Homo sapiens Protein: ORC4 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-244809.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | ORC4 | ||||||||||||||||||
Protein Name | origin recognition complex, subunit 4 | ||||||||||||||||||
Synonyms | ORC4L; ORC4P; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000376597 | ||||||||||||||||||
InnateDB Gene | IDBG-71780 (ORC4) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Component of the origin recognition complex (ORC) that binds origins of replication. DNA-binding is ATP-dependent. The specific DNA sequences that define origins of replication have not been identified yet. ORC is required to assemble the pre- replication complex necessary to initiate DNA replication. Binds histone H3 and H4 trimethylation marks H3K9me3, H3K27me3 and H4K20me3. {ECO:0000269PubMed:22427655}. | ||||||||||||||||||
Subcellular Localization | Nucleus. | ||||||||||||||||||
Disease Associations | Meier-Gorlin syndrome 2 (MGORS2) [MIM:613800]: A syndrome characterized by bilateral microtia, aplasia/hypoplasia of the patellae, and severe intrauterine and postnatal growth retardation with short stature and poor weight gain. Additional clinical findings include anomalies of cranial sutures, microcephaly, apparently low-set and simple ears, microstomia, full lips, highly arched or cleft palate, micrognathia, genitourinary tract anomalies, and various skeletal anomalies. While almost all cases have primordial dwarfism with substantial prenatal and postnatal growth retardation, not all cases have microcephaly, and microtia and absent/hypoplastic patella are absent in some. Despite the presence of microcephaly, intellect is usually normal. {ECO:0000269PubMed:21358631, ECO:0000269PubMed:21358632}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | |||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 39 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR003593
AAA+ ATPase domain IPR003959 ATPase, AAA-type, core IPR011579 ATPase domain, prokaryote IPR016527 Origin recognition complex, subunit 4 IPR027417 P-loop containing nucleoside triphosphate hydrolase |
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PFAM |
PF00004
PF07724 PF13304 PF01637 |
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PRINTS | |||||||||||||||||||
PIRSF |
PIRSF007858
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SMART |
SM00382
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | O43929 | ||||||||||||||||||
PhosphoSite | PhosphoSite-O43929 | ||||||||||||||||||
TrEMBL | Q96B14 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 5000 | ||||||||||||||||||
UniGene | Hs.558364 | ||||||||||||||||||
RefSeq | NP_859525 | ||||||||||||||||||
HUGO | HGNC:8490 | ||||||||||||||||||
OMIM | 603056 | ||||||||||||||||||
CCDS | CCDS2187 | ||||||||||||||||||
HPRD | 09118 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AC009480 AC019226 AF022108 AF047598 AF132596 AK295721 AK298862 AK299749 AY600302 BC014847 BC016177 CH471058 | ||||||||||||||||||
GenPept | AAC01957 AAC80282 AAD22110 AAH14847 AAH16177 AAS94326 AAX93051 AAY24232 BAH12166 BAH12887 BAH13118 EAX11555 EAX11556 EAX11557 EAX11558 EAX11560 | ||||||||||||||||||