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Ligands
Code Name Style Show Link
MG Magnesium ion
GNP Phosphoaminophosphonic acid-guanylate ester
F8T [4-[[4-(3-methoxyphenyl)phenyl]amino]phenyl]methyl-dimethyl-azanium
Non-standard Residues
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Glycosylation
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Code : 6GQW   PDBj   RCSB PDB   PDBe
Header : ONCOPROTEIN
Title : KRAS-169 Q61H GPPNHP + CH-1
Release Data : 2019-02-06
Compound :
mol_id molecule chains synonym
1 GTPase KRas A,B,C,D,F K-Ras 2,Ki-Ras,c-K-ras,c-Ki-ras
mutation: Q61H
mol_id molecule chains synonym
2 GTPase KRas E K-Ras 2,Ki-Ras,c-K-ras,c-Ki-ras
mutation: Q61H
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: KRAS, KRAS2, RASK2
mol_id organism_scientific organism_common expression_system
2 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: KRAS, KRAS2, RASK2
Authors : Cruz-Migoni, A., Quevedo, C.E., Carr, S.B., Phillips, S.E.V., Rabbitts, T.H.
Keywords : KRAS, ONCOPROTEIN
Exp. method : X-RAY DIFFRACTION ( 2.8 Å )
Citation :

Structure-based development of new RAS-effector inhibitors from a combination of active and inactive RAS-binding compounds.

Cruz-Migoni, A.,Canning, P.,Quevedo, C.E.  et al.
(2019)  Proc. Natl. Acad. Sci. U.S.A.  116 : 2545 - 2550

PubMed: 30683716
DOI: 10.1073/pnas.1811360116

Chain : E
UniProt : P01116 (RASK_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
GTP + H2O = GDP + H(+) + phosphate 3.6.5.2 PubMed:20949621
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