6YVS: FOCAL ADHESION KINASE CATALYTIC DOMAIN

FOCAL ADHESION KINASE CATALYTIC DOMAIN IN COMPLEX WITH 5-{4-[(Pyridin-3-ylmethyl)-amino]-5-trifluoromethyl-pyrimidin-2-ylamino}-1,3-dihydro-indol-2-one. Determined by X-ray diffraction at 1.81 Å resolution. Released 10 Feb 2021.

Method
X-ray diffraction
Resolution
1.81 Å
Organism
Homo sapiens
Chains
4
Atoms
9,136
Mol. weight
130.91 kDa
Ligands
PVT
Released
10 Feb 2021

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

Secondary structure: helices and β-sheets

6YVS contains 75 α-helices and 40 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: 17 helices, 10 β-strands

ElementResiduesLengthSheet
β-strand41611
α-helix419-4213
β-strand422-43091
β-strand435-44171
β-strand449-45571
α-helix462-47514
β-strand48312
α-helix484-4852
β-strand486-49051
α-helix4951
β-strand496-50051
β-strand505-50622
α-helix507-5137
α-helix520-53920
α-helix549-5513
β-strand552-55652
β-strand559-56242
α-helix586-5883
α-helix591-5966
α-helix601-61616
α-helix620-6212
α-helix628-6369
α-helix641-6444
α-helix649-65810
α-helix663-6653
α-helix667-6682
α-helix669-68416
Chain B: 19 helices, 10 β-strands
ElementResiduesLengthSheet
β-strand41613
α-helix419-4213
β-strand422-43093
β-strand435-44173
β-strand449-45573
α-helix462-47615
β-strand48314
α-helix484-4852
β-strand486-49053
α-helix4951
β-strand496-50053
β-strand505-50624
α-helix507-5148
α-helix515-5173
α-helix520-53920
α-helix549-5513
β-strand552-55654
β-strand559-56244
α-helix586-5883
α-helix591-5966
α-helix601-61616
α-helix620-6212
α-helix628-6303
α-helix631-6366
α-helix641-6444
α-helix649-65810
α-helix663-6653
α-helix667-6682
α-helix669-68416
Chain C: 18 helices, 10 β-strands
ElementResiduesLengthSheet
β-strand41615
α-helix419-4213
β-strand422-43095
β-strand435-44175
β-strand449-45575
α-helix462-47615
β-strand48316
α-helix484-4852
β-strand486-49055
α-helix4951
β-strand496-50055
β-strand505-50626
α-helix507-5137
α-helix520-53920
α-helix549-5513
β-strand552-55656
β-strand559-56246
α-helix586-5883
α-helix591-5966
α-helix601-61616
α-helix620-6212
α-helix628-6303
α-helix631-6366
α-helix641-6444
α-helix649-65810
α-helix663-6653
α-helix667-6682
α-helix669-68416
Chain D: 21 helices, 10 β-strands
ElementResiduesLengthSheet
α-helix413-4153
β-strand41611
α-helix419-4213
β-strand422-43091
β-strand435-44171
α-helix447-4482
β-strand449-45571
α-helix462-47615
β-strand48317
α-helix484-4852
β-strand486-49051
α-helix4951
β-strand496-50051
β-strand505-50627
α-helix507-5148
α-helix515-5173
α-helix520-53920
α-helix549-5513
β-strand552-55657
β-strand559-56247
α-helix586-5883
α-helix591-5966
α-helix601-61616
α-helix620-6212
α-helix628-6303
α-helix631-6366
α-helix641-6444
α-helix649-65810
α-helix663-6653
α-helix667-6682
α-helix669-68416

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Focal adhesion kinase 1A, B, C, Dprotein282Homo sapiensQ05397 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>6YVS_1 Focal adhesion kinase 1 (chains A, B, C, D)
GSGSTRDYEIQRERIELGRCIGEGQFGDVHQGIYMSPENPALAVAIKTCKNCTSDSVREK
FLQEALTMRQFDHPHIVKLIGVITENPVWIIMELCTLGELRSFLQVRKYSLDLASLILYA
YQLSTALAYLESKRFVHRDIAARNVLVSSNDCVKLGDFGLSRYMEDSTYYKASKGKLPIK
WMAPESINFRRFTSASDVWMFGVCMWEILMHGVKPFQGVKNNDVIGRIENGERLPMPPNC
PPTLYSLMTKCWAYDPSRRPRFTELKAQLSTILEEEKAQQEE

Ligands and cofactors

IDNameFormulaCopies
PVT5-[[4-(pyridin-3-ylmethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]-1,3-di…C19 H15 F3 N6 O4

Water and common crystallization additives (SO4) are not listed.

Primary citation

Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2. Berger, B.T., Amaral, M., Kokh, D.B. et al. Cell Chem Biol (2021) 28:686. DOI 10.1016/j.chembiol.2021.01.003 · PubMed

Other PDB entries of the same protein (UniProt Q05397 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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