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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X7E3
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 10 |
GO:0006623 | protein targeting to vacuole | 5 | 10 |
GO:0006810 | transport | 3 | 10 |
GO:0006886 | intracellular protein transport | 4 | 10 |
GO:0007034 | vacuolar transport | 4 | 10 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0016192 | vesicle-mediated transport | 4 | 10 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0033365 | protein localization to organelle | 5 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0046907 | intracellular transport | 3 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0051649 | establishment of localization in cell | 3 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0072594 | establishment of protein localization to organelle | 4 | 10 |
GO:0072665 | protein localization to vacuole | 6 | 10 |
GO:0072666 | establishment of protein localization to vacuole | 5 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 257 | 261 | PF00656 | 0.649 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 665 | 667 | PF00675 | 0.650 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 665 | 667 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.728 |
DEG_APCC_DBOX_1 | 212 | 220 | PF00400 | 0.589 |
DEG_APCC_DBOX_1 | 96 | 104 | PF00400 | 0.439 |
DEG_SPOP_SBC_1 | 547 | 551 | PF00917 | 0.641 |
DOC_CKS1_1 | 432 | 437 | PF01111 | 0.577 |
DOC_CKS1_1 | 570 | 575 | PF01111 | 0.641 |
DOC_MAPK_gen_1 | 18 | 25 | PF00069 | 0.574 |
DOC_PP1_RVXF_1 | 508 | 514 | PF00149 | 0.687 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.586 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.538 |
DOC_PP4_FxxP_1 | 583 | 586 | PF00568 | 0.707 |
DOC_PP4_FxxP_1 | 590 | 593 | PF00568 | 0.662 |
DOC_SPAK_OSR1_1 | 610 | 614 | PF12202 | 0.528 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 614 | 618 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.688 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 643 | 648 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 107 | 115 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 345 | 353 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 559 | 568 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 610 | 614 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 619 | 624 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 665 | 671 | PF00244 | 0.498 |
LIG_Actin_WH2_2 | 528 | 546 | PF00022 | 0.679 |
LIG_APCC_ABBA_1 | 64 | 69 | PF00400 | 0.554 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.753 |
LIG_CSL_BTD_1 | 337 | 340 | PF09270 | 0.485 |
LIG_EABR_CEP55_1 | 282 | 291 | PF12180 | 0.597 |
LIG_EH_1 | 587 | 591 | PF12763 | 0.737 |
LIG_EH1_1 | 652 | 660 | PF00400 | 0.607 |
LIG_EH1_1 | 668 | 676 | PF00400 | 0.653 |
LIG_eIF4E_1 | 133 | 139 | PF01652 | 0.457 |
LIG_eIF4E_1 | 275 | 281 | PF01652 | 0.558 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.605 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.502 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.344 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.672 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.670 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.691 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.634 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.564 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.407 |
LIG_LIR_Apic_2 | 429 | 435 | PF02991 | 0.538 |
LIG_LIR_Apic_2 | 581 | 586 | PF02991 | 0.699 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 406 | 417 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 272 | 276 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 397 | 402 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 531 | 535 | PF02991 | 0.622 |
LIG_NRBOX | 59 | 65 | PF00104 | 0.594 |
LIG_NRP_CendR_1 | 678 | 679 | PF00754 | 0.635 |
LIG_SH2_CRK | 432 | 436 | PF00017 | 0.555 |
LIG_SH2_CRK | 468 | 472 | PF00017 | 0.625 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.617 |
LIG_SH2_SRC | 414 | 417 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 325 | 329 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 623 | 627 | PF00017 | 0.624 |
LIG_SH2_STAT3 | 539 | 542 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.574 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.609 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.679 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.529 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.700 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.401 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.565 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.653 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.739 |
LIG_SUMO_SIM_anti_2 | 383 | 389 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 637 | 642 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 185 | 191 | PF11976 | 0.572 |
LIG_SUMO_SIM_par_1 | 235 | 240 | PF11976 | 0.557 |
LIG_SUMO_SIM_par_1 | 32 | 37 | PF11976 | 0.473 |
LIG_TYR_ITIM | 466 | 471 | PF00017 | 0.638 |
LIG_UBA3_1 | 270 | 277 | PF00899 | 0.495 |
LIG_UBA3_1 | 63 | 70 | PF00899 | 0.560 |
LIG_WRC_WIRS_1 | 270 | 275 | PF05994 | 0.415 |
MOD_CDK_SPK_2 | 450 | 455 | PF00069 | 0.481 |
MOD_CDK_SPK_2 | 582 | 587 | PF00069 | 0.702 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.627 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.507 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.642 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.444 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.646 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.786 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.554 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.733 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.536 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.559 |
MOD_Cter_Amidation | 16 | 19 | PF01082 | 0.559 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.568 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.644 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.511 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.714 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.444 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.674 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.646 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.632 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.634 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.759 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.641 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.608 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.549 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.593 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.736 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.766 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.344 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.344 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.704 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.544 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.484 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.444 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.444 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.444 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.635 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.665 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.656 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.486 |
MOD_NEK2_2 | 140 | 145 | PF00069 | 0.481 |
MOD_NEK2_2 | 505 | 510 | PF00069 | 0.705 |
MOD_OFUCOSY | 253 | 258 | PF10250 | 0.520 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.369 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.622 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.672 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.818 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.549 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.444 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.656 |
MOD_PKA_2 | 664 | 670 | PF00069 | 0.596 |
MOD_PKB_1 | 107 | 115 | PF00069 | 0.506 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.669 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.369 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.401 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.531 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.594 |
MOD_Plk_2-3 | 380 | 386 | PF00069 | 0.459 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.460 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.454 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.544 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.531 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.593 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.624 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.586 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.602 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.588 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.642 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.614 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.549 |
MOD_ProDKin_1 | 643 | 649 | PF00069 | 0.532 |
MOD_SUMO_rev_2 | 288 | 297 | PF00179 | 0.663 |
MOD_SUMO_rev_2 | 486 | 491 | PF00179 | 0.695 |
TRG_DiLeu_BaEn_1 | 137 | 142 | PF01217 | 0.321 |
TRG_DiLeu_BaEn_1 | 30 | 35 | PF01217 | 0.578 |
TRG_DiLeu_BaEn_4 | 380 | 386 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 507 | 512 | PF01217 | 0.686 |
TRG_DiLeu_BaLyEn_6 | 516 | 521 | PF01217 | 0.664 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.625 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 407 | 409 | PF00400 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 332 | 336 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 510 | 514 | PF00026 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 672 | 677 | PF00026 | 0.611 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKG6 | Leptomonas seymouri | 54% | 95% |
A0A1X0P9E4 | Trypanosomatidae | 27% | 94% |
A0A422N7B5 | Trypanosoma rangeli | 24% | 95% |
A4H7E1 | Leishmania braziliensis | 78% | 100% |
A4I9J9 | Leishmania infantum | 100% | 100% |
E9B4J7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q3H9 | Leishmania major | 89% | 100% |
V5BM77 | Trypanosoma cruzi | 25% | 93% |