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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005795 | Golgi stack | 4 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IKK0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022411 | cellular component disassembly | 4 | 12 |
GO:0032984 | protein-containing complex disassembly | 5 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0035494 | SNARE complex disassembly | 6 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006893 | Golgi to plasma membrane transport | 5 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0043001 | Golgi to plasma membrane protein transport | 5 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0061951 | establishment of protein localization to plasma membrane | 5 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0072659 | protein localization to plasma membrane | 5 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:0098876 | vesicle-mediated transport to the plasma membrane | 4 | 1 |
GO:1990778 | protein localization to cell periphery | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.258 |
CLV_C14_Caspase3-7 | 505 | 509 | PF00656 | 0.410 |
CLV_C14_Caspase3-7 | 647 | 651 | PF00656 | 0.276 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.341 |
CLV_PCSK_FUR_1 | 516 | 520 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.356 |
CLV_PCSK_PC1ET2_1 | 518 | 520 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 529 | 531 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 628 | 630 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.165 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.377 |
DOC_ANK_TNKS_1 | 628 | 635 | PF00023 | 0.276 |
DOC_CYCLIN_RxL_1 | 69 | 79 | PF00134 | 0.372 |
DOC_CYCLIN_RxL_1 | 698 | 710 | PF00134 | 0.349 |
DOC_MAPK_DCC_7 | 661 | 669 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 173 | 183 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 384 | 394 | PF00069 | 0.248 |
DOC_MAPK_gen_1 | 529 | 536 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 134 | 143 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 387 | 396 | PF00069 | 0.242 |
DOC_MAPK_MEF2A_6 | 529 | 538 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 661 | 669 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 674 | 683 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 703 | 711 | PF00069 | 0.337 |
DOC_MAPK_RevD_3 | 255 | 271 | PF00069 | 0.242 |
DOC_PP1_RVXF_1 | 602 | 609 | PF00149 | 0.258 |
DOC_PP2B_LxvP_1 | 662 | 665 | PF13499 | 0.345 |
DOC_SPAK_OSR1_1 | 387 | 391 | PF12202 | 0.242 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 731 | 735 | PF00917 | 0.355 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.374 |
DOC_USP7_UBL2_3 | 514 | 518 | PF12436 | 0.545 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.258 |
LIG_14-3-3_CanoR_1 | 134 | 142 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 176 | 183 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 614 | 620 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 720 | 726 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 82 | 86 | PF00244 | 0.485 |
LIG_Actin_WH2_2 | 368 | 386 | PF00022 | 0.247 |
LIG_APCC_ABBA_1 | 323 | 328 | PF00400 | 0.242 |
LIG_APCC_ABBA_1 | 388 | 393 | PF00400 | 0.242 |
LIG_APCC_ABBAyCdc20_2 | 387 | 393 | PF00400 | 0.242 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.475 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.242 |
LIG_Clathr_ClatBox_1 | 323 | 327 | PF01394 | 0.242 |
LIG_DLG_GKlike_1 | 530 | 537 | PF00625 | 0.482 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.420 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.245 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.349 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.385 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.247 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.466 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.396 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.413 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.499 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.356 |
LIG_GBD_Chelix_1 | 268 | 276 | PF00786 | 0.242 |
LIG_LIR_Apic_2 | 587 | 593 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 25 | 36 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 288 | 294 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 42 | 51 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 558 | 567 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 607 | 615 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 643 | 654 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 724 | 731 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 42 | 46 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 508 | 513 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 558 | 564 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 607 | 611 | PF02991 | 0.266 |
LIG_MAD2 | 98 | 106 | PF02301 | 0.327 |
LIG_NRBOX | 619 | 625 | PF00104 | 0.242 |
LIG_NRBOX | 704 | 710 | PF00104 | 0.474 |
LIG_PCNA_yPIPBox_3 | 614 | 624 | PF02747 | 0.242 |
LIG_Pex14_2 | 226 | 230 | PF04695 | 0.317 |
LIG_Rb_LxCxE_1 | 274 | 288 | PF01857 | 0.388 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.236 |
LIG_SH2_CRK | 590 | 594 | PF00017 | 0.276 |
LIG_SH2_GRB2like | 615 | 618 | PF00017 | 0.242 |
LIG_SH2_PTP2 | 561 | 564 | PF00017 | 0.258 |
LIG_SH2_STAP1 | 520 | 524 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 615 | 619 | PF00017 | 0.242 |
LIG_SH2_STAT3 | 128 | 131 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 520 | 523 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.217 |
LIG_SH3_2 | 397 | 402 | PF14604 | 0.412 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.428 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.242 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.417 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.310 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 532 | 539 | PF11976 | 0.366 |
LIG_SUMO_SIM_anti_2 | 690 | 697 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 622 | 627 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 636 | 643 | PF11976 | 0.235 |
LIG_SUMO_SIM_par_1 | 705 | 710 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 83 | 88 | PF11976 | 0.398 |
LIG_SxIP_EBH_1 | 665 | 674 | PF03271 | 0.438 |
LIG_TRAF2_1 | 424 | 427 | PF00917 | 0.388 |
LIG_TRAF2_1 | 480 | 483 | PF00917 | 0.360 |
LIG_TRAF2_1 | 491 | 494 | PF00917 | 0.418 |
LIG_UBA3_1 | 619 | 628 | PF00899 | 0.242 |
LIG_UBA3_1 | 707 | 716 | PF00899 | 0.417 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.567 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.370 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.361 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.292 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.257 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.370 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.488 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.480 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.398 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.194 |
MOD_Cter_Amidation | 527 | 530 | PF01082 | 0.455 |
MOD_Cter_Amidation | 633 | 636 | PF01082 | 0.276 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.511 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.364 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.412 |
MOD_GlcNHglycan | 163 | 167 | PF01048 | 0.438 |
MOD_GlcNHglycan | 187 | 191 | PF01048 | 0.527 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.242 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.246 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.269 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.432 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.378 |
MOD_GlcNHglycan | 717 | 720 | PF01048 | 0.547 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.483 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.554 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.297 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.558 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.121 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.480 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.351 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.376 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.394 |
MOD_N-GLC_1 | 13 | 18 | PF02516 | 0.511 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.534 |
MOD_N-GLC_1 | 433 | 438 | PF02516 | 0.242 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.375 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.250 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.331 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.392 |
MOD_NEK2_2 | 656 | 661 | PF00069 | 0.430 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.379 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.485 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.388 |
MOD_PIKK_1 | 682 | 688 | PF00454 | 0.400 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.473 |
MOD_PKA_1 | 518 | 524 | PF00069 | 0.409 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.359 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.301 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.464 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.258 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.487 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.242 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.489 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.302 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.340 |
MOD_Plk_1 | 606 | 612 | PF00069 | 0.253 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.438 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.358 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.242 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.308 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.488 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.406 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.522 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.258 |
MOD_SUMO_for_1 | 491 | 494 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 157 | 164 | PF00179 | 0.567 |
MOD_SUMO_rev_2 | 274 | 284 | PF00179 | 0.388 |
MOD_SUMO_rev_2 | 710 | 718 | PF00179 | 0.459 |
MOD_SUMO_rev_2 | 9 | 18 | PF00179 | 0.494 |
TRG_DiLeu_BaEn_1 | 633 | 638 | PF01217 | 0.243 |
TRG_DiLeu_BaEn_4 | 493 | 499 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 601 | 606 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 70 | 75 | PF01217 | 0.355 |
TRG_DiLeu_BaLyEn_6 | 718 | 723 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 646 | 649 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 725 | 728 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.251 |
TRG_Pf-PMV_PEXEL_1 | 302 | 307 | PF00026 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 98 | 103 | PF00026 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P640 | Leptomonas seymouri | 83% | 100% |
A0A0N0P6X6 | Leptomonas seymouri | 33% | 72% |
A0A0S4JAU3 | Bodo saltans | 26% | 100% |
A0A0S4JTC3 | Bodo saltans | 57% | 100% |
A0A1X0NXR8 | Trypanosomatidae | 63% | 100% |
A0A1X0P437 | Trypanosomatidae | 29% | 79% |
A0A3S7X0L3 | Leishmania donovani | 26% | 100% |
A0A422MWC2 | Trypanosoma rangeli | 28% | 83% |
A0A422NPR7 | Trypanosoma rangeli | 63% | 100% |
A4HFM9 | Leishmania braziliensis | 26% | 100% |
A4HFN1 | Leishmania braziliensis | 34% | 74% |
A4HYS3 | Leishmania infantum | 100% | 100% |
A4I2Q7 | Leishmania infantum | 26% | 100% |
C9ZI97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
D0A5W2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 83% |
E9AD83 | Leishmania major | 26% | 100% |
E9AID2 | Leishmania braziliensis | 94% | 100% |
E9AUL9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9AZ07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
O14325 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 95% |
O28972 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 32% | 100% |
P18708 | Cricetulus griseus | 40% | 99% |
P18759 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 40% | 97% |
P34732 | Candida albicans | 42% | 93% |
P46459 | Homo sapiens | 40% | 99% |
P46460 | Mus musculus | 40% | 99% |
P46461 | Drosophila melanogaster | 41% | 99% |
P54351 | Drosophila melanogaster | 42% | 98% |
Q07844 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 88% |
Q0DGP6 | Oryza sativa subsp. japonica | 44% | 99% |
Q4QCW5 | Leishmania major | 98% | 100% |
Q54SY2 | Dictyostelium discoideum | 24% | 85% |
Q58556 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 30% | 82% |
Q5R410 | Pongo abelii | 40% | 99% |
Q75JI3 | Dictyostelium discoideum | 44% | 100% |
Q94392 | Caenorhabditis elegans | 44% | 90% |
Q9M0Y8 | Arabidopsis thaliana | 44% | 99% |
Q9NAG4 | Caenorhabditis elegans | 26% | 91% |
Q9P7Q4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 41% | 93% |
Q9QUL6 | Rattus norvegicus | 42% | 99% |
V5DS04 | Trypanosoma cruzi | 64% | 92% |