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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QA96
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 2 |
GO:0002128 | tRNA nucleoside ribose methylation | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 2 |
GO:0006400 | tRNA modification | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008033 | tRNA processing | 8 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0030488 | tRNA methylation | 5 | 2 |
GO:0032259 | methylation | 2 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 10 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008171 | O-methyltransferase activity | 5 | 2 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0008175 | tRNA methyltransferase activity | 5 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016300 | tRNA (uracil) methyltransferase activity | 6 | 2 |
GO:0016427 | tRNA (cytosine) methyltransferase activity | 6 | 2 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0052665 | tRNA (uracil-2'-O-)-methyltransferase activity | 7 | 2 |
GO:0052666 | tRNA (cytosine-2'-O-)-methyltransferase activity | 7 | 2 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0106050 | tRNA 2'-O-methyltransferase activity | 6 | 2 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.517 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.492 |
CLV_PCSK_PC7_1 | 286 | 292 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.274 |
DEG_APCC_DBOX_1 | 402 | 410 | PF00400 | 0.477 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.576 |
DOC_CDC14_PxL_1 | 326 | 334 | PF14671 | 0.424 |
DOC_CYCLIN_RxL_1 | 235 | 243 | PF00134 | 0.533 |
DOC_CYCLIN_RxL_1 | 311 | 321 | PF00134 | 0.361 |
DOC_CYCLIN_yClb1_LxF_4 | 86 | 91 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 324 | 330 | PF00134 | 0.361 |
DOC_MAPK_gen_1 | 102 | 109 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 244 | 252 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 402 | 413 | PF00069 | 0.416 |
DOC_MAPK_HePTP_8 | 401 | 413 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 102 | 109 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 245 | 254 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 404 | 413 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 75 | 84 | PF00069 | 0.535 |
DOC_PP1_RVXF_1 | 36 | 42 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 86 | 92 | PF00149 | 0.474 |
DOC_PP2B_LxvP_1 | 411 | 414 | PF13499 | 0.311 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.429 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 204 | 212 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 244 | 249 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.325 |
LIG_Actin_WH2_2 | 391 | 409 | PF00022 | 0.473 |
LIG_Actin_WH2_2 | 449 | 464 | PF00022 | 0.363 |
LIG_APCC_ABBA_1 | 254 | 259 | PF00400 | 0.330 |
LIG_BIR_III_4 | 18 | 22 | PF00653 | 0.450 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.577 |
LIG_BRCT_BRCA1_1 | 435 | 439 | PF00533 | 0.368 |
LIG_deltaCOP1_diTrp_1 | 121 | 130 | PF00928 | 0.474 |
LIG_deltaCOP1_diTrp_1 | 18 | 26 | PF00928 | 0.377 |
LIG_eIF4E_1 | 50 | 56 | PF01652 | 0.428 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.400 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.491 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.410 |
LIG_FXI_DFP_1 | 14 | 18 | PF00024 | 0.430 |
LIG_LIR_Gen_1 | 278 | 283 | PF02991 | 0.341 |
LIG_LIR_LC3C_4 | 371 | 376 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.431 |
LIG_LYPXL_yS_3 | 329 | 332 | PF13949 | 0.357 |
LIG_LYPXL_yS_3 | 378 | 381 | PF13949 | 0.391 |
LIG_PCNA_yPIPBox_3 | 234 | 246 | PF02747 | 0.473 |
LIG_PTB_Apo_2 | 298 | 305 | PF02174 | 0.440 |
LIG_REV1ctd_RIR_1 | 59 | 66 | PF16727 | 0.513 |
LIG_RPA_C_Fungi | 97 | 109 | PF08784 | 0.241 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.264 |
LIG_SH2_PTP2 | 279 | 282 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.337 |
LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.264 |
LIG_SH2_STAT3 | 22 | 25 | PF00017 | 0.527 |
LIG_SH2_STAT3 | 248 | 251 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.336 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.298 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.405 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.471 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.334 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.339 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 409 | 416 | PF11976 | 0.314 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.455 |
LIG_TYR_ITIM | 255 | 260 | PF00017 | 0.367 |
LIG_TYR_ITIM | 376 | 381 | PF00017 | 0.407 |
LIG_UBA3_1 | 31 | 38 | PF00899 | 0.399 |
LIG_UBA3_1 | 89 | 97 | PF00899 | 0.290 |
MOD_CDC14_SPxK_1 | 215 | 218 | PF00782 | 0.597 |
MOD_CDK_SPxK_1 | 212 | 218 | PF00069 | 0.599 |
MOD_CDK_SPxxK_3 | 3 | 10 | PF00069 | 0.435 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.264 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.595 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.463 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.516 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.356 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.419 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.389 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.264 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.326 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.505 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.526 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.575 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.585 |
MOD_LATS_1 | 66 | 72 | PF00433 | 0.410 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.632 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.305 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.461 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.248 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.395 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.329 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.298 |
MOD_OFUCOSY | 463 | 469 | PF10250 | 0.300 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.427 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.520 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.462 |
MOD_PKA_1 | 244 | 250 | PF00069 | 0.369 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.664 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.594 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.351 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.205 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.391 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.347 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.303 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.225 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.294 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.514 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.479 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.277 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.727 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.470 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.496 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.367 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.387 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.282 |
MOD_SUMO_rev_2 | 40 | 49 | PF00179 | 0.258 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.544 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.556 |
TRG_NLS_MonoCore_2 | 401 | 406 | PF00514 | 0.485 |
TRG_NLS_MonoExtN_4 | 402 | 408 | PF00514 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 238 | 242 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUK1 | Leptomonas seymouri | 64% | 100% |
A0A0S4IV97 | Bodo saltans | 46% | 93% |
A0A1X0NN27 | Trypanosomatidae | 50% | 100% |
A0A3S7WYP3 | Leishmania donovani | 90% | 100% |
A0A422NV05 | Trypanosoma rangeli | 50% | 100% |
A4I142 | Leishmania infantum | 91% | 100% |
C9ZI50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 98% |
E9AIR3 | Leishmania braziliensis | 80% | 100% |
E9AX80 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 98% |
V5AZL8 | Trypanosoma cruzi | 50% | 100% |