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 | 2 |
GO:0005730 | nucleolus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q892
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 2 |
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
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:0016072 | rRNA metabolic process | 7 | 2 |
GO:0031167 | rRNA methylation | 5 | 2 |
GO:0032259 | methylation | 2 | 12 |
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 | 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:0070475 | rRNA base methylation | 6 | 2 |
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 | 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 | 0.574 |
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.250 |
CLV_PCSK_FUR_1 | 136 | 140 | PF00082 | 0.704 |
CLV_PCSK_FUR_1 | 172 | 176 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 181 | 183 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.761 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.271 |
CLV_PCSK_PC7_1 | 423 | 429 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.730 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.681 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.250 |
CLV_Separin_Metazoa | 522 | 526 | PF03568 | 0.536 |
DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.423 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.397 |
DOC_CYCLIN_RxL_1 | 19 | 29 | PF00134 | 0.423 |
DOC_CYCLIN_RxL_1 | 486 | 498 | PF00134 | 0.494 |
DOC_MAPK_gen_1 | 155 | 164 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 158 | 166 | PF00069 | 0.404 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.448 |
DOC_PP2B_PxIxI_1 | 335 | 341 | PF00149 | 0.528 |
DOC_SPAK_OSR1_1 | 563 | 567 | PF12202 | 0.502 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.450 |
DOC_USP7_UBL2_3 | 28 | 32 | PF12436 | 0.433 |
DOC_USP7_UBL2_3 | 284 | 288 | PF12436 | 0.763 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.674 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 210 | 219 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 257 | 265 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 356 | 361 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 381 | 389 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 427 | 432 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.523 |
LIG_Actin_WH2_2 | 159 | 176 | PF00022 | 0.433 |
LIG_BIR_III_2 | 268 | 272 | PF00653 | 0.516 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.472 |
LIG_Clathr_ClatBox_1 | 499 | 503 | PF01394 | 0.461 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.405 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.450 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.402 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.466 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.452 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.536 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.461 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.459 |
LIG_IRF3_LxIS_1 | 159 | 165 | PF10401 | 0.481 |
LIG_LIR_Gen_1 | 36 | 44 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 364 | 373 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 36 | 40 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 364 | 368 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.390 |
LIG_REV1ctd_RIR_1 | 57 | 63 | PF16727 | 0.434 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.358 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.390 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.372 |
LIG_SH2_GRB2like | 365 | 368 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 156 | 160 | PF00017 | 0.358 |
LIG_SH2_PTP2 | 365 | 368 | PF00017 | 0.475 |
LIG_SH2_SRC | 365 | 368 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.372 |
LIG_SH2_STAT3 | 62 | 65 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.468 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.528 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.661 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.425 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.445 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 51 | 58 | PF11976 | 0.526 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.489 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.748 |
LIG_WRC_WIRS_1 | 499 | 504 | PF05994 | 0.461 |
LIG_WW_3 | 115 | 119 | PF00397 | 0.552 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.678 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.482 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.394 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.409 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.724 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.591 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.475 |
MOD_Cter_Amidation | 136 | 139 | PF01082 | 0.704 |
MOD_Cter_Amidation | 284 | 287 | PF01082 | 0.569 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.704 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.534 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.443 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.266 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.755 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.447 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.662 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.476 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.745 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.681 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.441 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.769 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.451 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.458 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.410 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.504 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.712 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.250 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.564 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.559 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.509 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.450 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.574 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.475 |
MOD_PKA_1 | 138 | 144 | PF00069 | 0.783 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.762 |
MOD_PKA_1 | 33 | 39 | PF00069 | 0.409 |
MOD_PKA_1 | 427 | 433 | PF00069 | 0.635 |
MOD_PKA_1 | 436 | 442 | PF00069 | 0.597 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.486 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.725 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.582 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.747 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.362 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.635 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.597 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.545 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.502 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.622 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.497 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.511 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.484 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.660 |
MOD_SUMO_for_1 | 479 | 482 | PF00179 | 0.527 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.362 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.608 |
TRG_NLS_MonoExtC_3 | 137 | 143 | PF00514 | 0.700 |
TRG_NLS_MonoExtC_3 | 179 | 184 | PF00514 | 0.607 |
TRG_NLS_MonoExtC_3 | 285 | 290 | PF00514 | 0.539 |
TRG_NLS_MonoExtN_4 | 136 | 142 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 284 | 291 | PF00514 | 0.694 |
TRG_Pf-PMV_PEXEL_1 | 218 | 222 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I291 | Leptomonas seymouri | 70% | 100% |
A0A0S4JC42 | Bodo saltans | 53% | 100% |
A0A1X0NQY2 | Trypanosomatidae | 58% | 100% |
A0A3S7X1L9 | Leishmania donovani | 92% | 100% |
A0A422NZ09 | Trypanosoma rangeli | 57% | 100% |
A4HGM7 | Leishmania braziliensis | 82% | 100% |
A4I3Q1 | Leishmania infantum | 91% | 100% |
D0A8B0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AZZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
O14039 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q8GYE8 | Arabidopsis thaliana | 28% | 100% |
V5BAN7 | Trypanosoma cruzi | 59% | 100% |