by homology
Contact email: handman@wehi.edu.au
Publication title: A Leucine-Rich Repeat Motif of Leishmania Parasite Surface Antigen 2 Binds to Macrophages through the Complement Receptor 3
Publication 1st author(s): Kedzierski
Publication Identifier(s): 15067069
Host organism: -1
Interaction detection method(s): fluorescence activated cell sorting
Interaction type: physical association
Identification method participant A: identification by antibody
Identification method participant B: identification by antibody
ID(s) interactor A: P11215
ID(s) interactor B: E9AGG4
Taxid interactor A: Homo sapiens
Taxid interactor B: Leishmania infantum
Biological role(s) interactor A: unspecified role
Biological role(s) interactor B: unspecified role
Experimental role(s) interactor A: unspecified role
                
| 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. | yes | yes: 105 | 
| 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 | yes | yes: 39, no: 4 | 
| NetGPI | no | yes: 0, no: 43 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005929 | cilium | 4 | 44 | 
| GO:0016020 | membrane | 2 | 26 | 
| GO:0042995 | cell projection | 2 | 44 | 
| GO:0043226 | organelle | 2 | 44 | 
| GO:0043227 | membrane-bounded organelle | 3 | 44 | 
| GO:0110165 | cellular anatomical entity | 1 | 44 | 
| GO:0120025 | plasma membrane bounded cell projection | 3 | 44 | 
| GO:0005886 | plasma membrane | 3 | 6 | 
Related structures:
AlphaFold database: Q4QGK4
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 3 | 
| GO:0004672 | protein kinase activity | 3 | 3 | 
| GO:0004674 | protein serine/threonine kinase activity | 4 | 3 | 
| GO:0016301 | kinase activity | 4 | 3 | 
| GO:0016740 | transferase activity | 2 | 3 | 
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 3 | 
| GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 3 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 3 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.467 | 
| CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.480 | 
| CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.490 | 
| CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.511 | 
| CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.684 | 
| CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.462 | 
| CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.475 | 
| CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.489 | 
| CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.684 | 
| CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.462 | 
| CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.652 | 
| CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.503 | 
| CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.483 | 
| CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.592 | 
| CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.510 | 
| CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.666 | 
| DEG_SCF_FBW7_2 | 596 | 601 | PF00400 | 0.474 | 
| DEG_SPOP_SBC_1 | 449 | 453 | PF00917 | 0.463 | 
| DEG_SPOP_SBC_1 | 464 | 468 | PF00917 | 0.576 | 
| DEG_SPOP_SBC_1 | 474 | 478 | PF00917 | 0.540 | 
| DEG_SPOP_SBC_1 | 489 | 493 | PF00917 | 0.431 | 
| DEG_SPOP_SBC_1 | 499 | 503 | PF00917 | 0.528 | 
| DEG_SPOP_SBC_1 | 509 | 513 | PF00917 | 0.529 | 
| DEG_SPOP_SBC_1 | 524 | 528 | PF00917 | 0.428 | 
| DEG_SPOP_SBC_1 | 539 | 543 | PF00917 | 0.435 | 
| DEG_SPOP_SBC_1 | 554 | 558 | PF00917 | 0.547 | 
| DEG_SPOP_SBC_1 | 566 | 570 | PF00917 | 0.470 | 
| DEG_SPOP_SBC_1 | 576 | 580 | PF00917 | 0.489 | 
| DOC_CYCLIN_RxL_1 | 162 | 172 | PF00134 | 0.319 | 
| DOC_CYCLIN_RxL_1 | 210 | 218 | PF00134 | 0.268 | 
| DOC_CYCLIN_RxL_1 | 226 | 237 | PF00134 | 0.266 | 
| DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.545 | 
| DOC_CYCLIN_RxL_1 | 373 | 384 | PF00134 | 0.287 | 
| DOC_CYCLIN_yClb5_NLxxxL_5 | 236 | 245 | PF00134 | 0.296 | 
| DOC_CYCLIN_yCln2_LP_2 | 196 | 199 | PF00134 | 0.273 | 
| DOC_CYCLIN_yCln2_LP_2 | 217 | 223 | PF00134 | 0.288 | 
| DOC_CYCLIN_yCln2_LP_2 | 76 | 82 | PF00134 | 0.261 | 
| DOC_MAPK_gen_1 | 132 | 139 | PF00069 | 0.260 | 
| DOC_MAPK_gen_1 | 325 | 332 | PF00069 | 0.358 | 
| DOC_MAPK_MEF2A_6 | 420 | 427 | PF00069 | 0.404 | 
| DOC_PP1_RVXF_1 | 227 | 234 | PF00149 | 0.276 | 
| DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.279 | 
| DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.264 | 
| DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.272 | 
| DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.363 | 
| DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.417 | 
| DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.446 | 
| DOC_USP7_MATH_2 | 150 | 156 | PF00917 | 0.331 | 
| DOC_USP7_MATH_2 | 198 | 204 | PF00917 | 0.291 | 
| DOC_USP7_MATH_2 | 294 | 300 | PF00917 | 0.349 | 
| DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.276 | 
| DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.501 | 
| DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.447 | 
| LIG_14-3-3_CanoR_1 | 133 | 138 | PF00244 | 0.424 | 
| LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.370 | 
| LIG_14-3-3_CanoR_1 | 278 | 283 | PF00244 | 0.383 | 
| LIG_14-3-3_CanoR_1 | 325 | 332 | PF00244 | 0.261 | 
| LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.459 | 
| LIG_Actin_WH2_2 | 155 | 170 | PF00022 | 0.297 | 
| LIG_Actin_WH2_2 | 200 | 218 | PF00022 | 0.274 | 
| LIG_Actin_WH2_2 | 272 | 287 | PF00022 | 0.293 | 
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.576 | 
| LIG_deltaCOP1_diTrp_1 | 62 | 69 | PF00928 | 0.334 | 
| LIG_FHA_1 | 133 | 139 | PF00498 | 0.278 | 
| LIG_FHA_1 | 144 | 150 | PF00498 | 0.465 | 
| LIG_FHA_1 | 159 | 165 | PF00498 | 0.346 | 
| LIG_FHA_1 | 192 | 198 | PF00498 | 0.349 | 
| LIG_FHA_1 | 216 | 222 | PF00498 | 0.332 | 
| LIG_FHA_1 | 279 | 285 | PF00498 | 0.308 | 
| LIG_FHA_1 | 326 | 332 | PF00498 | 0.303 | 
| LIG_FHA_1 | 42 | 48 | PF00498 | 0.358 | 
| LIG_FHA_1 | 632 | 638 | PF00498 | 0.442 | 
| LIG_FHA_1 | 81 | 87 | PF00498 | 0.309 | 
| LIG_FHA_2 | 566 | 572 | PF00498 | 0.478 | 
| LIG_FHA_2 | 576 | 582 | PF00498 | 0.486 | 
| LIG_FHA_2 | 600 | 606 | PF00498 | 0.560 | 
| LIG_FHA_2 | 92 | 98 | PF00498 | 0.482 | 
| LIG_FXI_DFP_1 | 139 | 143 | PF00024 | 0.456 | 
| LIG_LIR_Gen_1 | 127 | 134 | PF02991 | 0.486 | 
| LIG_LIR_Gen_1 | 140 | 150 | PF02991 | 0.394 | 
| LIG_LIR_Gen_1 | 152 | 159 | PF02991 | 0.430 | 
| LIG_LIR_Gen_1 | 176 | 183 | PF02991 | 0.357 | 
| LIG_LIR_Gen_1 | 296 | 304 | PF02991 | 0.324 | 
| LIG_LIR_Gen_1 | 344 | 353 | PF02991 | 0.321 | 
| LIG_LIR_Gen_1 | 391 | 400 | PF02991 | 0.479 | 
| LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.343 | 
| LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.348 | 
| LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.369 | 
| LIG_LIR_Nem_3 | 176 | 180 | PF02991 | 0.366 | 
| LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.280 | 
| LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.334 | 
| LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.435 | 
| LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.387 | 
| LIG_NRBOX | 326 | 332 | PF00104 | 0.257 | 
| LIG_PDZ_Class_2 | 663 | 668 | PF00595 | 0.284 | 
| LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.356 | 
| LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.403 | 
| LIG_SH3_3 | 217 | 223 | PF00018 | 0.285 | 
| LIG_SH3_3 | 570 | 576 | PF00018 | 0.483 | 
| LIG_SH3_3 | 580 | 586 | PF00018 | 0.634 | 
| LIG_SH3_3 | 93 | 99 | PF00018 | 0.466 | 
| LIG_Sin3_3 | 652 | 659 | PF02671 | 0.277 | 
| LIG_SUMO_SIM_anti_2 | 350 | 355 | PF11976 | 0.262 | 
| LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.347 | 
| LIG_SUMO_SIM_par_1 | 423 | 429 | PF11976 | 0.337 | 
| LIG_SUMO_SIM_par_1 | 78 | 83 | PF11976 | 0.258 | 
| LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.365 | 
| LIG_UBA3_1 | 353 | 360 | PF00899 | 0.268 | 
| MOD_CDC14_SPxK_1 | 226 | 229 | PF00782 | 0.279 | 
| MOD_CDK_SPxK_1 | 223 | 229 | PF00069 | 0.276 | 
| MOD_CK1_1 | 179 | 185 | PF00069 | 0.368 | 
| MOD_CK1_1 | 254 | 260 | PF00069 | 0.338 | 
| MOD_CK1_1 | 299 | 305 | PF00069 | 0.355 | 
| MOD_CK1_1 | 359 | 365 | PF00069 | 0.351 | 
| MOD_CK1_1 | 370 | 376 | PF00069 | 0.356 | 
| MOD_CK1_1 | 388 | 394 | PF00069 | 0.383 | 
| MOD_CK2_1 | 565 | 571 | PF00069 | 0.456 | 
| MOD_CK2_1 | 575 | 581 | PF00069 | 0.530 | 
| MOD_CK2_1 | 599 | 605 | PF00069 | 0.571 | 
| MOD_CK2_1 | 91 | 97 | PF00069 | 0.349 | 
| MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.569 | 
| MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.616 | 
| MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.560 | 
| MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.737 | 
| MOD_GlcNHglycan | 264 | 268 | PF01048 | 0.545 | 
| MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.601 | 
| MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.646 | 
| MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.655 | 
| MOD_GlcNHglycan | 344 | 348 | PF01048 | 0.624 | 
| MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.681 | 
| MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.527 | 
| MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.523 | 
| MOD_GlcNHglycan | 384 | 388 | PF01048 | 0.648 | 
| MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.607 | 
| MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.689 | 
| MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.430 | 
| MOD_GSK3_1 | 120 | 127 | PF00069 | 0.458 | 
| MOD_GSK3_1 | 141 | 148 | PF00069 | 0.423 | 
| MOD_GSK3_1 | 175 | 182 | PF00069 | 0.412 | 
| MOD_GSK3_1 | 232 | 239 | PF00069 | 0.363 | 
| MOD_GSK3_1 | 247 | 254 | PF00069 | 0.358 | 
| MOD_GSK3_1 | 274 | 281 | PF00069 | 0.335 | 
| MOD_GSK3_1 | 295 | 302 | PF00069 | 0.330 | 
| MOD_GSK3_1 | 32 | 39 | PF00069 | 0.506 | 
| MOD_GSK3_1 | 343 | 350 | PF00069 | 0.379 | 
| MOD_GSK3_1 | 370 | 377 | PF00069 | 0.374 | 
| MOD_GSK3_1 | 385 | 392 | PF00069 | 0.330 | 
| MOD_GSK3_1 | 440 | 447 | PF00069 | 0.533 | 
| MOD_GSK3_1 | 448 | 455 | PF00069 | 0.578 | 
| MOD_GSK3_1 | 459 | 466 | PF00069 | 0.464 | 
| MOD_GSK3_1 | 469 | 476 | PF00069 | 0.495 | 
| MOD_GSK3_1 | 477 | 484 | PF00069 | 0.513 | 
| MOD_GSK3_1 | 488 | 495 | PF00069 | 0.482 | 
| MOD_GSK3_1 | 498 | 505 | PF00069 | 0.464 | 
| MOD_GSK3_1 | 508 | 515 | PF00069 | 0.495 | 
| MOD_GSK3_1 | 519 | 526 | PF00069 | 0.451 | 
| MOD_GSK3_1 | 527 | 534 | PF00069 | 0.464 | 
| MOD_GSK3_1 | 538 | 545 | PF00069 | 0.513 | 
| MOD_GSK3_1 | 549 | 556 | PF00069 | 0.527 | 
| MOD_GSK3_1 | 584 | 591 | PF00069 | 0.665 | 
| MOD_GSK3_1 | 627 | 634 | PF00069 | 0.430 | 
| MOD_GSK3_1 | 87 | 94 | PF00069 | 0.415 | 
| MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.507 | 
| MOD_NEK2_1 | 10 | 15 | PF00069 | 0.591 | 
| MOD_NEK2_1 | 167 | 172 | PF00069 | 0.384 | 
| MOD_NEK2_1 | 21 | 26 | PF00069 | 0.536 | 
| MOD_NEK2_1 | 215 | 220 | PF00069 | 0.332 | 
| MOD_NEK2_1 | 236 | 241 | PF00069 | 0.439 | 
| MOD_NEK2_1 | 284 | 289 | PF00069 | 0.352 | 
| MOD_NEK2_1 | 306 | 311 | PF00069 | 0.428 | 
| MOD_NEK2_1 | 332 | 337 | PF00069 | 0.403 | 
| MOD_NEK2_1 | 354 | 359 | PF00069 | 0.334 | 
| MOD_NEK2_1 | 361 | 366 | PF00069 | 0.346 | 
| MOD_NEK2_1 | 385 | 390 | PF00069 | 0.367 | 
| MOD_NEK2_1 | 398 | 403 | PF00069 | 0.337 | 
| MOD_NEK2_1 | 80 | 85 | PF00069 | 0.347 | 
| MOD_NEK2_1 | 87 | 92 | PF00069 | 0.371 | 
| MOD_NEK2_2 | 400 | 405 | PF00069 | 0.294 | 
| MOD_PIKK_1 | 308 | 314 | PF00454 | 0.454 | 
| MOD_PIKK_1 | 325 | 331 | PF00454 | 0.306 | 
| MOD_PKA_1 | 132 | 138 | PF00069 | 0.253 | 
| MOD_PKA_1 | 325 | 331 | PF00069 | 0.266 | 
| MOD_PKA_2 | 132 | 138 | PF00069 | 0.266 | 
| MOD_PKA_2 | 284 | 290 | PF00069 | 0.335 | 
| MOD_Plk_1 | 151 | 157 | PF00069 | 0.496 | 
| MOD_Plk_1 | 175 | 181 | PF00069 | 0.394 | 
| MOD_Plk_1 | 295 | 301 | PF00069 | 0.365 | 
| MOD_Plk_1 | 343 | 349 | PF00069 | 0.430 | 
| MOD_Plk_1 | 631 | 637 | PF00069 | 0.546 | 
| MOD_Plk_2-3 | 200 | 206 | PF00069 | 0.292 | 
| MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.342 | 
| MOD_Plk_4 | 133 | 139 | PF00069 | 0.343 | 
| MOD_Plk_4 | 251 | 257 | PF00069 | 0.400 | 
| MOD_Plk_4 | 332 | 338 | PF00069 | 0.301 | 
| MOD_Plk_4 | 347 | 353 | PF00069 | 0.415 | 
| MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.282 | 
| MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.501 | 
| MOD_SUMO_rev_2 | 415 | 421 | PF00179 | 0.329 | 
| MOD_SUMO_rev_2 | 625 | 634 | PF00179 | 0.339 | 
| TRG_DiLeu_BaEn_1 | 632 | 637 | PF01217 | 0.347 | 
| TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.363 | 
| TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.266 | 
| TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.285 | 
| TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.576 | 
| TRG_Pf-PMV_PEXEL_1 | 232 | 237 | PF00026 | 0.474 | 
| TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.472 | 
| TRG_Pf-PMV_PEXEL_1 | 376 | 381 | PF00026 | 0.496 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0S4IRQ2 | Bodo saltans | 31% | 78% | 
| A0A0S4IWB9 | Bodo saltans | 32% | 81% | 
| A0A0S4J206 | Bodo saltans | 32% | 100% | 
| A0A0S4J954 | Bodo saltans | 21% | 90% | 
| A0A0S4J985 | Bodo saltans | 30% | 67% | 
| A0A0S4JQZ4 | Bodo saltans | 32% | 67% | 
| A0A0S4JTM6 | Bodo saltans | 27% | 90% | 
| A0A0S4KK37 | Bodo saltans | 30% | 100% | 
| A0A3Q8I9B4 | Leishmania donovani | 43% | 100% | 
| A0A3Q8I9D9 | Leishmania donovani | 43% | 100% | 
| A0A3Q8IC27 | Leishmania donovani | 33% | 100% | 
| A0A3S5H6L9 | Leishmania donovani | 43% | 100% | 
| A0A3S5H6M3 | Leishmania donovani | 59% | 97% | 
| A0A3S5H6M4 | Leishmania donovani | 51% | 100% | 
| A0A3S7WS66 | Leishmania donovani | 51% | 100% | 
| A4H6Y8 | Leishmania braziliensis | 50% | 73% | 
| A4HBX3 | Leishmania braziliensis | 37% | 100% | 
| A4HZ93 | Leishmania infantum | 33% | 100% | 
| D1GJ51 | Leishmania infantum | 51% | 100% | 
| E9AGG2 | Leishmania infantum | 59% | 100% | 
| E9AGG7 | Leishmania infantum | 49% | 100% | 
| E9AGG9 | Leishmania infantum | 52% | 100% | 
| E9ANZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 94% | 
| E9AP04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 96% | 
| E9AP05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% | 
| E9AVA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% | 
| Q4QC79 | Leishmania major | 35% | 100% | 
| Q4QGI0 | Leishmania major | 58% | 100% | 
| Q4QGI2 | Leishmania major | 54% | 100% | 
| Q4QGI4 | Leishmania major | 50% | 100% | 
| Q4QGI6 | Leishmania major | 57% | 100% | 
| Q4QGI8 | Leishmania major | 53% | 88% | 
| Q4QGJ0 | Leishmania major | 55% | 100% | 
| Q4QGJ2 | Leishmania major | 97% | 100% | 
| Q4QGJ9 | Leishmania major | 55% | 100% | 
| Q4QGK0 | Leishmania major | 69% | 100% | 
| Q4QGK1 | Leishmania major | 64% | 95% | 
| Q4QGK2 | Leishmania major | 46% | 100% | 
| Q4QGK8 | Leishmania major | 57% | 100% | 
| Q4QGL2 | Leishmania major | 57% | 100% | 
| Q4QGL8 | Leishmania major | 50% | 100% | 
| Q4QGM1 | Leishmania major | 55% | 86% |