Cytochrome b5, type A

2I961528109672ENSG00000166347ENSMUSG00000024646P00167P56395NM_001190807NM_001914NM_148923NM_025797NM_001348159NP_001177736NP_001905NP_683725NP_080073NP_001335088Cytochrome b5, form A (gene name CYB5A), is a human microsomal cytochrome b5.1cyo: BOVINE CYTOCHROME B(5)1do9: SOLUTION STRUCTURE OF OXIDIZED MICROSOMAL RABBIT CYTOCHROME B5. FACTORS DETERMINING THE HETEROGENEOUS BINDING OF THE HEME.1ehb: CRYSTAL STRUCTURE OF RECOMBINANT TRYPSIN-SOLUBILIZED FRAGMENT OF CYTOCHROME B51es1: CRYSTAL STRUCTURE OF VAL61HIS MUTANT OF TRYPSIN-SOLUBILIZED FRAGMENT OF CYTOCHROME B51f03: SOLUTION STRUCTURE OF OXIDIZED BOVINE MICROSOMAL CYTOCHROME B5 MUTANT (E44A, E48A, E56A, D60A) AND ITS INTERACTION WITH CYTOCHROME C1f04: SOLUTION STRUCTURE OF OXIDIZED BOVINE MICROSOMAL CYTOCHROME B5 MUTANT (E44A, E48A, E56A, D60A) AND ITS INTERACTION WITH CYTOCHROME C1i5u: SOLUTION STRUCTURE OF CYTOCHROME B5 TRIPLE MUTANT (E48A/E56A/D60A)1j0q: Solution Structure of Oxidized Bovine Microsomal Cytochrome b5 mutant V61H1lqx: Crystal structure of V45E mutant of cytochrome b51lr6: Crystal structure of V45Y mutant of cytochrome b51m20: Crystal Structure of F35Y Mutant of Trypsin-solubilized Fragment of Cytochrome b51m2i: Crystal structure of E44A/E56A mutant of cytochrome b51m2m: Crystal structure of E44A/E48A/E56A/D60A mutant of cytochrome b51m59: Crystal Structure of P40V Mutant of Trypsin-solubilized Fragment of Cytochrome b51nx7: Solution Structure of Oxidized Bovine Microsomal Cytochrome B51sh4: Solution structure of oxidized bovine microsomal cytochrome B5 Mutant V45H1u9m: Crystal structure of F58W mutant of cytochrome b51u9u: Crystal structure of F58Y mutant of cytochrome b5 Cytochrome b5, form A (gene name CYB5A), is a human microsomal cytochrome b5. Cytochrome b5 is a membrane bound hemoprotein which functions as an electron carrier for several membrane bound oxygenases. It has two isoforms produced by alternative splicing. Isoform 1 is bound to the cytoplasmic side of the endoplasmic reticulum. It has a C-terminal transmembrane alpha-helix. Isoform 2 was found in cytoplasm. Defects in CYB5A are the cause of type IV hereditary methemoglobinemia.