Sortilin-Progranulin Interaction With Compound 24. Determined by X-ray diffraction at 2.9 Å resolution. Released 12 Aug 2020.
Explore 6X4H in 3D Show helices and sheets RCSB PDB PDBe
6X4H contains 18 α-helices and 64 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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 59-64 | 6 | |
| β-strand | 67-68 | 2 | 1 |
| β-strand | 71-72 | 2 | 1 |
| β-strand | 80-84 | 5 | 2 |
| β-strand | 90-96 | 7 | 2 |
| β-strand | 109-114 | 6 | 2 |
| β-strand | 121-123 | 3 | 2 |
| α-helix | 125-128 | 4 | |
| β-strand | 133 | 1 | 3 |
| β-strand | 139-141 | 3 | 3 |
| α-helix | 142 | 1 | |
| β-strand | 149-153 | 5 | 3 |
| α-helix | 154 | 1 | |
| β-strand | 163-167 | 5 | 3 |
| β-strand | 175-178 | 4 | 3 |
| β-strand | 183 | 1 | 4 |
| β-strand | 188-189 | 2 | 5 |
| β-strand | 197-200 | 4 | 5 |
| β-strand | 201 | 1 | 4 |
| β-strand | 206-209 | 4 | 5 |
| β-strand | 216-220 | 5 | 5 |
| β-strand | 223-228 | 6 | 6 |
| β-strand | 234-238 | 5 | 6 |
| β-strand | 251-256 | 6 | 6 |
| β-strand | 267-276 | 10 | 6 |
| β-strand | 279-285 | 7 | 6 |
| α-helix | 286 | 1 | |
| β-strand | 292-297 | 6 | 6 |
| β-strand | 305-306 | 2 | 6 |
| β-strand | 312 | 1 | 6 |
| β-strand | 318-323 | 6 | 7 |
| β-strand | 328-333 | 6 | 7 |
| α-helix | 334 | 1 | |
| β-strand | 340-346 | 7 | 7 |
| β-strand | 353-361 | 9 | 7 |
| β-strand | 362 | 1 | 8 |
| β-strand | 369 | 1 | 8 |
| β-strand | 372-373 | 2 | 7 |
| β-strand | 381-386 | 6 | 7 |
| β-strand | 392-397 | 6 | 7 |
| β-strand | 404-406 | 3 | 7 |
| β-strand | 407-408 | 2 | 9 |
| α-helix | 409-410 | 2 | |
| β-strand | 426-430 | 5 | 9 |
| α-helix | 432-436 | 5 | |
| β-strand | 446 | 1 | 9 |
| β-strand | 455-462 | 8 | 9 |
| α-helix | 470 | 1 | |
| β-strand | 471-475 | 5 | 9 |
| β-strand | 483-486 | 4 | 9 |
| β-strand | 490-495 | 6 | 10 |
| α-helix | 496-498 | 3 | |
| β-strand | 500-505 | 6 | 10 |
| β-strand | 511 | 1 | 11 |
| β-strand | 513-517 | 5 | 10 |
| β-strand | 525-528 | 4 | 10 |
| β-strand | 534 | 1 | 11 |
| β-strand | 535-541 | 7 | 1 |
| β-strand | 549-555 | 7 | 1 |
| β-strand | 564-570 | 7 | 1 |
| β-strand | 578 | 1 | 12 |
| α-helix | 579 | 1 | |
| α-helix | 581-583 | 3 | |
| β-strand | 584-588 | 5 | 13 |
| β-strand | 602 | 1 | 13 |
| β-strand | 605-612 | 8 | 13 |
| β-strand | 619 | 1 | 12 |
| β-strand | 628-632 | 5 | 13 |
| α-helix | 633 | 1 | |
| β-strand | 634-635 | 2 | 14 |
| α-helix | 637-639 | 3 | |
| β-strand | 640-642 | 3 | 15 |
| β-strand | 646-647 | 2 | 16 |
| β-strand | 656-657 | 2 | 16 |
| α-helix | 663-671 | 9 | |
| α-helix | 674-677 | 4 | |
| β-strand | 679 | 1 | 17 |
| β-strand | 682-684 | 3 | 15 |
| α-helix | 685 | 1 | |
| β-strand | 691-693 | 3 | 14 |
| β-strand | 701 | 1 | 17 |
| α-helix | 712-714 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Sortilin | A | protein | 663 | Homo sapiens | Q99523 (AlphaFold model) |
>6X4H_1 Sortilin (chains A) CGRVRDFVAKLANNTHQHVFDDLRGSVSLSWVGDSTGVILVLTTFHVPLVIMTFGQSKLY RSEDYGKNFKDITDLINNTFIRTEFGMAIGPENSGKVVLTAEVSGGSRGGRIFRSSDFAK NFVQTDLPFHPLTQMMYSPQNSDYLLALSTENGLWVSKNFGGKWEEIHKAVCLAKWGSDN TIFFTTYANGSCKADLGALELWRTSDLGKSFKTIGVKIYSFGLGGRFLFASVMADKDTTR RIHVSTDQGDTWSMAQLPSVGQEQFYSILAANDDMVFMHVDEPGDTGFGTIFTSDDRGIV YSKSLDRHLYTTTGGETDFTNVTSLRGVYITSVLSEDNSIQTMITFDQGGRWTHLRKPEN SECDATAKNKNECSLHIHASYSISQKLNVPMAPLSEPNAVGIVIAHGSVGDAISVMVPDV YISDDGGYSWTKMLEGPHYYTILDSGGIIVAIEHSSRPINVIKFSTDEGQCWQTYTFTRD PIYFTGLASEPGARSMNISIWGFTESFLTSQWVSYTIDFKDILERNCEEKDYTIWLAHST DPEDYEDGCILGYKEQFLRLRKSSMCQNGRDYVVTKQPSICLCSLEDFLCDFGYYRPEND SKCVEQPELKGHDLEFCLYGREEHLTTNGYRKIPGDKCQGGVNPVREVKDLKKKCTSNFL SPE
| ID | Name | Formula | Copies |
|---|---|---|---|
| UOY | 4-methyl-N-(6-phenoxypyridine-3-carbonyl)-L-leucine | C19 H22 N2 O4 | 1 |
Water and common crystallization additives (GOL) are not listed.
Identification of potent inhibitors of the sortilin-progranulin interaction. Stachel, S.J., Ginnetti, A.T., Johnson, S.A. et al. Bioorg Med Chem Lett (2020) 30:127403-127403. DOI 10.1016/j.bmcl.2020.127403 · PubMed
Other PDB entries of the same protein (UniProt Q99523 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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