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:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 13 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 13 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009451 | RNA modification | 5 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016070 | RNA metabolic process | 5 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0046483 | heterocycle metabolic process | 3 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0090304 | nucleic acid metabolic process | 4 | 13 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0003723 | RNA binding | 4 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0009982 | pseudouridine synthase activity | 4 | 13 |
GO:0016853 | isomerase activity | 2 | 13 |
GO:0016866 | intramolecular transferase activity | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.574 |
CLV_C14_Caspase3-7 | 458 | 462 | PF00656 | 0.365 |
CLV_C14_Caspase3-7 | 87 | 91 | PF00656 | 0.432 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.565 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 552 | 554 | PF00082 | 0.596 |
CLV_PCSK_PC7_1 | 356 | 362 | PF00082 | 0.278 |
CLV_PCSK_PC7_1 | 573 | 579 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.512 |
CLV_Separin_Metazoa | 235 | 239 | PF03568 | 0.539 |
CLV_Separin_Metazoa | 357 | 361 | PF03568 | 0.532 |
DEG_APCC_DBOX_1 | 248 | 256 | PF00400 | 0.346 |
DEG_APCC_DBOX_1 | 264 | 272 | PF00400 | 0.365 |
DEG_APCC_DBOX_1 | 355 | 363 | PF00400 | 0.532 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.478 |
DEG_ODPH_VHL_1 | 241 | 252 | PF01847 | 0.254 |
DEG_SPOP_SBC_1 | 494 | 498 | PF00917 | 0.490 |
DOC_CYCLIN_RxL_1 | 107 | 120 | PF00134 | 0.503 |
DOC_CYCLIN_RxL_1 | 261 | 270 | PF00134 | 0.511 |
DOC_MAPK_DCC_7 | 216 | 225 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 107 | 117 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 170 | 179 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 264 | 271 | PF00069 | 0.531 |
DOC_PP1_RVXF_1 | 407 | 414 | PF00149 | 0.539 |
DOC_PP2B_LxvP_1 | 177 | 180 | PF13499 | 0.493 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.411 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.440 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.436 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 111 | 116 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 134 | 139 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 238 | 242 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 424 | 432 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 493 | 503 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 51 | 56 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 78 | 86 | PF00244 | 0.488 |
LIG_Actin_WH2_2 | 141 | 158 | PF00022 | 0.437 |
LIG_APCC_ABBA_1 | 157 | 162 | PF00400 | 0.364 |
LIG_APCC_ABBAyCdc20_2 | 156 | 162 | PF00400 | 0.381 |
LIG_BIR_III_4 | 90 | 94 | PF00653 | 0.490 |
LIG_BRCT_BRCA1_1 | 532 | 536 | PF00533 | 0.477 |
LIG_BRCT_BRCA1_1 | 563 | 567 | PF00533 | 0.453 |
LIG_eIF4E_1 | 218 | 224 | PF01652 | 0.429 |
LIG_eIF4E_1 | 246 | 252 | PF01652 | 0.485 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.453 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.559 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.439 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.481 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.500 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.467 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.471 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.478 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.419 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.426 |
LIG_HP1_1 | 596 | 600 | PF01393 | 0.496 |
LIG_Integrin_RGD_1 | 372 | 374 | PF01839 | 0.432 |
LIG_LIR_Apic_2 | 122 | 127 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 193 | 202 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 227 | 237 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 341 | 349 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 474 | 481 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 594 | 604 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 610 | 617 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 193 | 197 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 341 | 345 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 610 | 614 | PF02991 | 0.333 |
LIG_NRBOX | 246 | 252 | PF00104 | 0.387 |
LIG_Pex14_1 | 547 | 551 | PF04695 | 0.546 |
LIG_Pex14_2 | 274 | 278 | PF04695 | 0.347 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.244 |
LIG_SH2_GRB2like | 327 | 330 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 327 | 331 | PF00017 | 0.534 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.560 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.408 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.445 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.441 |
LIG_SUMO_SIM_par_1 | 112 | 120 | PF11976 | 0.465 |
LIG_TYR_ITIM | 275 | 280 | PF00017 | 0.336 |
LIG_WRC_WIRS_1 | 410 | 415 | PF05994 | 0.555 |
LIG_WRC_WIRS_1 | 608 | 613 | PF05994 | 0.447 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.391 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.319 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.428 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.530 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.481 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.556 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.586 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.491 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.473 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.458 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.440 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.411 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.538 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.598 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.581 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.581 |
MOD_GlcNHglycan | 394 | 398 | PF01048 | 0.422 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.520 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.727 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.462 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.379 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.513 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.596 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.328 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.546 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.427 |
MOD_N-GLC_1 | 484 | 489 | PF02516 | 0.291 |
MOD_N-GLC_1 | 561 | 566 | PF02516 | 0.461 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.602 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.391 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.606 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.355 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.476 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.374 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.568 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.371 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.279 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.468 |
MOD_PKA_1 | 424 | 430 | PF00069 | 0.415 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.534 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.464 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.594 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.610 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.535 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.567 |
MOD_PKB_1 | 265 | 273 | PF00069 | 0.527 |
MOD_PKB_1 | 424 | 432 | PF00069 | 0.414 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.556 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.452 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.558 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.415 |
MOD_Plk_1 | 580 | 586 | PF00069 | 0.516 |
MOD_Plk_2-3 | 162 | 168 | PF00069 | 0.500 |
MOD_Plk_2-3 | 38 | 44 | PF00069 | 0.312 |
MOD_Plk_2-3 | 436 | 442 | PF00069 | 0.559 |
MOD_Plk_2-3 | 545 | 551 | PF00069 | 0.546 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.457 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.352 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.446 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.462 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.430 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.499 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.481 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.628 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.416 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.414 |
MOD_SUMO_for_1 | 531 | 534 | PF00179 | 0.267 |
TRG_DiLeu_BaEn_1 | 354 | 359 | PF01217 | 0.413 |
TRG_DiLeu_BaLyEn_6 | 219 | 224 | PF01217 | 0.339 |
TRG_DiLeu_BaLyEn_6 | 246 | 251 | PF01217 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 406 | 411 | PF01217 | 0.371 |
TRG_DiLeu_LyEn_5 | 150 | 155 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.394 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 264 | 267 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 359 | 361 | PF00400 | 0.285 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 553 | 556 | PF00400 | 0.500 |
TRG_NLS_MonoExtC_3 | 551 | 556 | PF00514 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 37 | 42 | PF00026 | 0.324 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P414 | Leptomonas seymouri | 62% | 98% |
A0A0S4JV05 | Bodo saltans | 38% | 94% |
A0A1X0NUT8 | Trypanosomatidae | 44% | 100% |
A0A3S7WRT6 | Leishmania donovani | 80% | 100% |
A0A422N563 | Trypanosoma rangeli | 46% | 100% |
A4HV43 | Leishmania infantum | 80% | 100% |
C9ZZ88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A7A5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 99% |
E9ANS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QGU5 | Leishmania major | 79% | 100% |
V5BBF7 | Trypanosoma cruzi | 43% | 100% |