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5H1D

Crystal structure of C-terminal of RhoGDI2

Summary for 5H1D
Entry DOI10.2210/pdb5h1d/pdb
DescriptorRho GDP-dissociation inhibitor 2 (2 entities in total)
Functional Keywordssignaling protein
Biological sourceHomo sapiens (Human)
Cellular locationCytoplasm, cytosol : P52566
Total number of polymer chains1
Total formula weight16427.71
Authors
Liu, J. (deposition date: 2016-10-08, release date: 2016-10-26, Last modification date: 2023-11-08)
Primary citationLiu, J.,Gao, J.,Li, F.,Ma, R.,Wei, Q.,Wang, A.,Wu, J.,Ruan, K.
NMR characterization of weak interactions between RhoGDI2 and fragment screening hits.
Biochim. Biophys. Acta, 1861:3061-3070, 2017
Cited by
PubMed Abstract: The delineation of intrinsically weak interactions between novel targets and fragment screening hits has long limited the pace of hit-to-lead evolution. Rho guanine-nucleotide dissociation inhibitor 2 (RhoGDI2) is a novel target that lacks any chemical probes for the treatment of tumor metastasis.
PubMed: 27721047
DOI: 10.1016/j.bbagen.2016.10.003
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.494 Å)
Structure validation

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数据于2024-10-30公开中

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