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: 10 |
NetGPI | no | yes: 0, no: 10 |
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 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q0I6
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006399 | tRNA metabolic process | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008033 | tRNA processing | 8 | 10 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009451 | RNA modification | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0034470 | ncRNA processing | 7 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0009982 | pseudouridine synthase activity | 4 | 11 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016866 | intramolecular transferase activity | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
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 | 226 | 230 | PF00656 | 0.246 |
CLV_C14_Caspase3-7 | 596 | 600 | PF00656 | 0.293 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.460 |
CLV_PCSK_PC7_1 | 202 | 208 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.387 |
DEG_APCC_DBOX_1 | 379 | 387 | PF00400 | 0.379 |
DEG_APCC_DBOX_1 | 423 | 431 | PF00400 | 0.246 |
DEG_APCC_DBOX_1 | 521 | 529 | PF00400 | 0.370 |
DEG_APCC_KENBOX_2 | 224 | 228 | PF00400 | 0.246 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.532 |
DEG_SCF_FBW7_1 | 619 | 625 | PF00400 | 0.512 |
DOC_CKS1_1 | 498 | 503 | PF01111 | 0.245 |
DOC_CKS1_1 | 601 | 606 | PF01111 | 0.473 |
DOC_CKS1_1 | 619 | 624 | PF01111 | 0.584 |
DOC_MAPK_gen_1 | 254 | 261 | PF00069 | 0.246 |
DOC_MAPK_gen_1 | 27 | 33 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 378 | 387 | PF00069 | 0.310 |
DOC_PP1_RVXF_1 | 244 | 251 | PF00149 | 0.246 |
DOC_PP1_RVXF_1 | 489 | 495 | PF00149 | 0.179 |
DOC_PP2B_LxvP_1 | 530 | 533 | PF13499 | 0.246 |
DOC_PP4_FxxP_1 | 647 | 650 | PF00568 | 0.293 |
DOC_PP4_FxxP_1 | 662 | 665 | PF00568 | 0.313 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.766 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 15 | 24 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 257 | 262 | PF00244 | 0.250 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.262 |
LIG_Actin_WH2_2 | 368 | 386 | PF00022 | 0.359 |
LIG_APCC_ABBA_1 | 221 | 226 | PF00400 | 0.246 |
LIG_BIR_III_2 | 496 | 500 | PF00653 | 0.267 |
LIG_BIR_III_4 | 304 | 308 | PF00653 | 0.324 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.324 |
LIG_EH1_1 | 453 | 461 | PF00400 | 0.246 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.503 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.257 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.209 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.334 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.433 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.364 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.361 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.256 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.522 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.506 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.379 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.267 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.370 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.443 |
LIG_FHA_2 | 513 | 519 | PF00498 | 0.277 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.427 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.379 |
LIG_Integrin_RGD_1 | 35 | 37 | PF01839 | 0.434 |
LIG_LIR_Apic_2 | 599 | 604 | PF02991 | 0.444 |
LIG_LIR_Apic_2 | 646 | 650 | PF02991 | 0.293 |
LIG_LIR_Apic_2 | 661 | 665 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 215 | 224 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 458 | 469 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 550 | 559 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 415 | 421 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 458 | 464 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 550 | 555 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 580 | 584 | PF02991 | 0.381 |
LIG_PCNA_PIPBox_1 | 397 | 406 | PF02747 | 0.310 |
LIG_PCNA_yPIPBox_3 | 457 | 468 | PF02747 | 0.359 |
LIG_Rb_pABgroove_1 | 398 | 406 | PF01858 | 0.267 |
LIG_SH2_CRK | 552 | 556 | PF00017 | 0.379 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.264 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.223 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 654 | 658 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.135 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.429 |
LIG_SH3_1 | 315 | 321 | PF00018 | 0.286 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.585 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.299 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.264 |
LIG_SH3_3 | 633 | 639 | PF00018 | 0.503 |
LIG_SUMO_SIM_anti_2 | 567 | 573 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 399 | 405 | PF11976 | 0.267 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.510 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.375 |
LIG_TRAF2_1 | 487 | 490 | PF00917 | 0.267 |
LIG_TRFH_1 | 647 | 651 | PF08558 | 0.303 |
LIG_WRC_WIRS_1 | 644 | 649 | PF05994 | 0.399 |
MOD_CDK_SPxxK_3 | 600 | 607 | PF00069 | 0.407 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.295 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.257 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.215 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.431 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.323 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.201 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.338 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.660 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.517 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.508 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.379 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.436 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.433 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.306 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.652 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.716 |
MOD_GlcNHglycan | 120 | 124 | PF01048 | 0.665 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.671 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.667 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.573 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.557 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.760 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.246 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.445 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.232 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.379 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.230 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.365 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.503 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.454 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.616 |
MOD_LATS_1 | 240 | 246 | PF00433 | 0.379 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.417 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.265 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.325 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.293 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.310 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.379 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.541 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.385 |
MOD_NEK2_2 | 47 | 52 | PF00069 | 0.336 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.412 |
MOD_PK_1 | 20 | 26 | PF00069 | 0.399 |
MOD_PKA_1 | 15 | 21 | PF00069 | 0.375 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.624 |
MOD_PKA_1 | 512 | 518 | PF00069 | 0.379 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.513 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.500 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.338 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.407 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.305 |
MOD_PKB_1 | 206 | 214 | PF00069 | 0.506 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.424 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.267 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.310 |
MOD_Plk_1 | 589 | 595 | PF00069 | 0.245 |
MOD_Plk_2-3 | 674 | 680 | PF00069 | 0.592 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.475 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.259 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.344 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.338 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.405 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.306 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.489 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.560 |
TRG_DiLeu_BaEn_1 | 478 | 483 | PF01217 | 0.379 |
TRG_DiLeu_BaEn_1 | 567 | 572 | PF01217 | 0.359 |
TRG_DiLeu_BaEn_4 | 295 | 301 | PF01217 | 0.310 |
TRG_DiLeu_BaLyEn_6 | 133 | 138 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.246 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.356 |
TRG_NES_CRM1_1 | 373 | 388 | PF08389 | 0.267 |
TRG_NLS_Bipartite_1 | 15 | 31 | PF00514 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 512 | 517 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P912 | Leptomonas seymouri | 60% | 95% |
A0A1X0NMC1 | Trypanosomatidae | 38% | 94% |
A0A3Q8IJ87 | Leishmania donovani | 93% | 100% |
A0A3S7X658 | Leishmania donovani | 23% | 95% |
A0A422NSE9 | Trypanosoma rangeli | 42% | 100% |
A4HQ91 | Leishmania braziliensis | 75% | 100% |
A4I8G2 | Leishmania infantum | 23% | 72% |
A4IDY9 | Leishmania infantum | 93% | 100% |
D0A420 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 99% |
E9AU09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
O74343 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
Q08647 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q08DI8 | Bos taurus | 30% | 100% |
Q17426 | Caenorhabditis elegans | 27% | 100% |
Q1L8I0 | Danio rerio | 25% | 100% |
Q4Q4T4 | Leishmania major | 22% | 96% |
Q5V1E6 | Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) | 26% | 100% |
Q91VU7 | Mus musculus | 29% | 100% |
Q96PZ0 | Homo sapiens | 30% | 100% |
Q9VSK9 | Drosophila melanogaster | 27% | 93% |
V5BT95 | Trypanosoma cruzi | 42% | 92% |