Journal:IUCrJ:S2052252520001840
From Proteopedia
(Difference between revisions)

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We presented the crystal structure of an <scene name='83/835837/Cv/1'>apo human MICU1-MICU2 heterodimer</scene>. The heterodimer had an asymmetric interface. Interestingly, the rigid <scene name='83/835837/Cv/5'>interface 1</scene> included a <scene name='83/835837/Cv/6'>D231(MICU1)-R352(MICU2) salt bridge</scene>, and D231 is a highly conserved residue for Ca<sup>2+</sup> coordination in MICU1 EF-hand 1. Thus, MICU1 EF-hand 1 can bind calcium when the salt bridge dissociates. The tight interaction in apo state of MICU1-MICU2 might hinder the conformational changes required for the Ca<sup>2+</sup> binding, resulting in a lower Ca<sup>2+</sup> binding affinity in the MICU1-MICU2 heterodimer as compared to that of MICU1 homodimer. | We presented the crystal structure of an <scene name='83/835837/Cv/1'>apo human MICU1-MICU2 heterodimer</scene>. The heterodimer had an asymmetric interface. Interestingly, the rigid <scene name='83/835837/Cv/5'>interface 1</scene> included a <scene name='83/835837/Cv/6'>D231(MICU1)-R352(MICU2) salt bridge</scene>, and D231 is a highly conserved residue for Ca<sup>2+</sup> coordination in MICU1 EF-hand 1. Thus, MICU1 EF-hand 1 can bind calcium when the salt bridge dissociates. The tight interaction in apo state of MICU1-MICU2 might hinder the conformational changes required for the Ca<sup>2+</sup> binding, resulting in a lower Ca<sup>2+</sup> binding affinity in the MICU1-MICU2 heterodimer as compared to that of MICU1 homodimer. | ||
- | + | <scene name='83/835837/Cv/9'>Interface 2</scene>. | |
<b>References</b><br> | <b>References</b><br> | ||
<references/> | <references/> | ||
</StructureSection> | </StructureSection> | ||
__NOEDITSECTION__ | __NOEDITSECTION__ |
Revision as of 13:27, 20 February 2020
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