Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H6U0
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006399 | tRNA metabolic process | 7 | 11 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 11 |
GO:0006423 | cysteinyl-tRNA aminoacylation | 7 | 11 |
GO:0006520 | amino acid metabolic process | 3 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0019752 | carboxylic acid metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0043038 | amino acid activation | 4 | 11 |
GO:0043039 | tRNA aminoacylation | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043436 | oxoacid metabolic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 11 |
GO:0004817 | cysteine-tRNA ligase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 609 | 613 | PF00656 | 0.494 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.247 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 686 | 688 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 745 | 749 | PF00082 | 0.401 |
DEG_APCC_DBOX_1 | 436 | 444 | PF00400 | 0.460 |
DOC_CYCLIN_RxL_1 | 448 | 457 | PF00134 | 0.420 |
DOC_MAPK_gen_1 | 428 | 436 | PF00069 | 0.447 |
DOC_PP1_RVXF_1 | 134 | 141 | PF00149 | 0.404 |
DOC_PP1_RVXF_1 | 449 | 455 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 55 | 62 | PF00149 | 0.444 |
DOC_PP4_FxxP_1 | 344 | 347 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 696 | 699 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.325 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.459 |
DOC_USP7_UBL2_3 | 734 | 738 | PF12436 | 0.451 |
DOC_USP7_UBL2_3 | 741 | 745 | PF12436 | 0.413 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.388 |
LIG_14-3-3_CanoR_1 | 260 | 268 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 311 | 318 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 553 | 559 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 60 | 69 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.386 |
LIG_ActinCP_TwfCPI_2 | 344 | 351 | PF01115 | 0.478 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.458 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.392 |
LIG_BRCT_BRCA1_1 | 700 | 704 | PF00533 | 0.447 |
LIG_deltaCOP1_diTrp_1 | 349 | 356 | PF00928 | 0.447 |
LIG_deltaCOP1_diTrp_1 | 691 | 696 | PF00928 | 0.520 |
LIG_EVH1_2 | 699 | 703 | PF00568 | 0.311 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.447 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.483 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.534 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.378 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.481 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.404 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.544 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.447 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.447 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.449 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.518 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.375 |
LIG_FHA_2 | 711 | 717 | PF00498 | 0.486 |
LIG_FHA_2 | 725 | 731 | PF00498 | 0.423 |
LIG_LIR_Apic_2 | 349 | 355 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 457 | 462 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 201 | 210 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 277 | 288 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 526 | 534 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 593 | 604 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 713 | 722 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 749 | 754 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 82 | 90 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 301 | 305 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 526 | 531 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 567 | 573 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 691 | 696 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 709 | 715 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 749 | 753 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.447 |
LIG_LYPXL_yS_3 | 28 | 31 | PF13949 | 0.442 |
LIG_LYPXL_yS_3 | 302 | 305 | PF13949 | 0.460 |
LIG_MLH1_MIPbox_1 | 286 | 290 | PF16413 | 0.447 |
LIG_MLH1_MIPbox_1 | 700 | 704 | PF16413 | 0.447 |
LIG_MYND_1 | 303 | 307 | PF01753 | 0.460 |
LIG_PCNA_PIPBox_1 | 617 | 626 | PF02747 | 0.337 |
LIG_PCNA_TLS_4 | 87 | 94 | PF02747 | 0.447 |
LIG_PCNA_yPIPBox_3 | 611 | 624 | PF02747 | 0.334 |
LIG_Pex14_1 | 386 | 390 | PF04695 | 0.460 |
LIG_Pex14_1 | 409 | 413 | PF04695 | 0.447 |
LIG_Pex14_2 | 203 | 207 | PF04695 | 0.447 |
LIG_REV1ctd_RIR_1 | 701 | 710 | PF16727 | 0.355 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.460 |
LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.542 |
LIG_SH2_NCK_1 | 715 | 719 | PF00017 | 0.511 |
LIG_SH2_SRC | 715 | 718 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 505 | 509 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 746 | 750 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.503 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.447 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.449 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.447 |
LIG_SH3_3 | 643 | 649 | PF00018 | 0.492 |
LIG_SH3_3 | 694 | 700 | PF00018 | 0.355 |
LIG_SUMO_SIM_anti_2 | 486 | 491 | PF11976 | 0.373 |
LIG_TRAF2_1 | 313 | 316 | PF00917 | 0.457 |
LIG_TRAF2_1 | 669 | 672 | PF00917 | 0.513 |
LIG_TRAF2_1 | 727 | 730 | PF00917 | 0.549 |
LIG_TYR_ITIM | 26 | 31 | PF00017 | 0.285 |
LIG_TYR_ITSM | 711 | 718 | PF00017 | 0.410 |
LIG_UBA3_1 | 179 | 185 | PF00899 | 0.221 |
LIG_WRC_WIRS_1 | 80 | 85 | PF05994 | 0.282 |
MOD_CDK_SPK_2 | 443 | 448 | PF00069 | 0.199 |
MOD_CDK_SPxxK_3 | 454 | 461 | PF00069 | 0.204 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.261 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.300 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.222 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.331 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.345 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.282 |
MOD_CK2_1 | 724 | 730 | PF00069 | 0.545 |
MOD_CK2_1 | 746 | 752 | PF00069 | 0.401 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.387 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.323 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.431 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.339 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.598 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.315 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.392 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.161 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.557 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.462 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.282 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.419 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.282 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.300 |
MOD_N-GLC_2 | 395 | 397 | PF02516 | 0.282 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.204 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.309 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.282 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.415 |
MOD_NEK2_2 | 284 | 289 | PF00069 | 0.330 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.325 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.458 |
MOD_PKA_1 | 333 | 339 | PF00069 | 0.204 |
MOD_PKA_1 | 677 | 683 | PF00069 | 0.412 |
MOD_PKA_1 | 710 | 716 | PF00069 | 0.405 |
MOD_PKA_1 | 737 | 743 | PF00069 | 0.460 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.282 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.415 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.208 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.357 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.325 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.282 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.282 |
MOD_Plk_1 | 591 | 597 | PF00069 | 0.345 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.300 |
MOD_Plk_2-3 | 729 | 735 | PF00069 | 0.524 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.330 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.282 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.413 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.350 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.244 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.282 |
MOD_Plk_4 | 757 | 763 | PF00069 | 0.568 |
MOD_Plk_4 | 768 | 774 | PF00069 | 0.474 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.346 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.293 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.199 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.199 |
MOD_SUMO_rev_2 | 106 | 112 | PF00179 | 0.282 |
MOD_SUMO_rev_2 | 174 | 180 | PF00179 | 0.283 |
MOD_SUMO_rev_2 | 383 | 391 | PF00179 | 0.300 |
MOD_SUMO_rev_2 | 612 | 620 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 708 | 713 | PF00179 | 0.530 |
MOD_SUMO_rev_2 | 729 | 739 | PF00179 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 448 | 453 | PF01217 | 0.282 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.204 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 750 | 753 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.282 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 687 | 689 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 704 | 706 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.282 |
TRG_NLS_Bipartite_1 | 661 | 680 | PF00514 | 0.405 |
TRG_NLS_MonoExtC_3 | 153 | 158 | PF00514 | 0.295 |
TRG_NLS_MonoExtC_3 | 685 | 691 | PF00514 | 0.418 |
TRG_NLS_MonoExtN_4 | 110 | 117 | PF00514 | 0.282 |
TRG_NLS_MonoExtN_4 | 154 | 159 | PF00514 | 0.295 |
TRG_NLS_MonoExtN_4 | 675 | 680 | PF00514 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 662 | 666 | PF00026 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 687 | 691 | PF00026 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 87 | 91 | PF00026 | 0.250 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U0 | Leptomonas seymouri | 81% | 99% |
A0A0S4JIJ5 | Bodo saltans | 64% | 100% |
A0A1X0NM71 | Trypanosomatidae | 69% | 98% |
A0A3S7WRW6 | Leishmania donovani | 89% | 99% |
A0A422N5J6 | Trypanosoma rangeli | 68% | 99% |
C9ZQB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 99% |
E9AGB4 | Leishmania infantum | 89% | 99% |
E9ANV2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
P49589 | Homo sapiens | 40% | 100% |
P53852 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 39% | 100% |
Q09860 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 40% | 100% |
Q291L4 | Drosophila pseudoobscura pseudoobscura | 41% | 100% |
Q4QGR8 | Leishmania major | 89% | 100% |
Q4R550 | Macaca fascicularis | 41% | 100% |
Q54KR1 | Dictyostelium discoideum | 45% | 100% |
Q5F408 | Gallus gallus | 40% | 100% |
Q5M7N8 | Xenopus tropicalis | 41% | 100% |
Q7KN90 | Drosophila melanogaster | 41% | 100% |
Q7ZWR2 | Xenopus laevis | 41% | 100% |
Q9ER72 | Mus musculus | 39% | 94% |