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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q3P1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.517 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.710 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 597 | 599 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.617 |
CLV_Separin_Metazoa | 606 | 610 | PF03568 | 0.472 |
DOC_AGCK_PIF_1 | 599 | 604 | PF00069 | 0.519 |
DOC_ANK_TNKS_1 | 550 | 557 | PF00023 | 0.484 |
DOC_MAPK_gen_1 | 263 | 270 | PF00069 | 0.657 |
DOC_MAPK_gen_1 | 416 | 426 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 419 | 428 | PF00069 | 0.491 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.713 |
DOC_USP7_UBL2_3 | 265 | 269 | PF12436 | 0.720 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.587 |
DOC_USP7_UBL2_3 | 348 | 352 | PF12436 | 0.573 |
DOC_USP7_UBL2_3 | 507 | 511 | PF12436 | 0.393 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.494 |
LIG_14-3-3_CanoR_1 | 194 | 204 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 263 | 270 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.718 |
LIG_Actin_WH2_2 | 423 | 440 | PF00022 | 0.487 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.560 |
LIG_CaM_IQ_9 | 399 | 414 | PF13499 | 0.516 |
LIG_Clathr_ClatBox_1 | 324 | 328 | PF01394 | 0.348 |
LIG_Clathr_ClatBox_1 | 468 | 472 | PF01394 | 0.508 |
LIG_CtBP_PxDLS_1 | 31 | 35 | PF00389 | 0.529 |
LIG_DLG_GKlike_1 | 36 | 43 | PF00625 | 0.661 |
LIG_EH1_1 | 318 | 326 | PF00400 | 0.380 |
LIG_eIF4E_1 | 319 | 325 | PF01652 | 0.377 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.617 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.683 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.491 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.472 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.724 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.734 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.532 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.478 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.502 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.473 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.548 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.453 |
LIG_LIR_Gen_1 | 452 | 458 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.736 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.520 |
LIG_PCNA_yPIPBox_3 | 312 | 325 | PF02747 | 0.419 |
LIG_REV1ctd_RIR_1 | 501 | 511 | PF16727 | 0.362 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.591 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.707 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.646 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.412 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.404 |
LIG_SUMO_SIM_anti_2 | 323 | 328 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 323 | 328 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 334 | 340 | PF11976 | 0.388 |
LIG_TRAF2_1 | 514 | 517 | PF00917 | 0.520 |
LIG_UBA3_1 | 468 | 474 | PF00899 | 0.456 |
LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.689 |
LIG_WRC_WIRS_1 | 483 | 488 | PF05994 | 0.429 |
LIG_WW_3 | 589 | 593 | PF00397 | 0.448 |
MOD_CDC14_SPxK_1 | 545 | 548 | PF00782 | 0.507 |
MOD_CDK_SPxK_1 | 542 | 548 | PF00069 | 0.528 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.700 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.734 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.686 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.676 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.476 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.466 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.439 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.405 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.431 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.470 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.467 |
MOD_CK2_1 | 641 | 647 | PF00069 | 0.527 |
MOD_Cter_Amidation | 232 | 235 | PF01082 | 0.680 |
MOD_Cter_Amidation | 349 | 352 | PF01082 | 0.582 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.655 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.796 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.592 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.681 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.543 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.390 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.641 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.401 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.462 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.531 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.616 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.758 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.622 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.716 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.675 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.631 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.796 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.724 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.640 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.607 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.415 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.768 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.462 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.485 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.520 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.551 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.716 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.703 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.669 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.686 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.748 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.698 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.637 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.732 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.350 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.409 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.628 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.510 |
MOD_NEK2_2 | 148 | 153 | PF00069 | 0.689 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.583 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.541 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.745 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.485 |
MOD_PKA_1 | 263 | 269 | PF00069 | 0.697 |
MOD_PKA_1 | 351 | 357 | PF00069 | 0.487 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.643 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.694 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.765 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.684 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.351 |
MOD_Plk_1 | 600 | 606 | PF00069 | 0.522 |
MOD_Plk_2-3 | 334 | 340 | PF00069 | 0.410 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.593 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.626 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.638 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.680 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.583 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.776 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.346 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.525 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.374 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.452 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.742 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.421 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.537 |
MOD_ProDKin_1 | 642 | 648 | PF00069 | 0.501 |
MOD_SUMO_rev_2 | 266 | 270 | PF00179 | 0.713 |
MOD_SUMO_rev_2 | 285 | 290 | PF00179 | 0.777 |
MOD_SUMO_rev_2 | 575 | 583 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 615 | 624 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 633 | 642 | PF00179 | 0.407 |
TRG_DiLeu_BaEn_4 | 515 | 521 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.727 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.629 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.750 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.715 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 604 | 607 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.729 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.648 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.558 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF45 | Leptomonas seymouri | 63% | 76% |
A0A1X0NRD1 | Trypanosomatidae | 42% | 80% |
A0A1X0NST4 | Trypanosomatidae | 31% | 80% |
A0A3Q8II25 | Leishmania donovani | 33% | 93% |
A0A3S7X791 | Leishmania donovani | 95% | 100% |
A4HM05 | Leishmania braziliensis | 79% | 100% |
A4HM06 | Leishmania braziliensis | 34% | 100% |
A4I9D6 | Leishmania infantum | 95% | 100% |
A4I9D8 | Leishmania infantum | 33% | 100% |
C9ZJQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 86% |
E9B4D6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B4D7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
V5B7N5 | Trypanosoma cruzi | 26% | 100% |
V5D844 | Trypanosoma cruzi | 38% | 100% |