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2D38

The Crystal Structure of Flavin Reductase HpaC complexed with NADP+

Summary for 2D38
Entry DOI10.2210/pdb2d38/pdb
Related2D36 2D37
Descriptorhypothetical NADH-dependent FMN oxidoreductase, FLAVIN MONONUCLEOTIDE, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ... (4 entities in total)
Functional Keywordsflavin reductase, oxidoreductase
Biological sourceSulfolobus tokodaii
Total number of polymer chains1
Total formula weight21356.89
Authors
Okai, M.,Kudo, N.,Lee, W.C.,Kamo, M.,Nagata, K.,Tanokura, M. (deposition date: 2005-09-26, release date: 2006-05-30, Last modification date: 2024-03-13)
Primary citationOkai, M.,Kudo, N.,Lee, W.C.,Kamo, M.,Nagata, K.,Tanokura, M.
Crystal structures of the short-chain flavin reductase HpaC from Sulfolobus tokodaii strain 7 in its three states: NAD(P)(+)(-)free, NAD(+)(-)bound, and NADP(+)(-)bound
Biochemistry, 45:5103-5110, 2006
Cited by
PubMed Abstract: 4-Hydroxyphenylacetate (4-HPA) is oxidized as an energy source by two component enzymes, the large component (HpaB) and the small component (HpaC). HpaB is a 4-HPA monooxygenase that utilizes FADH(2) supplied by a flavin reductase HpaC. We determined the crystal structure of HpaC (ST0723) from the aerobic thermoacidophilic crenarchaeon Sulfolobus tokodaii strain 7 in its three states [NAD(P)(+)-free, NAD(+)-bound, and NADP(+)-bound]. HpaC exists as a homodimer, and each monomer was found to contain an FMN. HpaC preferred FMN to FAD because there was not enough space to accommodate the AMP moiety of FAD in its flavin-binding site. The most striking difference between the NAD(P)(+)-free and the NAD(+)/NADP(+)-bound structures was observed in the N-terminal helix. The N-terminal helices in the NAD(+)/NADP(+)-bound structures rotated ca. 20 degrees relative to the NAD(P)(+)-free structure. The bound NAD(+) has a compact folded conformation with nearly parallel stacking rings of nicotinamide and adenine. The nicotinamide of NAD(+) stacked the isoalloxazine ring of FMN so that NADH could directly transfer hydride. The bound NADP(+) also had a compact conformation but was bound in a reverse direction, which was not suitable for hydride transfer.
PubMed: 16618099
DOI: 10.1021/bi052313i
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.05 Å)
Structure validation

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数据于2024-12-25公开中

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