6QSW: Complement factor B protease domain

Complement factor B protease domain in complex with the reversible inhibitor N-(2-bromo-4-methylnaphthalen-1-yl)-4,5-dihydro-1H-imidazol-2-amine. Determined by X-ray diffraction at 1.64 Å resolution. Released 27 Mar 2019.

Method
X-ray diffraction
Resolution
1.64 Å
Organism
Homo sapiens
Chains
3
Atoms
6,884
Mol. weight
100.74 kDa
Ligands
JGT
Released
27 Mar 2019

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

Secondary structure: helices and β-sheets

6QSW contains 40 α-helices and 45 β-strands across 3 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 AAA: 13 helices, 15 β-strands

ElementResiduesLengthSheet
β-strand30-3561
β-strand40-4891
β-strand51-5441
α-helix56-583
β-strand64-6851
α-helix81-844
β-strand85-9061
α-helix97C-97E3
β-strand104-10851
α-helix120-1212
β-strand12212
β-strand125A13
α-helix125B-125G6
α-helix125P-1288
β-strand133-142102
β-strand154-163102
α-helix165-1706
α-helix171-172B4
α-helix172L-1743
β-strand180-18452
α-helix192-1943
α-helix1971
β-strand198-20362
β-strand206-216112
β-strand225-23062
α-helix231-2333
α-helix235-2417
β-strand24913
Chain BBB: 13 helices, 15 β-strands
ElementResiduesLengthSheet
β-strand30-3564
β-strand40-4894
β-strand51-5444
α-helix56-583
β-strand65-6844
α-helix81-844
β-strand85-9064
α-helix97C-97E3
β-strand104-10854
α-helix120-1212
β-strand12215
β-strand125A16
α-helix125B-125G6
α-helix125P-1288
β-strand133-14085
β-strand156-16385
α-helix165-1706
α-helix171-172B4
α-helix172L-1743
β-strand180-18455
α-helix192-1943
α-helix1971
β-strand198-20365
β-strand206-216115
β-strand225-23065
α-helix231-2333
α-helix235-2417
β-strand24916
Chain CCC: 14 helices, 15 β-strands
ElementResiduesLengthSheet
β-strand30-3567
β-strand40-4897
β-strand51-5447
α-helix56-583
β-strand64-6857
α-helix81-844
β-strand85-9067
α-helix97C-97E3
β-strand104-10857
α-helix120-1212
β-strand12218
α-helix1231
β-strand125A19
α-helix125B-125G6
α-helix125P-1288
β-strand133-142108
β-strand154-163108
α-helix165-1706
α-helix171-172B4
α-helix172L-1743
β-strand180-18458
α-helix192-1943
α-helix1971
β-strand198-20368
β-strand206-216118
β-strand225-23068
α-helix231-2333
α-helix235-2417
β-strand24919

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Complement factor BAAA, BBB, CCCprotein291Homo sapiensP00751 (AlphaFold model)
Sequence of entity 1 (AAA, BBB, CCC), FASTA
>6QSW_1 Complement factor B (chains AAA, BBB, CCC)
SLSLCGMVWEHRKGTDYHKQPWQAKISVIRPSKGHESCMGAVVSEYFVLTAAHCFTVDDK
EHSIKVSVGGEKRDLEIEVVLFHPNYNINGKKEAGIPEFYDYDVALIKLKNKLKYGQTIR
PICLPCTEGTTRALRLPPTTTCQQQKEELLPAQDIKALFVSEEEKKLTRKEVYIKNGDKK
GSCERDAQYAPGYDKVKDISEVVTPRFLCTGGVSPYADPNTCRGDSGGPLIVHKRSRFIQ
VGVISWGVVDVCKNQKRQKQVPAHARDFHINLFQVLPWLKEKLQDEDLGFL

Ligands and cofactors

IDNameFormulaCopies
JGT~{N}-(2-bromanyl-4-methyl-naphthalen-1-yl)-4,5-dihydro-1~{H}-imidazol-2-amineC14 H14 Br N33

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

Primary citation

Small-molecule factor B inhibitor for the treatment of complement-mediated diseases. Schubart, A., Anderson, K., Mainolfi, N. et al. Proc Natl Acad Sci U S A (2019) 116:7926-7931. DOI 10.1073/pnas.1820892116 · PubMed

Other PDB entries of the same protein (UniProt P00751 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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