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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QD72
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 12 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 591 | 595 | PF00656 | 0.761 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.508 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.442 |
DEG_APCC_DBOX_1 | 341 | 349 | PF00400 | 0.622 |
DEG_SPOP_SBC_1 | 479 | 483 | PF00917 | 0.670 |
DEG_SPOP_SBC_1 | 7 | 11 | PF00917 | 0.775 |
DOC_CYCLIN_RxL_1 | 244 | 254 | PF00134 | 0.413 |
DOC_MAPK_gen_1 | 105 | 117 | PF00069 | 0.581 |
DOC_MAPK_gen_1 | 393 | 400 | PF00069 | 0.694 |
DOC_MAPK_HePTP_8 | 390 | 402 | PF00069 | 0.709 |
DOC_MAPK_MEF2A_6 | 393 | 402 | PF00069 | 0.648 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.413 |
DOC_PP4_FxxP_1 | 542 | 545 | PF00568 | 0.677 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.317 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.745 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 531 | 537 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 547 | 551 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 553 | 558 | PF00244 | 0.604 |
LIG_Actin_WH2_2 | 333 | 348 | PF00022 | 0.666 |
LIG_BRCT_BRCA1_1 | 498 | 502 | PF00533 | 0.732 |
LIG_BRCT_BRCA1_1 | 581 | 585 | PF00533 | 0.547 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.387 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.438 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.596 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.645 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.633 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.789 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.700 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.404 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.410 |
LIG_FHA_2 | 589 | 595 | PF00498 | 0.721 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.601 |
LIG_LIR_Apic_2 | 454 | 459 | PF02991 | 0.583 |
LIG_LIR_Apic_2 | 541 | 545 | PF02991 | 0.701 |
LIG_LIR_Gen_1 | 145 | 156 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 216 | 223 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 445 | 452 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 538 | 546 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 83 | 93 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 97 | 103 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 538 | 542 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.344 |
LIG_PCNA_yPIPBox_3 | 229 | 237 | PF02747 | 0.347 |
LIG_Pex14_2 | 397 | 401 | PF04695 | 0.650 |
LIG_SH2_GRB2like | 327 | 330 | PF00017 | 0.662 |
LIG_SH2_NCK_1 | 418 | 422 | PF00017 | 0.664 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.396 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.662 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.754 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.364 |
LIG_SUMO_SIM_anti_2 | 428 | 435 | PF11976 | 0.619 |
LIG_SUMO_SIM_anti_2 | 77 | 83 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 413 | 420 | PF11976 | 0.608 |
LIG_SUMO_SIM_par_1 | 448 | 454 | PF11976 | 0.693 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.568 |
LIG_TRAF2_1 | 535 | 538 | PF00917 | 0.668 |
LIG_TRAF2_1 | 549 | 552 | PF00917 | 0.481 |
LIG_TYR_ITIM | 416 | 421 | PF00017 | 0.654 |
LIG_TYR_ITIM | 96 | 101 | PF00017 | 0.328 |
LIG_WRC_WIRS_1 | 539 | 544 | PF05994 | 0.695 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.577 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.788 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.695 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.794 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.731 |
MOD_CK1_1 | 559 | 565 | PF00069 | 0.666 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.800 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.605 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.282 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.464 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.781 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.734 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.664 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.467 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.664 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.372 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.777 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.329 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.575 |
MOD_GlcNHglycan | 331 | 336 | PF01048 | 0.482 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.565 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.437 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.459 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.589 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.385 |
MOD_GlcNHglycan | 509 | 513 | PF01048 | 0.489 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.457 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.522 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.543 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.548 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.519 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.327 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.559 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.599 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.787 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.748 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.640 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.653 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.635 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.678 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.674 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.337 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.727 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.723 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.512 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.540 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.540 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.342 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.476 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.328 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.476 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.706 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.387 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.651 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.465 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.624 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.681 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.639 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.777 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.711 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.668 |
MOD_Plk_2-3 | 568 | 574 | PF00069 | 0.647 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.369 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.385 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.467 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.564 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.644 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.536 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.819 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.745 |
TRG_DiLeu_BaEn_1 | 428 | 433 | PF01217 | 0.666 |
TRG_DiLeu_BaLyEn_6 | 576 | 581 | PF01217 | 0.614 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.664 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.562 |
TRG_NLS_MonoExtC_3 | 104 | 109 | PF00514 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 439 | 444 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHD4 | Leptomonas seymouri | 61% | 97% |
A0A0S4IWL9 | Bodo saltans | 36% | 100% |
A0A1X0P615 | Trypanosomatidae | 49% | 100% |
A0A3Q8IBF0 | Leishmania donovani | 94% | 100% |
A0A3R7MPI1 | Trypanosoma rangeli | 44% | 100% |
A4HA88 | Leishmania braziliensis | 78% | 100% |
A4HYG8 | Leishmania infantum | 94% | 100% |
D0A0T8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AS92 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B132 | Trypanosoma cruzi | 45% | 100% |