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Structure paper

TitleIdentification of tetracycline combinations as EphB1 tyrosine kinase inhibitors for treatment of neuropathic pain.
Journal, issue, pagesProc. Natl. Acad. Sci. USA, Vol. 118, Year 2021
Publish dateOct 10, 2019 (structure data deposition date)
AuthorsAhmed, M.S. / Wang, P. / Nguyen, N.U.N. / Nakada, Y. / Menendez-Montes, I. / Ismail, M. / Bachoo, R. / Henkemeyer, M. / Sadek, H.A. / Kandil, E.S.
External linksProc. Natl. Acad. Sci. USA / PubMed:33627480
MethodsX-ray diffraction
Resolution1.608 - 2.705 Å
Structure data

PDB-6umw:
Crystal structure of hEphB1 bound with chlortetracycline
Method: X-RAY DIFFRACTION / Resolution: 1.982 Å

PDB-7kpl:
Crystal structure of hEphB1 in apo form
Method: X-RAY DIFFRACTION / Resolution: 2.705 Å

PDB-7kpm:
Crystal structure of hEphB1 bound with ADP
Method: X-RAY DIFFRACTION / Resolution: 1.608 Å

Chemicals

ChemComp-CTC:
7-CHLOROTETRACYCLINE / antibiotic*YM

ChemComp-HOH:
WATER

ChemComp-ADP:
ADENOSINE-5'-DIPHOSPHATE / ADP, energy-carrying molecule*YM

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / hEphB1 / Chlortetracycline / TRANSFERASE-TRANSFERASE INHIBITOR complex / TRANSFERASE / ADP

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