5IXS: Lactate Dehydrogenase

Lactate Dehydrogenase in complex with hydroxylactam inhibitor compound 9: (6R)-3-[(2-chlorophenyl)sulfanyl]-4-hydroxy-6-(3-hydroxyphenyl)-6-(thiophen-3-yl)-5,6-dihydropyridin-2(1H)-one. Determined by X-ray diffraction at 2.05 Å resolution. Released 14 Sept 2016.

Method
X-ray diffraction
Resolution
2.05 Å
Organism
Homo sapiens
Chains
4
Atoms
11,112
Mol. weight
151.9 kDa
Ligands
TXD, 6EY, NAI
Released
14 Sept 2016

Explore 5IXS in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5IXS contains 64 α-helices and 62 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: 16 helices, 14 β-strands

ElementResiduesLengthSheet
α-helix3-75
β-strand8-1031
α-helix16-183
β-strand21-2552
α-helix29-4012
β-strand46-5052
α-helix54-6613
α-helix68-703
β-strand75-7842
α-helix82-854
β-strand90-9342
α-helix106-12621
α-helix1301
β-strand131-13442
α-helix139-15012
α-helix154-1563
β-strand157-15932
α-helix163-17715
α-helix181-1833
β-strand185-18953
β-strand19012
β-strand197-20593
β-strand208-20923
α-helix210-2134
α-helix227-24418
α-helix249-26315
β-strand268-27582
β-strand287-29592
β-strand298-30362
α-helix309-32618
Chain B: 17 helices, 16 β-strands
ElementResiduesLengthSheet
α-helix3-75
β-strand8-1034
α-helix14-185
β-strand21-2555
α-helix29-4012
β-strand46-5055
α-helix54-6512
α-helix68-703
β-strand75-7845
α-helix82-854
β-strand90-9345
α-helix107-12620
α-helix1301
β-strand131-13445
α-helix139-15012
α-helix154-1563
β-strand157-15935
α-helix163-17715
α-helix181-1833
β-strand18516
β-strand188-18927
β-strand19015
β-strand197-19827
α-helix200-2023
β-strand204-20526
β-strand208-20926
α-helix210-2134
α-helix227-24418
α-helix249-26416
β-strand268-27585
β-strand287-29595
β-strand298-30365
α-helix309-32618
Chain C: 16 helices, 16 β-strands
ElementResiduesLengthSheet
α-helix3-75
β-strand8-1035
β-strand21-2554
α-helix29-4012
β-strand46-5054
α-helix54-6512
α-helix68-703
β-strand75-7844
α-helix82-854
β-strand88-9364
α-helix107-12620
α-helix1301
β-strand131-13444
α-helix139-15012
α-helix154-1563
β-strand157-15934
α-helix163-17715
α-helix181-1833
β-strand184-18528
β-strand188-18929
β-strand19014
β-strand197-19829
α-helix200-2023
β-strand204-20528
β-strand208-20928
α-helix210-2134
α-helix227-24418
α-helix249-26315
β-strand268-27584
β-strand287-29594
β-strand298-30364
α-helix309-32618
Chain D: 15 helices, 16 β-strands
ElementResiduesLengthSheet
α-helix3-75
β-strand8-1032
β-strand21-2551
α-helix29-4012
β-strand46-5051
α-helix54-6512
α-helix68-703
β-strand76-7831
α-helix82-854
β-strand90-9341
α-helix105-12622
β-strand131-13441
α-helix139-15012
α-helix154-1563
β-strand157-15931
α-helix163-17715
α-helix181-1833
β-strand185110
β-strand188-189211
β-strand19011
β-strand197-198211
α-helix200-2023
β-strand204-205210
β-strand208-209210
α-helix210-2134
α-helix227-24418
α-helix249-26315
β-strand268-27581
β-strand287-29591
β-strand298-30361
α-helix309-32618

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
L-lactate dehydrogenase A chainA, B, C, Dprotein331Homo sapiensP00338 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>5IXS_1 L-lactate dehydrogenase A chain (chains A, B, C, D)
ATLKDQLIYNLLKEEQTPQNKITVVGVGAVGMACAISILMKDLADELALVDVIEDKLKGE
MMDLQHGSLFLRTPKIVSGKDYNVTANSKLVIITAGARQQEGESRLNLVQRNVNIFKFII
PNVVKYSPNCKLLIVSNPVDILTYVAWKISGFPKNRVIGSGCNLDSARFRYLMGERLGVH
PLSCHGWVLGEHGDSSVPVWSGMNVAGVSLKTLHPDLGTDKDKEQWKEVHKQVVESAYEV
IKLKGYTSWAIGLSVADLAESIMKNLRRVHPVSTMIKGLYGIKDDVFLSVPCILGQNGIS
DLVKVTLTSEEEARLKKSADTLWGIQKELQF

Ligands and cofactors

IDNameFormulaCopies
TXD1,4,5,6-tetrahydronicotinamide adenine dinucleotideC21 H31 N7 O14 P23
6EY(6R)-3-[(2-chlorophenyl)sulfanyl]-4-hydroxy-6-(3-hydroxyphenyl)-6-(thiophen-3-y…C21 H16 Cl N O3 S24
NAI1,4-dihydronicotinamide adenine dinucleotideC21 H29 N7 O14 P21

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

Primary citation

Cell Active Hydroxylactam Inhibitors of Human Lactate Dehydrogenase with Oral Bioavailability in Mice. Purkey, H.E., Robarge, K., Chen, J. et al. ACS Med Chem Lett (2016) 7:896-901. DOI 10.1021/acsmedchemlett.6b00190 · PubMed

Other PDB entries of the same protein (UniProt P00338 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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