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4IT2

Mn(III)-PPIX bound Tt H-NOX

Summary for 4IT2
Entry DOI10.2210/pdb4it2/pdb
Related1U4H 1U55 1U56 3EEE 3M0B 3SJ5
DescriptorMethyl-accepting chemotaxis protein, MANGANESE PROTOPORPHYRIN IX (3 entities in total)
Functional Keywordso2-sensing heme domain, oxygen binding
Biological sourceCaldanaerobacter subterraneus subsp. tengcongensis (Thermoanaerobacter tengcongensis)
Total number of polymer chains2
Total formula weight45941.74
Authors
Winter, M.B.,Klemm, P.J.,Phillips-Piro, C.M.,Raymond, K.M.,Marletta, M.A. (deposition date: 2013-01-17, release date: 2013-02-27, Last modification date: 2023-09-20)
Primary citationWinter, M.B.,Klemm, P.J.,Phillips-Piro, C.M.,Raymond, K.N.,Marletta, M.A.
Porphyrin-Substituted H-NOX Proteins as High-Relaxivity MRI Contrast Agents.
Inorg.Chem., 52:2277-2279, 2013
Cited by
PubMed Abstract: Heme proteins are exquisitely tuned to carry out diverse biological functions while employing identical heme cofactors. Although heme protein properties are often altered through modification of the protein scaffold, protein function can be greatly expanded and diversified through replacement of the native heme with an unnatural porphyrin of interest. Thus, porphyrin substitution in proteins affords new opportunities to rationally tailor heme protein chemical properties for new biological applications. Here, a highly thermally stable Heme Nitric oxide/OXygen binding (H-NOX) protein is evaluated as a magnetic resonance imaging (MRI) contrast agent. T1 and T2 relaxivities measured for the H-NOX protein containing its native heme are compared to the protein substituted with unnatural manganese(II/III) and gadolinium(III) porphyrins. H-NOX proteins are found to provide unique porphyrin coordination environments and have enhanced relaxivities compared to commercial small-molecule agents. Porphyrin substitution is a promising strategy to encapsulate MRI-active metals in heme protein scaffolds for future imaging applications.
PubMed: 23394479
DOI: 10.1021/ic302685h
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.097 Å)
Structure validation

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数据于2025-06-25公开中

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