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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 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:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HFC4
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 1 |
GO:0042254 | ribosome biogenesis | 5 | 1 |
GO:0044085 | cellular component biogenesis | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 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:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 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 | 233 | 237 | PF00656 | 0.491 |
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.390 |
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 554 | 558 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 625 | 627 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 662 | 664 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.584 |
CLV_PCSK_FUR_1 | 333 | 337 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 642 | 644 | PF00082 | 0.754 |
CLV_PCSK_PC1ET2_1 | 672 | 674 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.727 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.584 |
DEG_APCC_DBOX_1 | 159 | 167 | PF00400 | 0.529 |
DOC_CKS1_1 | 167 | 172 | PF01111 | 0.463 |
DOC_CYCLIN_RxL_1 | 118 | 129 | PF00134 | 0.538 |
DOC_CYCLIN_RxL_1 | 675 | 689 | PF00134 | 0.656 |
DOC_MAPK_DCC_7 | 675 | 685 | PF00069 | 0.727 |
DOC_MAPK_gen_1 | 156 | 165 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 206 | 214 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 276 | 285 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 418 | 427 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 509 | 515 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 579 | 589 | PF00069 | 0.334 |
DOC_MAPK_gen_1 | 640 | 648 | PF00069 | 0.657 |
DOC_MAPK_MEF2A_6 | 108 | 117 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 158 | 167 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 267 | 275 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 276 | 285 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 582 | 591 | PF00069 | 0.199 |
DOC_PP1_RVXF_1 | 294 | 301 | PF00149 | 0.337 |
DOC_PP1_RVXF_1 | 358 | 365 | PF00149 | 0.492 |
DOC_PP1_RVXF_1 | 421 | 428 | PF00149 | 0.475 |
DOC_PP1_RVXF_1 | 438 | 444 | PF00149 | 0.417 |
DOC_PP1_RVXF_1 | 580 | 587 | PF00149 | 0.362 |
DOC_PP1_RVXF_1 | 60 | 66 | PF00149 | 0.477 |
DOC_PP1_RVXF_1 | 679 | 686 | PF00149 | 0.589 |
DOC_PP2B_LxvP_1 | 436 | 439 | PF13499 | 0.452 |
DOC_PP4_FxxP_1 | 260 | 263 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 475 | 478 | PF00568 | 0.346 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.262 |
DOC_USP7_MATH_2 | 578 | 584 | PF00917 | 0.199 |
DOC_USP7_UBL2_3 | 520 | 524 | PF12436 | 0.381 |
DOC_USP7_UBL2_3 | 675 | 679 | PF12436 | 0.711 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.421 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 278 | 282 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 336 | 345 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 420 | 426 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.429 |
LIG_Actin_WH2_2 | 195 | 211 | PF00022 | 0.538 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.458 |
LIG_BRCT_BRCA1_1 | 305 | 309 | PF00533 | 0.326 |
LIG_BRCT_BRCA1_1 | 423 | 427 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 471 | 475 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 582 | 586 | PF00533 | 0.425 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.468 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.474 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.419 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.452 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.481 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.713 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.435 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.505 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.355 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.511 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.574 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.598 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.593 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.388 |
LIG_LIR_Apic_2 | 258 | 263 | PF02991 | 0.463 |
LIG_LIR_Apic_2 | 472 | 478 | PF02991 | 0.340 |
LIG_LIR_Apic_2 | 86 | 92 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 306 | 317 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 363 | 371 | PF02991 | 0.711 |
LIG_LIR_Gen_1 | 508 | 518 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 583 | 594 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 651 | 658 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 363 | 367 | PF02991 | 0.719 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 508 | 514 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 583 | 589 | PF02991 | 0.399 |
LIG_MLH1_MIPbox_1 | 582 | 586 | PF16413 | 0.425 |
LIG_NRBOX | 278 | 284 | PF00104 | 0.444 |
LIG_NRBOX | 93 | 99 | PF00104 | 0.452 |
LIG_OCRL_FandH_1 | 585 | 597 | PF00620 | 0.315 |
LIG_PDZ_Class_2 | 685 | 690 | PF00595 | 0.582 |
LIG_Pex14_1 | 443 | 447 | PF04695 | 0.452 |
LIG_RPA_C_Fungi | 669 | 681 | PF08784 | 0.664 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.305 |
LIG_SH2_CRK | 574 | 578 | PF00017 | 0.334 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 447 | 451 | PF00017 | 0.219 |
LIG_SH2_NCK_1 | 89 | 93 | PF00017 | 0.425 |
LIG_SH2_PTP2 | 270 | 273 | PF00017 | 0.428 |
LIG_SH2_SRC | 447 | 450 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 511 | 515 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.581 |
LIG_SH3_1 | 447 | 453 | PF00018 | 0.362 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.390 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.434 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.362 |
LIG_SUMO_SIM_anti_2 | 112 | 118 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 163 | 169 | PF11976 | 0.339 |
LIG_TRAF2_1 | 363 | 366 | PF00917 | 0.648 |
LIG_UBA3_1 | 173 | 178 | PF00899 | 0.329 |
LIG_UBA3_1 | 199 | 206 | PF00899 | 0.343 |
LIG_UBA3_1 | 211 | 218 | PF00899 | 0.279 |
LIG_UBA3_1 | 515 | 520 | PF00899 | 0.396 |
LIG_WRC_WIRS_1 | 282 | 287 | PF05994 | 0.343 |
LIG_WRC_WIRS_1 | 361 | 366 | PF05994 | 0.598 |
MOD_CDK_SPxK_1 | 166 | 172 | PF00069 | 0.305 |
MOD_CDK_SPxxK_3 | 101 | 108 | PF00069 | 0.452 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.559 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.347 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.476 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.540 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.431 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.461 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.659 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.700 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.297 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.607 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.452 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.729 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.300 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.227 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.694 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.281 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.513 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.311 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.557 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.305 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.494 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.189 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.393 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.693 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.577 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.366 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.609 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.627 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.292 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.660 |
MOD_N-GLC_1 | 398 | 403 | PF02516 | 0.310 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.474 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.702 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.682 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.305 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.583 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.348 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.428 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.572 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.608 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.510 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.525 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.411 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.347 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.408 |
MOD_NEK2_2 | 555 | 560 | PF00069 | 0.535 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.622 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.574 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.353 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.290 |
MOD_PIKK_1 | 490 | 496 | PF00454 | 0.519 |
MOD_PIKK_1 | 656 | 662 | PF00454 | 0.683 |
MOD_PKA_1 | 626 | 632 | PF00069 | 0.698 |
MOD_PKA_1 | 663 | 669 | PF00069 | 0.597 |
MOD_PKA_1 | 674 | 680 | PF00069 | 0.602 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.643 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.375 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.362 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.475 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.290 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.421 |
MOD_Plk_2-3 | 365 | 371 | PF00069 | 0.598 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.301 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.329 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.305 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.348 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.452 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.398 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.229 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.380 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.342 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.270 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.305 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.590 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.452 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.305 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.400 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.421 |
MOD_SUMO_rev_2 | 323 | 331 | PF00179 | 0.688 |
MOD_SUMO_rev_2 | 448 | 455 | PF00179 | 0.238 |
MOD_SUMO_rev_2 | 493 | 503 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 548 | 558 | PF00179 | 0.575 |
MOD_SUMO_rev_2 | 605 | 613 | PF00179 | 0.371 |
TRG_DiLeu_BaEn_1 | 195 | 200 | PF01217 | 0.305 |
TRG_DiLeu_BaEn_1 | 210 | 215 | PF01217 | 0.305 |
TRG_DiLeu_BaEn_1 | 308 | 313 | PF01217 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 169 | 174 | PF01217 | 0.311 |
TRG_DiLeu_BaLyEn_6 | 93 | 98 | PF01217 | 0.425 |
TRG_DiLeu_LyEn_5 | 195 | 200 | PF01217 | 0.305 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.571 |
TRG_ER_diArg_1 | 333 | 336 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 44 | 46 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 643 | 646 | PF00400 | 0.693 |
TRG_NLS_Bipartite_1 | 626 | 646 | PF00514 | 0.730 |
TRG_NLS_MonoCore_2 | 639 | 644 | PF00514 | 0.684 |
TRG_NLS_MonoExtC_3 | 640 | 645 | PF00514 | 0.720 |
TRG_NLS_MonoExtN_4 | 640 | 646 | PF00514 | 0.718 |
TRG_Pf-PMV_PEXEL_1 | 121 | 126 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 619 | 624 | PF00026 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 663 | 668 | PF00026 | 0.710 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1U1 | Leptomonas seymouri | 80% | 88% |
A0A0N1PCZ7 | Leptomonas seymouri | 24% | 100% |
A0A0S4ISP4 | Bodo saltans | 50% | 93% |
A0A0S4JDN6 | Bodo saltans | 26% | 83% |
A0A1X0NMD6 | Trypanosomatidae | 58% | 84% |
A0A3Q8IE53 | Leishmania donovani | 85% | 88% |
A0A3R7N587 | Trypanosoma rangeli | 57% | 84% |
A0A3S5H7C7 | Leishmania donovani | 25% | 100% |
A1C7F7 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 24% | 100% |
A1CB55 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 32% | 91% |
A1DE84 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 31% | 91% |
A1DHV3 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 24% | 100% |
A2RA55 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 32% | 89% |
A3LWH3 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 32% | 94% |
A4H481 | Leishmania braziliensis | 27% | 100% |
A4HD81 | Leishmania braziliensis | 23% | 100% |
A4I2K1 | Leishmania infantum | 85% | 88% |
A4QX49 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 35% | 84% |
A5DAR2 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 33% | 92% |
A6R2L6 | Ajellomyces capsulatus (strain NAm1 / WU24) | 26% | 100% |
A6RMZ2 | Botryotinia fuckeliana (strain B05.10) | 28% | 100% |
A6RSH5 | Botryotinia fuckeliana (strain B05.10) | 32% | 79% |
A6ZZY8 | Saccharomyces cerevisiae (strain YJM789) | 30% | 93% |
A7F2S3 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 28% | 100% |
A7F8V8 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 33% | 79% |
A7TNT1 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 30% | 94% |
A7TS37 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 27% | 100% |
C9ZKU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 78% |
E9ACY2 | Leishmania major | 87% | 100% |
E9AH36 | Leishmania infantum | 25% | 100% |
E9AWL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AYQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 88% |
O60173 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 97% |
P0CQ94 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 28% | 73% |
P0CQ95 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 28% | 73% |
P0CR02 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 27% | 100% |
P26802 | Drosophila melanogaster | 25% | 100% |
P36120 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 93% |
Q0CF43 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 31% | 90% |
Q0CY48 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 25% | 100% |
Q0DLB9 | Oryza sativa subsp. japonica | 33% | 100% |
Q0UHM7 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 32% | 83% |
Q0UZ59 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 26% | 100% |
Q1E9T9 | Coccidioides immitis (strain RS) | 31% | 90% |
Q1K8F7 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 25% | 100% |
Q2GZU7 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 33% | 86% |
Q2UE66 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 32% | 91% |
Q4HZ68 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 30% | 93% |
Q4P0Y5 | Ustilago maydis (strain 521 / FGSC 9021) | 30% | 71% |
Q4P7M1 | Ustilago maydis (strain 521 / FGSC 9021) | 24% | 100% |
Q4PEX7 | Ustilago maydis (strain 521 / FGSC 9021) | 28% | 100% |
Q4QAV6 | Leishmania major | 24% | 100% |
Q4WV71 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 32% | 91% |
Q4X0C2 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 24% | 100% |
Q59S50 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 95% |
Q5BGX6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 33% | 89% |
Q6ATJ8 | Oryza sativa subsp. japonica | 26% | 100% |
Q6BKH3 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 32% | 86% |
Q6C835 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 32% | 86% |
Q6CCZ1 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 71% |
Q6CK32 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 30% | 93% |
Q754J2 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 33% | 97% |
Q7S873 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 33% | 85% |
Q7XJN0 | Arabidopsis thaliana | 32% | 100% |
Q869P0 | Dictyostelium discoideum | 34% | 76% |
Q86B47 | Drosophila melanogaster | 33% | 71% |
Q8TFL3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 30% | 97% |
Q9H8H2 | Homo sapiens | 36% | 81% |
V5BG99 | Trypanosoma cruzi | 57% | 83% |