Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | yes | yes: 2 |
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: 6 |
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 | 2 |
GO:0018444 | translation release factor complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QGW5
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 2 |
GO:0006518 | peptide metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043043 | peptide biosynthetic process | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0043604 | amide biosynthetic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003747 | translation release factor activity | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003924 | GTPase activity | 7 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005525 | GTP binding | 5 | 11 |
GO:0008079 | translation termination factor activity | 4 | 2 |
GO:0008135 | translation factor activity, RNA binding | 3 | 3 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0019001 | guanyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032561 | guanyl 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:0045182 | translation regulator activity | 1 | 3 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003746 | translation elongation factor activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.778 |
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.481 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 689 | 691 | PF00675 | 0.320 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.653 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 667 | 671 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 732 | 736 | PF00082 | 0.281 |
DEG_SPOP_SBC_1 | 269 | 273 | PF00917 | 0.725 |
DOC_ANK_TNKS_1 | 739 | 746 | PF00023 | 0.585 |
DOC_CKS1_1 | 244 | 249 | PF01111 | 0.726 |
DOC_CYCLIN_yCln2_LP_2 | 715 | 721 | PF00134 | 0.561 |
DOC_MAPK_gen_1 | 199 | 208 | PF00069 | 0.669 |
DOC_MAPK_gen_1 | 210 | 216 | PF00069 | 0.671 |
DOC_MAPK_gen_1 | 320 | 331 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 504 | 513 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 534 | 541 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 740 | 748 | PF00069 | 0.505 |
DOC_PP1_RVXF_1 | 504 | 511 | PF00149 | 0.495 |
DOC_PP1_RVXF_1 | 642 | 649 | PF00149 | 0.407 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 545 | 548 | PF13499 | 0.490 |
DOC_PP4_FxxP_1 | 557 | 560 | PF00568 | 0.473 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.806 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.774 |
DOC_USP7_MATH_2 | 221 | 227 | PF00917 | 0.720 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.699 |
DOC_USP7_UBL2_3 | 316 | 320 | PF12436 | 0.639 |
DOC_USP7_UBL2_3 | 566 | 570 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 683 | 687 | PF12436 | 0.481 |
DOC_USP7_UBL2_3 | 725 | 729 | PF12436 | 0.480 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 404 | 409 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 483 | 491 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 80 | 84 | PF00244 | 0.578 |
LIG_APCC_ABBA_1 | 721 | 726 | PF00400 | 0.533 |
LIG_APCC_ABBAyCdc20_2 | 80 | 86 | PF00400 | 0.725 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.639 |
LIG_BIR_III_2 | 241 | 245 | PF00653 | 0.699 |
LIG_BIR_III_4 | 410 | 414 | PF00653 | 0.481 |
LIG_BRCT_BRCA1_1 | 605 | 609 | PF00533 | 0.539 |
LIG_BRCT_BRCA1_2 | 605 | 611 | PF00533 | 0.530 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.681 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.481 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.726 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.481 |
LIG_FHA_1 | 739 | 745 | PF00498 | 0.481 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.756 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.831 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.809 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.681 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.555 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.481 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.481 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.481 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.506 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.449 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.463 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.383 |
LIG_FXI_DFP_1 | 724 | 728 | PF00024 | 0.295 |
LIG_IRF3_LxIS_1 | 430 | 436 | PF10401 | 0.481 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.649 |
LIG_LIR_Apic_2 | 554 | 560 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 82 | 87 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 374 | 381 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 482 | 491 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 678 | 688 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 726 | 735 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 571 | 577 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 678 | 684 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 726 | 730 | PF02991 | 0.517 |
LIG_PCNA_APIM_2 | 730 | 736 | PF02747 | 0.481 |
LIG_Pex14_1 | 373 | 377 | PF04695 | 0.481 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.495 |
LIG_Pex14_2 | 442 | 446 | PF04695 | 0.481 |
LIG_REV1ctd_RIR_1 | 646 | 656 | PF16727 | 0.533 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.812 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.665 |
LIG_SH2_CRK | 375 | 379 | PF00017 | 0.481 |
LIG_SH2_GRB2like | 24 | 27 | PF00017 | 0.688 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.715 |
LIG_SH2_NCK_1 | 37 | 41 | PF00017 | 0.730 |
LIG_SH2_SRC | 24 | 27 | PF00017 | 0.696 |
LIG_SH2_SRC | 375 | 378 | PF00017 | 0.481 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.751 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 375 | 379 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 484 | 488 | PF00017 | 0.445 |
LIG_SH2_STAT3 | 122 | 125 | PF00017 | 0.694 |
LIG_SH2_STAT3 | 141 | 144 | PF00017 | 0.337 |
LIG_SH2_STAT3 | 28 | 31 | PF00017 | 0.709 |
LIG_SH2_STAT3 | 49 | 52 | PF00017 | 0.682 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.705 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.738 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.749 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.388 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.783 |
LIG_SH3_3 | 717 | 723 | PF00018 | 0.533 |
LIG_SUMO_SIM_par_1 | 431 | 437 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 652 | 657 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 716 | 722 | PF11976 | 0.561 |
LIG_SxIP_EBH_1 | 632 | 644 | PF03271 | 0.445 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.757 |
LIG_TRAF2_1 | 257 | 260 | PF00917 | 0.722 |
LIG_TRAF2_1 | 296 | 299 | PF00917 | 0.582 |
LIG_TRAF2_1 | 382 | 385 | PF00917 | 0.512 |
LIG_TRAF2_1 | 674 | 677 | PF00917 | 0.470 |
LIG_UBA3_1 | 467 | 473 | PF00899 | 0.495 |
LIG_UBA3_1 | 538 | 546 | PF00899 | 0.585 |
LIG_UBA3_1 | 684 | 691 | PF00899 | 0.533 |
MOD_CDK_SPxxK_3 | 293 | 300 | PF00069 | 0.722 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.542 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.741 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.800 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.470 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.495 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.520 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.422 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.561 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.755 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.697 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.747 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.587 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.481 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.481 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.491 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.405 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.429 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.422 |
MOD_CK2_1 | 671 | 677 | PF00069 | 0.585 |
MOD_CK2_1 | 750 | 756 | PF00069 | 0.482 |
MOD_Cter_Amidation | 208 | 211 | PF01082 | 0.694 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.793 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.758 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.718 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.764 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.692 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.281 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.389 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.361 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.361 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.547 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.722 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.807 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.715 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.512 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.430 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.417 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.499 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.786 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.551 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.712 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.481 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.481 |
MOD_NEK2_1 | 750 | 755 | PF00069 | 0.469 |
MOD_NEK2_2 | 69 | 74 | PF00069 | 0.568 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.727 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.816 |
MOD_PIKK_1 | 423 | 429 | PF00454 | 0.481 |
MOD_PKA_1 | 300 | 306 | PF00069 | 0.649 |
MOD_PKA_1 | 404 | 410 | PF00069 | 0.481 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.540 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.490 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.461 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.434 |
MOD_PKA_2 | 689 | 695 | PF00069 | 0.528 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.578 |
MOD_PKB_1 | 310 | 318 | PF00069 | 0.708 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.557 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.550 |
MOD_Plk_1 | 677 | 683 | PF00069 | 0.495 |
MOD_Plk_2-3 | 549 | 555 | PF00069 | 0.476 |
MOD_Plk_2-3 | 600 | 606 | PF00069 | 0.425 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.539 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.490 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.461 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.499 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.565 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.527 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.731 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.761 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.793 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.806 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.626 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.671 |
MOD_SUMO_for_1 | 236 | 239 | PF00179 | 0.727 |
MOD_SUMO_for_1 | 304 | 307 | PF00179 | 0.589 |
MOD_SUMO_rev_2 | 229 | 238 | PF00179 | 0.783 |
MOD_SUMO_rev_2 | 239 | 245 | PF00179 | 0.793 |
MOD_SUMO_rev_2 | 475 | 480 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 540 | 548 | PF00179 | 0.589 |
MOD_SUMO_rev_2 | 567 | 571 | PF00179 | 0.519 |
TRG_DiLeu_BaEn_1 | 454 | 459 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.402 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.480 |
TRG_NLS_Bipartite_1 | 199 | 214 | PF00514 | 0.778 |
TRG_NLS_MonoExtN_4 | 198 | 203 | PF00514 | 0.649 |
TRG_Pf-PMV_PEXEL_1 | 623 | 627 | PF00026 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAZ5 | Leptomonas seymouri | 79% | 100% |
A0A0S4IX91 | Bodo saltans | 63% | 100% |
A0A1X0NV54 | Trypanosomatidae | 71% | 100% |
A0A3Q8ICH2 | Leishmania donovani | 94% | 100% |
A0A3R7MLL0 | Trypanosoma rangeli | 71% | 100% |
A0A3S7X9T0 | Leishmania donovani | 30% | 100% |
A4H6P3 | Leishmania braziliensis | 88% | 100% |
A4HN87 | Leishmania braziliensis | 32% | 100% |
A4HV24 | Leishmania infantum | 94% | 100% |
A4IBV5 | Leishmania infantum | 30% | 100% |
C9ZYQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A7C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9AFP2 | Leishmania major | 31% | 100% |
E9ANQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 99% |
E9B6U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O74718 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
P05453 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 100% |
P23637 | Ogataea pini | 40% | 100% |
Q9HGI7 | Candida maltosa | 38% | 100% |
Q9HGI8 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 38% | 100% |
Q9W074 | Drosophila melanogaster | 35% | 100% |