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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AIR3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
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 |
GO:0001510 | RNA methylation | 4 | 1 |
GO:0002128 | tRNA nucleoside ribose methylation | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0030488 | tRNA methylation | 5 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
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:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0008171 | O-methyltransferase activity | 5 | 1 |
GO:0008175 | tRNA methyltransferase activity | 5 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016300 | tRNA (uracil) methyltransferase activity | 6 | 1 |
GO:0016427 | tRNA (cytosine) methyltransferase activity | 6 | 1 |
GO:0052665 | tRNA (uracil-2'-O-)-methyltransferase activity | 7 | 1 |
GO:0052666 | tRNA (cytosine-2'-O-)-methyltransferase activity | 7 | 1 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 1 |
GO:0106050 | tRNA 2'-O-methyltransferase activity | 6 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.518 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.610 |
CLV_PCSK_PC1ET2_1 | 399 | 401 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.530 |
CLV_PCSK_PC7_1 | 283 | 289 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.284 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.477 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.583 |
DOC_CDC14_PxL_1 | 323 | 331 | PF14671 | 0.417 |
DOC_CYCLIN_RxL_1 | 308 | 318 | PF00134 | 0.507 |
DOC_CYCLIN_yClb1_LxF_4 | 342 | 348 | PF00134 | 0.365 |
DOC_CYCLIN_yClb1_LxF_4 | 83 | 88 | PF00134 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 321 | 327 | PF00134 | 0.368 |
DOC_MAPK_gen_1 | 239 | 249 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 399 | 410 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 99 | 106 | PF00069 | 0.452 |
DOC_MAPK_HePTP_8 | 398 | 410 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 401 | 410 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 99 | 106 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 33 | 39 | PF00149 | 0.414 |
DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.484 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.314 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.528 |
DOC_USP7_UBL2_3 | 235 | 239 | PF12436 | 0.259 |
DOC_USP7_UBL2_3 | 99 | 103 | PF12436 | 0.373 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.474 |
LIG_14-3-3_CanoR_1 | 130 | 138 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 201 | 209 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 215 | 221 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 241 | 246 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 389 | 398 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.409 |
LIG_Actin_RPEL_3 | 234 | 253 | PF02755 | 0.333 |
LIG_Actin_WH2_2 | 388 | 406 | PF00022 | 0.479 |
LIG_Actin_WH2_2 | 446 | 461 | PF00022 | 0.367 |
LIG_Actin_WH2_2 | 82 | 100 | PF00022 | 0.373 |
LIG_APCC_ABBA_1 | 251 | 256 | PF00400 | 0.334 |
LIG_BIR_III_4 | 15 | 19 | PF00653 | 0.501 |
LIG_deltaCOP1_diTrp_1 | 118 | 127 | PF00928 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 15 | 23 | PF00928 | 0.407 |
LIG_eIF4E_1 | 325 | 331 | PF01652 | 0.346 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.480 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.349 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.495 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.398 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.395 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.488 |
LIG_LIR_Gen_1 | 275 | 280 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 339 | 348 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 47 | 58 | PF02991 | 0.373 |
LIG_LIR_LC3C_4 | 368 | 373 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 5 | 9 | PF02991 | 0.407 |
LIG_LYPXL_yS_3 | 326 | 329 | PF13949 | 0.344 |
LIG_LYPXL_yS_3 | 375 | 378 | PF13949 | 0.393 |
LIG_PDZ_Class_3 | 460 | 465 | PF00595 | 0.283 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.420 |
LIG_PTB_Apo_2 | 270 | 277 | PF02174 | 0.295 |
LIG_PTB_Phospho_1 | 270 | 276 | PF10480 | 0.295 |
LIG_REV1ctd_RIR_1 | 56 | 63 | PF16727 | 0.517 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.434 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.376 |
LIG_SH2_PTP2 | 276 | 279 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.373 |
LIG_SH2_STAT3 | 158 | 161 | PF00017 | 0.434 |
LIG_SH2_STAT3 | 245 | 248 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.373 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.434 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.426 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.465 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.381 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.488 |
LIG_SUMO_SIM_anti_2 | 275 | 281 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.316 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.568 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.400 |
LIG_TYR_ITIM | 252 | 257 | PF00017 | 0.377 |
LIG_TYR_ITIM | 373 | 378 | PF00017 | 0.409 |
LIG_UBA3_1 | 28 | 35 | PF00899 | 0.421 |
LIG_WRC_WIRS_1 | 3 | 8 | PF05994 | 0.414 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.402 |
MOD_CDC14_SPxK_1 | 212 | 215 | PF00782 | 0.608 |
MOD_CDK_SPxK_1 | 209 | 215 | PF00069 | 0.593 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.453 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.589 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.473 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.413 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.544 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.359 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.346 |
MOD_Cter_Amidation | 334 | 337 | PF01082 | 0.563 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.315 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.323 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.254 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.353 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.461 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.567 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.373 |
MOD_LATS_1 | 63 | 69 | PF00433 | 0.537 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.557 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.197 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.279 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.486 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.537 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.319 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.481 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.533 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.589 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.549 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.261 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.524 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.494 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.418 |
MOD_PKA_1 | 241 | 247 | PF00069 | 0.355 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.379 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.455 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.628 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.337 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.441 |
MOD_PKB_1 | 457 | 465 | PF00069 | 0.243 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.547 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.407 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.405 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.314 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.454 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.443 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.711 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.505 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.370 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.468 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.474 |
MOD_SUMO_rev_2 | 41 | 46 | PF00179 | 0.505 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.528 |
TRG_NLS_MonoCore_2 | 398 | 403 | PF00514 | 0.485 |
TRG_NLS_MonoExtN_4 | 399 | 405 | PF00514 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 311 | 315 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUK1 | Leptomonas seymouri | 63% | 99% |
A0A0S4IV97 | Bodo saltans | 44% | 92% |
A0A1X0NN27 | Trypanosomatidae | 51% | 99% |
A0A3S7WYP3 | Leishmania donovani | 80% | 99% |
A0A422NV05 | Trypanosoma rangeli | 50% | 99% |
A4I142 | Leishmania infantum | 82% | 99% |
C9ZI50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 97% |
E9AX80 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 97% |
Q4QA96 | Leishmania major | 80% | 100% |
V5AZL8 | Trypanosoma cruzi | 52% | 99% |