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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0005759 | mitochondrial matrix | 5 | 7 |
GO:0031974 | membrane-enclosed lumen | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0043233 | organelle lumen | 3 | 7 |
GO:0070013 | intracellular organelle lumen | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4H8F7
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 1 |
GO:0002939 | tRNA N1-guanine methylation | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0030488 | tRNA methylation | 5 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0008168 | methyltransferase activity | 4 | 7 |
GO:0008173 | RNA methyltransferase activity | 4 | 7 |
GO:0008175 | tRNA methyltransferase activity | 5 | 7 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 7 |
GO:0009019 | tRNA (guanine-N1-)-methyltransferase activity | 7 | 7 |
GO:0016423 | tRNA (guanine) methyltransferase activity | 6 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 7 |
GO:0052906 | tRNA (guanine(37)-N(1))-methyltransferase activity | 8 | 7 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 7 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.775 |
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.293 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 638 | 640 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 638 | 640 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 686 | 688 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 686 | 690 | PF00082 | 0.667 |
DEG_APCC_DBOX_1 | 495 | 503 | PF00400 | 0.590 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.552 |
DOC_AGCK_PIF_1 | 593 | 598 | PF00069 | 0.261 |
DOC_CKS1_1 | 124 | 129 | PF01111 | 0.650 |
DOC_CYCLIN_yClb3_PxF_3 | 124 | 130 | PF00134 | 0.446 |
DOC_CYCLIN_yCln2_LP_2 | 387 | 393 | PF00134 | 0.359 |
DOC_MAPK_DCC_7 | 203 | 213 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 20 | 29 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 530 | 537 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 55 | 63 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 638 | 645 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 638 | 645 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 414 | 420 | PF00149 | 0.517 |
DOC_PP1_SILK_1 | 44 | 49 | PF00149 | 0.585 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.496 |
DOC_PP4_FxxP_1 | 410 | 413 | PF00568 | 0.517 |
DOC_PP4_FxxP_1 | 450 | 453 | PF00568 | 0.517 |
DOC_PP4_FxxP_1 | 645 | 648 | PF00568 | 0.405 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.560 |
DOC_USP7_UBL2_3 | 456 | 460 | PF12436 | 0.396 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 114 | 124 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 422 | 426 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 530 | 536 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 95 | 101 | PF00244 | 0.529 |
LIG_AP2alpha_1 | 544 | 548 | PF02296 | 0.590 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.759 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_1 | 500 | 504 | PF00533 | 0.590 |
LIG_EH1_1 | 263 | 271 | PF00400 | 0.555 |
LIG_eIF4E_1 | 264 | 270 | PF01652 | 0.452 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.531 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.472 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.481 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.427 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.512 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.234 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.517 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.469 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.472 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.452 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.433 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.643 |
LIG_LIR_Apic_2 | 149 | 154 | PF02991 | 0.590 |
LIG_LIR_Apic_2 | 644 | 648 | PF02991 | 0.405 |
LIG_LIR_Apic_2 | 84 | 88 | PF02991 | 0.703 |
LIG_LIR_Gen_1 | 286 | 295 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 438 | 449 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 487 | 493 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 501 | 512 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 543 | 551 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 573 | 582 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 487 | 491 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 501 | 507 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 543 | 547 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 573 | 578 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 591 | 596 | PF02991 | 0.250 |
LIG_PCNA_yPIPBox_3 | 262 | 270 | PF02747 | 0.303 |
LIG_PCNA_yPIPBox_3 | 48 | 61 | PF02747 | 0.335 |
LIG_Pex14_2 | 544 | 548 | PF04695 | 0.517 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.517 |
LIG_SH2_CRK | 473 | 477 | PF00017 | 0.517 |
LIG_SH2_CRK | 618 | 622 | PF00017 | 0.468 |
LIG_SH2_GRB2like | 418 | 421 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 618 | 622 | PF00017 | 0.468 |
LIG_SH2_SRC | 306 | 309 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 596 | 600 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.732 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.728 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.766 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.440 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.517 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.386 |
LIG_SUMO_SIM_anti_2 | 319 | 325 | PF11976 | 0.517 |
LIG_SUMO_SIM_anti_2 | 59 | 65 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 254 | 260 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 281 | 286 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 62 | 70 | PF11976 | 0.646 |
LIG_SUMO_SIM_par_1 | 626 | 633 | PF11976 | 0.431 |
LIG_TRAF2_1 | 373 | 376 | PF00917 | 0.323 |
LIG_TRAF2_1 | 624 | 627 | PF00917 | 0.313 |
LIG_TRFH_1 | 618 | 622 | PF08558 | 0.468 |
LIG_TRFH_1 | 645 | 649 | PF08558 | 0.519 |
LIG_TYR_ITIM | 304 | 309 | PF00017 | 0.517 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.446 |
LIG_TYR_ITIM | 412 | 417 | PF00017 | 0.517 |
LIG_UBA3_1 | 43 | 50 | PF00899 | 0.574 |
LIG_WRC_WIRS_1 | 595 | 600 | PF05994 | 0.270 |
MOD_CDK_SPxxK_3 | 232 | 239 | PF00069 | 0.519 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.594 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.745 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.507 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.365 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.517 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.498 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.725 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.637 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.500 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.799 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.369 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.463 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.487 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.447 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.606 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.410 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.439 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.324 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.615 |
MOD_Cter_Amidation | 528 | 531 | PF01082 | 0.317 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.761 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.487 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.317 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.648 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.447 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.438 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.514 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.686 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.747 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.481 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.746 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.404 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.515 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.601 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.540 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.475 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.635 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.658 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.735 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.403 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.309 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.317 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.317 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.515 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.640 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.657 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.454 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.387 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.517 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.638 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.560 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.410 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.363 |
MOD_NEK2_2 | 223 | 228 | PF00069 | 0.561 |
MOD_NEK2_2 | 330 | 335 | PF00069 | 0.517 |
MOD_NEK2_2 | 484 | 489 | PF00069 | 0.521 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.464 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.493 |
MOD_PIKK_1 | 655 | 661 | PF00454 | 0.363 |
MOD_PKA_1 | 240 | 246 | PF00069 | 0.568 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.593 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.336 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.517 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.658 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.517 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.564 |
MOD_PKB_1 | 20 | 28 | PF00069 | 0.570 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.540 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.376 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.487 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.364 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.562 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.576 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.405 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.418 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.453 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.517 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.469 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.472 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.517 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.403 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.742 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.504 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.621 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.594 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.501 |
MOD_SUMO_rev_2 | 332 | 340 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 370 | 379 | PF00179 | 0.347 |
TRG_DiLeu_BaEn_1 | 278 | 283 | PF01217 | 0.593 |
TRG_DiLeu_BaEn_1 | 28 | 33 | PF01217 | 0.549 |
TRG_DiLeu_BaEn_1 | 426 | 431 | PF01217 | 0.517 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.571 |
TRG_NLS_MonoExtC_3 | 685 | 691 | PF00514 | 0.663 |
TRG_NLS_MonoExtN_4 | 236 | 243 | PF00514 | 0.740 |
TRG_NLS_MonoExtN_4 | 683 | 690 | PF00514 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I219 | Leptomonas seymouri | 52% | 100% |
A0A3S7WTS8 | Leishmania donovani | 73% | 100% |
A4H8F7 | Leishmania braziliensis | 100% | 100% |
A4HWT0 | Leishmania infantum | 73% | 100% |
A9T6G5 | Physcomitrium patens | 29% | 100% |
E9AQI8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4QEY9 | Leishmania major | 73% | 99% |