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:0005730 | nucleolus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9B4Z0
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:0003723 | RNA binding | 4 | 12 |
GO:0003724 | RNA helicase activity | 3 | 12 |
GO:0003743 | translation initiation factor activity | 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:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
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 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
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 | 13 | 17 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 630 | 634 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 731 | 735 | PF00656 | 0.445 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.202 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 756 | 758 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 778 | 780 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.464 |
CLV_PCSK_FUR_1 | 567 | 571 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.202 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.202 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 718 | 720 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 760 | 762 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 778 | 780 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 258 | 260 | PF00082 | 0.248 |
CLV_PCSK_PC1ET2_1 | 318 | 320 | PF00082 | 0.226 |
CLV_PCSK_PC1ET2_1 | 427 | 429 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 569 | 571 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 718 | 720 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 760 | 762 | PF00082 | 0.671 |
CLV_PCSK_PC7_1 | 314 | 320 | PF00082 | 0.269 |
CLV_PCSK_PC7_1 | 496 | 502 | PF00082 | 0.415 |
CLV_PCSK_PC7_1 | 563 | 569 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 718 | 722 | PF00082 | 0.612 |
DEG_APCC_DBOX_1 | 473 | 481 | PF00400 | 0.427 |
DEG_SPOP_SBC_1 | 574 | 578 | PF00917 | 0.555 |
DOC_CKS1_1 | 147 | 152 | PF01111 | 0.398 |
DOC_CKS1_1 | 44 | 49 | PF01111 | 0.280 |
DOC_CYCLIN_RxL_1 | 197 | 206 | PF00134 | 0.402 |
DOC_CYCLIN_RxL_1 | 28 | 35 | PF00134 | 0.473 |
DOC_CYCLIN_RxL_1 | 329 | 340 | PF00134 | 0.426 |
DOC_CYCLIN_RxL_1 | 500 | 513 | PF00134 | 0.568 |
DOC_CYCLIN_RxL_1 | 549 | 558 | PF00134 | 0.457 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 24 | 33 | PF00134 | 0.350 |
DOC_CYCLIN_yCln2_LP_2 | 219 | 225 | PF00134 | 0.326 |
DOC_MAPK_FxFP_2 | 345 | 348 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 318 | 326 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 489 | 497 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 500 | 509 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 657 | 667 | PF00069 | 0.250 |
DOC_MAPK_gen_1 | 696 | 705 | PF00069 | 0.399 |
DOC_MAPK_JIP1_4 | 503 | 509 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 249 | 257 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 503 | 511 | PF00069 | 0.575 |
DOC_MAPK_RevD_3 | 703 | 719 | PF00069 | 0.548 |
DOC_PP1_RVXF_1 | 550 | 557 | PF00149 | 0.603 |
DOC_PP2B_LxvP_1 | 334 | 337 | PF13499 | 0.402 |
DOC_PP2B_PxIxI_1 | 142 | 148 | PF00149 | 0.332 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.426 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.433 |
DOC_PP4_FxxP_1 | 76 | 79 | PF00568 | 0.409 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.660 |
DOC_USP7_UBL2_3 | 696 | 700 | PF12436 | 0.330 |
DOC_USP7_UBL2_3 | 760 | 764 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 800 | 804 | PF12436 | 0.640 |
DOC_USP7_UBL2_3 | 85 | 89 | PF12436 | 0.409 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.409 |
LIG_14-3-3_CanoR_1 | 200 | 210 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 391 | 397 | PF00244 | 0.465 |
LIG_Actin_WH2_2 | 224 | 240 | PF00022 | 0.359 |
LIG_Actin_WH2_2 | 660 | 677 | PF00022 | 0.276 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.469 |
LIG_CaM_IQ_9 | 440 | 456 | PF13499 | 0.276 |
LIG_Clathr_ClatBox_1 | 274 | 278 | PF01394 | 0.383 |
LIG_DLG_GKlike_1 | 102 | 109 | PF00625 | 0.409 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.503 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.424 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.298 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.397 |
LIG_FHA_2 | 640 | 646 | PF00498 | 0.381 |
LIG_FXI_DFP_1 | 376 | 380 | PF00024 | 0.332 |
LIG_GBD_Chelix_1 | 223 | 231 | PF00786 | 0.386 |
LIG_LIR_Apic_2 | 73 | 79 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 120 | 127 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 133 | 143 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 369 | 379 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 506 | 515 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 612 | 622 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 738 | 747 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 770 | 777 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 506 | 511 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 612 | 618 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 738 | 744 | PF02991 | 0.623 |
LIG_NRBOX | 252 | 258 | PF00104 | 0.251 |
LIG_Pex14_2 | 281 | 285 | PF04695 | 0.492 |
LIG_Pex14_2 | 345 | 349 | PF04695 | 0.469 |
LIG_PTB_Apo_2 | 341 | 348 | PF02174 | 0.402 |
LIG_PTB_Apo_2 | 623 | 630 | PF02174 | 0.665 |
LIG_PTB_Phospho_1 | 623 | 629 | PF10480 | 0.666 |
LIG_SH2_CRK | 411 | 415 | PF00017 | 0.387 |
LIG_SH2_PTP2 | 382 | 385 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.270 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.398 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.426 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.394 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.365 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.507 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.619 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.440 |
LIG_SUMO_SIM_anti_2 | 320 | 328 | PF11976 | 0.403 |
LIG_TRAF2_1 | 461 | 464 | PF00917 | 0.420 |
LIG_TRAF2_1 | 642 | 645 | PF00917 | 0.270 |
LIG_TRAF2_1 | 770 | 773 | PF00917 | 0.508 |
LIG_UBA3_1 | 253 | 258 | PF00899 | 0.251 |
LIG_UBA3_1 | 33 | 39 | PF00899 | 0.446 |
LIG_UBA3_1 | 507 | 516 | PF00899 | 0.485 |
LIG_UBA3_1 | 77 | 85 | PF00899 | 0.232 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.392 |
LIG_WRC_WIRS_1 | 313 | 318 | PF05994 | 0.381 |
LIG_WRC_WIRS_1 | 373 | 378 | PF05994 | 0.300 |
LIG_WRC_WIRS_1 | 768 | 773 | PF05994 | 0.514 |
MOD_CDC14_SPxK_1 | 99 | 102 | PF00782 | 0.246 |
MOD_CDK_SPxK_1 | 146 | 152 | PF00069 | 0.232 |
MOD_CDK_SPxK_1 | 96 | 102 | PF00069 | 0.246 |
MOD_CDK_SPxxK_3 | 43 | 50 | PF00069 | 0.246 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.379 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.303 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.299 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.754 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.558 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.277 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.232 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.493 |
MOD_CK2_1 | 639 | 645 | PF00069 | 0.291 |
MOD_CK2_1 | 724 | 730 | PF00069 | 0.466 |
MOD_CK2_1 | 767 | 773 | PF00069 | 0.518 |
MOD_Cter_Amidation | 749 | 752 | PF01082 | 0.535 |
MOD_Cter_Amidation | 755 | 758 | PF01082 | 0.567 |
MOD_Cter_Amidation | 797 | 800 | PF01082 | 0.624 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.258 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.423 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.302 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.286 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.356 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.518 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.597 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.564 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.170 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.232 |
MOD_GlcNHglycan | 794 | 797 | PF01048 | 0.716 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.673 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.260 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.438 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.621 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.626 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.671 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.287 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.236 |
MOD_N-GLC_1 | 450 | 455 | PF02516 | 0.539 |
MOD_N-GLC_1 | 678 | 683 | PF02516 | 0.163 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.265 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.286 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.236 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.298 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.236 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.236 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.409 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.460 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.587 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.244 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.402 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.347 |
MOD_NEK2_2 | 627 | 632 | PF00069 | 0.585 |
MOD_PIKK_1 | 724 | 730 | PF00454 | 0.543 |
MOD_PK_1 | 319 | 325 | PF00069 | 0.272 |
MOD_PKA_1 | 318 | 324 | PF00069 | 0.236 |
MOD_PKA_1 | 455 | 461 | PF00069 | 0.422 |
MOD_PKA_1 | 620 | 626 | PF00069 | 0.534 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.251 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.564 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.246 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.245 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.336 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.236 |
MOD_Plk_1 | 600 | 606 | PF00069 | 0.571 |
MOD_Plk_1 | 632 | 638 | PF00069 | 0.532 |
MOD_Plk_1 | 783 | 789 | PF00069 | 0.583 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.236 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.271 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.286 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.232 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.280 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.383 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.246 |
MOD_SUMO_for_1 | 317 | 320 | PF00179 | 0.381 |
MOD_SUMO_for_1 | 677 | 680 | PF00179 | 0.236 |
MOD_SUMO_rev_2 | 228 | 234 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 493 | 502 | PF00179 | 0.409 |
TRG_DiLeu_BaEn_1 | 710 | 715 | PF01217 | 0.549 |
TRG_DiLeu_BaEn_1 | 784 | 789 | PF01217 | 0.418 |
TRG_DiLeu_BaEn_4 | 416 | 422 | PF01217 | 0.347 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.246 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.372 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.236 |
TRG_DiLeu_LyEn_5 | 784 | 789 | PF01217 | 0.357 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 662 | 665 | PF00928 | 0.270 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 567 | 570 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 777 | 779 | PF00400 | 0.650 |
TRG_ER_diLys_1 | 799 | 804 | PF00400 | 0.595 |
TRG_NES_CRM1_1 | 272 | 284 | PF08389 | 0.241 |
TRG_NLS_Bipartite_1 | 778 | 795 | PF00514 | 0.435 |
TRG_NLS_MonoCore_2 | 798 | 803 | PF00514 | 0.433 |
TRG_NLS_MonoExtC_3 | 499 | 504 | PF00514 | 0.542 |
TRG_NLS_MonoExtC_3 | 656 | 661 | PF00514 | 0.227 |
TRG_NLS_MonoExtC_3 | 756 | 761 | PF00514 | 0.564 |
TRG_NLS_MonoExtC_3 | 789 | 794 | PF00514 | 0.517 |
TRG_NLS_MonoExtC_3 | 799 | 804 | PF00514 | 0.617 |
TRG_NLS_MonoExtN_4 | 452 | 458 | PF00514 | 0.405 |
TRG_NLS_MonoExtN_4 | 657 | 662 | PF00514 | 0.227 |
TRG_NLS_MonoExtN_4 | 716 | 722 | PF00514 | 0.601 |
TRG_NLS_MonoExtN_4 | 754 | 761 | PF00514 | 0.564 |
TRG_NLS_MonoExtN_4 | 787 | 794 | PF00514 | 0.433 |
TRG_NLS_MonoExtN_4 | 799 | 804 | PF00514 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 102 | 107 | PF00026 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.309 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE92 | Leptomonas seymouri | 85% | 99% |
A0A0S4JD47 | Bodo saltans | 59% | 98% |
A0A1X0P9U0 | Trypanosomatidae | 66% | 97% |
A0A3Q8ID91 | Leishmania donovani | 33% | 100% |
A0A3Q8IQY6 | Leishmania donovani | 34% | 100% |
A0A3R7NR45 | Trypanosoma rangeli | 67% | 98% |
A0A3S5H7C7 | Leishmania donovani | 24% | 100% |
A0A3S7X7Z2 | Leishmania donovani | 96% | 100% |
A1CTZ6 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 34% | 86% |
A1DNG2 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 33% | 86% |
A2QRY2 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 34% | 86% |
A2YV85 | Oryza sativa subsp. indica | 37% | 94% |
A3BT52 | Oryza sativa subsp. japonica | 37% | 94% |
A3LZT3 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 32% | 86% |
A4HAR7 | Leishmania braziliensis | 89% | 100% |
A4HGR1 | Leishmania braziliensis | 33% | 100% |
A4I3T6 | Leishmania infantum | 33% | 100% |
A4I9Y2 | Leishmania infantum | 96% | 100% |
A4IDI7 | Leishmania infantum | 34% | 100% |
A4R5B8 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 35% | 88% |
A5DLR3 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 32% | 88% |
A5DZT7 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 30% | 85% |
A6QUM7 | Ajellomyces capsulatus (strain NAm1 / WU24) | 36% | 89% |
A6ZXU0 | Saccharomyces cerevisiae (strain YJM789) | 31% | 81% |
A7TGW7 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 31% | 82% |
C9ZMQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 95% |
E9AH36 | Leishmania infantum | 24% | 100% |
E9ASZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AWL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
O49289 | Arabidopsis thaliana | 37% | 95% |
P0CR06 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 33% | 100% |
P0CR07 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 33% | 100% |
Q09719 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 95% |
Q0CMM8 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 34% | 87% |
Q0UMB6 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 32% | 92% |
Q12389 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 81% |
Q4HZ42 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 35% | 90% |
Q4Q1K8 | Leishmania major | 34% | 100% |
Q4Q2Z6 | Leishmania major | 95% | 100% |
Q4Q858 | Leishmania major | 33% | 100% |
Q4QAV6 | Leishmania major | 24% | 100% |
Q5ANB2 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 89% |
Q5BFU7 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 34% | 86% |
Q6BL34 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 31% | 86% |
Q6C7X8 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 31% | 87% |
Q6CIR0 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 31% | 83% |
Q6FNA2 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 33% | 83% |
Q757U8 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 33% | 84% |
Q8K4L0 | Mus musculus | 38% | 92% |
Q8NJM2 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 33% | 93% |
Q8TDD1 | Homo sapiens | 39% | 91% |
V5DJX8 | Trypanosoma cruzi | 70% | 100% |