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Fig. 1 | BMC Neurology

Fig. 1

From: Diagnostic journey and genetic analysis of a novel homozygous CYP2U1 mutation causing autosomal recessive spastic paraplegia type 56 (SPG56) in a consanguineous family

Fig. 1

Prediction diagram of the CYP2U1 protein structure. (a) The overall structure of the CYP2U1 protein; (b) Local structural diagram of the histidine residue at position 305; (c) Local structural diagram of the tyrosine residue at position 305; (d) Hydrogen bonding between histidine at position 305 and adjacent amino acids; (e) Hydrogen bonding between tyrosine at position 305 and adjacent amino acids; Black represents hydrogen bonds

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BMC Neurology

ISSN: 1471-2377

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