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Fig. 2 | BMC Medical Genomics

Fig. 2

From: Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family

Fig. 2

a Complete ribbon representation of adenylate kinase protein (PDB ID-1Z83) with chains A, B, and C. b Secondary structure of the protein (PDB ID-1Z83) showing the amino acid residue at position 101 (Q101). c Wild type amino acid residue glutamine 101 (Q101). d Mutant type amino acid residue Lysine101 (K101). e The residue (Q) at position 101 of AK-1 is highly conserved across species

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