[English] 日本語
Yorodumi Papers
- Database of articles cited by EMDB/PDB/SASBDB data -

+
Search query

Keywords
Structure methods
Author
Journal
IF

-
Structure paper

TitleDifferential BET Bromodomain Inhibition by Dihydropteridinone and Pyrimidodiazepinone Kinase Inhibitors.
Journal, issue, pagesJ. Med. Chem., Year 2021
Publish dateMar 16, 2017 (structure data deposition date)
AuthorsKarim, R.M. / Bikowitz, M.J. / Chan, A. / Zhu, J.Y. / Grassie, D. / Becker, A. / Berndt, N. / Gunawan, S. / Lawrence, N.J. / Schonbrunn, E.
External linksJ. Med. Chem. / PubMed:34710325
MethodsX-ray diffraction
Resolution1.3 - 2.75 Å
Structure data

PDB-5v67:
CRYSTAL STRUCTURE OF THE FIRST BROMODOMAIN OF HUMAN BRD4 IN COMPLEX WITH Volasertib
Method: X-RAY DIFFRACTION / Resolution: 1.78 Å

PDB-5vbo:
CRYSTAL STRUCTURE OF THE FIRST BROMODOMAIN OF HUMAN BRD4 IN COMPLEX WITH LRRK2-IN-1
Method: X-RAY DIFFRACTION / Resolution: 1.3 Å

PDB-5vbp:
CRYSTAL STRUCTURE OF THE FIRST BROMODOMAIN OF HUMAN BRD4 IN COMPLEX WITH RO3280
Method: X-RAY DIFFRACTION / Resolution: 1.83 Å

PDB-5vbq:
CRYSTAL STRUCTURE OF THE FIRST BROMODOMAIN OF HUMAN BRDT IN COMPLEX WITH BI2536
Method: X-RAY DIFFRACTION / Resolution: 1.65 Å

PDB-5vbr:
CRYSTAL STRUCTURE OF THE FIRST BROMODOMAIN OF HUMAN BRDT IN COMPLEX WITH Volasertib
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

PDB-7bjy:
Crystal structure of the first bromodomain (BD1) of human BRDT bound to Ro3280
Method: X-RAY DIFFRACTION / Resolution: 2.22 Å

PDB-7k6g:
Crystal structure of the first bromodomain (BD1) of human BRD4 bound to ERK5-IN-1
Method: X-RAY DIFFRACTION / Resolution: 1.7 Å

PDB-7k6h:
Crystal structure of the first bromodomain (BD1) of human BRD4 bound to XMD8-92
Method: X-RAY DIFFRACTION / Resolution: 1.5 Å

PDB-7ko0:
Crystal structure of the second bromodomain (BD2) of human BRD4 bound to SG3-179
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

PDB-7l6d:
Crystal structure of the second bromodomain (BD2) of human BRD2 bound to bromosporine
Method: X-RAY DIFFRACTION / Resolution: 1.55 Å

PDB-7l72:
Crystal structure of the second bromodomain (BD2) of human BRD3 bound to Ro3280
Method: X-RAY DIFFRACTION / Resolution: 1.5 Å

PDB-7l73:
Crystal structure of the first bromodomain (BD1) of human BRDT bound to ERK5-IN-1
Method: X-RAY DIFFRACTION / Resolution: 1.46 Å

PDB-7l9g:
Crystal structure of the second bromodomain (BD2) of human BRD2 bound to BI2536
Method: X-RAY DIFFRACTION / Resolution: 1.36 Å

PDB-7l9j:
Crystal structure of the second bromodomain (BD2) of human BRD2 bound to Ro3280
Method: X-RAY DIFFRACTION / Resolution: 1.85 Å

PDB-7l9k:
Crystal structure of the second bromodomain (BD2) of human BRD2 bound to LRRK2-IN-1
Method: X-RAY DIFFRACTION / Resolution: 1.95 Å

PDB-7l9l:
Crystal structure of the second bromodomain (BD2) of human BRD3 bound to BI2536
Method: X-RAY DIFFRACTION / Resolution: 1.55 Å

PDB-7lah:
Crystal structure of the first bromodomain (BD1) of human BRD2 bound to bromosporine
Method: X-RAY DIFFRACTION / Resolution: 1.6 Å

PDB-7lai:
Crystal structure of the first bromodomain (BD1) of human BRD2 bound to BI2536
Method: X-RAY DIFFRACTION / Resolution: 1.85 Å

PDB-7laj:
Crystal structure of the first bromodomain (BD1) of human BRD2 bound to Ro3280
Method: X-RAY DIFFRACTION / Resolution: 1.854 Å

PDB-7lak:
Crystal structure of the first bromodomain (BD1) of human BRD2 bound to volasertib
Method: X-RAY DIFFRACTION / Resolution: 1.831 Å

PDB-7lau:
Crystal structure of the first bromodomain (BD1) of human BRD2 bound to ERK5-IN-1
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

PDB-7lay:
Crystal structure of the first bromodomain (BD1) of human BRD3 bound to SG3-179
Method: X-RAY DIFFRACTION / Resolution: 1.45 Å

PDB-7laz:
Crystal structure of the first bromodomain (BD1) of human BRD3 bound to ERK5-IN-1
Method: X-RAY DIFFRACTION / Resolution: 2.302 Å

PDB-7lb4:
Crystal structure of the second bromodomain (BD2) of human BRD3 bound to bromosporine
Method: X-RAY DIFFRACTION / Resolution: 2.004 Å

PDB-7lbt:
Crystal structure of the second bromodomain (BD2) of human BRD3 bound to ERK5-IN-1
Method: X-RAY DIFFRACTION / Resolution: 2.7 Å

PDB-7lej:
Crystal structure of the second bromodomain (BD2) of human BRDT bound to Volasertib
Method: X-RAY DIFFRACTION / Resolution: 1.73 Å

PDB-7lek:
Crystal structure of the second bromodomain (BD2) of human BRDT bound to ERK5-IN-1
Method: X-RAY DIFFRACTION / Resolution: 2.75 Å

PDB-7lel:
Crystal structure of the second bromodomain (BD2) of human BRDT bound to Bromosporine
Method: X-RAY DIFFRACTION / Resolution: 2.15 Å

PDB-7lem:
Crystal structure of the first bromodomain (BD1) of human BRDT bound to LRRK2-IN-1
Method: X-RAY DIFFRACTION / Resolution: 1.89 Å

Chemicals

ChemComp-IBI:
N-{trans-4-[4-(cyclopropylmethyl)piperazin-1-yl]cyclohexyl}-4-{[(7R)-7-ethyl-5-methyl-8-(1-methylethyl)-6-oxo-5,6,7,8-tetrahydropteridin-2-yl]amino}-3-methoxybenzamide / anticancer, inhibitor*YM

ChemComp-EDO:
1,2-ETHANEDIOL

ChemComp-DMS:
DIMETHYL SULFOXIDE / DMSO, precipitant*YM

ChemComp-HOH:
WATER

ChemComp-4K4:
2-[(2-methoxy-4-{[4-(4-methylpiperazin-1-yl)piperidin-1-yl]carbonyl}phenyl)amino]-5,11-dimethyl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one

ChemComp-CL:
Unknown entry

ChemComp-PEG:
DI(HYDROXYETHYL)ETHER

ChemComp-79C:
4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-N-(1-methylpiperidin-4-yl)benzamide

ChemComp-R78:
4-{[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl]amino}-3-methoxy-N-(1-methylpiperidin-4-yl)benzamide

ChemComp-VYJ:
11-cyclopentyl-2-({2-ethoxy-4-[4-(4-methylpiperazin-1-yl)piperidine-1-carbonyl]phenyl}amino)-5-methyl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one

ChemComp-4WG:
2-{[2-ethoxy-4-(4-hydroxypiperidin-1-yl)phenyl]amino}-5,11-dimethyl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one

ChemComp-5W2:
4-[[4-[[3-(~{tert}-butylsulfonylamino)-4-chloranyl-phenyl]amino]-5-methyl-pyrimidin-2-yl]amino]-2-fluoranyl-~{N}-(1-methylpiperidin-4-yl)benzamide

ChemComp-BMF:
Bromosporine

ChemComp-SO4:
SULFATE ION

ChemComp-BU1:
1,4-BUTANEDIOL

ChemComp-PO4:
PHOSPHATE ION

Source
  • homo sapiens (human)
KeywordsTRANSCRIPTION/INHIBITOR / BROMODOMAIN / CAP / HUNK1 / MCAP / PROTEIN BINDING-INHIBITOR COMPLEX / MITOTIC CHROMOSOME ASSOCIATED PROTEIN / INHIBITOR / TRANSCRIPTION-INHIBITOR COMPLEX / GENE REGULATION / kinase / Ro3280 / BET / ERK5 / dual BRD-kinase inhibitor / PLK1 / epigenetics / BRDT / testis specific / TRANSCRIPTION/TRANSCRIPTION INHIBITOR / TRANSCRIPTION-TRANSCRIPTION INHIBITOR complex / GENE REGULATION/INHIBITOR / GENE REGULATION-INHIBITOR complex / LRRK

+
About Yorodumi Papers

-
News

-
Feb 9, 2022. New format data for meta-information of EMDB entries

New format data for meta-information of EMDB entries

  • Version 3 of the EMDB header file is now the official format.
  • The previous official version 1.9 will be removed from the archive.

Related info.:EMDB header

External links:wwPDB to switch to version 3 of the EMDB data model

-
Aug 12, 2020. Covid-19 info

Covid-19 info

URL: https://pdbj.org/emnavi/covid19.php

New page: Covid-19 featured information page in EM Navigator.

Related info.:Covid-19 info / Mar 5, 2020. Novel coronavirus structure data

+
Mar 5, 2020. Novel coronavirus structure data

Novel coronavirus structure data

Related info.:Yorodumi Speices / Aug 12, 2020. Covid-19 info

External links:COVID-19 featured content - PDBj / Molecule of the Month (242)：Coronavirus Proteases

+
Jan 31, 2019. EMDB accession codes are about to change! (news from PDBe EMDB page)

EMDB accession codes are about to change! (news from PDBe EMDB page)

  • The allocation of 4 digits for EMDB accession codes will soon come to an end. Whilst these codes will remain in use, new EMDB accession codes will include an additional digit and will expand incrementally as the available range of codes is exhausted. The current 4-digit format prefixed with “EMD-” (i.e. EMD-XXXX) will advance to a 5-digit format (i.e. EMD-XXXXX), and so on. It is currently estimated that the 4-digit codes will be depleted around Spring 2019, at which point the 5-digit format will come into force.
  • The EM Navigator/Yorodumi systems omit the EMD- prefix.

Related info.:Q: What is EMD? / ID/Accession-code notation in Yorodumi/EM Navigator

External links:EMDB Accession Codes are Changing Soon! / Contact to PDBj

+
Jul 12, 2017. Major update of PDB

Major update of PDB

  • wwPDB released updated PDB data conforming to the new PDBx/mmCIF dictionary.
  • This is a major update changing the version number from 4 to 5, and with Remediation, in which all the entries are updated.
  • In this update, many items about electron microscopy experimental information are reorganized (e.g. em_software).
  • Now, EM Navigator and Yorodumi are based on the updated data.

External links:wwPDB Remediation / Enriched Model Files Conforming to OneDep Data Standards Now Available in the PDB FTP Archive

-
Yorodumi Papers

Database of articles cited by EMDB/PDB/SASBDB data

  • Database of articles cited by EMDB, PDB, and SASBDB entries
  • Using PubMed data

Related info.:EMDB / PDB / SASBDB / Yorodumi / EMN Papers / Changes in new EM Navigator and Yorodumi

Read more