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1CYN

CYCLOPHILIN B COMPLEXED WITH [D-(CHOLINYLESTER)SER8]-CYCLOSPORIN

Summary for 1CYN
Entry DOI10.2210/pdb1cyn/pdb
Related1BCK 1C5F 1CSA 1CWA 1CWB 1CWC 1CWF 1CWH 1CWI 1CWJ 1CWK 1CWL 1CWM 1CWO 1CYA 1CYB 1IKF 1M63 1MF8 1MIK 1QNG 1QNH 1XQ7 2ESL 2OJU 2POY 2RMA 2RMB 2RMC 2WFJ 2X2C 2X7K 2Z6W 3BO7 3CYS 3EOV
Related PRD IDPRD_002324
DescriptorPEPTIDYL-PROLYL CIS-TRANS ISOMERASE B, CYCLOSPORIN A (3 entities in total)
Functional Keywordsisomerase-immunosuppressant complex, cyclosporin, isomerase, rotamase, isomerase/immunosuppressant
Biological sourceHOMO SAPIENS (HUMAN)
More
Total number of polymer chains2
Total formula weight20929.22
Authors
Mikol, V.,Kallen, J.,Walkinshaw, M.D. (deposition date: 1995-05-22, release date: 1996-01-29, Last modification date: 2025-03-26)
Primary citationMikol, V.,Kallen, J.,Walkinshaw, M.D.
X-Ray Structure of a Cyclophilin B/Cyclosporin Complex: Comparison with Cyclophilin a and Delineation of its Calcineurin-Binding Domain.
Proc.Natl.Acad.Sci.USA, 91:5183-, 1994
Cited by
PubMed Abstract: The crystal structure of a complex between recombinant human cyclophilin B (CypB) and a cyclosporin A (CsA) analog has been determined and refined at 1.85-A resolution to a crystallographic R factor of 16.0%. The overall structures of CypB and of cyclophilin A (CypA) are similar; however, significant differences occur in two loops and at the N and C termini. The CsA-binding pocket in CypB has the same structure as in CypA and cyclosporin shows a similar bound conformation and network of interactions in both CypB and CypA complexes. The network of the water-mediated contacts is also essentially conserved. The higher potency of the CypB/CsA complex versus CypA/CsA in inhibiting the Ca(2+)- and calmodulin-dependent protein phosphatase calcineurin is discussed in terms of the structural differences between the two complexes. The three residues Arg90, Lys113, and Ala128 and the loop containing Arg158 on the surface of CypB are likely to modulate the differences in calcineurin inhibition between CypA and CypB.
PubMed: 8197205
DOI: 10.1073/PNAS.91.11.5183
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.85 Å)
Structure validation

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