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6GIM

Structure of the DNA duplex d(AAATTT)2 with [N-(3-chloro-4-((4,5-dihydro-1H-imidazol-2-yl)amino)phenyl)-4-((4,5-dihydro-1H-imidazol-2- yl)amino)benzamide] - (drug JNI18)

Summary for 6GIM
Entry DOI10.2210/pdb6gim/pdb
DescriptorDNA (5'-D(*AP*AP*AP*TP*TP*T)-3'), [4-[(3-chloranyl-4-imidazolidin-2-ylideneazaniumyl-phenyl)carbamoyl]phenyl]-imidazolidin-2-ylidene-azanium, MAGNESIUM ION, ... (4 entities in total)
Functional Keywordsat-rich dna, dna binding drugs, minor groove binding drugs, antiparasitic drugs, trypanosoma brucei, dna
Biological sourceTrypanosoma brucei
Total number of polymer chains4
Total formula weight8501.51
Authors
Millan, C.R.,Dardonvile, C.,de Koning, H.P.,Saperas, N.,Campos, J.L. (deposition date: 2018-05-14, release date: 2018-08-08, Last modification date: 2024-05-01)
Primary citationMillan, C.R.,Acosta-Reyes, F.J.,Lagartera, L.,Ebiloma, G.U.,Lemgruber, L.,Nue Martinez, J.J.,Saperas, N.,Dardonville, C.,de Koning, H.P.,Campos, J.L.
Functional and structural analysis of AT-specific minor groove binders that disrupt DNA-protein interactions and cause disintegration of the Trypanosoma brucei kinetoplast.
Nucleic Acids Res., 45:8378-8391, 2017
Cited by
PubMed: 28637278
DOI: 10.1093/nar/gkx521
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.43 Å)
Structure validation

221051

數據於2024-06-12公開中

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