RBY1A_HUMAN
| Gene | |
| Sequence | MVEADHPGKLFIGGLNRETNEKMLKAVFGKHGPISEVLLIKDRTSKSRGFAFITFENPADAKNAAKDMNGKSLHGKAIKVEQAKKPSFQSGGRRRPPASSRNRSPSGSLRSARGSRGGTRGWLPSHEGHLDDGGYTPDLKMSYSRGLIPVKRGPSSRSGGPPPKKSAPSAVARSNSWMGSQGPMSQRRENYGVPPRRATISSWRNDRMSTRHDGYATNDGNHPSCQETRDYAPPSRGYAYRDNGHSNRDEHSSRGYRNHRSSRETRDYAPPSRGHAYRDYGHSRRDESYSRGYRNRRSSRETREYAPPSRGHGYRDYGHSRRHESYSRGYRNHPSSRETRDYAPPHRDYAYRDYGHSSWDEHSSRGYSYHDGYGEALGRDHSEHLSGSSYRDALQRYGTSHGAPPARGPRMSYGGSTCHAYSNTRDRYGRSWESYSSCGDFHYCDREHVCRKDQRNPPSLGRVLPDPREACGSSSYVASIVDGGESRSEKGDSSRY |
| Molecular Function | F:mRNA binding;F:RNA binding;mRNA cis splicing, via spliceosome;regulation of alternative mRNA splicing, via spliceosome; |
| EMBL Protein ID | CAA53659.1; AAH47768.1; AAH70298.1; - |
| UniProt | RBY1A_HUMAN from Homo sapiens (Human) / Seqs with 100%, 90%, 50% identity / |
| iProClass | P0DJD3 |
| Pfam | PF08081 PF00076 |
| Google Search | scholar keyword |
| PDBj | 2FY1 |
| Info & Models | GTOP SWISS-MODEL |
| CBRC workflows | Annotation Comparative Modeling |
| PCI | P0DJD3 |
| CasaDB | RBY1A_HUMAN |