tRNA synthetase, N(2), N(2)-dimethylguanosine tRNA methyltransferase
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WSL8
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 1 |
GO:0002940 | tRNA N2-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:0000049 | tRNA binding | 5 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004809 | tRNA (guanine-N2-)-methyltransferase activity | 6 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008170 | N-methyltransferase activity | 5 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0008175 | tRNA methyltransferase activity | 5 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016423 | tRNA (guanine) methyltransferase activity | 6 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 279 | 283 | PF00656 | 0.266 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 716 | 720 | PF00656 | 0.711 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.302 |
CLV_PCSK_FUR_1 | 437 | 441 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.806 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.754 |
CLV_PCSK_KEX2_1 | 697 | 699 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 443 | 445 | PF00082 | 0.758 |
CLV_PCSK_PC7_1 | 390 | 396 | PF00082 | 0.655 |
CLV_PCSK_PC7_1 | 439 | 445 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 657 | 661 | PF00082 | 0.577 |
DEG_APCC_DBOX_1 | 313 | 321 | PF00400 | 0.281 |
DEG_APCC_DBOX_1 | 552 | 560 | PF00400 | 0.411 |
DEG_SCF_FBW7_2 | 659 | 666 | PF00400 | 0.501 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.592 |
DEG_SPOP_SBC_1 | 493 | 497 | PF00917 | 0.254 |
DOC_ANK_TNKS_1 | 677 | 684 | PF00023 | 0.432 |
DOC_CKS1_1 | 580 | 585 | PF01111 | 0.360 |
DOC_CKS1_1 | 660 | 665 | PF01111 | 0.497 |
DOC_CYCLIN_RxL_1 | 309 | 321 | PF00134 | 0.266 |
DOC_CYCLIN_RxL_1 | 654 | 662 | PF00134 | 0.561 |
DOC_CYCLIN_yCln2_LP_2 | 511 | 517 | PF00134 | 0.325 |
DOC_MAPK_DCC_7 | 329 | 337 | PF00069 | 0.269 |
DOC_MAPK_DCC_7 | 607 | 616 | PF00069 | 0.277 |
DOC_MAPK_gen_1 | 268 | 278 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 326 | 334 | PF00069 | 0.266 |
DOC_MAPK_MEF2A_6 | 329 | 337 | PF00069 | 0.269 |
DOC_MAPK_MEF2A_6 | 547 | 556 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 607 | 616 | PF00069 | 0.328 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.418 |
DOC_PP4_FxxP_1 | 330 | 333 | PF00568 | 0.393 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.314 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.627 |
DOC_USP7_UBL2_3 | 643 | 647 | PF12436 | 0.566 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.281 |
DOC_WW_Pin1_4 | 659 | 664 | PF00397 | 0.445 |
LIG_14-3-3_CanoR_1 | 378 | 388 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 473 | 477 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 536 | 542 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.393 |
LIG_Actin_WH2_2 | 100 | 118 | PF00022 | 0.281 |
LIG_Actin_WH2_2 | 75 | 92 | PF00022 | 0.331 |
LIG_APCC_ABBA_1 | 335 | 340 | PF00400 | 0.266 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.634 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.491 |
LIG_FAT_LD_1 | 526 | 534 | PF03623 | 0.355 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.557 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.404 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.369 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.343 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.266 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.403 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.266 |
LIG_GSK3_LRP6_1 | 579 | 584 | PF00069 | 0.271 |
LIG_IRF3_LxIS_1 | 74 | 81 | PF10401 | 0.403 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 573 | 581 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 84 | 94 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 573 | 577 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.325 |
LIG_LYPXL_yS_3 | 156 | 159 | PF13949 | 0.529 |
LIG_MYND_1 | 237 | 241 | PF01753 | 0.460 |
LIG_NRBOX | 525 | 531 | PF00104 | 0.266 |
LIG_PCNA_yPIPBox_3 | 240 | 251 | PF02747 | 0.329 |
LIG_PTB_Apo_2 | 123 | 130 | PF02174 | 0.411 |
LIG_PTB_Apo_2 | 143 | 150 | PF02174 | 0.145 |
LIG_PTB_Phospho_1 | 123 | 129 | PF10480 | 0.411 |
LIG_PTB_Phospho_1 | 143 | 149 | PF10480 | 0.145 |
LIG_REV1ctd_RIR_1 | 344 | 352 | PF16727 | 0.325 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.552 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.411 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.281 |
LIG_SH2_CRK | 516 | 520 | PF00017 | 0.281 |
LIG_SH2_NCK_1 | 516 | 520 | PF00017 | 0.266 |
LIG_SH2_NCK_1 | 68 | 72 | PF00017 | 0.280 |
LIG_SH2_PTP2 | 574 | 577 | PF00017 | 0.411 |
LIG_SH2_SRC | 129 | 132 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.626 |
LIG_SH2_STAT3 | 365 | 368 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.386 |
LIG_SH3_1 | 686 | 692 | PF00018 | 0.426 |
LIG_SH3_2 | 468 | 473 | PF14604 | 0.525 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.533 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.599 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.379 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.517 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.296 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.186 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.426 |
LIG_SUMO_SIM_anti_2 | 102 | 108 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 79 | 84 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 249 | 254 | PF11976 | 0.272 |
LIG_SUMO_SIM_par_1 | 81 | 87 | PF11976 | 0.331 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.287 |
LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.582 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.606 |
LIG_TRAF2_1 | 555 | 558 | PF00917 | 0.281 |
LIG_TRFH_1 | 565 | 569 | PF08558 | 0.331 |
LIG_TYR_ITIM | 154 | 159 | PF00017 | 0.457 |
LIG_UBA3_1 | 615 | 623 | PF00899 | 0.337 |
MOD_CDC14_SPxK_1 | 470 | 473 | PF00782 | 0.665 |
MOD_CDK_SPK_2 | 184 | 189 | PF00069 | 0.577 |
MOD_CDK_SPxK_1 | 467 | 473 | PF00069 | 0.611 |
MOD_CDK_SPxxK_3 | 233 | 240 | PF00069 | 0.446 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.657 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.277 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.474 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.603 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.717 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.693 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.266 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.393 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.370 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.557 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.746 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.700 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.420 |
MOD_Cter_Amidation | 220 | 223 | PF01082 | 0.542 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.282 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.669 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.584 |
MOD_GlcNHglycan | 232 | 236 | PF01048 | 0.703 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.288 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.305 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.411 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.411 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.494 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.640 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.622 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.308 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.817 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.522 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.515 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.266 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.505 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.678 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.578 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.326 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.621 |
MOD_LATS_1 | 295 | 301 | PF00433 | 0.266 |
MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.476 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.724 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.274 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.615 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.276 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.266 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.325 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.430 |
MOD_NEK2_2 | 333 | 338 | PF00069 | 0.266 |
MOD_PIKK_1 | 517 | 523 | PF00454 | 0.281 |
MOD_PIKK_1 | 594 | 600 | PF00454 | 0.266 |
MOD_PK_1 | 76 | 82 | PF00069 | 0.266 |
MOD_PKA_1 | 439 | 445 | PF00069 | 0.580 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.401 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.720 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.627 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.353 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.295 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.281 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.337 |
MOD_PKB_1 | 437 | 445 | PF00069 | 0.576 |
MOD_PKB_1 | 95 | 103 | PF00069 | 0.411 |
MOD_Plk_1 | 667 | 673 | PF00069 | 0.366 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.266 |
MOD_Plk_2-3 | 102 | 108 | PF00069 | 0.360 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.410 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.356 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.266 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.505 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.690 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.692 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.266 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.599 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.586 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.281 |
MOD_ProDKin_1 | 659 | 665 | PF00069 | 0.450 |
MOD_SUMO_rev_2 | 414 | 422 | PF00179 | 0.734 |
MOD_SUMO_rev_2 | 642 | 650 | PF00179 | 0.650 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 330 | 335 | PF01217 | 0.267 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 677 | 680 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 696 | 699 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.292 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.278 |
TRG_Pf-PMV_PEXEL_1 | 240 | 244 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.300 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF43 | Leptomonas seymouri | 68% | 99% |
A0A0S4IT52 | Bodo saltans | 47% | 100% |
A0A1X0NNC1 | Trypanosomatidae | 49% | 96% |
A0A3R7KAT5 | Trypanosoma rangeli | 51% | 100% |
A4H782 | Leishmania braziliensis | 79% | 100% |
A4HVM2 | Leishmania infantum | 100% | 100% |
D0A6N2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9APB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QG60 | Leishmania major | 93% | 99% |
V5BB27 | Trypanosoma cruzi | 52% | 100% |