4JNK: Lactate Dehydrogenase A

Lactate Dehydrogenase A in complex with inhibitor compound 22. Determined by X-ray diffraction at 1.9 Å resolution. Released 22 May 2013.

Method
X-ray diffraction
Resolution
1.9 Å
Organism
Homo sapiens
Chains
4
Atoms
11,949
Mol. weight
151.74 kDa
Ligands
LAC, ZHK, NAI
Released
22 May 2013

Explore 4JNK in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4JNK contains 69 α-helices and 64 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: 18 helices, 16 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-strand76-7832
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-strand184-18523
β-strand188-18924
β-strand19012
α-helix193-1953
β-strand197-19824
α-helix200-2023
β-strand204-20523
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: 19 helices, 16 β-strands
ElementResiduesLengthSheet
α-helix3-75
β-strand8-1035
β-strand21-2556
α-helix29-4012
β-strand46-5056
α-helix54-6613
α-helix68-703
β-strand75-7846
α-helix82-854
β-strand90-9346
α-helix99-1002
α-helix105-1084
α-helix109-12618
α-helix1301
β-strand131-13446
α-helix139-15012
α-helix154-1563
β-strand157-15936
α-helix163-17715
α-helix181-1833
β-strand184-18527
β-strand188-18928
β-strand19016
β-strand197-19828
α-helix200-2023
β-strand204-20527
β-strand208-20927
α-helix210-2134
α-helix227-24418
α-helix249-26315
β-strand268-27586
β-strand287-29596
β-strand298-30366
α-helix305-3084
α-helix309-32618
Chain C: 16 helices, 16 β-strands
ElementResiduesLengthSheet
α-helix3-75
β-strand8-1036
β-strand21-2555
α-helix29-4012
β-strand46-5055
α-helix54-6613
α-helix68-703
β-strand75-7845
α-helix82-854
β-strand90-9345
α-helix105-12622
α-helix1301
β-strand131-13445
α-helix139-15012
α-helix154-1563
β-strand157-15935
α-helix163-17715
α-helix181-1833
β-strand184-18529
β-strand188-189210
β-strand19015
β-strand197-198210
α-helix200-2023
β-strand204-20529
β-strand208-20929
α-helix210-2134
α-helix227-24418
α-helix249-26416
β-strand268-27585
β-strand287-29595
β-strand298-30365
α-helix309-32618
Chain D: 16 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-helix98-1003
α-helix105-12622
β-strand131-13441
α-helix139-15012
α-helix154-1563
β-strand157-15931
α-helix163-17715
α-helix181-1833
β-strand184-185211
β-strand188-189212
β-strand19011
β-strand197-198212
α-helix200-2023
β-strand204-205211
β-strand208-209211
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
>4JNK_1 L-lactate dehydrogenase A chain (chains A, B, C, D)
ATLKDQLIYNLLKEEQTPQNKITVVGVGAVGMACAISILMKDLADELALVDVIEDKLKGE
MMDLQHGSLFLRTPKIVSGKDYNVTANSKLVIITAGARQQEGESRLNLVQRNVNIFKFII
PNVVKYSPNCKLLIVSNPVDILTYVAWKISGFPKNRVIGSGCNLDSARFRYLMGERLGVH
PLSCHGWVLGEHGDSSVPVWSGMNVAGVSLKTLHPDLGTDKDKEQWKEVHKQVVESAYEV
IKLKGYTSWAIGLSVADLAESIMKNLRRVHPVSTMIKGLYGIKDDVFLSVPCILGQNGIS
DLVKVTLTSEEEARLKKSADTLWGIQKELQF

Ligands and cofactors

IDNameFormulaCopies
LACLactic acidC3 H6 O31
ZHK(2R)-2-{[5-cyano-4-(3,4-dichlorophenyl)-6-oxo-1,6-dihydropyrimidin-2-yl]sulfany…C20 H15 Cl2 N5 O4 S23
NAI1,4-dihydronicotinamide adenine dinucleotideC21 H29 N7 O14 P24

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

Primary citation

Identification of substituted 2-thio-6-oxo-1,6-dihydropyrimidines as inhibitors of human lactate dehydrogenase. Dragovich, P.S., Fauber, B.P., Corson, L.B. et al. Bioorg Med Chem Lett (2013) 23:3186-3194. DOI 10.1016/j.bmcl.2013.04.001 · 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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