001     62893
005     20200402210514.0
024 7 _ |2 pmid
|a pmid:18567048
024 7 _ |2 DOI
|a 10.1002/cbic.200800117
024 7 _ |2 WOS
|a WOS:000258092300014
037 _ _ |a PreJuSER-62893
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Biochemistry & Molecular Biology
084 _ _ |2 WoS
|a Chemistry, Medicinal
100 1 _ |a Thielmann, Y.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB77156
245 _ _ |a An indole binding site is a major determinant of the ligand specificity of the GABA type A receptor-associated protein GABARAP
260 _ _ |a Weinheim
|b Wiley-VCH
|c 2008
300 _ _ |a 1767 - 1775
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a ChemBioChem
|x 1439-4227
|0 8962
|v 9
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a The role of tryptophan as a key residue for ligand binding to the ubiquitin-like modifier GABA(A) receptor associated protein (GABARAP) was investigated. Two tryptophan-binding hydrophobic patches were identified on the conserved face of the GABARAP structure by NMR spectroscopy and molecular docking. GABARAP binding of indole and indole derivatives, including the free amino acid tryptophan was quantified. The two tryptophan binding sites can be clearly distinguished by mapping the NMR spectroscopy-derived residue-specific apparent dissociation constant, K(d), onto the three-dimensional structure of GABARAP. The biological relevance of tryptophan-binding pockets of GABARAP was supported by a highly conserved tryptophan residue in the GABARAP binding region of calreticulin, clathrin heavy chain, and the gamma2 subunit of the GABA(A) receptor. Replacement of tryptophan by alanine abolished ligand binding to GABARAP.
536 _ _ |a Funktion und Dysfunktion des Nervensystems
|c P33
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK409
|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Adaptor Proteins, Signal Transducing: chemistry
650 _ 2 |2 MeSH
|a Adaptor Proteins, Signal Transducing: metabolism
650 _ 2 |2 MeSH
|a Amino Acid Sequence
650 _ 2 |2 MeSH
|a Animals
650 _ 2 |2 MeSH
|a Binding Sites
650 _ 2 |2 MeSH
|a Humans
650 _ 2 |2 MeSH
|a Hydrophobic and Hydrophilic Interactions
650 _ 2 |2 MeSH
|a Indoles: chemistry
650 _ 2 |2 MeSH
|a Indoles: metabolism
650 _ 2 |2 MeSH
|a Ligands
650 _ 2 |2 MeSH
|a Microtubule-Associated Proteins: chemistry
650 _ 2 |2 MeSH
|a Microtubule-Associated Proteins: metabolism
650 _ 2 |2 MeSH
|a Models, Molecular
650 _ 2 |2 MeSH
|a Molecular Sequence Data
650 _ 2 |2 MeSH
|a Protein Conformation
650 _ 2 |2 MeSH
|a Receptors, GABA-A: metabolism
650 _ 2 |2 MeSH
|a Substrate Specificity
650 _ 2 |2 MeSH
|a Titrimetry
650 _ 2 |2 MeSH
|a Tryptophan: metabolism
650 _ 7 |0 0
|2 NLM Chemicals
|a Adaptor Proteins, Signal Transducing
650 _ 7 |0 0
|2 NLM Chemicals
|a Indoles
650 _ 7 |0 0
|2 NLM Chemicals
|a Ligands
650 _ 7 |0 0
|2 NLM Chemicals
|a Microtubule-Associated Proteins
650 _ 7 |0 0
|2 NLM Chemicals
|a Receptors, GABA-A
650 _ 7 |0 73-22-3
|2 NLM Chemicals
|a Tryptophan
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a GABARAP
653 2 0 |2 Author
|a indole-binding pocket
653 2 0 |2 Author
|a molecular modeling
653 2 0 |2 Author
|a molecular recognition
653 2 0 |2 Author
|a NMR spectroscopy
700 1 _ |a Mohrlüder, J.
|b 1
|u FZJ
|0 P:(DE-Juel1)132012
700 1 _ |a Koenig, B. W.
|b 2
|u FZJ
|0 P:(DE-Juel1)132009
700 1 _ |a Stangler, T.
|b 3
|0 P:(DE-HGF)0
700 1 _ |a Hartmann, R.
|b 4
|u FZJ
|0 P:(DE-Juel1)VDB57647
700 1 _ |a Becker, K.
|b 5
|u FZJ
|0 P:(DE-Juel1)VDB3486
700 1 _ |a Höltje, H.-D.
|b 6
|0 P:(DE-HGF)0
700 1 _ |a Willbold, D.
|b 7
|u FZJ
|0 P:(DE-Juel1)132029
773 _ _ |a 10.1002/cbic.200800117
|g Vol. 9, p. 1767 - 1775
|p 1767 - 1775
|q 9<1767 - 1775
|0 PERI:(DE-600)2020469-3
|t ChemBioChem
|v 9
|y 2008
|x 1439-4227
856 7 _ |u http://dx.doi.org/10.1002/cbic.200800117
909 C O |o oai:juser.fz-juelich.de:62893
|p VDB
913 1 _ |k P33
|v Funktion und Dysfunktion des Nervensystems
|l Funktion und Dysfunktion des Nervensystems
|b Gesundheit
|0 G:(DE-Juel1)FUEK409
|x 0
914 1 _ |y 2008
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k INB-2
|l Molekulare Biophysik
|d 31.12.2008
|g INB
|0 I:(DE-Juel1)VDB805
|x 0
970 _ _ |a VDB:(DE-Juel1)99806
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)ISB-2-20090406
980 _ _ |a UNRESTRICTED
980 _ _ |a I:(DE-Juel1)ICS-6-20110106
981 _ _ |a I:(DE-Juel1)IBI-7-20200312
981 _ _ |a I:(DE-Juel1)ISB-2-20090406
981 _ _ |a I:(DE-Juel1)ICS-6-20110106


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