6CQA

E. coli DHFR complex with inhibitor AMPQD

6CQA の概要

• エントリーDOI: 10.2210/pdb6cqa/pdb
• 分子名称: Dihydrofolate reductase, SULFATE ION, 7-[(3-aminophenyl)methyl]-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine, ... (4 entities in total)
• 機能のキーワード: dhfr, dihydrofolate reductase, inhibitor, complex, oxidoreductase
• 由来する生物種: Escherichia coli
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 19344.70

構造登録者

Cao, H.,Rodrigues, J.,Benach, J.,Wasserman, S.,Morisco, L.,Koss, J.,Shakhnovich, E.,Skolnick, J. (登録日: 2018-03-14, 公開日: 2019-01-09, 最終更新日: 2023-10-04)

主引用文献

Cao, H.,Gao, M.,Zhou, H.,Skolnick, J.
The crystal structure of a tetrahydrofolate-bound dihydrofolate reductase reveals the origin of slow product release.
Commun Biol, 1:226-226, 2018

PubMed Abstract: Dihydrofolate reductase (DHFR) catalyzes the stereospecific reduction of 7,8-dihydrofolate (FH2) to (6s)-5,6,7,8-tetrahydrofolate (FH4) via hydride transfer from NADPH. The consensus DHFR mechanism involves conformational changes between closed and occluded states occurring during the rate-limiting product release step. Although the Protein Data Bank (PDB) contains over 250 DHFR structures, the FH4 complex structure responsible for rate-limiting product release is unknown. We report to our knowledge the first crystal structure of an . DHFR:FH4 complex at 1.03 Å resolution showing distinct stabilizing interactions absent in FH2 or related (6R)-5,10-dideaza-FH4 complexes. We discover the time course of decay of the co-purified endogenous FH4 during crystal growth, with conversion from FH4 to FH2 occurring in 2-3 days. We also determine another occluded complex structure of DHFR with a slow-onset nanomolar inhibitor that contrasts with the methotrexate complex, suggesting a plausible strategy for designing DHFR antibiotics by targeting FH4 product conformations.

PubMed: 30564747
DOI: 10.1038/s42003-018-0236-y

実験手法

X-RAY DIFFRACTION (2.2 Å)