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: A4HDF5
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 | 134 | 138 | PF00656 | 0.249 |
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.474 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.345 |
CLV_C14_Caspase3-7 | 659 | 663 | PF00656 | 0.685 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.504 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.612 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.603 |
CLV_PCSK_PC1ET2_1 | 512 | 514 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 618 | 620 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.397 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.361 |
DEG_APCC_DBOX_1 | 222 | 230 | PF00400 | 0.314 |
DEG_APCC_DBOX_1 | 394 | 402 | PF00400 | 0.324 |
DEG_SPOP_SBC_1 | 347 | 351 | PF00917 | 0.380 |
DEG_SPOP_SBC_1 | 600 | 604 | PF00917 | 0.713 |
DEG_SPOP_SBC_1 | 640 | 644 | PF00917 | 0.625 |
DEG_SPOP_SBC_1 | 645 | 649 | PF00917 | 0.573 |
DOC_CYCLIN_RxL_1 | 165 | 178 | PF00134 | 0.369 |
DOC_CYCLIN_RxL_1 | 205 | 213 | PF00134 | 0.361 |
DOC_MAPK_gen_1 | 62 | 69 | PF00069 | 0.507 |
DOC_MAPK_RevD_3 | 544 | 560 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 375 | 382 | PF00149 | 0.249 |
DOC_PP2B_LxvP_1 | 432 | 435 | PF13499 | 0.380 |
DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.465 |
DOC_PP4_MxPP_1 | 479 | 482 | PF00568 | 0.191 |
DOC_SPAK_OSR1_1 | 344 | 348 | PF12202 | 0.380 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.715 |
DOC_USP7_UBL2_3 | 508 | 512 | PF12436 | 0.568 |
DOC_USP7_UBL2_3 | 558 | 562 | PF12436 | 0.687 |
DOC_USP7_UBL2_3 | 579 | 583 | PF12436 | 0.639 |
DOC_USP7_UBL2_3 | 597 | 601 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.119 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.263 |
LIG_14-3-3_CanoR_1 | 117 | 126 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 581 | 587 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 593 | 600 | PF00244 | 0.477 |
LIG_Actin_WH2_2 | 137 | 154 | PF00022 | 0.464 |
LIG_Actin_WH2_2 | 219 | 237 | PF00022 | 0.265 |
LIG_CtBP_PxDLS_1 | 203 | 208 | PF00389 | 0.371 |
LIG_deltaCOP1_diTrp_1 | 337 | 345 | PF00928 | 0.262 |
LIG_eIF4E_1 | 126 | 132 | PF01652 | 0.249 |
LIG_eIF4E_1 | 286 | 292 | PF01652 | 0.466 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.345 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.249 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.228 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.249 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.305 |
LIG_FHA_2 | 516 | 522 | PF00498 | 0.639 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.545 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.547 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.382 |
LIG_Integrin_RGD_1 | 513 | 515 | PF01839 | 0.570 |
LIG_LIR_Apic_2 | 179 | 185 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 124 | 133 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 343 | 353 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 452 | 460 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 500 | 511 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.574 |
LIG_NRBOX | 169 | 175 | PF00104 | 0.393 |
LIG_PCNA_yPIPBox_3 | 285 | 295 | PF02747 | 0.239 |
LIG_Pex14_1 | 23 | 27 | PF04695 | 0.339 |
LIG_Pex14_1 | 47 | 51 | PF04695 | 0.355 |
LIG_Pex14_2 | 493 | 497 | PF04695 | 0.249 |
LIG_PTB_Apo_2 | 113 | 120 | PF02174 | 0.267 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.327 |
LIG_SH2_GRB2like | 286 | 289 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.267 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.209 |
LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.267 |
LIG_SH2_STAT3 | 303 | 306 | PF00017 | 0.387 |
LIG_SH2_STAT3 | 335 | 338 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.277 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.273 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.500 |
LIG_SH3_4 | 208 | 215 | PF00018 | 0.485 |
LIG_SH3_4 | 579 | 586 | PF00018 | 0.668 |
LIG_SUMO_SIM_anti_2 | 127 | 135 | PF11976 | 0.331 |
LIG_SUMO_SIM_anti_2 | 542 | 548 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 127 | 135 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 545 | 550 | PF11976 | 0.471 |
LIG_SxIP_EBH_1 | 152 | 162 | PF03271 | 0.347 |
LIG_TRAF2_1 | 629 | 632 | PF00917 | 0.546 |
LIG_TYR_ITSM | 122 | 129 | PF00017 | 0.324 |
LIG_UBA3_1 | 210 | 216 | PF00899 | 0.488 |
LIG_WRC_WIRS_1 | 362 | 367 | PF05994 | 0.249 |
LIG_WRC_WIRS_1 | 503 | 508 | PF05994 | 0.524 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.249 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.273 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.445 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.513 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.598 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.588 |
MOD_CK1_1 | 633 | 639 | PF00069 | 0.592 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.572 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.614 |
MOD_CK1_1 | 655 | 661 | PF00069 | 0.486 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.229 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.554 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.389 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.338 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.594 |
MOD_CK2_1 | 658 | 664 | PF00069 | 0.772 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.297 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.446 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.422 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.296 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.634 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.253 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.442 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.754 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.728 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.302 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.262 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.288 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.502 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.483 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.265 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.512 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.495 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.760 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.670 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.526 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.557 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.504 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.583 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.249 |
MOD_LATS_1 | 167 | 173 | PF00433 | 0.370 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.249 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.249 |
MOD_N-GLC_1 | 387 | 392 | PF02516 | 0.267 |
MOD_N-GLC_1 | 483 | 488 | PF02516 | 0.278 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.337 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.398 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.249 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.342 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.410 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.344 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.327 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.623 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.271 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.184 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.408 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.447 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.327 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.407 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.616 |
MOD_PK_1 | 28 | 34 | PF00069 | 0.470 |
MOD_PKA_1 | 235 | 241 | PF00069 | 0.375 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.308 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.382 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.354 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.445 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.504 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.734 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.521 |
MOD_PKB_1 | 621 | 629 | PF00069 | 0.640 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.249 |
MOD_Plk_1 | 630 | 636 | PF00069 | 0.497 |
MOD_Plk_2-3 | 275 | 281 | PF00069 | 0.504 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.250 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.262 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.249 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.469 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.249 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.334 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.510 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.782 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.630 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.119 |
MOD_SUMO_rev_2 | 56 | 64 | PF00179 | 0.557 |
TRG_DiLeu_BaLyEn_6 | 206 | 211 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.292 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.249 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.324 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.397 |
TRG_NLS_MonoCore_2 | 577 | 582 | PF00514 | 0.722 |
TRG_NLS_MonoCore_2 | 617 | 622 | PF00514 | 0.639 |
TRG_NLS_MonoExtC_3 | 557 | 562 | PF00514 | 0.588 |
TRG_NLS_MonoExtC_3 | 618 | 623 | PF00514 | 0.617 |
TRG_NLS_MonoExtN_4 | 558 | 563 | PF00514 | 0.588 |
TRG_NLS_MonoExtN_4 | 618 | 624 | PF00514 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 197 | 202 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 30 | 34 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5X2 | Leptomonas seymouri | 79% | 100% |
A0A1X0NVJ4 | Trypanosomatidae | 68% | 100% |
A0A3R7KMZ0 | Trypanosoma rangeli | 66% | 100% |
A0A3S7WYE5 | Leishmania donovani | 89% | 100% |
A4I0T7 | Leishmania infantum | 89% | 100% |
D0A768 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9AWU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 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 | 88% | 100% |
Q9C587 | Arabidopsis thaliana | 31% | 69% |
V5BAM4 | Trypanosoma cruzi | 61% | 100% |