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:0032991 | protein-containing complex | 1 | 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 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4H575
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003724 | RNA helicase activity | 3 | 10 |
GO:0003743 | translation initiation factor activity | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004386 | helicase activity | 2 | 11 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 10 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 10 |
GO:0016787 | hydrolase activity | 2 | 11 |
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 | 10 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003723 | RNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 684 | 688 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 777 | 781 | PF00656 | 0.595 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 804 | 806 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 818 | 820 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 818 | 820 | PF00082 | 0.644 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.673 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 818 | 822 | PF00082 | 0.571 |
DEG_APCC_DBOX_1 | 209 | 217 | PF00400 | 0.549 |
DEG_APCC_DBOX_1 | 842 | 850 | PF00400 | 0.551 |
DEG_SPOP_SBC_1 | 50 | 54 | PF00917 | 0.591 |
DOC_CKS1_1 | 359 | 364 | PF01111 | 0.459 |
DOC_CYCLIN_RxL_1 | 361 | 370 | PF00134 | 0.447 |
DOC_CYCLIN_RxL_1 | 476 | 487 | PF00134 | 0.405 |
DOC_CYCLIN_RxL_1 | 742 | 753 | PF00134 | 0.649 |
DOC_CYCLIN_yCln2_LP_2 | 260 | 266 | PF00134 | 0.466 |
DOC_CYCLIN_yCln2_LP_2 | 434 | 440 | PF00134 | 0.391 |
DOC_MAPK_DCC_7 | 556 | 565 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 298 | 308 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 349 | 359 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 587 | 597 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 649 | 658 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 856 | 863 | PF00069 | 0.376 |
DOC_MAPK_HePTP_8 | 553 | 565 | PF00069 | 0.459 |
DOC_MAPK_JIP1_4 | 825 | 831 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 301 | 310 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 556 | 565 | PF00069 | 0.447 |
DOC_MIT_MIM_1 | 506 | 515 | PF04212 | 0.552 |
DOC_PP1_RVXF_1 | 379 | 385 | PF00149 | 0.474 |
DOC_PP1_RVXF_1 | 591 | 598 | PF00149 | 0.391 |
DOC_PP1_RVXF_1 | 743 | 750 | PF00149 | 0.647 |
DOC_PP1_RVXF_1 | 804 | 811 | PF00149 | 0.479 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.373 |
DOC_PP2B_LxvP_1 | 558 | 561 | PF13499 | 0.459 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.615 |
DOC_USP7_UBL2_3 | 821 | 825 | PF12436 | 0.629 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 127 | 136 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 381 | 385 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 511 | 516 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 520 | 525 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 593 | 598 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 708 | 713 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 768 | 775 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 121 | 136 | PF00022 | 0.512 |
LIG_Actin_WH2_2 | 320 | 336 | PF00022 | 0.459 |
LIG_Actin_WH2_2 | 411 | 429 | PF00022 | 0.472 |
LIG_Actin_WH2_2 | 621 | 638 | PF00022 | 0.533 |
LIG_APCC_ABBA_1 | 656 | 661 | PF00400 | 0.424 |
LIG_APCC_ABBAyCdc20_2 | 655 | 661 | PF00400 | 0.423 |
LIG_APCC_ABBAyCdc20_2 | 805 | 811 | PF00400 | 0.439 |
LIG_BRCT_BRCA1_1 | 644 | 648 | PF00533 | 0.565 |
LIG_BRCT_BRCA1_1 | 787 | 791 | PF00533 | 0.510 |
LIG_CtBP_PxDLS_1 | 198 | 202 | PF00389 | 0.561 |
LIG_EVH1_1 | 163 | 167 | PF00568 | 0.372 |
LIG_FAT_LD_1 | 505 | 513 | PF03623 | 0.552 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.588 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.451 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.504 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.512 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.417 |
LIG_FHA_1 | 858 | 864 | PF00498 | 0.581 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.492 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.421 |
LIG_LIR_Apic_2 | 192 | 198 | PF02991 | 0.420 |
LIG_LIR_Apic_2 | 282 | 288 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 33 | 43 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 383 | 390 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 383 | 387 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 645 | 651 | PF02991 | 0.498 |
LIG_MLH1_MIPbox_1 | 644 | 648 | PF16413 | 0.599 |
LIG_NRBOX | 364 | 370 | PF00104 | 0.447 |
LIG_NRBOX | 476 | 482 | PF00104 | 0.419 |
LIG_Pex14_2 | 394 | 398 | PF04695 | 0.447 |
LIG_REV1ctd_RIR_1 | 595 | 604 | PF16727 | 0.378 |
LIG_REV1ctd_RIR_1 | 645 | 653 | PF16727 | 0.612 |
LIG_SH2_CRK | 187 | 191 | PF00017 | 0.558 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.535 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.508 |
LIG_SH2_CRK | 569 | 573 | PF00017 | 0.533 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.472 |
LIG_SH2_GRB2like | 517 | 520 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 626 | 630 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 76 | 80 | PF00017 | 0.601 |
LIG_SH2_PTP2 | 195 | 198 | PF00017 | 0.423 |
LIG_SH2_SRC | 179 | 182 | PF00017 | 0.366 |
LIG_SH2_SRC | 187 | 190 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 517 | 521 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 575 | 579 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 809 | 812 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 828 | 831 | PF00017 | 0.360 |
LIG_SH3_1 | 161 | 167 | PF00018 | 0.428 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.584 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.412 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.458 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.462 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.502 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.459 |
LIG_SH3_4 | 134 | 141 | PF00018 | 0.502 |
LIG_SUMO_SIM_anti_2 | 140 | 146 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 307 | 313 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 364 | 370 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 436 | 441 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 493 | 499 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 859 | 864 | PF11976 | 0.391 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.508 |
LIG_TRAF2_1 | 711 | 714 | PF00917 | 0.643 |
LIG_TRAF2_1 | 737 | 740 | PF00917 | 0.646 |
LIG_TYR_ITIM | 560 | 565 | PF00017 | 0.459 |
LIG_TYR_ITIM | 74 | 79 | PF00017 | 0.479 |
LIG_UBA3_1 | 212 | 220 | PF00899 | 0.445 |
LIG_UBA3_1 | 494 | 502 | PF00899 | 0.426 |
MOD_CDK_SPK_2 | 471 | 476 | PF00069 | 0.567 |
MOD_CDK_SPxK_1 | 358 | 364 | PF00069 | 0.459 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.525 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.655 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.668 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.418 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.460 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.542 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.552 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.519 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.571 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.405 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.598 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.589 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.513 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.468 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.386 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.431 |
MOD_CK2_1 | 688 | 694 | PF00069 | 0.710 |
MOD_CK2_1 | 708 | 714 | PF00069 | 0.709 |
MOD_CK2_1 | 734 | 740 | PF00069 | 0.564 |
MOD_CK2_1 | 791 | 797 | PF00069 | 0.447 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.487 |
MOD_GlcNHglycan | 148 | 153 | PF01048 | 0.503 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.677 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.250 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.246 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.497 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.245 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.247 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.277 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.520 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.562 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.516 |
MOD_GlcNHglycan | 736 | 739 | PF01048 | 0.553 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.451 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.606 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.682 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.565 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.689 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.502 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.723 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.435 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.488 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.509 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.596 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.580 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.658 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.377 |
MOD_GSK3_1 | 857 | 864 | PF00069 | 0.585 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.541 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.587 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.536 |
MOD_N-GLC_1 | 696 | 701 | PF02516 | 0.772 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.512 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.650 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.459 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.473 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.371 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.663 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.490 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.444 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.612 |
MOD_NEK2_1 | 733 | 738 | PF00069 | 0.505 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.430 |
MOD_NEK2_1 | 798 | 803 | PF00069 | 0.428 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.358 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.508 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.488 |
MOD_PK_1 | 708 | 714 | PF00069 | 0.497 |
MOD_PK_1 | 859 | 865 | PF00069 | 0.610 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.473 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.523 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.472 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.582 |
MOD_PKA_2 | 741 | 747 | PF00069 | 0.605 |
MOD_PKB_1 | 706 | 714 | PF00069 | 0.751 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.430 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.742 |
MOD_Plk_1 | 696 | 702 | PF00069 | 0.730 |
MOD_Plk_1 | 799 | 805 | PF00069 | 0.458 |
MOD_Plk_2-3 | 21 | 27 | PF00069 | 0.622 |
MOD_Plk_2-3 | 689 | 695 | PF00069 | 0.744 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.495 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.438 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.454 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.533 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.361 |
MOD_Plk_4 | 787 | 793 | PF00069 | 0.455 |
MOD_Plk_4 | 799 | 805 | PF00069 | 0.382 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.468 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.459 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.451 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.555 |
MOD_SUMO_for_1 | 128 | 131 | PF00179 | 0.539 |
MOD_SUMO_for_1 | 849 | 852 | PF00179 | 0.451 |
MOD_SUMO_rev_2 | 847 | 851 | PF00179 | 0.488 |
TRG_DiLeu_BaEn_1 | 208 | 213 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_1 | 504 | 509 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 285 | 290 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 361 | 366 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 69 | 74 | PF01217 | 0.483 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.659 |
TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 828 | 831 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 818 | 820 | PF00400 | 0.644 |
TRG_NES_CRM1_1 | 472 | 487 | PF08389 | 0.420 |
TRG_NLS_Bipartite_1 | 161 | 176 | PF00514 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.297 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P942 | Leptomonas seymouri | 75% | 100% |
A0A0S4IVE5 | Bodo saltans | 46% | 92% |
A0A1X0NPK0 | Trypanosomatidae | 57% | 87% |
A0A3Q8IF94 | Leishmania donovani | 33% | 100% |
A0A3R7LQQ6 | Trypanosoma rangeli | 57% | 91% |
A0A3S7WQ33 | Leishmania donovani | 92% | 100% |
A0A3S7X579 | Leishmania donovani | 29% | 100% |
A2QQA8 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 33% | 74% |
A3LQ55 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 34% | 99% |
A4H4Y0 | Leishmania braziliensis | 36% | 100% |
A4HK20 | Leishmania braziliensis | 33% | 100% |
A4HK38 | Leishmania braziliensis | 30% | 100% |
A4HTF8 | Leishmania infantum | 92% | 100% |
A4I7K4 | Leishmania infantum | 33% | 100% |
A4I7M5 | Leishmania infantum | 30% | 100% |
A6RW79 | Botryotinia fuckeliana (strain B05.10) | 34% | 75% |
A6ZLH6 | Saccharomyces cerevisiae (strain YJM789) | 29% | 100% |
A7TJK8 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 29% | 100% |
C9ZPN4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 92% |
E9AM86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9AWL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B2I0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
P21372 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
Q0D1K3 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 34% | 73% |
Q0J7Y8 | Oryza sativa subsp. japonica | 33% | 92% |
Q0UN57 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 32% | 73% |
Q2HAD8 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 34% | 82% |
Q2U2J6 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 33% | 73% |
Q4IP34 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 36% | 72% |
Q4Q1K8 | Leishmania major | 35% | 100% |
Q4Q5M6 | Leishmania major | 30% | 100% |
Q4Q5P5 | Leishmania major | 33% | 100% |
Q4QAV6 | Leishmania major | 24% | 100% |
Q4QHK6 | Leishmania major | 26% | 100% |
Q4QIG1 | Leishmania major | 91% | 100% |
Q4QIQ9 | Leishmania major | 35% | 100% |
Q4TVV3 | Danio rerio | 32% | 85% |
Q569Z5 | Mus musculus | 32% | 84% |
Q5R6D8 | Pongo abelii | 32% | 84% |
Q62780 | Rattus norvegicus | 32% | 84% |
Q6BML1 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 34% | 95% |
Q6CCZ1 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 33% | 89% |
Q6FML5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 28% | 100% |
Q754U8 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 29% | 100% |
Q7L014 | Homo sapiens | 32% | 84% |
Q7SH33 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 35% | 73% |
Q84UQ1 | Oryza sativa subsp. japonica | 36% | 83% |
Q8H0U8 | Arabidopsis thaliana | 36% | 74% |
Q9P7C7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 86% |
Q9SF41 | Arabidopsis thaliana | 34% | 88% |
V5DDC5 | Trypanosoma cruzi | 57% | 92% |