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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005663 | DNA replication factor C complex | 2 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AWU0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006260 | DNA replication | 5 | 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:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 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:0006281 | DNA repair | 5 | 5 |
GO:0006950 | response to stress | 2 | 5 |
GO:0006974 | DNA damage response | 4 | 5 |
GO:0033554 | cellular response to stress | 3 | 5 |
GO:0050896 | response to stimulus | 1 | 5 |
GO:0051716 | cellular response to stimulus | 2 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0003689 | DNA clamp loader activity | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 9 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 9 |
GO:0016887 | ATP hydrolysis activity | 7 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 9 |
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:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 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 | 133 | 137 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 250 | 254 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.370 |
CLV_C14_Caspase3-7 | 630 | 634 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 654 | 658 | PF00656 | 0.712 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.664 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 511 | 513 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 558 | 560 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 619 | 621 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.739 |
DEG_APCC_DBOX_1 | 169 | 177 | PF00400 | 0.419 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.370 |
DEG_APCC_DBOX_1 | 393 | 401 | PF00400 | 0.450 |
DEG_APCC_KENBOX_2 | 105 | 109 | PF00400 | 0.373 |
DEG_SPOP_SBC_1 | 346 | 350 | PF00917 | 0.417 |
DEG_SPOP_SBC_1 | 567 | 571 | PF00917 | 0.703 |
DEG_SPOP_SBC_1 | 600 | 604 | PF00917 | 0.749 |
DEG_SPOP_SBC_1 | 639 | 643 | PF00917 | 0.755 |
DOC_CYCLIN_RxL_1 | 164 | 177 | PF00134 | 0.426 |
DOC_CYCLIN_RxL_1 | 204 | 212 | PF00134 | 0.415 |
DOC_MAPK_gen_1 | 61 | 68 | PF00069 | 0.541 |
DOC_PP1_RVXF_1 | 374 | 381 | PF00149 | 0.306 |
DOC_PP2B_LxvP_1 | 431 | 434 | PF13499 | 0.417 |
DOC_PP4_FxxP_1 | 181 | 184 | PF00568 | 0.500 |
DOC_PP4_MxPP_1 | 478 | 481 | PF00568 | 0.236 |
DOC_SPAK_OSR1_1 | 343 | 347 | PF12202 | 0.417 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.799 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 625 | 629 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.611 |
DOC_USP7_UBL2_3 | 507 | 511 | PF12436 | 0.649 |
DOC_USP7_UBL2_3 | 558 | 562 | PF12436 | 0.761 |
DOC_USP7_UBL2_3 | 579 | 583 | PF12436 | 0.663 |
DOC_USP7_UBL2_3 | 615 | 619 | PF12436 | 0.704 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 116 | 125 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 180 | 184 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 235 | 239 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 581 | 587 | PF00244 | 0.784 |
LIG_14-3-3_CanoR_1 | 606 | 614 | PF00244 | 0.559 |
LIG_Actin_WH2_2 | 136 | 153 | PF00022 | 0.504 |
LIG_CtBP_PxDLS_1 | 202 | 207 | PF00389 | 0.430 |
LIG_DLG_GKlike_1 | 501 | 509 | PF00625 | 0.575 |
LIG_eIF4E_1 | 125 | 131 | PF01652 | 0.306 |
LIG_eIF4E_1 | 285 | 291 | PF01652 | 0.493 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.398 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.302 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.702 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.306 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.362 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.495 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.718 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.417 |
LIG_Integrin_RGD_1 | 512 | 514 | PF01839 | 0.745 |
LIG_LIR_Apic_2 | 178 | 184 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 123 | 132 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 342 | 352 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 451 | 459 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 499 | 510 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 342 | 347 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 458 | 463 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.585 |
LIG_NRBOX | 168 | 174 | PF00104 | 0.448 |
LIG_Pex14_1 | 22 | 26 | PF04695 | 0.400 |
LIG_Pex14_1 | 46 | 50 | PF04695 | 0.415 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.306 |
LIG_PTB_Apo_2 | 112 | 119 | PF02174 | 0.325 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.378 |
LIG_SH2_GRB2like | 125 | 128 | PF00017 | 0.359 |
LIG_SH2_GRB2like | 285 | 288 | PF00017 | 0.491 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.325 |
LIG_SH2_STAT3 | 302 | 305 | PF00017 | 0.524 |
LIG_SH2_STAT3 | 334 | 337 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.306 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.306 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.627 |
LIG_SH3_4 | 207 | 214 | PF00018 | 0.518 |
LIG_SH3_4 | 579 | 586 | PF00018 | 0.721 |
LIG_SUMO_SIM_anti_2 | 126 | 134 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 126 | 134 | PF11976 | 0.351 |
LIG_SxIP_EBH_1 | 151 | 161 | PF03271 | 0.406 |
LIG_TYR_ITSM | 121 | 128 | PF00017 | 0.450 |
LIG_UBA3_1 | 209 | 216 | PF00899 | 0.529 |
LIG_WRC_WIRS_1 | 361 | 366 | PF05994 | 0.306 |
LIG_WRC_WIRS_1 | 502 | 507 | PF05994 | 0.584 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.306 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.597 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.439 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.361 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.661 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.648 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.625 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.669 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.306 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.603 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.509 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.441 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.394 |
MOD_CK2_1 | 625 | 631 | PF00069 | 0.628 |
MOD_CK2_1 | 653 | 659 | PF00069 | 0.742 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.358 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.464 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.439 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.326 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.657 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.306 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.350 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.721 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.745 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.293 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.318 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.324 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.640 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.519 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.519 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.304 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.630 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.754 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.742 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.779 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.677 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.627 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.576 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.635 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.297 |
MOD_LATS_1 | 166 | 172 | PF00433 | 0.427 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.329 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.306 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.306 |
MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.454 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.306 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.403 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.460 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.560 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.401 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.378 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.313 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.450 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.534 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.375 |
MOD_NEK2_2 | 506 | 511 | PF00069 | 0.641 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.539 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.365 |
MOD_PIKK_1 | 514 | 520 | PF00454 | 0.705 |
MOD_PK_1 | 151 | 157 | PF00069 | 0.231 |
MOD_PK_1 | 27 | 33 | PF00069 | 0.506 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.348 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.120 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.410 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.508 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.505 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.737 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.695 |
MOD_PKB_1 | 622 | 630 | PF00069 | 0.690 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.306 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.532 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.411 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.320 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.325 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.306 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.302 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.383 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.551 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.694 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.417 |
MOD_SUMO_rev_2 | 55 | 63 | PF00179 | 0.598 |
TRG_DiLeu_BaLyEn_6 | 205 | 210 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 392 | 397 | PF01217 | 0.348 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.327 |
TRG_NLS_Bipartite_1 | 583 | 601 | PF00514 | 0.783 |
TRG_NLS_MonoCore_2 | 577 | 582 | PF00514 | 0.756 |
TRG_NLS_MonoCore_2 | 618 | 623 | PF00514 | 0.689 |
TRG_NLS_MonoExtC_3 | 557 | 562 | PF00514 | 0.687 |
TRG_NLS_MonoExtC_3 | 619 | 624 | PF00514 | 0.673 |
TRG_NLS_MonoExtN_4 | 558 | 563 | PF00514 | 0.688 |
TRG_NLS_MonoExtN_4 | 594 | 601 | PF00514 | 0.739 |
TRG_NLS_MonoExtN_4 | 619 | 625 | PF00514 | 0.697 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 196 | 201 | PF00026 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5X2 | Leptomonas seymouri | 77% | 100% |
A0A1X0NVJ4 | Trypanosomatidae | 68% | 100% |
A0A3R7KMZ0 | Trypanosoma rangeli | 65% | 100% |
A0A3S7WYE5 | Leishmania donovani | 94% | 100% |
A4HDF5 | Leishmania braziliensis | 89% | 100% |
A4I0T7 | Leishmania infantum | 94% | 100% |
D0A768 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
O60182 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 71% |
P35600 | Drosophila melanogaster | 31% | 67% |
P38630 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 77% |
Q4QAN4 | Leishmania major | 92% | 100% |
Q9C587 | Arabidopsis thaliana | 32% | 69% |
V5BAM4 | Trypanosoma cruzi | 65% | 100% |