Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 6 |
Silverman et al. | no | yes: 4 |
Pissara et al. | no | yes: 16 |
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: 24 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 4 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0016592 | mediator complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: A4I4S4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 25 |
GO:0006793 | phosphorus metabolic process | 3 | 25 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 25 |
GO:0006807 | nitrogen compound metabolic process | 2 | 25 |
GO:0008152 | metabolic process | 1 | 25 |
GO:0009987 | cellular process | 1 | 25 |
GO:0016310 | phosphorylation | 5 | 25 |
GO:0019538 | protein metabolic process | 3 | 25 |
GO:0036211 | protein modification process | 4 | 25 |
GO:0043170 | macromolecule metabolic process | 3 | 25 |
GO:0043412 | macromolecule modification | 4 | 25 |
GO:0044237 | cellular metabolic process | 2 | 25 |
GO:0044238 | primary metabolic process | 2 | 25 |
GO:0071704 | organic substance metabolic process | 2 | 25 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 25 |
GO:0051301 | cell division | 2 | 1 |
GO:0007165 | signal transduction | 2 | 3 |
GO:0009266 | response to temperature stimulus | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 3 |
GO:0050789 | regulation of biological process | 2 | 3 |
GO:0050794 | regulation of cellular process | 3 | 3 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0065007 | biological regulation | 1 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 25 |
GO:0003824 | catalytic activity | 1 | 25 |
GO:0004672 | protein kinase activity | 3 | 25 |
GO:0005488 | binding | 1 | 25 |
GO:0005524 | ATP binding | 5 | 25 |
GO:0016301 | kinase activity | 4 | 25 |
GO:0016740 | transferase activity | 2 | 25 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 25 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 25 |
GO:0017076 | purine nucleotide binding | 4 | 25 |
GO:0030554 | adenyl nucleotide binding | 5 | 25 |
GO:0032553 | ribonucleotide binding | 3 | 25 |
GO:0032555 | purine ribonucleotide binding | 4 | 25 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 25 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 25 |
GO:0036094 | small molecule binding | 2 | 25 |
GO:0043167 | ion binding | 2 | 25 |
GO:0043168 | anion binding | 3 | 25 |
GO:0097159 | organic cyclic compound binding | 2 | 25 |
GO:0097367 | carbohydrate derivative binding | 2 | 25 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 25 |
GO:1901265 | nucleoside phosphate binding | 3 | 25 |
GO:1901363 | heterocyclic compound binding | 2 | 25 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 14 |
GO:0004707 | MAP kinase activity | 5 | 11 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 1 |
GO:0097472 | cyclin-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.385 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.343 |
CLV_PCSK_PC7_1 | 150 | 156 | PF00082 | 0.413 |
CLV_PCSK_PC7_1 | 191 | 197 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.762 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.345 |
DEG_APCC_DBOX_1 | 149 | 157 | PF00400 | 0.423 |
DEG_APCC_DBOX_1 | 267 | 275 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 281 | 289 | PF00400 | 0.395 |
DEG_APCC_DBOX_1 | 528 | 536 | PF00400 | 0.268 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.541 |
DEG_SPOP_SBC_1 | 241 | 245 | PF00917 | 0.596 |
DEG_SPOP_SBC_1 | 309 | 313 | PF00917 | 0.222 |
DEG_SPOP_SBC_1 | 76 | 80 | PF00917 | 0.348 |
DOC_CYCLIN_RxL_1 | 542 | 552 | PF00134 | 0.359 |
DOC_MAPK_gen_1 | 266 | 274 | PF00069 | 0.341 |
DOC_MAPK_gen_1 | 323 | 332 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 347 | 356 | PF00069 | 0.297 |
DOC_MAPK_gen_1 | 527 | 534 | PF00069 | 0.281 |
DOC_MAPK_HePTP_8 | 324 | 336 | PF00069 | 0.343 |
DOC_MAPK_JIP1_4 | 350 | 356 | PF00069 | 0.288 |
DOC_MAPK_MEF2A_6 | 326 | 334 | PF00069 | 0.305 |
DOC_MIT_MIM_1 | 541 | 549 | PF04212 | 0.258 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.771 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.261 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.693 |
LIG_14-3-3_CanoR_1 | 25 | 30 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 310 | 316 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 326 | 331 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 553 | 558 | PF00244 | 0.353 |
LIG_Actin_WH2_2 | 158 | 173 | PF00022 | 0.610 |
LIG_BIR_III_2 | 101 | 105 | PF00653 | 0.359 |
LIG_BIR_III_2 | 49 | 53 | PF00653 | 0.549 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 312 | 316 | PF00533 | 0.258 |
LIG_BRCT_BRCA1_1 | 364 | 368 | PF00533 | 0.244 |
LIG_Clathr_ClatBox_1 | 546 | 550 | PF01394 | 0.343 |
LIG_CtBP_PxDLS_1 | 539 | 545 | PF00389 | 0.300 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.539 |
LIG_deltaCOP1_diTrp_1 | 297 | 301 | PF00928 | 0.343 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.556 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.530 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.326 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.351 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.391 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.531 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.393 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.392 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.395 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.385 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.312 |
LIG_LIR_Apic_2 | 416 | 422 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 488 | 497 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 567 | 576 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 567 | 573 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 93 | 97 | PF02991 | 0.581 |
LIG_Pex14_2 | 217 | 221 | PF04695 | 0.510 |
LIG_PTB_Apo_2 | 425 | 432 | PF02174 | 0.341 |
LIG_PTB_Phospho_1 | 425 | 431 | PF10480 | 0.341 |
LIG_RPA_C_Fungi | 221 | 233 | PF08784 | 0.545 |
LIG_RPA_C_Fungi | 257 | 269 | PF08784 | 0.356 |
LIG_SH2_CRK | 94 | 98 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 570 | 574 | PF00017 | 0.417 |
LIG_SH2_SRC | 490 | 493 | PF00017 | 0.258 |
LIG_SH2_SRC | 497 | 500 | PF00017 | 0.233 |
LIG_SH2_SRC | 570 | 573 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 390 | 394 | PF00017 | 0.258 |
LIG_SH2_STAP1 | 431 | 435 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 490 | 494 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 570 | 574 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.525 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.579 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.661 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.548 |
LIG_SUMO_SIM_anti_2 | 172 | 178 | PF11976 | 0.509 |
LIG_SUMO_SIM_anti_2 | 329 | 334 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 545 | 550 | PF11976 | 0.258 |
LIG_TRAF2_1 | 506 | 509 | PF00917 | 0.272 |
LIG_WW_2 | 63 | 66 | PF00397 | 0.545 |
LIG_WW_3 | 50 | 54 | PF00397 | 0.538 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.634 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.573 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.244 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.530 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.392 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.834 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.288 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.384 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.322 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.511 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.356 |
MOD_DYRK1A_RPxSP_1 | 59 | 63 | PF00069 | 0.551 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.592 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.545 |
MOD_GlcNHglycan | 177 | 182 | PF01048 | 0.505 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.536 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.465 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.357 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.384 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.244 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.343 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.319 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.603 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.636 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.538 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.495 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.534 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.601 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.244 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.292 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.422 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.689 |
MOD_LATS_1 | 224 | 230 | PF00433 | 0.504 |
MOD_LATS_1 | 23 | 29 | PF00433 | 0.531 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.647 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.231 |
MOD_N-GLC_1 | 429 | 434 | PF02516 | 0.369 |
MOD_N-GLC_1 | 503 | 508 | PF02516 | 0.258 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.639 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.521 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.550 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.411 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.361 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.259 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.307 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.333 |
MOD_NEK2_2 | 81 | 86 | PF00069 | 0.303 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.523 |
MOD_PK_1 | 25 | 31 | PF00069 | 0.540 |
MOD_PK_1 | 326 | 332 | PF00069 | 0.258 |
MOD_PKA_1 | 262 | 268 | PF00069 | 0.342 |
MOD_PKA_1 | 326 | 332 | PF00069 | 0.510 |
MOD_PKA_1 | 553 | 559 | PF00069 | 0.401 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.453 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.504 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.340 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.490 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.258 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.351 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.534 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.381 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.552 |
MOD_Plk_2-3 | 157 | 163 | PF00069 | 0.532 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.516 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.629 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.261 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.321 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.322 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.343 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.403 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.656 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.688 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.261 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.405 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.694 |
TRG_DiLeu_BaLyEn_6 | 542 | 547 | PF01217 | 0.261 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 52 | 54 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 553 | 555 | PF00400 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 347 | 352 | PF00026 | 0.267 |
TRG_Pf-PMV_PEXEL_1 | 545 | 550 | PF00026 | 0.288 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P661 | Leptomonas seymouri | 51% | 92% |
A0A3Q8IIY5 | Leishmania donovani | 100% | 100% |
A0A3Q8ITZ9 | Leishmania donovani | 26% | 100% |
A0A3S7WR45 | Leishmania donovani | 27% | 100% |
A0A3S7X2Z6 | Leishmania donovani | 28% | 100% |
A4H641 | Leishmania braziliensis | 28% | 100% |
A4HHL5 | Leishmania braziliensis | 84% | 100% |
A4HHY4 | Leishmania braziliensis | 27% | 100% |
A4HIM5 | Leishmania braziliensis | 27% | 100% |
A4HLJ9 | Leishmania braziliensis | 26% | 100% |
A4HUG1 | Leishmania infantum | 27% | 100% |
A4I564 | Leishmania infantum | 28% | 100% |
A4I910 | Leishmania infantum | 26% | 100% |
C9ZW07 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AE77 | Leishmania major | 95% | 100% |
E9ALK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AN59 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B0G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B3X5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q449 | Leishmania major | 26% | 100% |
Q4Q7S2 | Leishmania major | 29% | 100% |
Q4QHG6 | Leishmania major | 27% | 100% |
V5DCN7 | Trypanosoma cruzi | 31% | 97% |