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PDB: 7 件
6XWU
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BU of 6xwu by Molmil
Crystal structure of drosophila melanogaster CENP-C cumin domain
分子名称: RE68959p
著者Jeyaprakash, A.A, Medina-Pritchard, B, Lazou, V, Zou, J, Byron, O, Abad, M.A, Rappsilber, J, Heun, P.
登録日2020-01-24
公開日2020-04-01
最終更新日2024-01-24
実験手法X-RAY DIFFRACTION (1.82 Å)
主引用文献Structural basis for centromere maintenance by Drosophila CENP-A chaperone CAL1.
Embo J., 39, 2020
6XWS
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BU of 6xws by Molmil
Crystal Structure of Drosophila CAL1 1-160 bound to CENP-A/H4
分子名称: Chromosome alignment defect 1,Chromosome alignment defect 1, Histone H3-like centromeric protein cid, Histone H4
著者Jeyaprakash, A.A, Medina-Pritchard, B, Lazou, V, Zou, J, Byron, O, Abad, M.A, Rappsilber, J, Heun, P.
登録日2020-01-24
公開日2020-04-15
最終更新日2024-01-24
実験手法X-RAY DIFFRACTION (4.36 Å)
主引用文献Structural basis for centromere maintenance by Drosophila CENP-A chaperone CAL1.
Embo J., 39, 2020
6XWV
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BU of 6xwv by Molmil
Crystal structure of drosophila melanogaster CENP-C bound to CAL1
分子名称: Calmodulin, Ryanodine Receptor 2
著者Jeyaprakash, A.A, Medina-Pritchard, B, Lazou, V, Zou, J, Byron, O, Abad, M.A, Rappsilber, J, Heun, P.
登録日2020-01-24
公開日2020-04-01
最終更新日2024-05-01
実験手法X-RAY DIFFRACTION (2.27 Å)
主引用文献Structural basis for centromere maintenance by Drosophila CENP-A chaperone CAL1.
Embo J., 39, 2020
6XWT
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BU of 6xwt by Molmil
drosophila melanogaster CENP-A/H4 bound to N-terminal CAL1 fragment
分子名称: Chromosome alignment defect 1, Histone H3-like centromeric protein cid, Histone H4
著者Jeyaprakash, A.A, Medina-Pritchard, B, Lazou, V, Zou, J, Byron, O, Abad, M.A, Rappsilber, J, Heun, P.
登録日2020-01-24
公開日2020-04-01
最終更新日2024-01-24
実験手法X-RAY DIFFRACTION (3.47 Å)
主引用文献Structural basis for centromere maintenance by Drosophila CENP-A chaperone CAL1.
Embo J., 39, 2020
8QSU
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BU of 8qsu by Molmil
Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease
分子名称: Putative methyltransferase C9orf114, S-ADENOSYL-L-HOMOCYSTEINE
著者Jeyaprakash, A.A, Abad, M.A.
登録日2023-10-11
公開日2024-10-23
実験手法X-RAY DIFFRACTION (2.38 Å)
主引用文献Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease
To Be Published
8QSW
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BU of 8qsw by Molmil
Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease
分子名称: Putative methyltransferase C9orf114
著者Jeyaprakash, A.A, Abad, M.A.
登録日2023-10-11
公開日2024-10-23
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Bi-allelic mutants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease
To Be Published
8QSV
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BU of 8qsv by Molmil
Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease
分子名称: Putative methyltransferase C9orf114, S-ADENOSYLMETHIONINE
著者Jeyaprakash, A.A, Abad, M.A.
登録日2023-10-11
公開日2024-10-23
実験手法X-RAY DIFFRACTION (2.62 Å)
主引用文献Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental disease
To Be Published

227111

件を2024-11-06に公開中

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