via a MetaCyc pathway. This annotation was also checked manually. Original annotation: Formiminoglutamic iminohydrolase (EC 3.5.3.13) Type 1: Protein-coding gene Located on scaffold scaffold1/0|quiver|pilon, + strand, nucleotides 385,111 to 386,475 See nucleotide sequence around PfGW456L13_330 or for all of scaffold scaffold1/0|quiver|pilon