2i96
From Proteopedia
Jump to navigationJump to search
Solution structure of the oxidized microsomal human cytochrome b5
| ||||||||||||
Structural highlights
DiseaseCYB5_HUMAN Defects in CYB5A are the cause of methemoglobinemia CYB5A-related (METHB-CYB5A) [MIM:250790. A form of methemoglobinemia, a hematologic disease characterized by the presence of excessive amounts of methemoglobin in blood cells, resulting in decreased oxygen carrying capacity of the blood, cyanosis and hypoxia.[1] FunctionCYB5_HUMAN Cytochrome b5 is a membrane bound hemoprotein which function as an electron carrier for several membrane bound oxygenases. Evolutionary ConservationCheck, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. See AlsoReferences | ||||||||||||||||||||
This page was last modified 08:14, 13 August 2026.