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: E9AQI8
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 | 108 | 112 | PF00656 | 0.493 |
CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.670 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.376 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 681 | 683 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 555 | 557 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 632 | 634 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 681 | 683 | PF00082 | 0.621 |
CLV_PCSK_PC7_1 | 520 | 526 | PF00082 | 0.186 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.680 |
DEG_APCC_DBOX_1 | 496 | 504 | PF00400 | 0.594 |
DEG_APCC_DBOX_1 | 582 | 590 | PF00400 | 0.402 |
DEG_SPOP_SBC_1 | 544 | 548 | PF00917 | 0.603 |
DOC_MAPK_gen_1 | 20 | 29 | PF00069 | 0.619 |
DOC_MAPK_gen_1 | 336 | 345 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 434 | 442 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 524 | 531 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 632 | 639 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 632 | 639 | PF00069 | 0.430 |
DOC_MAPK_RevD_3 | 42 | 55 | PF00069 | 0.558 |
DOC_PP1_RVXF_1 | 415 | 421 | PF00149 | 0.521 |
DOC_PP1_SILK_1 | 44 | 49 | PF00149 | 0.604 |
DOC_PP2B_PxIxI_1 | 531 | 537 | PF00149 | 0.506 |
DOC_PP4_FxxP_1 | 411 | 414 | PF00568 | 0.521 |
DOC_PP4_FxxP_1 | 451 | 454 | PF00568 | 0.521 |
DOC_PP4_FxxP_1 | 542 | 545 | PF00568 | 0.276 |
DOC_PP4_FxxP_1 | 639 | 642 | PF00568 | 0.413 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.645 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.515 |
LIG_14-3-3_CanoR_1 | 240 | 245 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 35 | 44 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 524 | 530 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 53 | 58 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 556 | 565 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 583 | 587 | PF00244 | 0.415 |
LIG_Actin_WH2_2 | 133 | 148 | PF00022 | 0.525 |
LIG_AP2alpha_1 | 538 | 542 | PF02296 | 0.594 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.780 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 501 | 505 | PF00533 | 0.594 |
LIG_DLG_GKlike_1 | 240 | 248 | PF00625 | 0.583 |
LIG_EH1_1 | 263 | 271 | PF00400 | 0.571 |
LIG_eIF4E_1 | 264 | 270 | PF01652 | 0.463 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.537 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.503 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.540 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.516 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.645 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.535 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.238 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.506 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.521 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.415 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.511 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.523 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.471 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.429 |
LIG_LIR_Apic_2 | 148 | 154 | PF02991 | 0.569 |
LIG_LIR_Apic_2 | 410 | 414 | PF02991 | 0.539 |
LIG_LIR_Apic_2 | 540 | 545 | PF02991 | 0.434 |
LIG_LIR_Apic_2 | 638 | 642 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 84 | 88 | PF02991 | 0.764 |
LIG_LIR_Gen_1 | 286 | 295 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 439 | 450 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 502 | 513 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 537 | 545 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 585 | 590 | PF02991 | 0.243 |
LIG_PDZ_Class_3 | 683 | 688 | PF00595 | 0.477 |
LIG_Pex14_2 | 538 | 542 | PF04695 | 0.521 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.507 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.521 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.521 |
LIG_SH2_CRK | 612 | 616 | PF00017 | 0.484 |
LIG_SH2_GRB2like | 419 | 422 | PF00017 | 0.521 |
LIG_SH2_NCK_1 | 389 | 393 | PF00017 | 0.528 |
LIG_SH2_NCK_1 | 415 | 419 | PF00017 | 0.521 |
LIG_SH2_NCK_1 | 549 | 553 | PF00017 | 0.632 |
LIG_SH2_NCK_1 | 612 | 616 | PF00017 | 0.484 |
LIG_SH2_SRC | 306 | 309 | PF00017 | 0.594 |
LIG_SH2_SRC | 549 | 552 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.784 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.772 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.789 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.457 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 319 | 325 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 281 | 286 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 62 | 68 | PF11976 | 0.682 |
LIG_SUMO_SIM_par_1 | 620 | 627 | PF11976 | 0.444 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.332 |
LIG_TRAF2_1 | 654 | 657 | PF00917 | 0.424 |
LIG_TRFH_1 | 612 | 616 | PF08558 | 0.484 |
LIG_TRFH_1 | 639 | 643 | PF08558 | 0.526 |
LIG_TYR_ITIM | 304 | 309 | PF00017 | 0.387 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.464 |
LIG_TYR_ITIM | 413 | 418 | PF00017 | 0.387 |
LIG_UBA3_1 | 43 | 50 | PF00899 | 0.604 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.721 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.611 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.517 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.790 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.387 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.721 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.783 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.646 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.533 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.797 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.387 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.484 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.492 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.448 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.615 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.764 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.439 |
MOD_Cter_Amidation | 522 | 525 | PF01082 | 0.387 |
MOD_Cter_Amidation | 553 | 556 | PF01082 | 0.462 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.778 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.675 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.577 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.593 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.496 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.387 |
MOD_GlcNHglycan | 363 | 367 | PF01048 | 0.612 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.458 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.554 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.439 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.702 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.643 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.749 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.526 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.606 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.357 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.764 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.761 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.535 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.387 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.387 |
MOD_N-GLC_1 | 557 | 562 | PF02516 | 0.609 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.643 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.471 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.333 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.456 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.387 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.574 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.418 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.372 |
MOD_NEK2_2 | 330 | 335 | PF00069 | 0.387 |
MOD_NEK2_2 | 485 | 490 | PF00069 | 0.391 |
MOD_PK_1 | 53 | 59 | PF00069 | 0.595 |
MOD_PKA_1 | 240 | 246 | PF00069 | 0.587 |
MOD_PKA_1 | 346 | 352 | PF00069 | 0.505 |
MOD_PKA_1 | 53 | 59 | PF00069 | 0.595 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.616 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.535 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.680 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.505 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.387 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.197 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.578 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.456 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.541 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.553 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.345 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.346 |
MOD_Plk_1 | 619 | 625 | PF00069 | 0.509 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.442 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.461 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.387 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.319 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.490 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.387 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.509 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.780 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.513 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.505 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.512 |
MOD_SUMO_rev_2 | 332 | 340 | PF00179 | 0.387 |
MOD_SUMO_rev_2 | 76 | 81 | PF00179 | 0.703 |
TRG_DiLeu_BaEn_1 | 278 | 283 | PF01217 | 0.612 |
TRG_DiLeu_BaEn_1 | 28 | 33 | PF01217 | 0.568 |
TRG_DiLeu_BaEn_1 | 427 | 432 | PF01217 | 0.387 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.294 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.634 |
TRG_NES_CRM1_1 | 329 | 341 | PF08389 | 0.365 |
TRG_NLS_MonoExtC_3 | 680 | 686 | PF00514 | 0.673 |
TRG_NLS_MonoExtN_4 | 236 | 243 | PF00514 | 0.757 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I219 | Leptomonas seymouri | 53% | 100% |
A0A3S7WTS8 | Leishmania donovani | 90% | 100% |
A4H8F7 | Leishmania braziliensis | 74% | 100% |
A4HWT0 | Leishmania infantum | 90% | 100% |
B7G5J1 | Phaeodactylum tricornutum (strain CCAP 1055/1) | 25% | 100% |
Q4QEY9 | Leishmania major | 91% | 100% |