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. Author manuscript; available in PMC: 2015 May 12.
Published in final edited form as: Toxicol Appl Pharmacol. 2007 Mar 12;221(1):29–41. doi: 10.1016/j.taap.2007.02.017

Fig 1.

Fig 1

Alignment of CYP1C1 and CYP1C2 sequences derived from the Danio rerio genome assembly version 6 (Zv6; ENS 1C1 and ENS 1C2), and cloned CYP1C1 and CYP1C2 cDNA sequences from zebrafish Tubingen Longfin (TL) and zebrafish purchased in a local pet store (pet store-obtained zebrafish, PS). Small rectangles, amino acids that are identical in sequences cloned from both TL and PS zebrafish but differ from the corresponding Zv6 sequence; pentagons, amino acids in sequences cloned from either TL or PS zebrafish that differ from the other strain and from the Zv6 sequence; “heme bind” means heme binding site; shaded areas labeled SRS1-6 = Substrate binding sites 1–6.