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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 4 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0005634 | nucleus | 5 | 3 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: E9AN20
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0030490 | maturation of SSU-rRNA | 9 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003676 | nucleic acid binding | 3 | 17 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004386 | helicase activity | 2 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
GO:0003724 | RNA helicase activity | 3 | 5 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 5 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0003723 | RNA binding | 4 | 3 |
GO:0003743 | translation initiation factor activity | 4 | 1 |
GO:0008135 | translation factor activity, RNA binding | 3 | 1 |
GO:0045182 | translation regulator activity | 1 | 1 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 113 | 117 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 199 | 203 | PF00656 | 0.614 |
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 683 | 687 | PF00656 | 0.375 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 675 | 677 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 713 | 715 | PF00675 | 0.586 |
CLV_PCSK_FUR_1 | 711 | 715 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.212 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.212 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 713 | 715 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 540 | 542 | PF00082 | 0.212 |
CLV_PCSK_PC1ET2_1 | 583 | 585 | PF00082 | 0.240 |
CLV_PCSK_PC1ET2_1 | 607 | 609 | PF00082 | 0.210 |
CLV_PCSK_PC7_1 | 398 | 404 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.470 |
DEG_APCC_DBOX_1 | 451 | 459 | PF00400 | 0.410 |
DEG_APCC_DBOX_1 | 512 | 520 | PF00400 | 0.352 |
DEG_APCC_KENBOX_2 | 465 | 469 | PF00400 | 0.463 |
DEG_Kelch_Keap1_1 | 343 | 348 | PF01344 | 0.367 |
DEG_SCF_FBW7_1 | 649 | 654 | PF00400 | 0.346 |
DEG_SPOP_SBC_1 | 341 | 345 | PF00917 | 0.423 |
DOC_ANK_TNKS_1 | 141 | 148 | PF00023 | 0.530 |
DOC_CKS1_1 | 411 | 416 | PF01111 | 0.454 |
DOC_CKS1_1 | 648 | 653 | PF01111 | 0.334 |
DOC_CKS1_1 | 691 | 696 | PF01111 | 0.586 |
DOC_MAPK_gen_1 | 283 | 290 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 402 | 411 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 490 | 498 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 540 | 546 | PF00069 | 0.437 |
DOC_MAPK_HePTP_8 | 488 | 500 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 304 | 312 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 491 | 500 | PF00069 | 0.434 |
DOC_PP2B_LxvP_1 | 565 | 568 | PF13499 | 0.412 |
DOC_PP4_FxxP_1 | 648 | 651 | PF00568 | 0.345 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.573 |
DOC_USP7_MATH_2 | 19 | 25 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 690 | 695 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.648 |
LIG_14-3-3_CanoR_1 | 362 | 366 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 641 | 651 | PF00244 | 0.452 |
LIG_Actin_WH2_2 | 351 | 369 | PF00022 | 0.411 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.548 |
LIG_BRCT_BRCA1_1 | 644 | 648 | PF00533 | 0.331 |
LIG_Clathr_ClatBox_1 | 442 | 446 | PF01394 | 0.406 |
LIG_CtBP_PxDLS_1 | 335 | 339 | PF00389 | 0.391 |
LIG_eIF4E_1 | 63 | 69 | PF01652 | 0.590 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.475 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.583 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.450 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.407 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.446 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.475 |
LIG_FHA_1 | 691 | 697 | PF00498 | 0.587 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.571 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.538 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.524 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.477 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.446 |
LIG_FHA_2 | 648 | 654 | PF00498 | 0.464 |
LIG_Integrin_isoDGR_2 | 450 | 452 | PF01839 | 0.210 |
LIG_LIR_Apic_2 | 23 | 29 | PF02991 | 0.648 |
LIG_LIR_Apic_2 | 645 | 651 | PF02991 | 0.338 |
LIG_LIR_Apic_2 | 688 | 694 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.597 |
LIG_PCNA_yPIPBox_3 | 311 | 325 | PF02747 | 0.410 |
LIG_Rb_LxCxE_1 | 199 | 218 | PF01857 | 0.520 |
LIG_Rb_LxCxE_1 | 475 | 494 | PF01857 | 0.338 |
LIG_Rb_pABgroove_1 | 527 | 535 | PF01858 | 0.341 |
LIG_RPA_C_Fungi | 137 | 149 | PF08784 | 0.505 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.314 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.314 |
LIG_SH2_CRK | 492 | 496 | PF00017 | 0.363 |
LIG_SH2_CRK | 620 | 624 | PF00017 | 0.257 |
LIG_SH2_NCK_1 | 620 | 624 | PF00017 | 0.259 |
LIG_SH2_SRC | 63 | 66 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.209 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.271 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.583 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.225 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.295 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.333 |
LIG_SUMO_SIM_anti_2 | 497 | 503 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 27 | 34 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 354 | 360 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 432 | 437 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 441 | 446 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 494 | 499 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 597 | 603 | PF11976 | 0.203 |
LIG_TRAF2_1 | 196 | 199 | PF00917 | 0.563 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.230 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.506 |
LIG_TRAF2_1 | 553 | 556 | PF00917 | 0.252 |
MOD_CDK_SPxxK_3 | 164 | 171 | PF00069 | 0.528 |
MOD_CDK_SPxxK_3 | 445 | 452 | PF00069 | 0.230 |
MOD_CDK_SPxxK_3 | 690 | 697 | PF00069 | 0.554 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.642 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.597 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.509 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.473 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.321 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.248 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.379 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.369 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.314 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.588 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.578 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.770 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.526 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.603 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.181 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.471 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.281 |
MOD_Cter_Amidation | 711 | 714 | PF01082 | 0.626 |
MOD_GlcNHglycan | 10 | 14 | PF01048 | 0.640 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.678 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.748 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.437 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.298 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.324 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.230 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.296 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.183 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.639 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.425 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.530 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.331 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.376 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.573 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.782 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.541 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.549 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.592 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.670 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.615 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.359 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.246 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.311 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.359 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.439 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.328 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.314 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.354 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.335 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.189 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.674 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.617 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.566 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.567 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.418 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.217 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.315 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.423 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.510 |
MOD_PIKK_1 | 631 | 637 | PF00454 | 0.230 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.584 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.445 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.320 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.349 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.292 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.533 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.696 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.569 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.388 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.340 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.443 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.344 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.291 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.342 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.378 |
MOD_Plk_4 | 687 | 693 | PF00069 | 0.466 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.526 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.526 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.540 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.292 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.292 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.425 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.330 |
MOD_ProDKin_1 | 690 | 696 | PF00069 | 0.638 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.648 |
MOD_SUMO_rev_2 | 729 | 735 | PF00179 | 0.537 |
TRG_DiLeu_BaEn_1 | 378 | 383 | PF01217 | 0.291 |
TRG_DiLeu_BaEn_4 | 316 | 322 | PF01217 | 0.203 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.255 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 557 | 559 | PF00400 | 0.230 |
TRG_ER_diArg_1 | 579 | 582 | PF00400 | 0.229 |
TRG_ER_diArg_1 | 710 | 713 | PF00400 | 0.604 |
TRG_ER_diLys_1 | 732 | 736 | PF00400 | 0.471 |
TRG_NES_CRM1_1 | 621 | 631 | PF08389 | 0.225 |
TRG_NLS_MonoExtC_3 | 402 | 408 | PF00514 | 0.225 |
TRG_NLS_MonoExtN_4 | 402 | 407 | PF00514 | 0.225 |
TRG_Pf-PMV_PEXEL_1 | 714 | 718 | PF00026 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I458 | Leptomonas seymouri | 23% | 100% |
A0A0N1I5R1 | Leptomonas seymouri | 60% | 93% |
A0A0S4JSZ9 | Bodo saltans | 24% | 100% |
A0A1X0NRS9 | Trypanosomatidae | 34% | 94% |
A0A3Q8ID91 | Leishmania donovani | 27% | 100% |
A0A3Q8IQY6 | Leishmania donovani | 25% | 100% |
A0A3S5H5X3 | Leishmania donovani | 23% | 100% |
A0A3S5H6T7 | Leishmania donovani | 23% | 100% |
A0A3S7WR01 | Leishmania donovani | 89% | 94% |
A0A3S7X579 | Leishmania donovani | 24% | 100% |
A1CHL3 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 21% | 92% |
A1DG51 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 25% | 100% |
A4H4Y0 | Leishmania braziliensis | 23% | 100% |
A4H5Z5 | Leishmania braziliensis | 68% | 98% |
A4HGR1 | Leishmania braziliensis | 27% | 100% |
A4HK38 | Leishmania braziliensis | 25% | 100% |
A4HP82 | Leishmania braziliensis | 24% | 100% |
A4HTF8 | Leishmania infantum | 25% | 100% |
A4HUC1 | Leishmania infantum | 89% | 94% |
A4HWB0 | Leishmania infantum | 24% | 100% |
A4HZF8 | Leishmania infantum | 22% | 100% |
A4I3T6 | Leishmania infantum | 27% | 100% |
A4I7M5 | Leishmania infantum | 25% | 100% |
A4IDI7 | Leishmania infantum | 25% | 100% |
D0A3C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A4H6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9AM86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ASZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AT30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B2I0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
P0CQ74 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 24% | 100% |
P0CQ75 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 24% | 100% |
Q4Q1G8 | Leishmania major | 23% | 100% |
Q4Q1K8 | Leishmania major | 24% | 100% |
Q4Q5M6 | Leishmania major | 26% | 100% |
Q4Q858 | Leishmania major | 28% | 100% |
Q4QHK6 | Leishmania major | 89% | 100% |
Q4QIG1 | Leishmania major | 26% | 100% |
Q4QIQ9 | Leishmania major | 23% | 100% |
Q8RXK6 | Arabidopsis thaliana | 22% | 100% |
V5BII0 | Trypanosoma cruzi | 35% | 100% |