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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HSF8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003724 | RNA helicase activity | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.728 |
CLV_PCSK_FUR_1 | 556 | 560 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.710 |
CLV_PCSK_PC1ET2_1 | 555 | 557 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 619 | 621 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.528 |
CLV_Separin_Metazoa | 349 | 353 | PF03568 | 0.415 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.429 |
DEG_SCF_FBW7_2 | 74 | 81 | PF00400 | 0.415 |
DOC_CDC14_PxL_1 | 319 | 327 | PF14671 | 0.385 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.472 |
DOC_CKS1_1 | 75 | 80 | PF01111 | 0.415 |
DOC_CYCLIN_RxL_1 | 144 | 158 | PF00134 | 0.407 |
DOC_CYCLIN_yCln2_LP_2 | 175 | 178 | PF00134 | 0.475 |
DOC_MAPK_DCC_7 | 397 | 406 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 130 | 137 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 180 | 187 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 428 | 438 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 452 | 460 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 98 | 105 | PF00069 | 0.436 |
DOC_MAPK_HePTP_8 | 394 | 406 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 347 | 355 | PF00069 | 0.415 |
DOC_MAPK_MEF2A_6 | 397 | 406 | PF00069 | 0.426 |
DOC_PP2B_LxvP_1 | 175 | 178 | PF13499 | 0.456 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.643 |
DOC_PP2B_LxvP_1 | 314 | 317 | PF13499 | 0.335 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.405 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.513 |
DOC_PP4_FxxP_1 | 56 | 59 | PF00568 | 0.415 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.475 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.540 |
DOC_USP7_UBL2_3 | 576 | 580 | PF12436 | 0.608 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.415 |
LIG_14-3-3_CanoR_1 | 11 | 20 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 159 | 166 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 194 | 199 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 299 | 304 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 352 | 356 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 559 | 568 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 595 | 603 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 98 | 103 | PF00244 | 0.436 |
LIG_APCC_ABBA_1 | 406 | 411 | PF00400 | 0.426 |
LIG_BIR_III_4 | 67 | 71 | PF00653 | 0.520 |
LIG_eIF4E_1 | 69 | 75 | PF01652 | 0.415 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.426 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.411 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.415 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.377 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.470 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.415 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.450 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.326 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.718 |
LIG_LIR_Apic_2 | 301 | 306 | PF02991 | 0.534 |
LIG_LIR_Apic_2 | 459 | 464 | PF02991 | 0.516 |
LIG_LIR_Apic_2 | 53 | 59 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 18 | 27 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 2 | 9 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 310 | 320 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 81 | 92 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.405 |
LIG_LYPXL_SIV_4 | 323 | 331 | PF13949 | 0.520 |
LIG_NRBOX | 130 | 136 | PF00104 | 0.475 |
LIG_NRBOX | 364 | 370 | PF00104 | 0.501 |
LIG_PDZ_Class_3 | 620 | 625 | PF00595 | 0.595 |
LIG_RPA_C_Fungi | 501 | 513 | PF08784 | 0.410 |
LIG_RPA_C_Plants | 496 | 507 | PF08784 | 0.609 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.267 |
LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.387 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.385 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 442 | 446 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.262 |
LIG_SH3_2 | 294 | 299 | PF14604 | 0.608 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.334 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.610 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.433 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.267 |
LIG_SUMO_SIM_anti_2 | 260 | 265 | PF11976 | 0.480 |
LIG_SUMO_SIM_anti_2 | 434 | 441 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 443 | 448 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 468 | 477 | PF11976 | 0.470 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.456 |
LIG_TYR_ITIM | 149 | 154 | PF00017 | 0.387 |
LIG_TYR_ITIM | 82 | 87 | PF00017 | 0.267 |
LIG_WRC_WIRS_1 | 378 | 383 | PF05994 | 0.283 |
MOD_CDC14_SPxK_1 | 615 | 618 | PF00782 | 0.743 |
MOD_CDK_SPK_2 | 516 | 521 | PF00069 | 0.505 |
MOD_CDK_SPxK_1 | 124 | 130 | PF00069 | 0.267 |
MOD_CDK_SPxK_1 | 612 | 618 | PF00069 | 0.744 |
MOD_CDK_SPxK_1 | 74 | 80 | PF00069 | 0.267 |
MOD_CDK_SPxxK_3 | 460 | 467 | PF00069 | 0.481 |
MOD_CDK_SPxxK_3 | 516 | 523 | PF00069 | 0.629 |
MOD_CDK_SPxxK_3 | 612 | 619 | PF00069 | 0.706 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.669 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.679 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.650 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.267 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.267 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.266 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.617 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.640 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.632 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.751 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.661 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.427 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.472 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.732 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.681 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.679 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.414 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.291 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.275 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.494 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.735 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.692 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.715 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.697 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.674 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.467 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.448 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.490 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.506 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.672 |
MOD_LATS_1 | 192 | 198 | PF00433 | 0.499 |
MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.662 |
MOD_N-GLC_2 | 343 | 345 | PF02516 | 0.267 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.270 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.608 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.745 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.312 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.429 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.283 |
MOD_PIKK_1 | 566 | 572 | PF00454 | 0.693 |
MOD_PIKK_1 | 596 | 602 | PF00454 | 0.636 |
MOD_PK_1 | 374 | 380 | PF00069 | 0.200 |
MOD_PKA_1 | 507 | 513 | PF00069 | 0.340 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.267 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.425 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.567 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.267 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.716 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.691 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.511 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.289 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.410 |
MOD_Plk_2-3 | 158 | 164 | PF00069 | 0.332 |
MOD_Plk_2-3 | 255 | 261 | PF00069 | 0.452 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.486 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.340 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.254 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.262 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.362 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.205 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.397 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.298 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.364 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.267 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.380 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.733 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.477 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.642 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.723 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.752 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.267 |
MOD_SUMO_rev_2 | 445 | 454 | PF00179 | 0.385 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 171 | 176 | PF01217 | 0.385 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.218 |
TRG_ER_diArg_1 | 520 | 523 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 556 | 559 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.751 |
TRG_ER_diArg_1 | 97 | 100 | PF00400 | 0.297 |
TRG_NLS_Bipartite_1 | 558 | 580 | PF00514 | 0.689 |
TRG_NLS_Bipartite_1 | 605 | 622 | PF00514 | 0.711 |
TRG_NLS_MonoExtC_3 | 554 | 559 | PF00514 | 0.629 |
TRG_NLS_MonoExtC_3 | 575 | 580 | PF00514 | 0.647 |
TRG_NLS_MonoExtC_3 | 617 | 622 | PF00514 | 0.710 |
TRG_NLS_MonoExtN_4 | 616 | 622 | PF00514 | 0.708 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 150 | 155 | PF00026 | 0.206 |
TRG_Pf-PMV_PEXEL_1 | 585 | 590 | PF00026 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 80 | 85 | PF00026 | 0.267 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2T9 | Leptomonas seymouri | 72% | 100% |
A0A0S4J5D6 | Bodo saltans | 49% | 100% |
A0A0S4KKU4 | Bodo saltans | 30% | 90% |
A0A1X0NJH3 | Trypanosomatidae | 26% | 100% |
A0A1X0P0F9 | Trypanosomatidae | 56% | 100% |
A0A1X0P7J3 | Trypanosomatidae | 23% | 89% |
A0A3R7M1K3 | Trypanosoma rangeli | 27% | 87% |
A0A3S5H5H4 | Leishmania donovani | 100% | 100% |
A0A3S5H6T7 | Leishmania donovani | 29% | 100% |
A0A3S7X5R1 | Leishmania donovani | 29% | 81% |
A0A422NDK5 | Trypanosoma rangeli | 54% | 100% |
A2XVF7 | Oryza sativa subsp. indica | 30% | 75% |
A3AVH5 | Oryza sativa subsp. japonica | 30% | 75% |
A4H481 | Leishmania braziliensis | 80% | 100% |
A4HWB0 | Leishmania infantum | 29% | 100% |
A4I846 | Leishmania infantum | 29% | 81% |
A4R5B8 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 32% | 68% |
A7ESL7 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 33% | 68% |
A7TJ71 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 27% | 81% |
C9ZNU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 98% |
D0A4H6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
D0AAB3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 86% |
E9AKE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
E9AQ10 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B304 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 81% |
P26802 | Drosophila melanogaster | 29% | 91% |
Q0CNX1 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 38% | 100% |
Q1EB38 | Coccidioides immitis (strain RS) | 32% | 67% |
Q4HZ42 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 31% | 70% |
Q4Q552 | Leishmania major | 28% | 81% |
Q4QFH1 | Leishmania major | 30% | 100% |
Q4QJG6 | Leishmania major | 95% | 100% |
Q54BD6 | Dictyostelium discoideum | 25% | 100% |
Q6C835 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 29% | 78% |
Q6FU81 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 94% |
Q7XJN0 | Arabidopsis thaliana | 28% | 100% |
Q8N8A6 | Homo sapiens | 28% | 94% |
Q93Y39 | Arabidopsis thaliana | 32% | 76% |
V5CZW7 | Trypanosoma cruzi | 58% | 100% |
V5DCA1 | Trypanosoma cruzi | 27% | 87% |