9BG0: GTPase NRas

Tri-complex of Daraxonrasib (RMC-6236), NRAS WT, and CypA. Determined by X-ray diffraction at 1.64 Å resolution. Released 19 Mar 2025.

Method: X-ray diffraction
Resolution: 1.64 Å
Organism: Homo sapiens
Chains: 4
Atoms: 6,019
Mol. weight: 77.57 kDa
Ligands: A1AHB, MG, GNP
Released: 19 Mar 2025

Explore 9BG0 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

9BG0 contains 21 α-helices and 39 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 6 helices, 6 β-strands

Element	Residues	Length	Sheet
β-strand	2-10	9	1
α-helix	16-25	10
β-strand	37-46	10	1
β-strand	49-58	10	1
α-helix	62-67	6
α-helix	69-74	6
β-strand	77-83	7	1
α-helix	87-104	18
β-strand	111-116	6	1
α-helix	127-137	11
β-strand	141-143	3	1
α-helix	152-168	17

Chain B: 6 helices, 8 β-strands

Element	Residues	Length	Sheet
β-strand	2-10	9	2
α-helix	16-25	10
β-strand	37-46	10	2
β-strand	49-58	10	2
α-helix	62-68	7
α-helix	69-74	6
β-strand	77-83	7	2
α-helix	87-104	18
β-strand	111-116	6	2
α-helix	127-137	11
β-strand	141-143	3	2
β-strand	145	1	3
β-strand	150	1	3
α-helix	152-167	16

Chain C: 5 helices, 13 β-strands

Element	Residues	Length	Sheet
α-helix	2-4	3
β-strand	5-12	8	4
β-strand	15-24	10	4
α-helix	30-41	12
β-strand	52	1	4
β-strand	55-57	3	4
β-strand	61-64	4	4
β-strand	77	1	5
β-strand	80	1	5
β-strand	83	1	6
β-strand	97-100	4	4
β-strand	108	1	6
β-strand	112-115	4	4
α-helix	120-122	3
β-strand	128-132	5	4
α-helix	136-142	7
α-helix	143-145	3
β-strand	156-163	8	4

Chain D: 4 helices, 12 β-strands

Element	Residues	Length	Sheet
β-strand	5-12	8	7
β-strand	15-24	10	7
α-helix	30-41	12
β-strand	52-57	6	7
β-strand	61-64	4	7
β-strand	77-78	2	8
β-strand	80	1	8
β-strand	83	1	9
β-strand	97-100	4	7
β-strand	108	1	9
β-strand	112-115	4	7
α-helix	120-122	3
β-strand	128-134	7	7
α-helix	136-142	7
α-helix	143-145	3
β-strand	156-164	9	7

Molecules and chains

Molecule	Chains	Type	Length	Organism	UniProt
GTPase NRas	A, B	protein	170	Homo sapiens	P01111 (AlphaFold model)
Peptidyl-prolyl cis-trans isomerase A	C, D	protein	166	Homo sapiens	P62937 (AlphaFold model)

Sequence of entity 1 (A, B), FASTA

>9BG0_1 GTPase NRas (chains A, B)
SMTEYKLVVVGAGGVGKSALTIQLIQNHFVDEYDPTIEDSYRKQVVIDGETCLLDILDTA
GQEEYSAMRDQYMRTGEGFLCVFAINNSKSFADINLYREQIKRVKDSDDVPMVLVGNKCD
LPTRTVDTKQAHELAKSYGIPFIETSAKTRQGVEDAFYTLVREIRQYRMK

Sequence of entity 2 (C, D), FASTA

>9BG0_2 Peptidyl-prolyl cis-trans isomerase A (chains C, D)
SMVNPTVFFDIAVDGEPLGRVSFELFADKVPKTAENFRALSTGEKGFGYKGSCFHRIIPG
FMCQGGDFTRHNGTGGKSIYGEKFEDENFILKHTGPGILSMANAGPNTNGSQFFICTAKT
EWLDGKHVVFGKVKEGMNIVEAMERFGSRNGKTSKKITIADCGQLE

Ligands and cofactors

ID	Name	Formula	Copies
A1AHB	(1R,2S)-N-[(1P,7S,9S,13R,20M)-21-ethyl-20-{2-[(1R)-1-methoxyethyl]-5-(4-methylp…	C44 H58 N8 O5 S	2
MG	Magnesium ion	Mg	2
GNP	Phosphoaminophosphonic acid-guanylate ester	C10 H17 N6 O13 P3	2

Primary citation

Discovery of Daraxonrasib (RMC-6236), a Potent and Orally Bioavailable RAS(ON) Multi-selective, Noncovalent Tri-complex Inhibitor for the Treatment of Patients with Multiple RAS-Addicted Cancers. Cregg, J., Edwards, A.V., Chang, S. et al. J Med Chem (2025) 68:6064-6083. DOI 10.1021/acs.jmedchem.4c02314 · PubMed

Other PDB entries of the same protein (UniProt P01111 (AlphaFold model), which also has an AlphaFold model), best resolution first:

9BG8 1.2 Å, Tri-complex of Daraxonrasib (RMC-6236), NRAS Q61R, and CypA
24SR 1.23 Å, Human NRAS WT (GDP-bound) in complex with macrocyclic peptide inhibitor AP6296
7F68 1.24 Å, Crystal structure of N-ras S89D
9BG3 1.33 Å, Tri-complex of Daraxonrasib (RMC-6236), NRAS Q61K, and CypA
6ZIO 1.55 Å, Crystal structure of NRAS (C118S) in complex with GDP
9Y3W 1.56 Å, Crystal structure of NRas-G12D in complex with GDP and compound 13
8TBI 1.59 Å, Tricomplex of RMC-7977, NRAS WT, and CypA
3CON 1.65 Å, Crystal structure of the human NRAS GTPase bound with GDP
6WGH 1.65 Å, Crystal structure of GDP-bound NRAS with ten residues long internal tandem duplication…
5UHV 1.67 Å, wild-type NRas bound to GppNHp
9Y1Y 1.7 Å, Crystal structure of NRas-G12D in complex with GDP and compound 7
9Y1X 1.72 Å, Crystal structure of NRas-G12D in complex with GDP and IACS-56676

Browse structure collections

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