1LK6: Dimeric antithrombin

Structure of dimeric antithrombin complexed with a P14-P9 reactive loop peptide and an exogenous tripeptide. Determined by X-ray diffraction at 2.8 Å resolution. Released 3 Jun 2003.

Method
X-ray diffraction
Resolution
2.8 Å
Organism
Homo sapiens
Chains
4
Atoms
6,763
Mol. weight
101.06 kDa
Ligands
NDG, NAG
Released
3 Jun 2003

Explore 1LK6 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

1LK6 contains 31 α-helices and 44 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 C: 0 helices, 1 β-strand

ElementResiduesLengthSheet
β-strand3-648
Chain D: 0 helices, 1 β-strand
ElementResiduesLengthSheet
β-strand1118
Chain I: 16 helices, 22 β-strands
ElementResiduesLengthSheet
α-helix7-93
α-helix12-143
β-strand2416
α-helix46-6823
β-strand76-7837
α-helix80-9112
α-helix96-10510
α-helix108-1103
β-strand11516
α-helix118-13013
β-strand139-149118
β-strand15419
α-helix156-16611
β-strand169-17358
α-helix175-19319
β-strand213-222108
β-strand225110
α-helix231-2333
β-strand235-24067
β-strand246-262177
α-helix264-2663
β-strand268-27367
β-strand274110
β-strand279-28577
α-helix292-2987
α-helix301-31010
β-strand312-321107
β-strand323-33088
α-helix332-3376
α-helix342-3443
β-strand35519
β-strand36618
β-strand368-37588
β-strand386-39051
β-strand400-40347
β-strand408-41477
α-helix415-4173
β-strand419-42687
Chain L: 15 helices, 20 β-strands
ElementResiduesLengthSheet
α-helix46-6823
β-strand76-7831
α-helix80-9112
α-helix96-10510
α-helix108-1103
α-helix118-13114
β-strand139-149112
β-strand153-15423
α-helix156-16510
β-strand169-17352
α-helix175-19319
α-helix204-2063
β-strand213-224122
β-strand22514
α-helix231-2333
β-strand235-23621
β-strand239-24025
β-strand246-24725
β-strand250-262131
α-helix264-2663
β-strand268-27361
β-strand27414
β-strand279-28571
α-helix286-2872
α-helix293-2964
α-helix301-3099
β-strand312-322111
β-strand323-33082
α-helix332-3376
α-helix342-3443
β-strand355-35733
β-strand364-375122
β-strand379-390122
β-strand408-41471
β-strand419-42681

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
antithrombin-IIII, Lprotein432Homo sapiensP01008 (AlphaFold model)
antithrombin P14-P9 peptideCprotein7
exogenous tripeptide formyl-MLFDprotein3
Sequence of entity 1 (I, L), FASTA
>1LK6_1 antithrombin-III (chains I, L)
HGSPVDICTAKPRDIPMNPMCIYRSPEKKATEDEGSEQKIPEATNRRVWELSKANSRFAT
TFYQHLADSKNDNDNIFLSPLSISTAFAMTKLGACNDTLQQLMEVFKFDTISEKTSDQIH
FFFAKLNCRLYRKANKSSKLVSANRLFGDKSLTFNETYQDISELVYGAKLQPLDFKENAE
QSRAAINKWVSNKTEGRITDVIPSEAINELTVLVLVNTIYFKGLWKSKFSPENTRKELFY
KADGESCSASMMYQEGKFRYRRVAEGTQVLELPFKGDDITMVLILPKPEKSLAKVEKELT
PEVLQEWLDELEEMMLVVHMPRFRIEDGFSLKEQLQDMGLVDLFSPEKSKLPGIVAEGRD
DLYVSDAFHKAFLEVNEEGSEAAASTAVVIAGRSLNPNRVTFKANRPFLVFIREVPLNTI
IFMGRVANPCVK
Sequence of entity 2 (C), FASTA
>1LK6_2 antithrombin P14-P9 peptide (chains C)
XSEAAAS
Sequence of entity 3 (D), FASTA
>1LK6_3 exogenous tripeptide formyl-MLF (chains D)
MLF

Ligands and cofactors

IDNameFormulaCopies
NDG2-acetamido-2-deoxy-alpha-D-glucopyranoseC8 H15 N O66
NAG2-acetamido-2-deoxy-beta-D-glucopyranoseC8 H15 N O62

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

Primary citation

Serpin Polymerization Is Prevented by a Hydrogen Bond Network That Is Centered on His-334 and Stabilized by Glycerol. Zhou, A., Stein, P.E., Huntington, J.A. et al. J Biol Chem (2003) 278:15116-15122. DOI 10.1074/jbc.M211663200 · PubMed

Other PDB entries of the same protein (UniProt P01008 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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