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:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 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:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 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 |
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:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
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 | 0.518 |
CLV_C14_Caspase3-7 | 87 | 91 | PF00656 | 0.402 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.544 |
CLV_PCSK_FUR_1 | 575 | 579 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 576 | 578 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.349 |
CLV_Separin_Metazoa | 235 | 239 | PF03568 | 0.521 |
CLV_Separin_Metazoa | 357 | 361 | PF03568 | 0.469 |
DEG_APCC_DBOX_1 | 248 | 256 | PF00400 | 0.315 |
DEG_APCC_DBOX_1 | 355 | 363 | PF00400 | 0.468 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.436 |
DOC_CDC14_PxL_1 | 233 | 241 | PF14671 | 0.494 |
DOC_CYCLIN_RxL_1 | 107 | 120 | PF00134 | 0.467 |
DOC_CYCLIN_RxL_1 | 246 | 256 | PF00134 | 0.385 |
DOC_MAPK_gen_1 | 107 | 117 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 172 | 179 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 482 | 488 | PF00069 | 0.514 |
DOC_PP1_RVXF_1 | 407 | 414 | PF00149 | 0.477 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.365 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.426 |
DOC_PP4_FxxP_1 | 588 | 591 | PF00568 | 0.457 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.409 |
DOC_USP7_MATH_2 | 543 | 549 | PF00917 | 0.514 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.676 |
LIG_14-3-3_CanoR_1 | 11 | 21 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 111 | 116 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 134 | 139 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 238 | 242 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 267 | 275 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 499 | 505 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 51 | 56 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 78 | 86 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 141 | 158 | PF00022 | 0.397 |
LIG_APCC_ABBA_1 | 157 | 162 | PF00400 | 0.321 |
LIG_APCC_ABBAyCdc20_2 | 156 | 162 | PF00400 | 0.341 |
LIG_BIR_III_4 | 90 | 94 | PF00653 | 0.458 |
LIG_BRCT_BRCA1_1 | 270 | 274 | PF00533 | 0.482 |
LIG_BRCT_BRCA1_1 | 484 | 488 | PF00533 | 0.355 |
LIG_BRCT_BRCA1_1 | 532 | 536 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_1 | 563 | 567 | PF00533 | 0.399 |
LIG_EH1_1 | 217 | 225 | PF00400 | 0.414 |
LIG_eIF4E_1 | 218 | 224 | PF01652 | 0.382 |
LIG_eIF4E_1 | 246 | 252 | PF01652 | 0.427 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.427 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.456 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.543 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.467 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.472 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.449 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.461 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.396 |
LIG_HP1_1 | 596 | 600 | PF01393 | 0.437 |
LIG_LIR_Gen_1 | 193 | 202 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 227 | 237 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 341 | 349 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 474 | 481 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 594 | 604 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 610 | 617 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 193 | 197 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 341 | 345 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 610 | 614 | PF02991 | 0.298 |
LIG_Pex14_1 | 547 | 551 | PF04695 | 0.537 |
LIG_Pex14_2 | 274 | 278 | PF04695 | 0.317 |
LIG_Pex14_2 | 476 | 480 | PF04695 | 0.420 |
LIG_SH2_CRK | 507 | 511 | PF00017 | 0.379 |
LIG_SH2_GRB2like | 327 | 330 | PF00017 | 0.383 |
LIG_SH2_NCK_1 | 327 | 331 | PF00017 | 0.512 |
LIG_SH2_SRC | 175 | 178 | PF00017 | 0.496 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.491 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.350 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.370 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.409 |
LIG_SUMO_SIM_par_1 | 112 | 120 | PF11976 | 0.426 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.398 |
LIG_TYR_ITIM | 275 | 280 | PF00017 | 0.319 |
LIG_WRC_WIRS_1 | 280 | 285 | PF05994 | 0.361 |
LIG_WRC_WIRS_1 | 410 | 415 | PF05994 | 0.495 |
LIG_WRC_WIRS_1 | 608 | 613 | PF05994 | 0.419 |
MOD_CDK_SPK_2 | 129 | 134 | PF00069 | 0.389 |
MOD_CDK_SPK_2 | 494 | 499 | PF00069 | 0.583 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.463 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.353 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.502 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.543 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.507 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.402 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.428 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.428 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.426 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.477 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.448 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.354 |
MOD_GlcNHglycan | 394 | 398 | PF01048 | 0.376 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.561 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.431 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.416 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.480 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.481 |
MOD_N-GLC_1 | 561 | 566 | PF02516 | 0.410 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.571 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.560 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.525 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.467 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.332 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.518 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.346 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.554 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.431 |
MOD_PKA_1 | 482 | 488 | PF00069 | 0.421 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.517 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.420 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.510 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.551 |
MOD_PKB_1 | 265 | 273 | PF00069 | 0.481 |
MOD_PKB_1 | 554 | 562 | PF00069 | 0.511 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.525 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.434 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.421 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.525 |
MOD_Plk_1 | 580 | 586 | PF00069 | 0.479 |
MOD_Plk_2-3 | 162 | 168 | PF00069 | 0.483 |
MOD_Plk_2-3 | 436 | 442 | PF00069 | 0.539 |
MOD_Plk_2-3 | 545 | 551 | PF00069 | 0.537 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.419 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.468 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.375 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.472 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.369 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.485 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.491 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.614 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.369 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.670 |
TRG_DiLeu_BaEn_1 | 354 | 359 | PF01217 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 406 | 411 | PF01217 | 0.341 |
TRG_DiLeu_LyEn_5 | 150 | 155 | PF01217 | 0.465 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 507 | 509 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 551 | 554 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.540 |
TRG_NLS_MonoCore_2 | 574 | 579 | PF00514 | 0.460 |
TRG_NLS_MonoExtC_3 | 575 | 581 | PF00514 | 0.459 |
TRG_NLS_MonoExtN_4 | 575 | 580 | PF00514 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P414 | Leptomonas seymouri | 61% | 98% |
A0A0S4JV05 | Bodo saltans | 39% | 94% |
A0A1X0NUT8 | Trypanosomatidae | 43% | 100% |
A0A3S7WRT6 | Leishmania donovani | 92% | 100% |
A0A422N563 | Trypanosoma rangeli | 45% | 100% |
A4H6R0 | Leishmania braziliensis | 79% | 100% |
A4HV43 | Leishmania infantum | 92% | 100% |
D0A7A5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 99% |
E9ANS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BBF7 | Trypanosoma cruzi | 44% | 100% |