Binding Site Information of Target
Target General Information | Top | ||||
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Target ID | T02259 | Target Info | |||
Target Name | Runt-related transcription factor 2 (RUNX2) | ||||
Synonyms | SL3/AKV core-binding factor alpha A subunit; SL3-3 enhancer factor 1 alpha A subunit; Polyomavirus enhancer-binding protein 2 alpha Asubunit; Polyomavirus enhancer-binding protein 2 alpha A subunit; PEBP2A; PEBP2-alpha A; PEA2-alpha A; Osteoblast-specific transcription factor 2; Oncogene AML-3; OSF2; OSF-2; Core-binding factor subunit alpha-1; CBFA1; CBF-alpha-1; Acute myeloid leukemia 3 protein; AML3 | ||||
Target Type | Literature-reported Target | ||||
Gene Name | RUNX2 | ||||
UniProt ID |
Drug Binding Sites of Target | Top | |||||
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Ligand Name: Plicamycin | Ligand Info | |||||
Structure Description | Crystal structure of the DNA binding domains of human transcription factor ERG, human Runx2 bound to core binding factor beta (Cbfb), and mithramycin, in complex with 16mer DNA CAGAGGATGTGGCTTC | PDB:6VGG | ||||
Method | X-ray diffraction | Resolution | 4.31 Å | Mutation | No | [1] |
PDB Sequence |
AELVRTDSPN
120 FLCSVLPSHW130 RCNKTLPVAF140 KVVALGEVPD150 GTVVTVMAGN160 DENYSAELRN 170 ASAVMKNQVA180 RFNDLRFVGR190 SGRGKSFTLT200 ITVFTNPPQV210 ATYHRAIKVT 220 VDGPREP
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References | Top | ||||
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REF 1 | Allosteric interference in oncogenic FLI1 and ERG transactions by mithramycins. Structure. 2021 May 6;29(5):404-412.e4. |
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