SHLD3_HUMAN
| Gene | |
| Sequence | MTTEVILHYRPCESDPTQLPKIAEKAIQDFPTRPLSRFIPWFPYDGSKLPLRPKRSPPVISEEAAEDVKQYLTISEHDAKSHSYDCTVDLLEFQPSLKKQHLTWSHTLKEQTNSGNLGKQSEKGKQHKRRSWSISLPSNNCTKNVSPLSKKLQDSLKALNLHSLYRARWTIEHTICNSQTLEDIWTKLNQIIRHNELPSCNATIQRHLGQIWVFCDIMYCEYVGSLLKGRLALTGKINLFVHKYGVIFSM |
| Molecular Function | DNA repair;negative regulation of double-strand break repair via homologous recombination;positive regulation of double-strand break repair via nonhomologous end joining;positive regulation of isotype switching; |
| EMBL Protein ID | BAC85360.1; - |
| UniProt | SHLD3_HUMAN from Homo sapiens (Human) / Seqs with 100%, 90%, 50% identity / |
| iProClass | Q6ZNX1 |
| Pfam | |
| Google Search | scholar keyword |
| PDBj | 6K07 6K08 6KTO |
| Info & Models | GTOP SWISS-MODEL |
| CBRC workflows | Annotation Comparative Modeling |
| PCI | Q6ZNX1 |
| CasaDB | SHLD3_HUMAN |