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:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 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 |
Related structures:
AlphaFold database: A4I7T1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043022 | ribosome binding | 4 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 346 | 350 | PF00656 | 0.716 |
CLV_C14_Caspase3-7 | 352 | 356 | PF00656 | 0.711 |
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.727 |
CLV_C14_Caspase3-7 | 543 | 547 | PF00656 | 0.496 |
CLV_C14_Caspase3-7 | 636 | 640 | PF00656 | 0.376 |
CLV_C14_Caspase3-7 | 76 | 80 | PF00656 | 0.706 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.595 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 183 | 191 | PF00400 | 0.448 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.518 |
DEG_SPOP_SBC_1 | 461 | 465 | PF00917 | 0.651 |
DOC_ANK_TNKS_1 | 321 | 328 | PF00023 | 0.563 |
DOC_CYCLIN_RxL_1 | 221 | 232 | PF00134 | 0.320 |
DOC_MAPK_gen_1 | 322 | 330 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 391 | 401 | PF00069 | 0.432 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.692 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 204 | 209 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 240 | 245 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 269 | 278 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 322 | 330 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 382 | 392 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 511 | 519 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 540 | 548 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 569 | 574 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 63 | 71 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.661 |
LIG_14-3-3_CterR_2 | 681 | 684 | PF00244 | 0.524 |
LIG_APCC_ABBA_1 | 646 | 651 | PF00400 | 0.378 |
LIG_BIR_III_2 | 79 | 83 | PF00653 | 0.597 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.465 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.740 |
LIG_BRCT_BRCA1_1 | 640 | 644 | PF00533 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 120 | 130 | PF00928 | 0.431 |
LIG_EVH1_2 | 95 | 99 | PF00568 | 0.542 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.516 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.312 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.252 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.546 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.390 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.490 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.379 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.454 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.341 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.372 |
LIG_FHA_1 | 661 | 667 | PF00498 | 0.460 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.746 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.516 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.484 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.592 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.508 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.425 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.514 |
LIG_LIR_Apic_2 | 417 | 423 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 177 | 188 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 2 | 9 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 239 | 250 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 407 | 415 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 501 | 510 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 514 | 524 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 578 | 586 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 407 | 411 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 501 | 506 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 514 | 519 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 578 | 582 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.376 |
LIG_MYND_1 | 92 | 96 | PF01753 | 0.496 |
LIG_NRBOX | 505 | 511 | PF00104 | 0.452 |
LIG_RPA_C_Fungi | 317 | 329 | PF08784 | 0.502 |
LIG_SH2_CRK | 408 | 412 | PF00017 | 0.404 |
LIG_SH2_PTP2 | 420 | 423 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 579 | 583 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 599 | 603 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 614 | 618 | PF00017 | 0.386 |
LIG_SH2_STAT3 | 108 | 111 | PF00017 | 0.515 |
LIG_SH2_STAT3 | 588 | 591 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.439 |
LIG_SH3_2 | 92 | 97 | PF14604 | 0.548 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.500 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.557 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.624 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.579 |
LIG_SUMO_SIM_anti_2 | 615 | 620 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 615 | 620 | PF11976 | 0.430 |
LIG_TRAF2_1 | 426 | 429 | PF00917 | 0.552 |
LIG_TRAF2_2 | 192 | 197 | PF00917 | 0.542 |
LIG_TYR_ITIM | 406 | 411 | PF00017 | 0.413 |
LIG_UBA3_1 | 298 | 304 | PF00899 | 0.508 |
LIG_UBA3_1 | 395 | 403 | PF00899 | 0.477 |
LIG_UBA3_1 | 506 | 513 | PF00899 | 0.408 |
LIG_WRC_WIRS_1 | 659 | 664 | PF05994 | 0.521 |
LIG_WW_3 | 190 | 194 | PF00397 | 0.522 |
LIG_WW_3 | 94 | 98 | PF00397 | 0.545 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.572 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.600 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.420 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.721 |
MOD_CK1_1 | 559 | 565 | PF00069 | 0.652 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.733 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.591 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.610 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.570 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.460 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.458 |
MOD_CMANNOS | 570 | 573 | PF00535 | 0.455 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.398 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.674 |
MOD_GlcNHglycan | 345 | 349 | PF01048 | 0.809 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.638 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.634 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.653 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.473 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.616 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.664 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.606 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.705 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.637 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.539 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.525 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.566 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.424 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.644 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.754 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.597 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.446 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.708 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.480 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.641 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.598 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.363 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.414 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.304 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.287 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.544 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.504 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.550 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.446 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.516 |
MOD_NEK2_2 | 449 | 454 | PF00069 | 0.527 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.740 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.712 |
MOD_PK_1 | 204 | 210 | PF00069 | 0.499 |
MOD_PK_1 | 240 | 246 | PF00069 | 0.428 |
MOD_PKA_1 | 268 | 274 | PF00069 | 0.468 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.576 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.628 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.322 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.462 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.528 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.719 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.506 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.520 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.635 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.500 |
MOD_PKA_2 | 607 | 613 | PF00069 | 0.429 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.663 |
MOD_PKB_1 | 674 | 682 | PF00069 | 0.475 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.461 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.665 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.457 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.541 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.476 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.542 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.589 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.481 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.601 |
TRG_DiLeu_BaEn_1 | 505 | 510 | PF01217 | 0.443 |
TRG_DiLeu_BaEn_2 | 175 | 181 | PF01217 | 0.375 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 614 | 617 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 649 | 652 | PF00928 | 0.370 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 652 | 654 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.622 |
TRG_NES_CRM1_1 | 390 | 404 | PF08389 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 286 | 290 | PF00026 | 0.655 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGR3 | Leptomonas seymouri | 48% | 91% |
A0A1X0NVZ4 | Trypanosomatidae | 30% | 100% |
A0A3Q8IG45 | Leishmania donovani | 99% | 100% |
A0A3R7NTQ6 | Trypanosoma rangeli | 32% | 100% |
A4HKA1 | Leishmania braziliensis | 68% | 100% |
D0A9Z2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B2N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q5G8 | Leishmania major | 88% | 100% |
V5BQR4 | Trypanosoma cruzi | 30% | 100% |