Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 2 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9B0Y5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0031123 | RNA 3'-end processing | 7 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071076 | RNA 3' uridylation | 8 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 3 |
GO:0016779 | nucleotidyltransferase activity | 4 | 3 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 3 |
GO:0070569 | uridylyltransferase activity | 5 | 3 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 3 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.672 |
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.585 |
CLV_MEL_PAP_1 | 128 | 134 | PF00089 | 0.674 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 446 | 448 | PF00082 | 0.549 |
CLV_PCSK_PC7_1 | 191 | 197 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.613 |
DOC_CYCLIN_RxL_1 | 191 | 201 | PF00134 | 0.699 |
DOC_CYCLIN_yCln2_LP_2 | 274 | 280 | PF00134 | 0.697 |
DOC_MAPK_gen_1 | 270 | 278 | PF00069 | 0.592 |
DOC_MAPK_gen_1 | 396 | 405 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 270 | 278 | PF00069 | 0.627 |
DOC_MAPK_MEF2A_6 | 356 | 364 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 461 | 468 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 34 | 41 | PF00149 | 0.539 |
DOC_PP2B_LxvP_1 | 274 | 277 | PF13499 | 0.682 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.685 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.798 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.779 |
DOC_USP7_UBL2_3 | 444 | 448 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 131 | 139 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 141 | 147 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 168 | 176 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 195 | 201 | PF00244 | 0.815 |
LIG_14-3-3_CanoR_1 | 25 | 34 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 293 | 297 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 447 | 456 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 88 | 97 | PF00244 | 0.657 |
LIG_Actin_WH2_2 | 27 | 45 | PF00022 | 0.618 |
LIG_APCC_ABBA_1 | 155 | 160 | PF00400 | 0.793 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.695 |
LIG_CaM_IQ_9 | 430 | 446 | PF13499 | 0.549 |
LIG_Clathr_ClatBox_1 | 361 | 365 | PF01394 | 0.632 |
LIG_eIF4E_1 | 525 | 531 | PF01652 | 0.616 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.793 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.617 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.682 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.549 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.503 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.685 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.657 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.693 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.800 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.572 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.708 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 354 | 364 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 409 | 417 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 451 | 462 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 413 | 417 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.379 |
LIG_Pex14_2 | 93 | 97 | PF04695 | 0.656 |
LIG_REV1ctd_RIR_1 | 37 | 47 | PF16727 | 0.629 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.507 |
LIG_SH2_SRC | 162 | 165 | PF00017 | 0.791 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.675 |
LIG_SH2_STAT3 | 139 | 142 | PF00017 | 0.685 |
LIG_SH2_STAT3 | 71 | 74 | PF00017 | 0.805 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.758 |
LIG_SH3_2 | 83 | 88 | PF14604 | 0.644 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.684 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.760 |
LIG_SH3_CIN85_PxpxPR_1 | 83 | 88 | PF14604 | 0.644 |
LIG_SUMO_SIM_par_1 | 315 | 321 | PF11976 | 0.679 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.691 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.703 |
LIG_TRAF2_1 | 298 | 301 | PF00917 | 0.780 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.814 |
LIG_UBA3_1 | 391 | 396 | PF00899 | 0.549 |
LIG_WRC_WIRS_1 | 319 | 324 | PF05994 | 0.681 |
LIG_WRC_WIRS_1 | 468 | 473 | PF05994 | 0.549 |
LIG_WW_3 | 85 | 89 | PF00397 | 0.641 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.664 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.800 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.791 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.790 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.549 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.723 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.704 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.549 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.704 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.663 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.652 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.671 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.547 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.769 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.704 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.675 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.824 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.724 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.656 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.549 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.504 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.724 |
MOD_LATS_1 | 194 | 200 | PF00433 | 0.822 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.678 |
MOD_N-GLC_2 | 55 | 57 | PF02516 | 0.800 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.651 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.814 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.639 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.679 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.549 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.677 |
MOD_NEK2_2 | 171 | 176 | PF00069 | 0.678 |
MOD_OFUCOSY | 57 | 63 | PF10250 | 0.666 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.783 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.690 |
MOD_PK_1 | 196 | 202 | PF00069 | 0.707 |
MOD_PKA_1 | 447 | 453 | PF00069 | 0.549 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.723 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.698 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.635 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.671 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.725 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.418 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.682 |
MOD_PKB_1 | 287 | 295 | PF00069 | 0.717 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.772 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.556 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.549 |
MOD_Plk_2-3 | 473 | 479 | PF00069 | 0.549 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.678 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.679 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.550 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.701 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.678 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.637 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.672 |
MOD_SUMO_rev_2 | 371 | 380 | PF00179 | 0.685 |
MOD_SUMO_rev_2 | 383 | 388 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 473 | 482 | PF00179 | 0.549 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.796 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 273 | 276 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.704 |
TRG_NES_CRM1_1 | 387 | 399 | PF08389 | 0.549 |
TRG_NLS_MonoExtC_3 | 377 | 382 | PF00514 | 0.678 |
TRG_NLS_MonoExtC_3 | 445 | 451 | PF00514 | 0.549 |
TRG_NLS_MonoExtN_4 | 444 | 450 | PF00514 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4I5P1 | Leishmania infantum | 83% | 100% |