Structure
atLeast majority ProS Experiment
:order disorder conflict PDB cluster ProS Pfam Domain SEG
1272
order/disorder by at least rule
disorder by at least rule
order/disorder by majority rule
Region 4cem A 121-428 order
Region 4cem A 429-486 disorder
Region 4cem B 121-429 order
Region 4cem B 430-486 disorder
Region 4cek A 455-456 disorder
Region 4cek A 457-480 order
Region 4cek A 481-530 disorder
Region 4cek A 531-534 order
Region 4cek A 535-536 disorder
Region 4cek A 537-551 order
Region 4cek A 552-558 disorder
Region 4cek A 559-655 order
Region 4cek A 656-657 disorder
Region 4cek A 658-757 order
Seq 768-1015 Hetero dimer : IID00251 Complex
Region 1uw4 D 768-1015 order
Seq 768-1015 Hetero tetramer : IID00251 Complex
Region 1uw4 B 768-1015 order
Seq 1105-1198 Hetero dimer : IID00325 Complex
Region 2wjv D 1105-1128 order
Region 2wjv D 1129-1166 disorder
Region 2wjv D 1167-1175 order
Region 2wjv D 1176-1180 disorder
Region 2wjv D 1181-1198 order
Region 2wjv E 1105-1129 order
Region 2wjv E 1130-1166 disorder
Region 2wjv E 1167-1198 order
Region 1105-1227 disorder
Seq ProS verified 1105-1129,1167-1198 Hetero dimer : IID00325 Complex
Region 2wjv D 1105-1128 order
Region 2wjv E 1105-1129 order
Region 2wjv E 1167-1198 order
Region 2wjv D 1167-1175 order
Region 2wjv D 1181-1198 order
Region 1105-1227 disorder
1088-1088 Phosphothreonine
1088-1088 Phosphothreonine
Prediction
Disorder 1-56,429-456,511-563,1009-1172,1205-1272
Order 57-428,457-510,564-758,768-1008,1173-1204
ProS 1-28,435-443,521-525,1009-1017,1091-1100,1112-1118,1138-1145,1169-1172,1205-1225,1240-1249,1255-1268
Disorder 1-63,65-65,68-68,386-387,389-389,430-457,484-561,759-766,1015-1107,1124-1125,1127-1167,1176-1177,1180-1180,1232-1232,1234-1272
Order 64-64,66-67,69-385,388-388,390-429,458-483,562-758,767-1014,1108-1123,1126-1126,1168-1175,1178-1179,1181-1231,1233-1233
PF04050 1036-1218 4.8e-121
SEG 54-126
,516-557
,1025-1044
,1046-1075
,1080-1094
,1153-1162
,1201-1208
Function
Function in SwissProt
Involved in nonsense-mediated decay (NMD) of mRNAs containing premature stop codons by associating with the nuclear exon junction complex (EJC). Recruited by UPF3B associated with the EJC core at the cytoplasmic side of the nuclear envelope and the subsequent formation of an UPF1-UPF2-UPF3 surveillance complex (including UPF1 bound to release factors at the stalled ribosome) is believed to activate NMD. In cooperation with UPF3B stimulates both ATPase and RNA helicase activities of UPF1. Binds spliced mRNA.