5JS5
Nitric oxide complex of the L16F mutant of cytochrome c prime from Alcaligenes xylosoxidans
Summary for 5JS5
Entry DOI | 10.2210/pdb5js5/pdb |
Descriptor | Cytochrome c', HEME C, ASCORBIC ACID, ... (5 entities in total) |
Functional Keywords | gas sensor, cytochrome, nitric oxide, electron transport |
Biological source | Alcaligenes xylosoxydans xylosoxydans |
Total number of polymer chains | 1 |
Total formula weight | 14231.73 |
Authors | Kekilli, D.,Strange, R.W.,Hough, M.A. (deposition date: 2016-05-07, release date: 2017-03-08, Last modification date: 2024-10-23) |
Primary citation | Kekilli, D.,Petersen, C.A.,Pixton, D.A.,Ghafoor, D.D.,Abdullah, G.H.,Dworkowski, F.S.N.,Wilson, M.T.,Heyes, D.J.,Hardman, S.J.O.,Murphy, L.M.,Strange, R.W.,Scrutton, N.S.,Andrew, C.R.,Hough, M.A. Engineering proximal vs. distal heme-NO coordination via dinitrosyl dynamics: implications for NO sensor design. Chem Sci, 8:1986-1994, 2017 Cited by PubMed Abstract: Proximal distal heme-NO coordination is a novel strategy for selective gas response in heme-based NO-sensors. In the case of cytochrome c' (AXCP), formation of a transient distal 6cNO complex is followed by scission of the Fe-His bond and conversion to a proximal 5cNO product a putative dinitrosyl species. Here we show that replacement of the AXCP distal Leu16 residue with smaller or similar sized residues (Ala, Val or Ile) traps the distal 6cNO complex, whereas Leu or Phe residues lead to a proximal 5cNO product with a transient or non-detectable distal 6cNO precursor. Crystallographic, spectroscopic, and kinetic measurements of 6cNO AXCP complexes show that increased distal steric hindrance leads to distortion of the Fe-N-O angle and flipping of the heme 7-propionate. However, it is the kinetic parameters of the distal NO ligand that determine whether 6cNO or proximal 5cNO end products are formed. Our data support a 'balance of affinities' mechanism in which proximal 5cNO coordination depends on relatively rapid release of the distal NO from the dinitrosyl precursor. This mechanism, which is applicable to other proteins that form transient dinitrosyls, represents a novel strategy for 5cNO formation that does not rely on an inherently weak Fe-His bond. Our data suggest a general means of engineering selective gas response into biologically-derived gas sensors in synthetic biology. PubMed: 28451315DOI: 10.1039/c6sc04190f PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.7 Å) |
Structure validation
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