159 related articles for article (PubMed ID: 17242432)
1. Comparative molecular dynamics analysis of tapasin-dependent and -independent MHC class I alleles.
Sieker F; Springer S; Zacharias M
Protein Sci; 2007 Feb; 16(2):299-308. PubMed ID: 17242432
[TBL] [Abstract][Full Text] [Related]
2. Differential tapasin dependence of MHC class I molecules correlates with conformational changes upon peptide dissociation: a molecular dynamics simulation study.
Sieker F; Straatsma TP; Springer S; Zacharias M
Mol Immunol; 2008 Aug; 45(14):3714-22. PubMed ID: 18639935
[TBL] [Abstract][Full Text] [Related]
3. Coupling between side chain interactions and binding pocket flexibility in HLA-B*44:02 molecules investigated by molecular dynamics simulations.
Ostermeir K; Springer S; Zacharias M
Mol Immunol; 2015 Feb; 63(2):312-9. PubMed ID: 25146482
[TBL] [Abstract][Full Text] [Related]
4. Conformational flexibility of the MHC class I alpha1-alpha2 domain in peptide bound and free states: a molecular dynamics simulation study.
Zacharias M; Springer S
Biophys J; 2004 Oct; 87(4):2203-14. PubMed ID: 15454423
[TBL] [Abstract][Full Text] [Related]
5. Molecular architecture of the MHC I peptide-loading complex: one tapasin molecule is essential and sufficient for antigen processing.
Hulpke S; Baldauf C; Tampé R
FASEB J; 2012 Dec; 26(12):5071-80. PubMed ID: 22923333
[TBL] [Abstract][Full Text] [Related]
6. Flexibility of the MHC class II peptide binding cleft in the bound, partially filled, and empty states: a molecular dynamics simulation study.
Yaneva R; Springer S; Zacharias M
Biopolymers; 2009 Jan; 91(1):14-27. PubMed ID: 18767126
[TBL] [Abstract][Full Text] [Related]
7. Computational characterization of residue couplings and micropolymorphism-induced changes in the dynamics of two differentially disease-associated human MHC class-I alleles.
Serçinoğlu O; Ozbek P
J Biomol Struct Dyn; 2018 Feb; 36(3):724-740. PubMed ID: 28278760
[TBL] [Abstract][Full Text] [Related]
8. A single polymorphic residue within the peptide-binding cleft of MHC class I molecules determines spectrum of tapasin dependence.
Park B; Lee S; Kim E; Ahn K
J Immunol; 2003 Jan; 170(2):961-8. PubMed ID: 12517962
[TBL] [Abstract][Full Text] [Related]
9. Aggregate formation by ERp57-deficient MHC class I peptide-loading complexes.
Stepensky D; Bangia N; Cresswell P
Traffic; 2007 Nov; 8(11):1530-42. PubMed ID: 17822402
[TBL] [Abstract][Full Text] [Related]
10. Successive crystal structure snapshots suggest the basis for MHC class I peptide loading and editing by tapasin.
Hafstrand I; Sayitoglu EC; Apavaloaei A; Josey BJ; Sun R; Han X; Pellegrino S; Ozkazanc D; Potens R; Janssen L; Nilvebrant J; Nygren PÅ; Sandalova T; Springer S; Georgoudaki AM; Duru AD; Achour A
Proc Natl Acad Sci U S A; 2019 Mar; 116(11):5055-5060. PubMed ID: 30808808
[TBL] [Abstract][Full Text] [Related]
11. Selective loading of high-affinity peptides onto major histocompatibility complex class I molecules by the tapasin-ERp57 heterodimer.
Wearsch PA; Cresswell P
Nat Immunol; 2007 Aug; 8(8):873-81. PubMed ID: 17603487
[TBL] [Abstract][Full Text] [Related]
12. Exchange catalysis by tapasin exploits conserved and allele-specific features of MHC-I molecules.
Lan H; Abualrous ET; Sticht J; Fernandez LMA; Werk T; Weise C; Ballaschk M; Schmieder P; Loll B; Freund C
Nat Commun; 2021 Jul; 12(1):4236. PubMed ID: 34244493
[TBL] [Abstract][Full Text] [Related]
13. Position 156 influences the peptide repertoire and tapasin dependency of human leukocyte antigen B*44 allotypes.
Badrinath S; Saunders P; Huyton T; Aufderbeck S; Hiller O; Blasczyk R; Bade-Doeding C
Haematologica; 2012 Jan; 97(1):98-106. PubMed ID: 21993680
[TBL] [Abstract][Full Text] [Related]
14. Interaction of ERp57 and tapasin in the generation of MHC class I-peptide complexes.
Garbi N; Hämmerling G; Tanaka S
Curr Opin Immunol; 2007 Feb; 19(1):99-105. PubMed ID: 17150345
[TBL] [Abstract][Full Text] [Related]
15. Changes at the floor of the peptide-binding groove induce a strong preference for proline at position 3 of the bound peptide: molecular dynamics simulations of HLA-A*0217.
Toh H; Savoie CJ; Kamikawaji N; Muta S; Sasazuki T; Kuhara S
Biopolymers; 2000 Oct; 54(5):318-27. PubMed ID: 10935972
[TBL] [Abstract][Full Text] [Related]
16. Tapasin edits peptides on MHC class I molecules by accelerating peptide exchange.
Praveen PV; Yaneva R; Kalbacher H; Springer S
Eur J Immunol; 2010 Jan; 40(1):214-24. PubMed ID: 20017190
[TBL] [Abstract][Full Text] [Related]
17. Tapasin dependence of major histocompatibility complex class I molecules correlates with their conformational flexibility.
Garstka MA; Fritzsche S; Lenart I; Hein Z; Jankevicius G; Boyle LH; Elliott T; Trowsdale J; Antoniou AN; Zacharias M; Springer S
FASEB J; 2011 Nov; 25(11):3989-98. PubMed ID: 21836024
[TBL] [Abstract][Full Text] [Related]
18. F pocket flexibility influences the tapasin dependence of two differentially disease-associated MHC Class I proteins.
Abualrous ET; Fritzsche S; Hein Z; Al-Balushi MS; Reinink P; Boyle LH; Wellbrock U; Antoniou AN; Springer S
Eur J Immunol; 2015 Apr; 45(4):1248-57. PubMed ID: 25615938
[TBL] [Abstract][Full Text] [Related]
19. Decamer-like conformation of a nona-peptide bound to HLA-B*3501 due to non-standard positioning of the C terminus.
Menssen R; Orth P; Ziegler A; Saenger W
J Mol Biol; 1999 Jan; 285(2):645-53. PubMed ID: 9878435
[TBL] [Abstract][Full Text] [Related]
20. A mechanistic basis for the co-evolution of chicken tapasin and major histocompatibility complex class I (MHC I) proteins.
van Hateren A; Carter R; Bailey A; Kontouli N; Williams AP; Kaufman J; Elliott T
J Biol Chem; 2013 Nov; 288(45):32797-32808. PubMed ID: 24078633
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
