6YF1: FKBP12

FKBP12 in complex with the BMP potentiator compound 8 at 1.12A resolution. Determined by X-ray diffraction at 1.12 Å resolution. Released 10 Mar 2021.

Method: X-ray diffraction
Resolution: 1.12 Å
Organism: Homo sapiens
Chains: 1
Atoms: 1,103
Mol. weight: 12.8 kDa
Ligands: OP8
Released: 10 Mar 2021

Explore 6YF1 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6YF1 contains 3 α-helices and 8 β-strands across 1 chain. 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: 3 helices, 8 β-strands

Element	Residues	Length	Sheet
β-strand	2-8	7	1
β-strand	21-30	10	1
β-strand	35-38	4	1
α-helix	39-42	4
β-strand	46-49	4	1
α-helix	57-63	7
β-strand	71-76	6	1
α-helix	78-80	3
β-strand	87	1	2
β-strand	91	1	2
β-strand	97-106	10	1

Molecules and chains

Molecule	Chains	Type	Length	Organism	UniProt
Peptidyl-prolyl cis-trans isomerase FKBP1A	A	protein	109	Homo sapiens	P62942 (AlphaFold model)

Sequence of entity 1 (A), FASTA

>6YF1_1 Peptidyl-prolyl cis-trans isomerase FKBP1A (chains A)
GPGVQVETISPGDGRTFPKRGQTCVVHYTGMLEDGKKFDSSRDRNKPFKFMLGKQEVIRG
WEEGVAQMSVGQRAKLTISPDYAYGATGHPGIIPPHATLVFDVELLKLE

Ligands and cofactors

ID	Name	Formula	Copies
OP8	(1aR,3R,5S,6R,7S,9R,10R,17aS,20S,21R,22S,25R,25aR)-25-Ethyl-10,22-dihydroxy-20-…	C43 H69 N O13	1

Primary citation

Phenotypic screen identifies calcineurin-sparing FK506 analogs as BMP potentiators for treatment of acute kidney injury. Larraufie, M.H., Gao, X., Xia, X. et al. Cell Chem Biol (2021) 28:1271. DOI 10.1016/j.chembiol.2021.04.001 · PubMed

Other PDB entries of the same protein (UniProt P62942 (AlphaFold model), which also has an AlphaFold model), best resolution first:

2PPN 0.92 Å, Crystal structure of FKBP12
2PPP 0.94 Å, Crystal structure of E60Q mutant of FKBP12
6YF3 1.0 Å, FKBP12 in complex with the BMP potentiator compound 10 at 1.00A resolution
6YF2 1.03 Å, FKBP12 in complex with the BMP potentiator compound 6 at 1.03A resolution
8X6P 1.05 Å, Isomerase Protein
8CHM 1.12 Å, Human FKBP12 in complex with (1S,5S,6R)-10-((S)-(3,5-dichlorophenyl)sulfinyl)-3-(pyridin-…
4N19 1.2 Å, Structural basis of conformational transitions in the active site and 80 s loop in the…
8PDF 1.2 Å, FKBP12 in complex with PROTAC 6a2
9LYG 1.26 Å, Crystal structure of FKBP12 complexed with Small Molecule Anchor for Protein-201
2PPO 1.29 Å, Crystal structure of E60A mutant of FKBP12
7U8D 1.39 Å, FKBP12 mutant V55G bound to Rapa*-3Z
9DTW 1.39 Å, Co-crystal structure of the ternary complex of human FKBP12, QDPR and Compound 4

Browse structure collections

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