Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 15 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0099080 | supramolecular complex | 2 | 15 |
GO:0099081 | supramolecular polymer | 3 | 15 |
GO:0099512 | supramolecular fiber | 4 | 15 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
Related structures:
AlphaFold database: Q9NF78
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0000902 | cell morphogenesis | 3 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 15 |
GO:0007018 | microtubule-based movement | 3 | 15 |
GO:0009653 | anatomical structure morphogenesis | 2 | 2 |
GO:0009987 | cellular process | 1 | 15 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 2 |
GO:0030865 | cortical cytoskeleton organization | 6 | 2 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 2 |
GO:0032502 | developmental process | 1 | 2 |
GO:0043622 | cortical microtubule organization | 5 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003774 | cytoskeletal motor activity | 1 | 15 |
GO:0003777 | microtubule motor activity | 2 | 15 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 15 |
GO:0005515 | protein binding | 2 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0008017 | microtubule binding | 5 | 15 |
GO:0008092 | cytoskeletal protein binding | 3 | 15 |
GO:0015631 | tubulin binding | 4 | 15 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140657 | ATP-dependent activity | 1 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 580 | 584 | PF00656 | 0.686 |
CLV_MEL_PAP_1 | 117 | 123 | PF00089 | 0.334 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 625 | 627 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.535 |
CLV_PCSK_FUR_1 | 626 | 630 | PF00082 | 0.645 |
CLV_PCSK_FUR_1 | 633 | 637 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 489 | 491 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 570 | 572 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 612 | 614 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 628 | 630 | PF00082 | 0.632 |
CLV_PCSK_PC7_1 | 485 | 491 | PF00082 | 0.481 |
CLV_PCSK_PC7_1 | 540 | 546 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.677 |
CLV_Separin_Metazoa | 562 | 566 | PF03568 | 0.670 |
CLV_Separin_Metazoa | 623 | 627 | PF03568 | 0.501 |
CLV_Separin_Metazoa | 638 | 642 | PF03568 | 0.667 |
DEG_APCC_DBOX_1 | 263 | 271 | PF00400 | 0.306 |
DEG_APCC_DBOX_1 | 410 | 418 | PF00400 | 0.674 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.556 |
DOC_MAPK_gen_1 | 143 | 152 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 376 | 383 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 454 | 461 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 120 | 129 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 325 | 332 | PF00069 | 0.319 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.720 |
DOC_USP7_UBL2_3 | 436 | 440 | PF12436 | 0.583 |
DOC_USP7_UBL2_3 | 513 | 517 | PF12436 | 0.595 |
DOC_USP7_UBL2_3 | 651 | 655 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.308 |
LIG_14-3-3_CanoR_1 | 219 | 226 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 350 | 354 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 378 | 384 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 418 | 422 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 46 | 52 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 641 | 647 | PF00244 | 0.629 |
LIG_Actin_WH2_2 | 155 | 173 | PF00022 | 0.319 |
LIG_APCC_ABBA_1 | 155 | 160 | PF00400 | 0.295 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.334 |
LIG_CaM_IQ_9 | 495 | 510 | PF13499 | 0.466 |
LIG_deltaCOP1_diTrp_1 | 24 | 32 | PF00928 | 0.420 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.557 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.365 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.308 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.308 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.531 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.351 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.249 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.485 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.346 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.495 |
LIG_LIR_Apic_2 | 187 | 192 | PF02991 | 0.334 |
LIG_LIR_Apic_2 | 37 | 42 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 124 | 133 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 151 | 162 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 497 | 505 | PF02991 | 0.736 |
LIG_LIR_Gen_1 | 634 | 643 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 64 | 74 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.742 |
LIG_LIR_Nem_3 | 634 | 640 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.332 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.320 |
LIG_PCNA_yPIPBox_3 | 544 | 558 | PF02747 | 0.438 |
LIG_PCNA_yPIPBox_3 | 55 | 69 | PF02747 | 0.341 |
LIG_PCNA_yPIPBox_3 | 561 | 572 | PF02747 | 0.385 |
LIG_PTB_Apo_2 | 120 | 127 | PF02174 | 0.319 |
LIG_Rb_pABgroove_1 | 97 | 105 | PF01858 | 0.460 |
LIG_RPA_C_Fungi | 567 | 579 | PF08784 | 0.414 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.326 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.334 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.354 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.354 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.306 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 533 | 537 | PF00017 | 0.634 |
LIG_SH2_STAT3 | 59 | 62 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.341 |
LIG_SH3_1 | 325 | 331 | PF00018 | 0.319 |
LIG_SH3_2 | 328 | 333 | PF14604 | 0.319 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.319 |
LIG_SUMO_SIM_par_1 | 15 | 21 | PF11976 | 0.397 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.575 |
LIG_UBA3_1 | 125 | 130 | PF00899 | 0.324 |
LIG_UBA3_1 | 599 | 607 | PF00899 | 0.686 |
LIG_UBA3_1 | 621 | 628 | PF00899 | 0.502 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.499 |
LIG_WW_3 | 140 | 144 | PF00397 | 0.311 |
MOD_CDK_SPxxK_3 | 355 | 362 | PF00069 | 0.319 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.314 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.308 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.399 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.326 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.319 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.360 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.276 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.599 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.454 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.538 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.530 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.333 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.320 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.334 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.411 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.445 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.274 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.306 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.306 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.262 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.458 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.594 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.432 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.354 |
MOD_LATS_1 | 438 | 444 | PF00433 | 0.459 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.379 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.251 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.307 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.316 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.308 |
MOD_N-GLC_2 | 82 | 84 | PF02516 | 0.295 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.601 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.334 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.366 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.312 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.400 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.298 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.306 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.319 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.584 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.493 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.513 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.429 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.456 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.295 |
MOD_PKA_1 | 489 | 495 | PF00069 | 0.631 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.320 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.379 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.320 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.308 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.308 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.639 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.608 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.631 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.470 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.334 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.308 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.496 |
MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.470 |
MOD_Plk_2-3 | 520 | 526 | PF00069 | 0.705 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.405 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.333 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.443 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.349 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.340 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.319 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.265 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.310 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.446 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.295 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.308 |
MOD_SUMO_for_1 | 516 | 519 | PF00179 | 0.634 |
MOD_SUMO_rev_2 | 131 | 139 | PF00179 | 0.364 |
MOD_SUMO_rev_2 | 432 | 441 | PF00179 | 0.658 |
MOD_SUMO_rev_2 | 519 | 528 | PF00179 | 0.639 |
MOD_SUMO_rev_2 | 616 | 622 | PF00179 | 0.660 |
TRG_DiLeu_BaEn_3 | 616 | 622 | PF01217 | 0.508 |
TRG_ENDOCYTIC_2 | 637 | 640 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 445 | 448 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 542 | 545 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 632 | 635 | PF00400 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.319 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDD6 | Leptomonas seymouri | 77% | 86% |
A0A0S4IP49 | Bodo saltans | 27% | 81% |
A0A0S4IR67 | Bodo saltans | 63% | 84% |
A0A0S4J2K1 | Bodo saltans | 32% | 69% |
A0A0S4JRN9 | Bodo saltans | 34% | 100% |
A0A1X0NQ03 | Trypanosomatidae | 28% | 79% |
A0A1X0NWZ8 | Trypanosomatidae | 62% | 88% |
A0A3Q8IAZ2 | Leishmania donovani | 97% | 100% |
A0A3Q8IEL2 | Leishmania donovani | 31% | 100% |
A0A3R7KHX7 | Trypanosoma rangeli | 30% | 89% |
A0A3S7X9Y1 | Leishmania donovani | 27% | 100% |
A0A422NEQ8 | Trypanosoma rangeli | 60% | 87% |
A0A422NMD1 | Trypanosoma rangeli | 24% | 100% |
A4HAQ7 | Leishmania braziliensis | 32% | 100% |
A4HCT2 | Leishmania braziliensis | 82% | 91% |
A4HHN8 | Leishmania braziliensis | 31% | 100% |
A4HND6 | Leishmania braziliensis | 26% | 100% |
A4HSA6 | Leishmania infantum | 30% | 100% |
A4I0A6 | Leishmania infantum | 97% | 100% |
A4I4V3 | Leishmania infantum | 31% | 100% |
A4IC09 | Leishmania infantum | 27% | 100% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 87% |
D0A8T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9AEA1 | Leishmania major | 30% | 100% |
E9AFU7 | Leishmania major | 27% | 100% |
E9AW71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P28743 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 93% |
Q4KLL9 | Rattus norvegicus | 31% | 79% |
Q6PFD6 | Mus musculus | 31% | 79% |
Q8LNZ2 | Arabidopsis thaliana | 29% | 70% |
Q9SCJ4 | Arabidopsis thaliana | 29% | 81% |
V5B6Q5 | Trypanosoma cruzi | 23% | 100% |
V5D733 | Trypanosoma cruzi | 62% | 87% |