3HS4: Human carbonic anhydrase II

Human carbonic anhydrase II complexed with acetazolamide. Determined by X-ray diffraction at 1.1 Å resolution. Released 8 Dec 2009.

Method
X-ray diffraction
Resolution
1.1 Å
Organism
Homo sapiens
Chains
1
Atoms
2,536
Mol. weight
30.11 kDa
Ligands
ZN, AZM
Released
8 Dec 2009

Explore 3HS4 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3HS4 contains 14 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: 14 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
β-strand24013
α-helix246-2483
β-strand257-25822

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Carbonic anhydrase 2Aprotein260Homo sapiensP00918 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>3HS4_1 Carbonic anhydrase 2 (chains A)
MSHHWGYGKHNGPEHWHKDFPIAKGERQSPVDIDTHTAKYDPSLKPLSVSYDQATSLRIL
NNGHAFNVEFDDSQDKAVLKGGPLDGTYRLIQFHFHWGSLDGQGSEHTVDKKKYAAELHL
VHWNTKYGDFGKAVQQPDGLAVLGIFLKVGSAKPGLQKVVDVLDSIKTKGKSADFTNFDP
RGLLPESLDYWTYPGSLTTPPLLECVTWIVLKEPISVSSEQVLKFRKLNFNGEGEPEELM
VDNWRPAQPLKNRQIKASFK

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn1
AZM5-acetamido-1,3,4-thiadiazole-2-sulfonamideC4 H6 N4 O3 S23

Water and common crystallization additives (GOL) are not listed.

Primary citation

High-resolution structure of human carbonic anhydrase II complexed with acetazolamide reveals insights into inhibitor drug design. Sippel, K.H., Robbins, A.H., Domsic, J. et al. Acta Crystallogr Sect F Struct Biol Cryst Commun (2009) 65:992-995. DOI 10.1107/S1744309109036665 · PubMed

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

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3HS4 is part of these collections:

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