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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0044232 | organelle membrane contact site | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140268 | endoplasmic reticulum-plasma membrane contact site | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7X3S1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006869 | lipid transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015850 | organic hydroxy compound transport | 5 | 1 |
GO:0015918 | sterol transport | 6 | 1 |
GO:0032365 | intracellular lipid transport | 4 | 1 |
GO:0032366 | intracellular sterol transport | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0005319 | lipid transporter activity | 2 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005496 | steroid binding | 3 | 1 |
GO:0008289 | lipid binding | 2 | 1 |
GO:0015248 | sterol transporter activity | 3 | 1 |
GO:0032934 | sterol binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0120013 | lipid transfer activity | 3 | 1 |
GO:0120015 | sterol transfer activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 520 | 524 | PF00656 | 0.564 |
CLV_C14_Caspase3-7 | 637 | 641 | PF00656 | 0.438 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.794 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 626 | 628 | PF00675 | 0.356 |
CLV_PCSK_FUR_1 | 532 | 536 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 245 | 247 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.763 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.765 |
CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.341 |
DOC_CKS1_1 | 658 | 663 | PF01111 | 0.349 |
DOC_CYCLIN_yCln2_LP_2 | 594 | 600 | PF00134 | 0.677 |
DOC_PP1_RVXF_1 | 542 | 549 | PF00149 | 0.688 |
DOC_PP2B_LxvP_1 | 594 | 597 | PF13499 | 0.671 |
DOC_PP4_FxxP_1 | 401 | 404 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 559 | 562 | PF00568 | 0.720 |
DOC_PP4_FxxP_1 | 658 | 661 | PF00568 | 0.373 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 722 | 726 | PF00917 | 0.438 |
DOC_USP7_UBL2_3 | 219 | 223 | PF12436 | 0.696 |
DOC_USP7_UBL2_3 | 683 | 687 | PF12436 | 0.438 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 657 | 662 | PF00397 | 0.349 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 627 | 631 | PF00244 | 0.324 |
LIG_Actin_WH2_2 | 26 | 43 | PF00022 | 0.595 |
LIG_AP2alpha_2 | 399 | 401 | PF02296 | 0.548 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.712 |
LIG_BIR_III_4 | 328 | 332 | PF00653 | 0.469 |
LIG_BIR_III_4 | 610 | 614 | PF00653 | 0.562 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.394 |
LIG_eIF4E_1 | 437 | 443 | PF01652 | 0.414 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.632 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.532 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.392 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.484 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.492 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.665 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.496 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.544 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.560 |
LIG_FHA_1 | 705 | 711 | PF00498 | 0.435 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.730 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.599 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.516 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.515 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.572 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.505 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.604 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.438 |
LIG_LIR_Apic_2 | 347 | 353 | PF02991 | 0.600 |
LIG_LIR_Apic_2 | 399 | 404 | PF02991 | 0.496 |
LIG_LIR_Apic_2 | 556 | 562 | PF02991 | 0.717 |
LIG_LIR_Gen_1 | 316 | 326 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 355 | 364 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 438 | 447 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 480 | 489 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 516 | 526 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 660 | 671 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 676 | 686 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 717 | 728 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 516 | 521 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 629 | 633 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 660 | 666 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 676 | 682 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 717 | 723 | PF02991 | 0.438 |
LIG_PCNA_yPIPBox_3 | 351 | 363 | PF02747 | 0.566 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.553 |
LIG_Pex14_2 | 626 | 630 | PF04695 | 0.357 |
LIG_Pex14_2 | 642 | 646 | PF04695 | 0.357 |
LIG_Pex14_2 | 709 | 713 | PF04695 | 0.357 |
LIG_REV1ctd_RIR_1 | 135 | 143 | PF16727 | 0.664 |
LIG_SH2_CRK | 543 | 547 | PF00017 | 0.546 |
LIG_SH2_CRK | 720 | 724 | PF00017 | 0.430 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.578 |
LIG_SH2_NCK_1 | 440 | 444 | PF00017 | 0.511 |
LIG_SH2_PTP2 | 358 | 361 | PF00017 | 0.399 |
LIG_SH2_SRC | 679 | 682 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.725 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 720 | 724 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.391 |
LIG_SH3_2 | 283 | 288 | PF14604 | 0.817 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.809 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.491 |
LIG_SUMO_SIM_anti_2 | 30 | 37 | PF11976 | 0.608 |
LIG_SUMO_SIM_par_1 | 470 | 476 | PF11976 | 0.511 |
LIG_TRAF2_1 | 549 | 552 | PF00917 | 0.723 |
LIG_TYR_ITIM | 677 | 682 | PF00017 | 0.491 |
LIG_TYR_ITSM | 436 | 443 | PF00017 | 0.447 |
LIG_WRC_WIRS_1 | 105 | 110 | PF05994 | 0.566 |
LIG_WRC_WIRS_1 | 345 | 350 | PF05994 | 0.545 |
LIG_WRC_WIRS_1 | 505 | 510 | PF05994 | 0.520 |
LIG_WRC_WIRS_1 | 639 | 644 | PF05994 | 0.391 |
LIG_WW_3 | 445 | 449 | PF00397 | 0.590 |
MOD_CDK_SPxxK_3 | 238 | 245 | PF00069 | 0.666 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.561 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.766 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.748 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.517 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.605 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.556 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.715 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.522 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.520 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.621 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.534 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.564 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.513 |
MOD_Cter_Amidation | 183 | 186 | PF01082 | 0.756 |
MOD_Cter_Amidation | 220 | 223 | PF01082 | 0.677 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.678 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.807 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.555 |
MOD_GlcNHglycan | 233 | 237 | PF01048 | 0.801 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.728 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.703 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.563 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.569 |
MOD_GlcNHglycan | 648 | 652 | PF01048 | 0.429 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.414 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.552 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.564 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.615 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.739 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.744 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.734 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.499 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.736 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.501 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.664 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.490 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.511 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.557 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.438 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.532 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.336 |
MOD_GSK3_1 | 718 | 725 | PF00069 | 0.351 |
MOD_LATS_1 | 25 | 31 | PF00433 | 0.571 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.564 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.524 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.504 |
MOD_N-GLC_1 | 704 | 709 | PF02516 | 0.438 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.557 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.570 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.523 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.526 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.541 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.698 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.563 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.288 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.363 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.464 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.336 |
MOD_NEK2_2 | 177 | 182 | PF00069 | 0.607 |
MOD_OFUCOSY | 69 | 75 | PF10250 | 0.594 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.553 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.795 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.571 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.640 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.557 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.556 |
MOD_PIKK_1 | 722 | 728 | PF00454 | 0.438 |
MOD_PK_1 | 139 | 145 | PF00069 | 0.631 |
MOD_PK_1 | 687 | 693 | PF00069 | 0.491 |
MOD_PKA_1 | 224 | 230 | PF00069 | 0.771 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.581 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.641 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.560 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.351 |
MOD_PKB_1 | 168 | 176 | PF00069 | 0.599 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.697 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.705 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.572 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.572 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.438 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.522 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.470 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.433 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.421 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.502 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.601 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.399 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.357 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.769 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.658 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.617 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.470 |
MOD_ProDKin_1 | 657 | 663 | PF00069 | 0.349 |
MOD_SUMO_rev_2 | 676 | 685 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 695 | 702 | PF00179 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 357 | 362 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 96 | 101 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 679 | 682 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 720 | 723 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.769 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 532 | 535 | PF00400 | 0.559 |
TRG_NLS_MonoCore_2 | 221 | 226 | PF00514 | 0.708 |
TRG_NLS_MonoExtC_3 | 218 | 223 | PF00514 | 0.723 |
TRG_NLS_MonoExtN_4 | 218 | 223 | PF00514 | 0.679 |
TRG_NLS_MonoExtN_4 | 532 | 539 | PF00514 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.622 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I443 | Leptomonas seymouri | 57% | 100% |
A0A3R7L2R2 | Trypanosoma rangeli | 35% | 100% |
A4HIK4 | Leishmania braziliensis | 69% | 97% |
A4I5U9 | Leishmania infantum | 100% | 100% |
E9B144 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q722 | Leishmania major | 90% | 100% |
V5B7B2 | Trypanosoma cruzi | 37% | 100% |