PDB ID 8QSW: Crystal structure of SPOUT1/CENP-32 | A356N catalytic site mutant
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Bi-allelic variants of SPOUT1, a novel RNA methyltransferase, cause chromosome missegregation and a rare neurodevelopmental diseasePDB DOI: https://doi.org/10.2210/pdb8QSW/pdbClassification: CELL CYCLEOrganism(s): Homo sapiensExpression System: Escherichia coliMutation(s): No
创建时间：
2024-10-23
