6NW2: Human RIPK1 kinase domain

Structure of human RIPK1 kinase domain in complex with compound 11. Determined by X-ray diffraction at 2.0 Å resolution. Released 1 May 2019.

Method: X-ray diffraction
Resolution: 2.0 Å
Organism: Homo sapiens
Chains: 2
Atoms: 4,289
Mol. weight: 71.56 kDa
Ligands: L4Y
Released: 1 May 2019

Explore 6NW2 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6NW2 contains 32 α-helices and 21 β-strands across 2 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: 15 helices, 10 β-strands

Element	Residues	Length	Sheet
β-strand	10-11	2	1
α-helix	14-16	3
β-strand	17	1	1
β-strand	31-36	6	1
β-strand	40-49	10	1
α-helix	57-68	12
β-strand	75	1	2
β-strand	78-84	7	1
β-strand	87-92	6	1
β-strand	99	1	2
α-helix	100-104	5
α-helix	112-131	20
α-helix	141-143	3
β-strand	144-146	3	2
β-strand	152-154	3	2
α-helix	163-169	7
α-helix	190-192	3
α-helix	195-197	3
α-helix	207-223	17
α-helix	234-242	9
α-helix	249-251	3
α-helix	258-267	10
α-helix	272-274	3
α-helix	278-288	11
α-helix	289-293	5

Chain B: 17 helices, 11 β-strands

Element	Residues	Length	Sheet
β-strand	12	1	3
α-helix	14-16	3
β-strand	17	1	3
β-strand	32-36	5	3
β-strand	40-46	7	3
α-helix	57-68	12
β-strand	72	1	4
β-strand	75	1	4
β-strand	78-82	5	3
β-strand	89-93	5	3
β-strand	99	1	4
α-helix	100-104	5
α-helix	109-111	3
α-helix	112-131	20
α-helix	141-143	3
β-strand	144-146	3	4
β-strand	152-154	3	4
α-helix	163-168	6
α-helix	195-197	3
α-helix	204-205	2
α-helix	207-223	17
α-helix	235-242	8
α-helix	249-251	3
α-helix	258-267	10
α-helix	272-274	3
α-helix	276-277	2
α-helix	278-288	11
α-helix	289-293	5

Molecules and chains

Molecule	Chains	Type	Length	Organism	UniProt
Receptor-interacting serine/threonine-protein kinase 1	A, B	protein	310	Homo sapiens	Q13546 (AlphaFold model)

Sequence of entity 1 (A, B), FASTA

>6NW2_1 Receptor-interacting serine/threonine-protein kinase 1 (chains A, B)
MHHHHHHGENLYFQGSMQPDMSLNVIKMKSSDFLESAELDSGGFGKVSLAFHRTQGLMIM
KTVYKGPNCIEHNEALLEEAKMMNRLRHSRVVKLLGVIIEEGKYSLVMEYMEKGNLMHVL
KAEMSTPLSVKGRIILEIIEGMAYLHGKGVIHKDLKPENILVDNDFHIKIADLGLASFKM
WSKLNNEEHNELREVDGTAKKNGGTLYYMAPEHLNDVNAKPTEKSDVYSFAVVLWAIFAN
KEPYENAIAEQQLIMAIKSGNRPDVDDITEYCPREIISLMKLCWEANPEARPTFPGIEEK
FRPFYLSQLE

Ligands and cofactors

ID	Name	Formula	Copies
L4Y	(5R)-5-methyl-N-[(3S)-5-methyl-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepin-3-yl]-…	C19 H22 N4 O3	2

Primary citation

Potent and selective inhibitors of receptor-interacting protein kinase 1 that lack an aromatic back pocket group. Hamilton, G.L., Chen, H., Deshmukh, G. et al. Bioorg Med Chem Lett (2019) 29:1497-1501. DOI 10.1016/j.bmcl.2019.04.014 · PubMed

Other PDB entries of the same protein (UniProt Q13546 (AlphaFold model), which also has an AlphaFold model), best resolution first:

5ZMZ 1.4 Å, Amyloid core of RIP1
6AC5 1.45 Å, Crystal structure of RIPK1 death domain GlcNAcylated by EPEC effector NleB
4ITJ 1.8 Å, Crystal structure of RIP1 kinase in complex with necrostatin-4
7FD0 2.0 Å, Crystal Structure of human RIPK1 kinase domain in complex with a novel inhibitor
24IB 2.05 Å, Crystal structure of human RIPK1 kinase domain in complex with compound HR10
9Q31 2.05 Å, RIP1 kinase domain in complex with GDC-8264
6NYH 2.1 Å, Structure of human RIPK1 kinase domain in complex with GNE684
9GTY 2.15 Å, RIPK1 in complex with AZ"320
7FCZ 2.21 Å, Crystal Structure of human RIPK1 kinase domain in complex with a novel inhibitor
5HX6 2.23 Å, Crystal structure of RIP1 kinase with a benzo[b][1,4]oxazepin-4-one
4ITH 2.25 Å, Crystal structure of RIP1 kinase in complex with necrostatin-1 analog
9GTG 2.25 Å, RIPK1 in complex with AZ"902

Browse structure collections

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