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 | 499 | 503 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 518 | 522 | PF00656 | 0.439 |
CLV_C14_Caspase3-7 | 616 | 620 | PF00656 | 0.357 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.416 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.312 |
DEG_APCC_KENBOX_2 | 170 | 174 | PF00400 | 0.522 |
DEG_SPOP_SBC_1 | 142 | 146 | PF00917 | 0.521 |
DEG_SPOP_SBC_1 | 214 | 218 | PF00917 | 0.586 |
DOC_CYCLIN_yCln2_LP_2 | 293 | 299 | PF00134 | 0.311 |
DOC_CYCLIN_yCln2_LP_2 | 573 | 579 | PF00134 | 0.589 |
DOC_MAPK_DCC_7 | 266 | 276 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 263 | 273 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 4 | 11 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.510 |
DOC_PP2B_LxvP_1 | 573 | 576 | PF13499 | 0.588 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.392 |
DOC_PP4_FxxP_1 | 538 | 541 | PF00568 | 0.637 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 701 | 705 | PF00917 | 0.416 |
DOC_USP7_MATH_2 | 285 | 291 | PF00917 | 0.387 |
DOC_USP7_UBL2_3 | 202 | 206 | PF12436 | 0.609 |
DOC_USP7_UBL2_3 | 662 | 666 | PF12436 | 0.357 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 413 | 419 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 532 | 542 | PF00244 | 0.516 |
LIG_Actin_WH2_2 | 26 | 43 | PF00022 | 0.485 |
LIG_AP2alpha_2 | 378 | 380 | PF02296 | 0.466 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.623 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.317 |
LIG_CtBP_PxDLS_1 | 285 | 289 | PF00389 | 0.403 |
LIG_deltaCOP1_diTrp_1 | 120 | 130 | PF00928 | 0.352 |
LIG_eIF4E_1 | 416 | 422 | PF01652 | 0.356 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.663 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.457 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.504 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.377 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.445 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.468 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.533 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.545 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.332 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.650 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.555 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.462 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.444 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.475 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.434 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.394 |
LIG_LIR_Apic_2 | 326 | 332 | PF02991 | 0.526 |
LIG_LIR_Apic_2 | 378 | 383 | PF02991 | 0.403 |
LIG_LIR_Apic_2 | 535 | 541 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 295 | 305 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 335 | 343 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 417 | 425 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 459 | 467 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 639 | 650 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 655 | 665 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 696 | 707 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 417 | 422 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 459 | 463 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 557 | 561 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 639 | 645 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 655 | 661 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 696 | 702 | PF02991 | 0.357 |
LIG_LRP6_Inhibitor_1 | 350 | 356 | PF00058 | 0.262 |
LIG_MLH1_MIPbox_1 | 112 | 116 | PF16413 | 0.317 |
LIG_PCNA_yPIPBox_3 | 168 | 180 | PF02747 | 0.519 |
LIG_PCNA_yPIPBox_3 | 330 | 342 | PF02747 | 0.444 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.465 |
LIG_Pex14_2 | 605 | 609 | PF04695 | 0.392 |
LIG_Pex14_2 | 621 | 625 | PF04695 | 0.298 |
LIG_Pex14_2 | 688 | 692 | PF04695 | 0.298 |
LIG_REV1ctd_RIR_1 | 113 | 121 | PF16727 | 0.330 |
LIG_REV1ctd_RIR_1 | 135 | 141 | PF16727 | 0.516 |
LIG_RPA_C_Fungi | 200 | 212 | PF08784 | 0.517 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.322 |
LIG_SH2_CRK | 699 | 703 | PF00017 | 0.346 |
LIG_SH2_NCK_1 | 419 | 423 | PF00017 | 0.405 |
LIG_SH2_PTP2 | 337 | 340 | PF00017 | 0.341 |
LIG_SH2_SRC | 658 | 661 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 416 | 420 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 699 | 703 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.368 |
LIG_SH3_2 | 262 | 267 | PF14604 | 0.689 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.682 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.560 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.334 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.329 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.664 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.446 |
LIG_SUMO_SIM_anti_2 | 30 | 37 | PF11976 | 0.495 |
LIG_SUMO_SIM_anti_2 | 97 | 102 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 449 | 455 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 586 | 591 | PF11976 | 0.440 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.310 |
LIG_TRAF2_1 | 443 | 446 | PF00917 | 0.302 |
LIG_TRAF2_1 | 528 | 531 | PF00917 | 0.641 |
LIG_TYR_ITIM | 656 | 661 | PF00017 | 0.371 |
LIG_TYR_ITSM | 415 | 422 | PF00017 | 0.415 |
LIG_Vh1_VBS_1 | 54 | 72 | PF01044 | 0.317 |
LIG_WRC_WIRS_1 | 105 | 110 | PF05994 | 0.476 |
LIG_WRC_WIRS_1 | 324 | 329 | PF05994 | 0.457 |
LIG_WRC_WIRS_1 | 484 | 489 | PF05994 | 0.432 |
LIG_WRC_WIRS_1 | 618 | 623 | PF05994 | 0.357 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.522 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.499 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.740 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.530 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.636 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.427 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.695 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.493 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.592 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.376 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.502 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.703 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.410 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.451 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.483 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.610 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.436 |
MOD_Cter_Amidation | 180 | 183 | PF01082 | 0.581 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.518 |
MOD_GlcNHglycan | 155 | 159 | PF01048 | 0.463 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.465 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.794 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.468 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.648 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.664 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.557 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.450 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.519 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.582 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.608 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.642 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.414 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.735 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.617 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.437 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.433 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.375 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.459 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.476 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.466 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.381 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.319 |
MOD_LATS_1 | 25 | 31 | PF00433 | 0.488 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.417 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.375 |
MOD_N-GLC_1 | 683 | 688 | PF02516 | 0.357 |
MOD_N-GLC_2 | 71 | 73 | PF02516 | 0.298 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.470 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.481 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.454 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.437 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.521 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.362 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.318 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.380 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.400 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.327 |
MOD_NEK2_2 | 522 | 527 | PF00069 | 0.486 |
MOD_OFUCOSY | 69 | 75 | PF10250 | 0.473 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.464 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.514 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.679 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.581 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.541 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.483 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.315 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.568 |
MOD_PIKK_1 | 701 | 707 | PF00454 | 0.371 |
MOD_PK_1 | 666 | 672 | PF00069 | 0.371 |
MOD_PKA_1 | 182 | 188 | PF00069 | 0.514 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.665 |
MOD_PKA_1 | 267 | 273 | PF00069 | 0.517 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.598 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.332 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.384 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.447 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.455 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.653 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.573 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.379 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.384 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.464 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.518 |
MOD_Plk_1 | 626 | 632 | PF00069 | 0.333 |
MOD_Plk_1 | 683 | 689 | PF00069 | 0.398 |
MOD_Plk_2-3 | 78 | 84 | PF00069 | 0.374 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.335 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.397 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.424 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.406 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.363 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.562 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.341 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.307 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.623 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.635 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.427 |
MOD_SUMO_rev_2 | 185 | 195 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 655 | 664 | PF00179 | 0.357 |
TRG_DiLeu_BaEn_1 | 190 | 195 | PF01217 | 0.518 |
TRG_DiLeu_BaEn_1 | 295 | 300 | PF01217 | 0.396 |
TRG_DiLeu_BaEn_1 | 97 | 102 | PF01217 | 0.438 |
TRG_DiLeu_BaEn_3 | 445 | 451 | PF01217 | 0.270 |
TRG_DiLeu_BaEn_4 | 286 | 292 | PF01217 | 0.379 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 699 | 702 | PF00928 | 0.287 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 605 | 607 | PF00400 | 0.317 |
TRG_NLS_MonoExtC_3 | 201 | 206 | PF00514 | 0.668 |
TRG_NLS_MonoExtN_4 | 202 | 209 | PF00514 | 0.594 |
TRG_NLS_MonoExtN_4 | 263 | 270 | PF00514 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I443 | Leptomonas seymouri | 54% | 98% |
A0A3R7L2R2 | Trypanosoma rangeli | 34% | 100% |
A0A3S7X3S1 | Leishmania donovani | 69% | 97% |
A4I5U9 | Leishmania infantum | 69% | 97% |
E9B144 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 97% |
Q4Q722 | Leishmania major | 69% | 100% |