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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AX80
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_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.483 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 399 | 401 | PF00082 | 0.524 |
CLV_PCSK_PC7_1 | 283 | 289 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.375 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.516 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.643 |
DOC_ANK_TNKS_1 | 286 | 293 | PF00023 | 0.285 |
DOC_CDC14_PxL_1 | 323 | 331 | PF14671 | 0.474 |
DOC_CYCLIN_RxL_1 | 232 | 240 | PF00134 | 0.502 |
DOC_CYCLIN_yClb1_LxF_4 | 83 | 88 | PF00134 | 0.575 |
DOC_CYCLIN_yCln2_LP_2 | 321 | 327 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 241 | 249 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 399 | 410 | PF00069 | 0.474 |
DOC_MAPK_HePTP_8 | 398 | 410 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 401 | 410 | PF00069 | 0.471 |
DOC_PP1_RVXF_1 | 33 | 39 | PF00149 | 0.478 |
DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.575 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.365 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.404 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.459 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 130 | 138 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 215 | 221 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 241 | 246 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 389 | 398 | PF00244 | 0.514 |
LIG_Actin_RPEL_3 | 234 | 253 | PF02755 | 0.424 |
LIG_Actin_WH2_2 | 388 | 406 | PF00022 | 0.484 |
LIG_Actin_WH2_2 | 446 | 461 | PF00022 | 0.419 |
LIG_APCC_ABBA_1 | 251 | 256 | PF00400 | 0.404 |
LIG_BIR_III_4 | 15 | 19 | PF00653 | 0.600 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.639 |
LIG_BRCT_BRCA1_1 | 343 | 347 | PF00533 | 0.625 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.486 |
LIG_deltaCOP1_diTrp_1 | 118 | 127 | PF00928 | 0.575 |
LIG_deltaCOP1_diTrp_1 | 15 | 23 | PF00928 | 0.452 |
LIG_EH1_1 | 113 | 121 | PF00400 | 0.450 |
LIG_eIF4E_1 | 47 | 53 | PF01652 | 0.477 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.353 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.409 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.502 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.384 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.469 |
LIG_HP1_1 | 370 | 374 | PF01393 | 0.258 |
LIG_LIR_Apic_2 | 196 | 202 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 275 | 280 | PF02991 | 0.468 |
LIG_LIR_LC3C_4 | 368 | 373 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.397 |
LIG_LYPXL_S_1 | 374 | 378 | PF13949 | 0.248 |
LIG_LYPXL_yS_3 | 326 | 329 | PF13949 | 0.420 |
LIG_LYPXL_yS_3 | 375 | 378 | PF13949 | 0.521 |
LIG_PCNA_yPIPBox_3 | 231 | 243 | PF02747 | 0.515 |
LIG_PTB_Apo_2 | 270 | 277 | PF02174 | 0.461 |
LIG_PTB_Apo_2 | 295 | 302 | PF02174 | 0.464 |
LIG_PTB_Phospho_1 | 270 | 276 | PF10480 | 0.462 |
LIG_REV1ctd_RIR_1 | 56 | 63 | PF16727 | 0.549 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.470 |
LIG_SH2_PTP2 | 276 | 279 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.410 |
LIG_SH2_STAT3 | 158 | 161 | PF00017 | 0.470 |
LIG_SH2_STAT3 | 19 | 22 | PF00017 | 0.577 |
LIG_SH2_STAT3 | 245 | 248 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.404 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.480 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.502 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.525 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.401 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.595 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.529 |
LIG_SUMO_SIM_anti_2 | 275 | 281 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.383 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.578 |
LIG_TYR_ITIM | 252 | 257 | PF00017 | 0.510 |
LIG_TYR_ITIM | 373 | 378 | PF00017 | 0.539 |
LIG_UBA3_1 | 28 | 35 | PF00899 | 0.542 |
LIG_UBA3_1 | 86 | 94 | PF00899 | 0.529 |
MOD_CDC14_SPxK_1 | 212 | 215 | PF00782 | 0.746 |
MOD_CDK_SPxK_1 | 209 | 215 | PF00069 | 0.727 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.479 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.506 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.620 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.426 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.560 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.353 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.280 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.375 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.631 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.641 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.565 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.469 |
MOD_LATS_1 | 63 | 69 | PF00433 | 0.562 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.649 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.234 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.321 |
MOD_N-GLC_2 | 154 | 156 | PF02516 | 0.250 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.548 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.544 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.350 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.417 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.353 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.516 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.504 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.411 |
MOD_NEK2_2 | 379 | 384 | PF00069 | 0.252 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.588 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.553 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.518 |
MOD_PKA_1 | 241 | 247 | PF00069 | 0.424 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.469 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.646 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.405 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.464 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.462 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.510 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.442 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.350 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.515 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.326 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.496 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.480 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.733 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.528 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.429 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.456 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.493 |
MOD_SUMO_rev_2 | 37 | 46 | PF00179 | 0.329 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 311 | 314 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.489 |
TRG_NLS_MonoCore_2 | 398 | 403 | PF00514 | 0.524 |
TRG_NLS_MonoExtN_4 | 399 | 405 | PF00514 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 235 | 239 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.614 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUK1 | Leptomonas seymouri | 65% | 100% |
A0A0S4IV97 | Bodo saltans | 44% | 95% |
A0A1X0NN27 | Trypanosomatidae | 50% | 100% |
A0A3S7WYP3 | Leishmania donovani | 88% | 100% |
A0A422NV05 | Trypanosoma rangeli | 50% | 100% |
A4I142 | Leishmania infantum | 90% | 100% |
C9ZI50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
D0AA55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 89% |
E9AIR3 | Leishmania braziliensis | 82% | 100% |
Q4QA96 | Leishmania major | 89% | 100% |
V5AZL8 | Trypanosoma cruzi | 51% | 100% |