Sws2 is the mitochondrial small-subunit ribosomal protein uS13m. Its conserved uS13 RNA-binding fold and mitochondrial localization support a structural role in the mitoribosome and mitochondrial protein synthesis.
Reason: The target has the diagnostic uS13 family domain and a mitochondrial localization record. The S. cerevisiae structural supplementary table identifies Sws2/P53937 as uS13m and its contact with rRNA helix H62. This grounds transfer of the conserved RNA-associated mitoribosomal role while leaving exact S. pombe bridge geometry unresolved.
Summary: structural constituent of ribosome is supported.
Reason: The target has the diagnostic uS13 family domain and a mitochondrial localization record. The S. cerevisiae structural supplementary table identifies Sws2/P53937 as uS13m and its contact with rRNA helix H62. This grounds transfer of the conserved RNA-associated mitoribosomal role while leaving exact S. pombe bridge geometry unresolved.
Summary: structural constituent of ribosome is supported.
Reason: The target has the diagnostic uS13 family domain and a mitochondrial localization record. The S. cerevisiae structural supplementary table identifies Sws2/P53937 as uS13m and its contact with rRNA helix H62. This grounds transfer of the conserved RNA-associated mitoribosomal role while leaving exact S. pombe bridge geometry unresolved.
HDA PMID:16823372 ORFeome cloning and global analysis of protein localization ...
ACCEPT
Summary: mitochondrion is supported.
Reason: Mitochondrial localization is concordant with the conserved mitochondrial ribosomal ortholog assignment. Retain the PomBase genome-scale localization annotation (PMID:16823372); the available abstract describes the screen but does not expose the target image. The source excerpt records the target HDA/IC annotation, not a reinspection of the individual microscopy image.
Reason: Mitochondrial localization is concordant with the conserved mitochondrial ribosomal ortholog assignment. Retain the PomBase genome-scale localization annotation (PMID:16823372); the available abstract describes the screen but does not expose the target image.
Reason: Mitochondrial localization is concordant with the conserved mitochondrial ribosomal ortholog assignment. Retain the PomBase genome-scale localization annotation (PMID:16823372); the available abstract describes the screen but does not expose the target image.
Summary: mitochondrial small ribosomal subunit is supported.
Reason: The target has the diagnostic uS13 family domain and a mitochondrial localization record. The S. cerevisiae structural supplementary table identifies Sws2/P53937 as uS13m and its contact with rRNA helix H62. This grounds transfer of the conserved RNA-associated mitoribosomal role while leaving exact S. pombe bridge geometry unresolved.
NAS PMID:18245278 Bot1p is required for mitochondrial translation, respiratory...
ACCEPT
Summary: mitochondrial small ribosomal subunit is supported.
Reason: The target has the diagnostic uS13 family domain and a mitochondrial localization record. The S. cerevisiae structural supplementary table identifies Sws2/P53937 as uS13m and its contact with rRNA helix H62. This grounds transfer of the conserved RNA-associated mitoribosomal role while leaving exact S. pombe bridge geometry unresolved.
Summary: ribosome is reviewed in the context of sws2.
Reason: The broad ribosome annotation is compatible with the biology, but mitochondrial small ribosomal subunit captures the supported sws2 function more precisely.
Summary: translation is reviewed in the context of sws2.
Reason: The broad translation annotation is compatible with the biology, but mitochondrial translation captures the supported sws2 function more precisely.
Summary: small ribosomal subunit is reviewed in the context of sws2.
Reason: The broad small ribosomal subunit annotation is compatible with the biology, but mitochondrial small ribosomal subunit captures the supported sws2 function more precisely.
Reason: The target has the diagnostic uS13 family domain and a mitochondrial localization record. The S. cerevisiae structural supplementary table identifies Sws2/P53937 as uS13m and its contact with rRNA helix H62. This grounds transfer of the conserved RNA-associated mitoribosomal role while leaving exact S. pombe bridge geometry unresolved.
NAS PMID:18245278 Bot1p is required for mitochondrial translation, respiratory...
ACCEPT
Summary: mitochondrial translation is supported.
Reason: The target has the diagnostic uS13 family domain and a mitochondrial localization record. The S. cerevisiae structural supplementary table identifies Sws2/P53937 as uS13m and its contact with rRNA helix H62. This grounds transfer of the conserved RNA-associated mitoribosomal role while leaving exact S. pombe bridge geometry unresolved.
These computational predictions are reviewed separately from the GOA annotation set used for this review. The assessments below are from this project and do not constitute official GO annotations or endorsement by GO/UniProt. They are not included in the existing annotation review above.
Review rationale: The target has the diagnostic uS13m family domain and mitochondrial localization. Characterized S. cerevisiae mitoribosome structures support transfer of the conserved mitochondrial ribosomal role. Translation is therefore supported, and the existing mitochondrial translation annotation (GO:0032543) is more specific within the biological-process aspect. The generic prediction is LSP.
Review rationale: The target has the diagnostic uS13m family domain and mitochondrial localization. Characterized S. cerevisiae mitoribosome structures support transfer of the conserved mitochondrial ribosomal role. Membership in the mitochondrial small ribosomal subunit is a supported cellular-component annotation and is more specific than ribosome. The predicted broad complex membership is LSP.
Review rationale: The target carries the diagnostic uS13 domain. In the experimentally determined S. cerevisiae mitoribosome, the homolog Sws2/P53937 is uS13m and contacts rRNA helix H62 (PMID:28154081, supplementary tables S2 and bridge table). This supports transfer of conserved RNA binding to fission-yeast Sws2, without asserting identical bridge geometry. The equivalent RNA-binding annotation already exists in target GOA, so CNN applies.
Review rationale: The target has the diagnostic uS13m family domain and mitochondrial localization. Characterized S. cerevisiae mitoribosome structures support transfer of the conserved mitochondrial ribosomal role. Membership in the mitochondrial small ribosomal subunit is a supported cellular-component annotation and is more specific than ribonucleoprotein complex. The predicted broad complex membership is LSP.