4F56: PDB entry 4F56

The bicyclic intermediate structure provides insights into the desuccinylation mechanism of SIRT5. Determined by X-ray diffraction at 1.7 Å resolution. Released 20 Jun 2012.

Method
X-ray diffraction
Resolution
1.7 Å
Organism
Homo sapiens
Chains
4
Atoms
4,785
Mol. weight
63.3 kDa
Ligands
ZN, CGK
Released
20 Jun 2012

Explore 4F56 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4F56 contains 37 α-helices and 36 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: 19 helices, 16 β-strands

ElementResiduesLengthSheet
β-strand3711
α-helix40-4910
β-strand52-5761
α-helix59-613
α-helix63-653
β-strand7712
β-strand8012
α-helix82-854
α-helix88-936
α-helix95-11016
α-helix116-13015
β-strand134-13961
α-helix145-1495
β-strand154-15631
β-strand159-16683
β-strand172-17433
α-helix182-1843
α-helix194-1963
α-helix201-2033
β-strand20614
α-helix2141
β-strand21514
β-strand216-22053
α-helix221-2222
β-strand22615
α-helix227-2282
α-helix229-24113
β-strand244-24851
β-strand25516
α-helix257-2593
α-helix260-2667
β-strand271-27551
α-helix282-2843
β-strand287-29041
α-helix293-3019
Chain B: 18 helices, 16 β-strands
ElementResiduesLengthSheet
β-strand3717
α-helix40-4910
β-strand52-5767
α-helix59-613
α-helix63-653
β-strand7718
β-strand8018
α-helix82-854
α-helix88-936
α-helix95-10915
α-helix116-12914
β-strand134-13967
α-helix145-1495
β-strand154-15637
β-strand159-16689
β-strand172-17439
α-helix182-1843
α-helix201-2033
β-strand206110
α-helix2141
β-strand215110
β-strand216-22059
α-helix221-2222
β-strand226111
α-helix227-2282
α-helix229-24113
β-strand244-24857
β-strand255112
α-helix257-2593
α-helix260-2667
β-strand271-27557
α-helix282-2843
β-strand287-29047
α-helix293-3008
Chains C and D: 0 helices, 2 β-strands
ElementResiduesLengthSheet
β-strand815
β-strand1016

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
NAD-dependent lysine demalonylase and desuccinylase sirtuin-5, mitochondrialA, Bprotein273Homo sapiensQ9NXA8 (AlphaFold model)
peptide from Histone H3.1C, Dprotein12Homo sapiensP68431 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>4F56_1 NAD-dependent lysine demalonylase and desuccinylase sirtuin-5, mitochondrial (chains A, B)
GSFTARPSSSMADFRKFFAKAKHIVIISGAGVSAESGVPTFRGAGGYWRKWQAQDLATPL
AFAHNPSRVWEFYHYRREVMGSKEPNAGHRAIAECETRLGKQGRRVVVITQNIDELHRKA
GTKNLLEIHGSLFKTRCTSCGVVAENYKSPICPALSGKGAPEPGTQDASIPVEKLPRCEE
AGCGGLLRPHVVWFGENLDPAILEEVDRELAHCDLCLVVGTSSVVYPAAMFAPQVAARGV
PVAEFNTETTPATNRFRFHFQGPCGTTLPEALA
Sequence of entity 2 (C, D), FASTA
>4F56_2 peptide from Histone H3.1 (chains C, D)
KQTARKSTGGKA

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn2
CGK3-[(2R,3aR,5R,6R,6aR)-5-({[(S)-{[(S)-{[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-…C19 H27 N5 O16 P2 S2

Primary citation

The Bicyclic Intermediate Structure Provides Insights into the Desuccinylation Mechanism of Human Sirtuin 5 (SIRT5). Zhou, Y., Zhang, H., He, B. et al. J Biol Chem (2012) 287:28307-28314. DOI 10.1074/jbc.M112.384511 · PubMed

Other PDB entries of the same protein (UniProt Q9NXA8 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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