6KAE: Hemoglobin subunit alpha

Crosslinked alpha(Fe-CO)-beta(Ni) human hemoglobin A in the T quaternary structure at 95 K: Light. Determined by X-ray diffraction at 1.45 Å resolution. Released 19 Feb 2020.

Method
X-ray diffraction
Resolution
1.45 Å
Organism
Homo sapiens
Chains
8
Atoms
10,498
Mol. weight
129.72 kDa
Ligands
2FU, HNI, CMO, HEM
Released
19 Feb 2020

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

Secondary structure: helices and β-sheets

6KAE contains 92 α-helices and 0 β-strands across 8 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: 11 helices, 0 β-strands

ElementResiduesLengthSheet
α-helix4-1714
α-helix18-203
α-helix21-3515
α-helix37-426
α-helix53-7119
α-helix76-794
α-helix81-855
α-helix86-916
α-helix95-973
α-helix98-11215
α-helix119-13618
Chain B: 12 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix5-1511
α-helix20-3415
α-helix36-416
α-helix43-453
α-helix51-555
α-helix58-7417
α-helix75-773
α-helix81-844
α-helix86-949
α-helix101-11818
α-helix119-1213
α-helix124-14219
Chain C: 10 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix4-1714
α-helix18-203
α-helix21-3515
α-helix37-426
α-helix53-7119
α-helix76-794
α-helix81-866
α-helix87-915
α-helix96-11217
α-helix119-13618
Chain D: 13 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix5-1511
α-helix20-3415
α-helix36-416
α-helix43-453
α-helix51-555
α-helix58-7417
α-helix75-806
α-helix81-844
α-helix86-905
α-helix91-955
α-helix101-11818
α-helix119-1213
α-helix124-14219
Chain E: 11 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix4-1714
α-helix18-203
α-helix21-3515
α-helix37-426
α-helix53-7119
α-helix73-753
α-helix76-794
α-helix81-866
α-helix87-915
α-helix97-11216
α-helix119-13618
Chain F: 12 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix5-1511
α-helix20-3415
α-helix36-416
α-helix43-453
α-helix51-555
α-helix58-7417
α-helix78-803
α-helix81-844
α-helix86-949
α-helix101-11818
α-helix119-1213
α-helix124-14219
Chain G: 11 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix4-1714
α-helix18-203
α-helix21-3515
α-helix37-426
α-helix53-7119
α-helix73-753
α-helix76-794
α-helix81-866
α-helix87-915
α-helix96-11217
α-helix119-13618
Chain H: 12 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix5-1511
α-helix20-3415
α-helix36-416
α-helix43-453
α-helix51-566
α-helix58-7417
α-helix75-773
α-helix81-844
α-helix86-949
α-helix101-11818
α-helix119-1213
α-helix124-14219

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Hemoglobin subunit alphaA, C, E, Gprotein141Homo sapiensP69905 (AlphaFold model)
Hemoglobin subunit betaB, D, F, Hprotein146Homo sapiensP68871 (AlphaFold model)
Sequence of entity 1 (A, C, E, G), FASTA
>6KAE_1 Hemoglobin subunit alpha (chains A, C, E, G)
VLSPADKTNVKAAWGKVGAHAGEYGAEALERMFLSFPTTKTYFPHFDLSHGSAQVKGHGK
KVADALTNAVAHVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAEFTPA
VHASLDKFLASVSTVLTSKYR
Sequence of entity 2 (B, D, F, H), FASTA
>6KAE_2 Hemoglobin subunit beta (chains B, D, F, H)
VHLTPEEKSAVTALWGKVNVDEVGGEALGRLLVVYPWTQRFFESFGDLSTPDAVMGNPKV
KAHGKKVLGAFSDGLAHLDNLKGTFATLSELHCDKLHVDPENFRLLGNVLVCVLAHHFGK
EFTPPVQAAYQKVVAGVANALAHKYH

Ligands and cofactors

IDNameFormulaCopies
2FUBut-2-enedialC4 H4 O22
HNIProtoporphyrin IX containing ni(ii)C34 H32 N4 Ni O44
CMOCarbon monoxideC O16
HEMProtoporphyrin IX containing FEC34 H32 Fe N4 O44

Primary citation

Direct observation of ligand migration within human hemoglobin at work. Shibayama, N., Sato-Tomita, A., Ohki, M. et al. Proc Natl Acad Sci U S A (2020) 117:4741-4748. DOI 10.1073/pnas.1913663117 · PubMed

Other PDB entries of the same protein (UniProt P69905 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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