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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4I5P1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006396 | RNA processing | 6 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016070 | RNA metabolic process | 5 | 5 |
GO:0031123 | RNA 3'-end processing | 7 | 5 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0071076 | RNA 3' uridylation | 8 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0090304 | nucleic acid metabolic process | 4 | 5 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016779 | nucleotidyltransferase activity | 4 | 5 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 5 |
GO:0070569 | uridylyltransferase activity | 5 | 5 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.211 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.211 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.422 |
CLV_PCSK_FUR_1 | 86 | 90 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.280 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.419 |
DOC_CKS1_1 | 130 | 135 | PF01111 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 219 | 225 | PF00134 | 0.502 |
DOC_MAPK_DCC_7 | 63 | 73 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 215 | 223 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 341 | 350 | PF00069 | 0.211 |
DOC_MAPK_MEF2A_6 | 129 | 137 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 215 | 223 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 301 | 309 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 406 | 413 | PF00069 | 0.255 |
DOC_PP1_RVXF_1 | 115 | 122 | PF00149 | 0.543 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.433 |
DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.354 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.387 |
DOC_PP2B_LxvP_1 | 66 | 69 | PF13499 | 0.371 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.452 |
DOC_USP7_UBL2_3 | 389 | 393 | PF12436 | 0.217 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.456 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 238 | 242 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.424 |
LIG_APCC_ABBA_1 | 100 | 105 | PF00400 | 0.456 |
LIG_CaM_IQ_9 | 375 | 391 | PF13499 | 0.224 |
LIG_Clathr_ClatBox_1 | 306 | 310 | PF01394 | 0.294 |
LIG_DLG_GKlike_1 | 87 | 95 | PF00625 | 0.402 |
LIG_eIF4E_1 | 11 | 17 | PF01652 | 0.296 |
LIG_eIF4E_1 | 470 | 476 | PF01652 | 0.282 |
LIG_EVH1_1 | 68 | 72 | PF00568 | 0.379 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.443 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.215 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.296 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.462 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.491 |
LIG_GBD_Chelix_1 | 91 | 99 | PF00786 | 0.407 |
LIG_LIR_Apic_2 | 64 | 70 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 299 | 309 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 354 | 362 | PF02991 | 0.211 |
LIG_LIR_Gen_1 | 396 | 407 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 358 | 362 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.286 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.385 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.455 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 19 | 22 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.384 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.544 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.393 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.380 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.369 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.557 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.516 |
LIG_TRAF2_1 | 283 | 286 | PF00917 | 0.490 |
LIG_UBA3_1 | 336 | 341 | PF00899 | 0.215 |
LIG_WRC_WIRS_1 | 413 | 418 | PF05994 | 0.255 |
LIG_WW_2 | 69 | 72 | PF00397 | 0.376 |
MOD_CDC14_SPxK_1 | 291 | 294 | PF00782 | 0.397 |
MOD_CDK_SPxK_1 | 288 | 294 | PF00069 | 0.414 |
MOD_CDK_SPxxK_3 | 129 | 136 | PF00069 | 0.444 |
MOD_CDK_SPxxK_3 | 185 | 192 | PF00069 | 0.417 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.531 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.577 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.219 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.496 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.494 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.211 |
MOD_Cter_Amidation | 84 | 87 | PF01082 | 0.396 |
MOD_DYRK1A_RPxSP_1 | 129 | 133 | PF00069 | 0.406 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.556 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.415 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.440 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.550 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.532 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.627 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.280 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.376 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.403 |
MOD_LATS_1 | 139 | 145 | PF00433 | 0.480 |
MOD_N-GLC_2 | 3 | 5 | PF02516 | 0.452 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.522 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.299 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.359 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.565 |
MOD_NEK2_2 | 39 | 44 | PF00069 | 0.361 |
MOD_OFUCOSY | 38 | 43 | PF10250 | 0.358 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.621 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.255 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.400 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.444 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.388 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.456 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.255 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.420 |
MOD_PKB_1 | 232 | 240 | PF00069 | 0.402 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.551 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.211 |
MOD_Plk_2-3 | 418 | 424 | PF00069 | 0.211 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.409 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.327 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.556 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.598 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.692 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.414 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.406 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.456 |
MOD_SUMO_rev_2 | 316 | 325 | PF00179 | 0.365 |
MOD_SUMO_rev_2 | 328 | 333 | PF00179 | 0.286 |
MOD_SUMO_rev_2 | 418 | 427 | PF00179 | 0.211 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.211 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.425 |
TRG_NES_CRM1_1 | 332 | 344 | PF08389 | 0.211 |
TRG_NLS_MonoExtC_3 | 322 | 328 | PF00514 | 0.345 |
TRG_NLS_MonoExtC_3 | 390 | 396 | PF00514 | 0.255 |
TRG_NLS_MonoExtN_4 | 389 | 395 | PF00514 | 0.255 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I395 | Leptomonas seymouri | 66% | 100% |
C9ZR09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9B0Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |