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: 7 |
NetGPI | no | yes: 0, no: 7 |
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 |
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 | 46 | 50 | PF00656 | 0.397 |
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 520 | 524 | PF00656 | 0.551 |
CLV_C14_Caspase3-7 | 637 | 641 | PF00656 | 0.429 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.815 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 626 | 628 | PF00675 | 0.375 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.823 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 649 | 653 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.371 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.493 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.586 |
DOC_CKS1_1 | 658 | 663 | PF01111 | 0.374 |
DOC_CYCLIN_yCln2_LP_2 | 594 | 600 | PF00134 | 0.660 |
DOC_MAPK_DCC_7 | 314 | 322 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 314 | 322 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 483 | 492 | PF00069 | 0.304 |
DOC_PP1_RVXF_1 | 542 | 549 | PF00149 | 0.696 |
DOC_PP2B_LxvP_1 | 594 | 597 | PF13499 | 0.664 |
DOC_PP4_FxxP_1 | 401 | 404 | PF00568 | 0.457 |
DOC_PP4_FxxP_1 | 559 | 562 | PF00568 | 0.718 |
DOC_PP4_FxxP_1 | 658 | 661 | PF00568 | 0.358 |
DOC_SPAK_OSR1_1 | 63 | 67 | PF12202 | 0.311 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.807 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 722 | 726 | PF00917 | 0.500 |
DOC_USP7_UBL2_3 | 220 | 224 | PF12436 | 0.699 |
DOC_USP7_UBL2_3 | 683 | 687 | PF12436 | 0.429 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 657 | 662 | PF00397 | 0.374 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 483 | 490 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 627 | 631 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 63 | 67 | PF00244 | 0.414 |
LIG_AP2alpha_2 | 399 | 401 | PF02296 | 0.530 |
LIG_BIR_III_4 | 610 | 614 | PF00653 | 0.575 |
LIG_deltaCOP1_diTrp_1 | 120 | 130 | PF00928 | 0.386 |
LIG_deltaCOP1_diTrp_1 | 206 | 213 | PF00928 | 0.540 |
LIG_eIF4E_1 | 437 | 443 | PF01652 | 0.424 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.523 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.486 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.434 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.494 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.486 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.654 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.569 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.604 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.499 |
LIG_FHA_1 | 705 | 711 | PF00498 | 0.384 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.609 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.515 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.489 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.598 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.429 |
LIG_LIR_Apic_2 | 347 | 353 | PF02991 | 0.580 |
LIG_LIR_Apic_2 | 399 | 404 | PF02991 | 0.469 |
LIG_LIR_Apic_2 | 556 | 562 | PF02991 | 0.718 |
LIG_LIR_Gen_1 | 316 | 326 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 355 | 364 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 438 | 447 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 480 | 488 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 516 | 526 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 660 | 671 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 676 | 686 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 717 | 728 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 516 | 521 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 578 | 582 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 629 | 633 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 660 | 666 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 676 | 682 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 717 | 723 | PF02991 | 0.429 |
LIG_PCNA_yPIPBox_3 | 351 | 363 | PF02747 | 0.570 |
LIG_PCNA_yPIPBox_3 | 716 | 728 | PF02747 | 0.212 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.521 |
LIG_Pex14_2 | 626 | 630 | PF04695 | 0.376 |
LIG_Pex14_2 | 642 | 646 | PF04695 | 0.376 |
LIG_Pex14_2 | 709 | 713 | PF04695 | 0.376 |
LIG_REV1ctd_RIR_1 | 135 | 143 | PF16727 | 0.649 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.391 |
LIG_SH2_PTP2 | 358 | 361 | PF00017 | 0.415 |
LIG_SH2_SRC | 679 | 682 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.723 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.429 |
LIG_SH3_2 | 283 | 288 | PF14604 | 0.822 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.542 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.770 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.493 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.716 |
LIG_SUMO_SIM_anti_2 | 30 | 37 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 470 | 476 | PF11976 | 0.497 |
LIG_TRAF2_2 | 549 | 554 | PF00917 | 0.588 |
LIG_TYR_ITIM | 677 | 682 | PF00017 | 0.429 |
LIG_TYR_ITSM | 436 | 443 | PF00017 | 0.477 |
LIG_WRC_WIRS_1 | 105 | 110 | PF05994 | 0.532 |
LIG_WRC_WIRS_1 | 345 | 350 | PF05994 | 0.522 |
LIG_WRC_WIRS_1 | 505 | 510 | PF05994 | 0.513 |
LIG_WRC_WIRS_1 | 639 | 644 | PF05994 | 0.429 |
LIG_WW_3 | 445 | 449 | PF00397 | 0.514 |
MOD_CDC14_SPxK_1 | 217 | 220 | PF00782 | 0.522 |
MOD_CDK_SPK_2 | 214 | 219 | PF00069 | 0.523 |
MOD_CDK_SPxK_1 | 214 | 220 | PF00069 | 0.526 |
MOD_CDK_SPxxK_3 | 238 | 245 | PF00069 | 0.661 |
MOD_CDK_SPxxK_3 | 253 | 260 | PF00069 | 0.545 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.662 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.503 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.763 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.695 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.511 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.482 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.519 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.610 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.485 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.504 |
MOD_Cter_Amidation | 183 | 186 | PF01082 | 0.784 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.841 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.544 |
MOD_GlcNHglycan | 233 | 237 | PF01048 | 0.741 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.738 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.721 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.596 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.580 |
MOD_GlcNHglycan | 648 | 652 | PF01048 | 0.438 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.516 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.602 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.636 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.756 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.488 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.768 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.782 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.608 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.473 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.451 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.509 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.486 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.429 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.228 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.543 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.350 |
MOD_LATS_1 | 25 | 31 | PF00433 | 0.560 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.527 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.809 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.465 |
MOD_N-GLC_1 | 704 | 709 | PF02516 | 0.413 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.523 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.591 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.521 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.517 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.522 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.719 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.571 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.283 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.311 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.459 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.366 |
MOD_OFUCOSY | 69 | 75 | PF10250 | 0.585 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.522 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.593 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.569 |
MOD_PIKK_1 | 722 | 728 | PF00454 | 0.459 |
MOD_PK_1 | 139 | 145 | PF00069 | 0.615 |
MOD_PK_1 | 687 | 693 | PF00069 | 0.500 |
MOD_PKA_1 | 151 | 157 | PF00069 | 0.523 |
MOD_PKA_1 | 224 | 230 | PF00069 | 0.805 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.544 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.657 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.671 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.561 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.406 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.377 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.329 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.615 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.724 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.572 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.595 |
MOD_Plk_1 | 647 | 653 | PF00069 | 0.377 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.413 |
MOD_Plk_2-3 | 78 | 84 | PF00069 | 0.430 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.472 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.478 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.431 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.554 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.380 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.376 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.683 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.555 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.714 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.749 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.642 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.586 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.452 |
MOD_ProDKin_1 | 657 | 663 | PF00069 | 0.374 |
MOD_SUMO_rev_2 | 676 | 685 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 695 | 702 | PF00179 | 0.415 |
TRG_DiLeu_BaEn_1 | 316 | 321 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 96 | 101 | PF01217 | 0.548 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 679 | 682 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I443 | Leptomonas seymouri | 57% | 100% |
A0A3R7L2R2 | Trypanosoma rangeli | 35% | 100% |
A0A3S7X3S1 | Leishmania donovani | 89% | 100% |
A4HIK4 | Leishmania braziliensis | 70% | 97% |
A4I5U9 | Leishmania infantum | 89% | 100% |
Q4Q722 | Leishmania major | 87% | 100% |