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. 2006 Jul;72(7):4871–4877. doi: 10.1128/AEM.00375-06

TABLE 3.

Characteristics of P. chrysosporium copper radical oxidase genes

Gene Previous gene modelsa
cDNA sequence analysis
v1.0 v2.1 Molecular massb pI SSc Best hitd Accession no.e Remarks
cro1 pc.120.7.1 + pc.120.6.1 124009 65 4.7 23/24 AHT-QT C. neoformans gi57227801 (607) (ct) DQ398767
cro2 pc.46.103.1 134241 69 4.6 16/17 VLA-QG U. maydis glo1 gi71013128 (522) DQ398768
cro3 pc.85.36.1 + gx.85.36.1 121818 80 4.6 20/21 ASA-FI M. grisea gi39952025 (746) (ct) DQ398769 Two WSC domains
cro4 gx.85.15.1 + pc.85.33.1 + pc.85.32.1 8882 106 4.6 21/22 SHA-SL M. grisea gi39952025 (842) (ct) DQ398770 Four WSC domains
cro5 gx.85.13.1 + pc.85.28.1 121730 106 4.4 21/22 VQA-SS M. grisea gi39952025 (817) (ct) DQ398771 Four WSC domains
cro6 pc.72.34.1 37905 82 5.3 21/22 VLA-SE P. chrysosporium glx gi1050304 (412) DQ398772
glx pc.52.9.1 11068 57 5.1 22/23 ASD-AP gi1050304
a

Automated gene models available at http://genome.jgi-psf.org/Phchr1/Phchr1.home.html, with v1.0 models archived. To directly access v2.1 model information, end the following URL with the model number: http://genome.jgi-psf.org/cgi-bin/dispGeneModel?db=Phchr1&id=___.

b

Predicted molecular mass of mature peptide in kilodaltons.

c

Secretion signals (SS) predicted by SignalP (www.cbs.dtu.dk/services/SignalP/) using both neural networks and hidden Markov models. Position and surrounding residues are shown. The glx signal was determined experimentally (23, 45).

d

BLASTP searches of nonredundant NCBI. ct, conceptual translation.

e

Deposited cDNA sequences were based on PCR-amplified products using RNA derived from standard carbon-starved cultures (cro1, cro3, cro4, and cro5), colonized wood wafers harvested on day 10 (cro2), and Avicel cultures harvested on day 6 (cro6). Subsequent RT-PCR and cDNA sequence analysis have shown that all seven copper radical oxidase transcripts are present in carbon-starved cultures and in colonized wood wafer after day 10.