2X25: Free acetyl-CypA orthorhombic form

Free acetyl-CypA orthorhombic form. Determined by X-ray diffraction at 1.2 Å resolution. Released 23 Mar 2010.

Method
X-ray diffraction
Resolution
1.2 Å
Organism
HOMO SAPIENS
Chains
1
Atoms
1,744
Mol. weight
18.64 kDa
Released
23 Mar 2010

Explore 2X25 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2X25 contains 4 α-helices and 12 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 B: 4 helices, 12 β-strands

ElementResiduesLengthSheet
α-helix0-12
β-strand5-1281
β-strand15-24101
α-helix30-4112
β-strand52-5761
β-strand61-6441
β-strand7712
β-strand8012
β-strand8313
β-strand97-10041
β-strand10813
β-strand112-11541
α-helix120-1223
β-strand128-13471
α-helix136-1438
β-strand156-16381

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Peptidyl-prolyl cis-trans isomerase aBprotein169HOMO SAPIENSP62937 (AlphaFold model)
Sequence of entity 1 (B), FASTA
>2X25_1 PEPTIDYL-PROLYL CIS-TRANS ISOMERASE A (chains B)
HHHHHVNPTVFFDIAVDGEPLGRVSFELFADKVPKTAENFRALSTGEKGFGYKGSCFHRI
IPGFMCQGGDFTRHNGTGGKSIYGEKFEDENFILKHTGPGILSMANAGPNTNGSQFFICT
AKTKWLDGKHVVFGKVKEGMNIVEAMERFGSRNGKTSKKITIADCGQLE

Primary citation

Acetylation Regulates Cyclophilin a Catalysis, Immunosuppression and HIV Isomerization. Lammers, M., Neumann, H., Chin, J.W. et al. Nat Chem Biol (2010) 6:331. DOI 10.1038/NCHEMBIO.342 · PubMed

Other PDB entries of the same protein (UniProt P62937 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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