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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000331 | contractile vacuole | 6 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0005777 | peroxisome | 6 | 1 |
GO:0020015 | glycosome | 7 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
Related structures:
AlphaFold database: A4HGZ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0051179 | localization | 1 | 5 |
GO:0051234 | establishment of localization | 2 | 5 |
GO:0055085 | transmembrane transport | 2 | 5 |
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006797 | polyphosphate metabolic process | 4 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006817 | phosphate ion transport | 7 | 1 |
GO:0006820 | monoatomic anion transport | 5 | 1 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0015698 | inorganic anion transport | 6 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030002 | intracellular monoatomic anion homeostasis | 5 | 1 |
GO:0030643 | intracellular phosphate ion homeostasis | 7 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0055062 | phosphate ion homeostasis | 8 | 1 |
GO:0055081 | monoatomic anion homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072502 | obsolete cellular trivalent inorganic anion homeostasis | 6 | 1 |
GO:0072506 | obsolete trivalent inorganic anion homeostasis | 7 | 1 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 6 |
GO:0005315 | inorganic phosphate transmembrane transporter activity | 4 | 1 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 604 | 608 | PF00656 | 0.370 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.491 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.399 |
CLV_PCSK_PC7_1 | 88 | 94 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.491 |
DEG_APCC_DBOX_1 | 213 | 221 | PF00400 | 0.569 |
DEG_APCC_DBOX_1 | 224 | 232 | PF00400 | 0.574 |
DEG_APCC_DBOX_1 | 381 | 389 | PF00400 | 0.286 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.613 |
DOC_CYCLIN_RxL_1 | 160 | 171 | PF00134 | 0.634 |
DOC_CYCLIN_RxL_1 | 222 | 232 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 237 | 243 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 5 | 13 | PF00069 | 0.679 |
DOC_MAPK_HePTP_8 | 340 | 352 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 343 | 352 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 426 | 435 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 641 | 647 | PF00149 | 0.347 |
DOC_PP4_FxxP_1 | 239 | 242 | PF00568 | 0.629 |
DOC_PP4_FxxP_1 | 315 | 318 | PF00568 | 0.416 |
DOC_PP4_FxxP_1 | 646 | 649 | PF00568 | 0.286 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.269 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 689 | 693 | PF00917 | 0.543 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.567 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.266 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 225 | 235 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 377 | 385 | PF00244 | 0.269 |
LIG_BRCT_BRCA1_1 | 231 | 235 | PF00533 | 0.630 |
LIG_deltaCOP1_diTrp_1 | 254 | 259 | PF00928 | 0.608 |
LIG_EH1_1 | 629 | 637 | PF00400 | 0.323 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.798 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.696 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.572 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.309 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.331 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.279 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.482 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.634 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.293 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.489 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.283 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.347 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.351 |
LIG_FHA_1 | 718 | 724 | PF00498 | 0.324 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.323 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.469 |
LIG_FHA_2 | 507 | 513 | PF00498 | 0.519 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.370 |
LIG_GBD_Chelix_1 | 525 | 533 | PF00786 | 0.387 |
LIG_LIR_Apic_2 | 236 | 242 | PF02991 | 0.627 |
LIG_LIR_Apic_2 | 417 | 422 | PF02991 | 0.469 |
LIG_LIR_Apic_2 | 532 | 537 | PF02991 | 0.464 |
LIG_LIR_Apic_2 | 720 | 724 | PF02991 | 0.324 |
LIG_LIR_Apic_2 | 726 | 731 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 244 | 251 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 289 | 299 | PF02991 | 0.192 |
LIG_LIR_Gen_1 | 41 | 52 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 494 | 504 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 55 | 65 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 565 | 575 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 608 | 619 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 14 | 18 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.192 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 494 | 499 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 565 | 570 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 608 | 614 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 679 | 684 | PF02991 | 0.374 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.652 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.634 |
LIG_NRBOX | 573 | 579 | PF00104 | 0.323 |
LIG_Pex14_1 | 15 | 19 | PF04695 | 0.550 |
LIG_Pex14_1 | 259 | 263 | PF04695 | 0.465 |
LIG_Pex14_1 | 572 | 576 | PF04695 | 0.323 |
LIG_Pex14_2 | 141 | 145 | PF04695 | 0.624 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.613 |
LIG_PTB_Apo_2 | 461 | 468 | PF02174 | 0.223 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.550 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.638 |
LIG_SH2_GRB2like | 246 | 249 | PF00017 | 0.688 |
LIG_SH2_NCK_1 | 246 | 250 | PF00017 | 0.691 |
LIG_SH2_PTP2 | 261 | 264 | PF00017 | 0.379 |
LIG_SH2_PTP2 | 501 | 504 | PF00017 | 0.540 |
LIG_SH2_PTP2 | 728 | 731 | PF00017 | 0.393 |
LIG_SH2_SRC | 246 | 249 | PF00017 | 0.688 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.652 |
LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 697 | 700 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 728 | 731 | PF00017 | 0.364 |
LIG_SH3_1 | 74 | 80 | PF00018 | 0.729 |
LIG_SH3_2 | 80 | 85 | PF14604 | 0.634 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.775 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.653 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.499 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.318 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.346 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.193 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.469 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 519 | 525 | PF11976 | 0.443 |
LIG_SUMO_SIM_anti_2 | 613 | 619 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 708 | 714 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 145 | 152 | PF11976 | 0.711 |
LIG_SUMO_SIM_par_1 | 475 | 481 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 488 | 494 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 521 | 527 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 617 | 622 | PF11976 | 0.267 |
LIG_SUMO_SIM_par_1 | 661 | 666 | PF11976 | 0.299 |
LIG_TRAF2_1 | 104 | 107 | PF00917 | 0.775 |
LIG_TRAF2_1 | 510 | 513 | PF00917 | 0.570 |
LIG_TYR_ITIM | 20 | 25 | PF00017 | 0.541 |
LIG_TYR_ITIM | 499 | 504 | PF00017 | 0.540 |
LIG_UBA3_1 | 593 | 602 | PF00899 | 0.340 |
LIG_UBA3_1 | 635 | 643 | PF00899 | 0.325 |
LIG_Vh1_VBS_1 | 617 | 635 | PF01044 | 0.318 |
LIG_WRC_WIRS_1 | 624 | 629 | PF05994 | 0.469 |
MOD_CDK_SPK_2 | 158 | 163 | PF00069 | 0.611 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.771 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.598 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.465 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.500 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.267 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.370 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.211 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.305 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.469 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.540 |
MOD_Cter_Amidation | 3 | 6 | PF01082 | 0.401 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.413 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.319 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.540 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.340 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.422 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.318 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.571 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.740 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.569 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.323 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.473 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.323 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.300 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.373 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.423 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.777 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.598 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.338 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.290 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.347 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.341 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.211 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.408 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.180 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.269 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.323 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.672 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.684 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.535 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.585 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.255 |
MOD_PKB_1 | 214 | 222 | PF00069 | 0.568 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.623 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.188 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.730 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.567 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.286 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.291 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.336 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.233 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.345 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.367 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.286 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.514 |
MOD_Plk_4 | 717 | 723 | PF00069 | 0.349 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.606 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.307 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.310 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.266 |
MOD_SUMO_for_1 | 52 | 55 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 230 | 239 | PF00179 | 0.561 |
TRG_DiLeu_BaEn_1 | 106 | 111 | PF01217 | 0.720 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.647 |
TRG_DiLeu_BaLyEn_6 | 404 | 409 | PF01217 | 0.323 |
TRG_DiLeu_BaLyEn_6 | 589 | 594 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.634 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.323 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.647 |
TRG_NES_CRM1_1 | 175 | 185 | PF08389 | 0.599 |
TRG_NLS_Bipartite_1 | 5 | 27 | PF00514 | 0.590 |
TRG_NLS_MonoExtC_3 | 191 | 196 | PF00514 | 0.581 |
TRG_NLS_MonoExtN_4 | 189 | 196 | PF00514 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 225 | 230 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 416 | 420 | PF00026 | 0.309 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWP2 | Leptomonas seymouri | 80% | 99% |
A0A1X0NQK1 | Trypanosomatidae | 64% | 100% |
A0A3Q8IB88 | Leishmania donovani | 91% | 100% |
A0A422NG32 | Trypanosoma rangeli | 71% | 100% |
A4I428 | Leishmania infantum | 91% | 100% |
D0A8X9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9B0B5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
P27514 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 82% |
Q21339 | Caenorhabditis elegans | 25% | 100% |
Q4Q7W9 | Leishmania major | 91% | 100% |
Q93655 | Caenorhabditis elegans | 21% | 100% |