6RH4: Human Carbonic Anhydrase II

Human Carbonic Anhydrase II in complex with 4-Nitrobenzenesulfonamide. Determined by X-ray diffraction at 0.95 Å resolution. Released 15 Apr 2020.

Method
X-ray diffraction
Resolution
0.95 Å
Organism
Homo sapiens
Chains
1
Atoms
2,717
Mol. weight
31.37 kDa
Ligands
4NZ, GLC, BGC, BE7
Released
15 Apr 2020

Explore 6RH4 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6RH4 contains 15 α-helices and 18 β-strands across 1 chain. 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: 15 helices, 18 β-strands

ElementResiduesLengthSheet
α-helix16-183
α-helix21-244
β-strand32-3321
β-strand39-4022
α-helix44-463
β-strand47-5042
β-strand56-6162
β-strand66-7052
β-strand78-8142
β-strand88-97102
β-strand108-10921
β-strand11211
α-helix113-1142
β-strand116-12492
α-helix125-1283
α-helix131-1344
β-strand141-150102
α-helix155-1573
α-helix158-1636
α-helix164-1674
β-strand173-17532
α-helix181-1844
β-strand191-19662
β-strand207-21262
α-helix2151
β-strand216-21832
α-helix220-2267
β-strand23013
α-helix2331
α-helix237-2382
β-strand24013
α-helix246-2483
β-strand257-25822

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Carbonic anhydrase 2Aprotein265Homo sapiensP00918 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>6RH4_1 Carbonic anhydrase 2 (chains A)
GSPEFMSHHWGYGKHNGPEHWHKDFPIAKGERQSPVDIDTHTAKYDPSLKPLSVSYDQAT
SLRILNNGHAFNVEFDDSQDKAVLKGGPLDGTYRLIQFHFHWGSLDGQGSEHTVDKKKYA
AELHLVHWNTKYGDFGKAVQQPDGLAVLGIFLKVGSAKPGLQKVVDVLDSIKTKGKSADF
TNFDPRGLLPESLDYWTYPGSLTTPPLLECVTWIVLKEPISVSSEQVLKFRKLNFNGEGE
PEELMVDNWRPAQPLKNRQIKASFK

Ligands and cofactors

IDNameFormulaCopies
4NZ4-nitrobenzenesulfonamideC6 H6 N2 O4 S2
GLCalpha-D-glucopyranoseC6 H12 O61
BGCbeta-D-glucopyranoseC6 H12 O62
BE7(4-carboxyphenyl)(chloro)mercuryC7 H5 Cl Hg O21
HGMercury (II) ionHg1
ZNZinc ionZn1

Primary citation

The Influence of Varying Fluorination Patterns on the Thermodynamics and Kinetics of Benzenesulfonamide Binding to Human Carbonic Anhydrase II. Glockner, S., Ngo, K., Wagner, B. et al. Biomolecules (2020) 10. DOI 10.3390/biom10040509 · PubMed

Other PDB entries of the same protein (UniProt P00918 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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