Nuclear proteins, Importin 1 (IMP1) Uncharacterized
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. | yes | yes: 20 |
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:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A4IBC5
Term | Name | Level | Count |
---|---|---|---|
GO:0006606 | protein import into nucleus | 5 | 12 |
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006913 | nucleocytoplasmic transport | 5 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0033365 | protein localization to organelle | 5 | 12 |
GO:0034504 | protein localization to nucleus | 6 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051169 | nuclear transport | 4 | 12 |
GO:0051170 | import into nucleus | 6 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0072594 | establishment of protein localization to organelle | 4 | 12 |
GO:0006405 | RNA export from nucleus | 5 | 1 |
GO:0006406 | mRNA export from nucleus | 6 | 1 |
GO:0015931 | nucleobase-containing compound transport | 5 | 1 |
GO:0050657 | nucleic acid transport | 6 | 1 |
GO:0050658 | RNA transport | 4 | 1 |
GO:0051028 | mRNA transport | 5 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051236 | establishment of RNA localization | 3 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005048 | signal sequence binding | 4 | 1 |
GO:0005488 | binding | 1 | 2 |
GO:0008139 | nuclear localization sequence binding | 5 | 1 |
GO:0033218 | amide binding | 2 | 1 |
GO:0042277 | peptide binding | 3 | 1 |
GO:0061608 | nuclear import signal receptor activity | 3 | 1 |
GO:0140104 | molecular carrier activity | 1 | 1 |
GO:0140142 | nucleocytoplasmic carrier activity | 2 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0031267 | small GTPase binding | 5 | 1 |
GO:0051020 | GTPase binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.566 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 851 | 853 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 908 | 910 | PF00675 | 0.514 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 883 | 887 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 898 | 902 | PF00082 | 0.502 |
DOC_CDC14_PxL_1 | 165 | 173 | PF14671 | 0.468 |
DOC_CDC14_PxL_1 | 401 | 409 | PF14671 | 0.505 |
DOC_CYCLIN_RxL_1 | 546 | 554 | PF00134 | 0.310 |
DOC_CYCLIN_yCln2_LP_2 | 159 | 165 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 69 | 75 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 187 | 196 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 384 | 391 | PF00069 | 0.332 |
DOC_MAPK_gen_1 | 56 | 63 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 189 | 198 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 242 | 250 | PF00069 | 0.302 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 402 | 405 | PF13499 | 0.343 |
DOC_PP2B_LxvP_1 | 577 | 580 | PF13499 | 0.426 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 732 | 736 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 738 | 742 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 767 | 771 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 856 | 860 | PF00917 | 0.474 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 689 | 694 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.474 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 242 | 247 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 384 | 391 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 535 | 544 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 623 | 628 | PF00244 | 0.466 |
LIG_Actin_WH2_2 | 341 | 359 | PF00022 | 0.414 |
LIG_APCC_ABBA_1 | 802 | 807 | PF00400 | 0.366 |
LIG_APCC_ABBA_1 | 861 | 866 | PF00400 | 0.305 |
LIG_APCC_ABBAyCdc20_2 | 320 | 326 | PF00400 | 0.383 |
LIG_BIR_III_2 | 149 | 153 | PF00653 | 0.302 |
LIG_BIR_III_2 | 690 | 694 | PF00653 | 0.483 |
LIG_BIR_III_4 | 155 | 159 | PF00653 | 0.466 |
LIG_BIR_III_4 | 663 | 667 | PF00653 | 0.354 |
LIG_BRCT_BRCA1_1 | 172 | 176 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 246 | 250 | PF00533 | 0.388 |
LIG_BRCT_BRCA1_1 | 658 | 662 | PF00533 | 0.295 |
LIG_BRCT_BRCA1_1 | 769 | 773 | PF00533 | 0.394 |
LIG_deltaCOP1_diTrp_1 | 292 | 300 | PF00928 | 0.331 |
LIG_eIF4E_1 | 397 | 403 | PF01652 | 0.393 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.374 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.355 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.330 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.232 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.295 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.387 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.412 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.450 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.510 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.367 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.375 |
LIG_FHA_2 | 728 | 734 | PF00498 | 0.427 |
LIG_GBD_Chelix_1 | 118 | 126 | PF00786 | 0.454 |
LIG_GBD_Chelix_1 | 4 | 12 | PF00786 | 0.364 |
LIG_LIR_Apic_2 | 337 | 342 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 321 | 332 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 436 | 447 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 461 | 471 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 597 | 607 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 624 | 632 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 659 | 669 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 677 | 688 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 734 | 744 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 770 | 780 | PF02991 | 0.448 |
LIG_LIR_LC3C_4 | 462 | 467 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 436 | 442 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 539 | 544 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 624 | 628 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 677 | 683 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 734 | 740 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 770 | 776 | PF02991 | 0.449 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.308 |
LIG_PCNA_PIPBox_1 | 769 | 778 | PF02747 | 0.434 |
LIG_PCNA_yPIPBox_3 | 211 | 221 | PF02747 | 0.352 |
LIG_Pex14_2 | 621 | 625 | PF04695 | 0.466 |
LIG_Pex14_2 | 821 | 825 | PF04695 | 0.290 |
LIG_PTB_Apo_2 | 619 | 626 | PF02174 | 0.474 |
LIG_Rb_pABgroove_1 | 593 | 601 | PF01858 | 0.446 |
LIG_Rb_pABgroove_1 | 656 | 664 | PF01858 | 0.307 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.400 |
LIG_SH2_CRK | 439 | 443 | PF00017 | 0.462 |
LIG_SH2_CRK | 737 | 741 | PF00017 | 0.337 |
LIG_SH2_NCK_1 | 737 | 741 | PF00017 | 0.354 |
LIG_SH2_SRC | 251 | 254 | PF00017 | 0.365 |
LIG_SH2_SRC | 805 | 808 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 439 | 443 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 916 | 919 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 805 | 808 | PF00017 | 0.396 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.417 |
LIG_SUMO_SIM_anti_2 | 192 | 199 | PF11976 | 0.331 |
LIG_SUMO_SIM_anti_2 | 400 | 405 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 244 | 249 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 315 | 321 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 465 | 470 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 549 | 554 | PF11976 | 0.402 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.464 |
LIG_TRAF2_1 | 646 | 649 | PF00917 | 0.505 |
LIG_TYR_ITSM | 247 | 254 | PF00017 | 0.456 |
LIG_UBA3_1 | 491 | 498 | PF00899 | 0.431 |
LIG_UBA3_1 | 772 | 778 | PF00899 | 0.379 |
MOD_CDK_SPxxK_3 | 689 | 696 | PF00069 | 0.412 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.385 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.387 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.496 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.309 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.325 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.447 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.449 |
MOD_CK1_1 | 887 | 893 | PF00069 | 0.477 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.333 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.369 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.342 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.430 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.436 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.382 |
MOD_CK2_1 | 834 | 840 | PF00069 | 0.513 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.464 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.316 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.455 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.395 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.586 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.200 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.439 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.505 |
MOD_GlcNHglycan | 854 | 857 | PF01048 | 0.460 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.496 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.313 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.359 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.464 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.463 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.371 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.396 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.314 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.490 |
MOD_GSK3_1 | 755 | 762 | PF00069 | 0.559 |
MOD_GSK3_1 | 763 | 770 | PF00069 | 0.492 |
MOD_GSK3_1 | 780 | 787 | PF00069 | 0.490 |
MOD_GSK3_1 | 852 | 859 | PF00069 | 0.541 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.446 |
MOD_N-GLC_1 | 500 | 505 | PF02516 | 0.294 |
MOD_N-GLC_1 | 589 | 594 | PF02516 | 0.381 |
MOD_N-GLC_1 | 621 | 626 | PF02516 | 0.403 |
MOD_N-GLC_1 | 727 | 732 | PF02516 | 0.468 |
MOD_N-GLC_1 | 794 | 799 | PF02516 | 0.414 |
MOD_N-GLC_1 | 887 | 892 | PF02516 | 0.553 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.490 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.353 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.435 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.486 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.350 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.406 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.421 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.323 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.362 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.491 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.354 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.352 |
MOD_NEK2_1 | 867 | 872 | PF00069 | 0.351 |
MOD_NEK2_2 | 732 | 737 | PF00069 | 0.430 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.493 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.436 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.377 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.390 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.479 |
MOD_PIKK_1 | 583 | 589 | PF00454 | 0.508 |
MOD_PIKK_1 | 767 | 773 | PF00454 | 0.347 |
MOD_PK_1 | 344 | 350 | PF00069 | 0.493 |
MOD_PKA_1 | 384 | 390 | PF00069 | 0.322 |
MOD_PKA_1 | 852 | 858 | PF00069 | 0.280 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.322 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.427 |
MOD_PKA_2 | 832 | 838 | PF00069 | 0.539 |
MOD_PKB_1 | 349 | 357 | PF00069 | 0.578 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.509 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.455 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.401 |
MOD_Plk_1 | 621 | 627 | PF00069 | 0.383 |
MOD_Plk_1 | 648 | 654 | PF00069 | 0.345 |
MOD_Plk_1 | 727 | 733 | PF00069 | 0.389 |
MOD_Plk_1 | 794 | 800 | PF00069 | 0.445 |
MOD_Plk_1 | 833 | 839 | PF00069 | 0.524 |
MOD_Plk_1 | 876 | 882 | PF00069 | 0.561 |
MOD_Plk_2-3 | 834 | 840 | PF00069 | 0.513 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.498 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.433 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.293 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.441 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.463 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.363 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.413 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.504 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.422 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.488 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.356 |
MOD_Plk_4 | 834 | 840 | PF00069 | 0.517 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.387 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.528 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.395 |
MOD_ProDKin_1 | 689 | 695 | PF00069 | 0.552 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.464 |
MOD_SUMO_rev_2 | 807 | 814 | PF00179 | 0.473 |
TRG_DiLeu_BaEn_1 | 192 | 197 | PF01217 | 0.434 |
TRG_DiLeu_BaEn_1 | 834 | 839 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.295 |
TRG_DiLeu_BaLyEn_6 | 590 | 595 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 737 | 740 | PF00928 | 0.342 |
TRG_ER_diArg_1 | 348 | 351 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.429 |
TRG_NLS_MonoExtC_3 | 908 | 914 | PF00514 | 0.438 |
TRG_NLS_MonoExtN_4 | 907 | 913 | PF00514 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 549 | 554 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 880 | 884 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 910 | 914 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1U2 | Leptomonas seymouri | 74% | 100% |
A0A0S4J991 | Bodo saltans | 37% | 100% |
A0A1X0P5L5 | Trypanosomatidae | 47% | 100% |
A0A3S7X9A3 | Leishmania donovani | 99% | 100% |
A0A422NM11 | Trypanosoma rangeli | 48% | 100% |
A4HMQ7 | Leishmania braziliensis | 91% | 100% |
B8ARW2 | Oryza sativa subsp. indica | 25% | 100% |
B9FDR3 | Oryza sativa subsp. japonica | 26% | 100% |
C9ZZC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 98% |
E9AF57 | Leishmania major | 97% | 100% |
E9B6B3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O14089 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
O14787 | Homo sapiens | 25% | 100% |
P38217 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q3SYU7 | Bos taurus | 24% | 100% |
Q8BFY9 | Mus musculus | 24% | 100% |
Q8H0U4 | Arabidopsis thaliana | 27% | 100% |
Q92973 | Homo sapiens | 24% | 100% |
Q99LG2 | Mus musculus | 25% | 100% |
V5BTG7 | Trypanosoma cruzi | 47% | 100% |