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:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HGM7
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0032259 | methylation | 2 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043414 | macromolecule methylation | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 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:0000154 | rRNA modification | 6 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031167 | rRNA methylation | 5 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0070475 | rRNA base methylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | 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 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 185 | 189 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.227 |
CLV_PCSK_FUR_1 | 172 | 176 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 181 | 183 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.711 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 33 | 35 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.154 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.508 |
CLV_Separin_Metazoa | 518 | 522 | PF03568 | 0.515 |
CLV_TASPASE1 | 450 | 456 | PF01112 | 0.493 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.393 |
DEG_COP1_1 | 224 | 232 | PF00400 | 0.279 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.355 |
DEG_SPOP_SBC_1 | 280 | 284 | PF00917 | 0.468 |
DOC_ANK_TNKS_1 | 136 | 143 | PF00023 | 0.674 |
DOC_ANK_TNKS_1 | 183 | 190 | PF00023 | 0.409 |
DOC_CYCLIN_RxL_1 | 482 | 494 | PF00134 | 0.459 |
DOC_MAPK_gen_1 | 155 | 164 | PF00069 | 0.313 |
DOC_MAPK_gen_1 | 206 | 216 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 158 | 166 | PF00069 | 0.350 |
DOC_MAPK_MEF2A_6 | 210 | 218 | PF00069 | 0.434 |
DOC_MAPK_NFAT4_5 | 211 | 219 | PF00069 | 0.419 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.451 |
DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.390 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.413 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.619 |
DOC_USP7_UBL2_3 | 28 | 32 | PF12436 | 0.403 |
DOC_USP7_UBL2_3 | 292 | 296 | PF12436 | 0.743 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 257 | 265 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 34 | 38 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 359 | 364 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 384 | 392 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.501 |
LIG_Actin_WH2_2 | 159 | 176 | PF00022 | 0.379 |
LIG_BIR_III_2 | 268 | 272 | PF00653 | 0.477 |
LIG_BIR_III_4 | 467 | 471 | PF00653 | 0.511 |
LIG_Clathr_ClatBox_1 | 495 | 499 | PF01394 | 0.424 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.374 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.437 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.357 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.432 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.436 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.390 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.515 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.429 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.427 |
LIG_IRF3_LxIS_1 | 159 | 165 | PF10401 | 0.455 |
LIG_LIR_Gen_1 | 36 | 44 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 367 | 376 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 36 | 40 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.344 |
LIG_PTB_Apo_2 | 370 | 377 | PF02174 | 0.370 |
LIG_REV1ctd_RIR_1 | 57 | 63 | PF16727 | 0.379 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.296 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.347 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.323 |
LIG_SH2_GRB2like | 368 | 371 | PF00017 | 0.424 |
LIG_SH2_NCK_1 | 156 | 160 | PF00017 | 0.296 |
LIG_SH2_PTP2 | 368 | 371 | PF00017 | 0.438 |
LIG_SH2_SRC | 368 | 371 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.338 |
LIG_SH2_STAT3 | 62 | 65 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.431 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.352 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.380 |
LIG_SUMO_SIM_par_1 | 51 | 58 | PF11976 | 0.404 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.489 |
LIG_WRC_WIRS_1 | 495 | 500 | PF05994 | 0.424 |
LIG_WW_3 | 115 | 119 | PF00397 | 0.504 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.617 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.516 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.448 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.372 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.349 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.565 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.438 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.665 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.401 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.624 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.213 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.715 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.400 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.460 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.686 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.691 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.712 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.441 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.413 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.424 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.425 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.391 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.453 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.544 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.213 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.551 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.493 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.413 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.697 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.507 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.438 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.473 |
MOD_PKA_1 | 174 | 180 | PF00069 | 0.424 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.686 |
MOD_PKA_1 | 33 | 39 | PF00069 | 0.364 |
MOD_PKA_1 | 358 | 364 | PF00069 | 0.354 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.544 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.664 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.304 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.377 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.494 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.550 |
MOD_PKB_1 | 172 | 180 | PF00069 | 0.431 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.633 |
MOD_Plk_2-3 | 452 | 458 | PF00069 | 0.492 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.496 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.439 |
MOD_SUMO_for_1 | 299 | 302 | PF00179 | 0.437 |
MOD_SUMO_for_1 | 475 | 478 | PF00179 | 0.453 |
MOD_SUMO_rev_2 | 273 | 281 | PF00179 | 0.571 |
MOD_SUMO_rev_2 | 302 | 309 | PF00179 | 0.667 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.315 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.413 |
TRG_NLS_MonoExtC_3 | 179 | 184 | PF00514 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 93 | 97 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I291 | Leptomonas seymouri | 70% | 100% |
A0A0S4JC42 | Bodo saltans | 52% | 100% |
A0A1X0NQY2 | Trypanosomatidae | 58% | 100% |
A0A3S7X1L9 | Leishmania donovani | 83% | 99% |
A0A422NZ09 | Trypanosoma rangeli | 59% | 100% |
A4I3Q1 | Leishmania infantum | 83% | 99% |
D0A8B0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AZZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |
O14039 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q4Q892 | Leishmania major | 82% | 99% |
Q8GYE8 | Arabidopsis thaliana | 27% | 100% |
Q8K4F6 | Mus musculus | 27% | 100% |
Q96P11 | Homo sapiens | 28% | 100% |
V5BAN7 | Trypanosoma cruzi | 58% | 100% |