MMS2/YGL087C Gene Ontology Annotations Help

This page displays GO annotations in different sections according to the annotation method used to add that annotation to SGD.

MMS2 Manually curated*:

Last Reviewed on: 2002-08-06    Molecular Function | Biological Process | Cellular Component

Manually curated Molecular Function
Annotation(s) Evidence Reference(s) Assigned By
ubiquitin-protein ligase activity ISS: Inferred from Sequence or structural Similarity
with SGD:RAD6, SGD:UBC4
Assigned on 2005-10-28
Broomfield S, et al.  (1998) MMS2, encoding a ubiquitin-conjugating-enzyme-like protein, is a member of the yeast error-free postreplication repair pathway. Proc Natl Acad Sci U S A 95(10):5678-83 SGD
contributes_to ubiquitin-protein ligase activity ISS: Inferred from Sequence or structural Similarity
Assigned on 2005-10-28
IDA: Inferred from Direct Assay
Assigned on 2005-10-28
Hofmann RM and Pickart CM  (1999) Noncanonical MMS2-encoded ubiquitin-conjugating enzyme functions in assembly of novel polyubiquitin chains for DNA repair. Cell 96(5):645-53 SGD

Manually curated Biological Process
Annotation(s) Evidence Reference(s) Assigned By
free ubiquitin chain polymerization IDA: Inferred from Direct Assay
Assigned on 2009-09-28
Carlile CM, et al.  (2009) Synthesis of free and proliferating cell nuclear antigen-bound polyubiquitin chains by the RING E3 ubiquitin ligase Rad5. J Biol Chem 284(43):29326-34 SGD
postreplication repair IGI: Inferred from Genetic Interaction
with SGD:RAD6, SGD:RAD18, SGD:REV3
Assigned on 2005-10-28
IMP: Inferred from Mutant Phenotype
Assigned on 2005-10-28
Broomfield S, et al.  (1998) MMS2, encoding a ubiquitin-conjugating-enzyme-like protein, is a member of the yeast error-free postreplication repair pathway. Proc Natl Acad Sci U S A 95(10):5678-83 SGD
IGI: Inferred from Genetic Interaction
with SGD:UBC13
Assigned on 2005-10-28
IMP: Inferred from Mutant Phenotype
Assigned on 2005-10-28
Hofmann RM and Pickart CM  (1999) Noncanonical MMS2-encoded ubiquitin-conjugating enzyme functions in assembly of novel polyubiquitin chains for DNA repair. Cell 96(5):645-53 SGD
protein polyubiquitination IDA: Inferred from Direct Assay
Assigned on 2005-10-26
IPI: Inferred from Physical Interaction
Assigned on 2005-10-26
Hofmann RM and Pickart CM  (1999) Noncanonical MMS2-encoded ubiquitin-conjugating enzyme functions in assembly of novel polyubiquitin chains for DNA repair. Cell 96(5):645-53 SGD

Manually curated Cellular Component
Annotation(s) Evidence Reference(s) Assigned By
cytoplasm IDA: Inferred from Direct Assay
Assigned on 2002-08-06
Ulrich HD and Jentsch S  (2000) Two RING finger proteins mediate cooperation between ubiquitin-conjugating enzymes in DNA repair. EMBO J 19(13):3388-97 SGD
nucleus IDA: Inferred from Direct Assay
Assigned on 2002-08-06
Ulrich HD and Jentsch S  (2000) Two RING finger proteins mediate cooperation between ubiquitin-conjugating enzymes in DNA repair. EMBO J 19(13):3388-97 SGD
ubiquitin conjugating enzyme complex IPI: Inferred from Physical Interaction
with SGD:UBC13
Assigned on 2005-10-28
Hofmann RM and Pickart CM  (1999) Noncanonical MMS2-encoded ubiquitin-conjugating enzyme functions in assembly of novel polyubiquitin chains for DNA repair. Cell 96(5):645-53 SGD

* Manually curated GO annotations reflect our best understanding of the basic molecular function, biological process, and cellular component for this gene product. Manually curated annotations are assigned by SGD curators based on published papers when available, or by curatorial statements if necessary. Curators periodically review all Manually curated GO annotations for accuracy and completeness. The "Last Reviewed on:" date at the top of this section indicates when these annotations were last reviewed.


MMS2 High-throughput**:

Biological Process

High-throughput Biological Process
Annotation(s) Evidence Reference(s) Assigned By
response to DNA damage stimulus IMP: Inferred from Mutant Phenotype
Assigned on 2006-04-06
Chang M, et al.  (2002) A genome-wide screen for methyl methanesulfonate-sensitive mutants reveals genes required for S phase progression in the presence of DNA damage. Proc Natl Acad Sci U S A 99(26):16934-9 SGD

** GO annotations from High-throughput experiments are made based on a variety of large scale high-throughput experiments, including genome-wide experiments. Many of these annotations are made based on GO annotations (or mappings to GO annotations) assigned by the authors, rather than SGD curators. While SGD curators read these publications and often work closely with authors to incorporate the information, each individual annotation may not necessarily be reviewed by a curator. GO Annotations from high-throughput experiments will be assigned only when this type of data is available, and thus may not be assigned in all three aspects of the Gene Ontologies.


MMS2 Computational***:

Molecular Function

Computational Molecular Function
Annotation(s) Evidence Reference(s) Assigned By
acid-amino acid ligase activity IEA: Inferred from Electronic Annotation
with EBI:IPR000608
Last updated 2013-03-02
DDB, et al.  (2001) Gene Ontology annotation through association of InterPro records with GO terms. InterPro
ligase activity IEA: Inferred from Electronic Annotation
with EBI:KW-0436
Last updated 2013-03-02
UniProt-GOA  (2011) Gene Ontology annotation based on manual assignment of UniProtKB keywords in UniProtKB/Swiss-Prot entries. UniProtKB

*** Computational GO Annotations are predictions. These annotations are NOT reviewed by a curator. Currently, all computational GO annotations for S. cerevisiae are assigned by an external source (for example, the Gene Ontology Annotation (GOA) project of the European Bioinformatics Institute (EBI)).