Nuclear proteins, nucleoporin interacting component (NUP93)
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:0005643 | nuclear pore | 3 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:0044612 | nuclear pore linkers | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IW16
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0015931 | nucleobase-containing compound transport | 5 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0050657 | nucleic acid transport | 6 | 12 |
GO:0050658 | RNA transport | 4 | 12 |
GO:0051028 | mRNA transport | 5 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051236 | establishment of RNA localization | 3 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0006405 | RNA export from nucleus | 5 | 1 |
GO:0006406 | mRNA export from nucleus | 6 | 1 |
GO:0006606 | protein import into nucleus | 5 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0016973 | poly(A)+ mRNA export from nucleus | 7 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0034504 | protein localization to nucleus | 6 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051170 | import into nucleus | 6 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 12 |
GO:0017056 | structural constituent of nuclear pore | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.461 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.589 |
CLV_C14_Caspase3-7 | 555 | 559 | PF00656 | 0.348 |
CLV_C14_Caspase3-7 | 789 | 793 | PF00656 | 0.488 |
CLV_MEL_PAP_1 | 386 | 392 | PF00089 | 0.475 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 603 | 605 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.540 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 712 | 714 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 861 | 863 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 861 | 863 | PF00082 | 0.455 |
CLV_PCSK_PC7_1 | 122 | 128 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.393 |
DEG_APCC_DBOX_1 | 337 | 345 | PF00400 | 0.328 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.663 |
DEG_APCC_DBOX_1 | 511 | 519 | PF00400 | 0.363 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.692 |
DEG_SCF_FBW7_1 | 501 | 506 | PF00400 | 0.359 |
DEG_SCF_FBW7_2 | 415 | 422 | PF00400 | 0.398 |
DEG_SPOP_SBC_1 | 848 | 852 | PF00917 | 0.262 |
DOC_CKS1_1 | 500 | 505 | PF01111 | 0.398 |
DOC_CYCLIN_yCln2_LP_2 | 580 | 586 | PF00134 | 0.443 |
DOC_CYCLIN_yCln2_LP_2 | 795 | 801 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 126 | 133 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 347 | 356 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.659 |
DOC_MAPK_MEF2A_6 | 163 | 170 | PF00069 | 0.632 |
DOC_MAPK_MEF2A_6 | 447 | 455 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 592 | 601 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 686 | 694 | PF00069 | 0.363 |
DOC_MAPK_NFAT4_5 | 163 | 171 | PF00069 | 0.632 |
DOC_PP2B_LxvP_1 | 580 | 583 | PF13499 | 0.443 |
DOC_PP2B_LxvP_1 | 726 | 729 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 795 | 798 | PF13499 | 0.449 |
DOC_PP4_FxxP_1 | 799 | 802 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 729 | 733 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 848 | 852 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 881 | 885 | PF00917 | 0.475 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 225 | 230 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 338 | 342 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 40 | 44 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 468 | 474 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 488 | 495 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 531 | 536 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 575 | 584 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 592 | 597 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 604 | 610 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 731 | 735 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 834 | 844 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 868 | 873 | PF00244 | 0.407 |
LIG_Actin_WH2_2 | 474 | 490 | PF00022 | 0.427 |
LIG_BIR_III_4 | 401 | 405 | PF00653 | 0.475 |
LIG_BRCT_BRCA1_1 | 783 | 787 | PF00533 | 0.342 |
LIG_Clathr_ClatBox_1 | 598 | 602 | PF01394 | 0.369 |
LIG_CSL_BTD_1 | 193 | 196 | PF09270 | 0.644 |
LIG_EH1_1 | 534 | 542 | PF00400 | 0.449 |
LIG_eIF4E_1 | 446 | 452 | PF01652 | 0.363 |
LIG_eIF4E_1 | 593 | 599 | PF01652 | 0.344 |
LIG_eIF4E_1 | 766 | 772 | PF01652 | 0.428 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.633 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.596 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.423 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.770 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.367 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.475 |
LIG_FHA_1 | 766 | 772 | PF00498 | 0.479 |
LIG_FHA_1 | 806 | 812 | PF00498 | 0.484 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.603 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.344 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.348 |
LIG_FHA_2 | 869 | 875 | PF00498 | 0.475 |
LIG_GBD_Chelix_1 | 532 | 540 | PF00786 | 0.321 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 483 | 492 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 591 | 601 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 613 | 624 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 765 | 772 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 792 | 802 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 892 | 899 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 285 | 290 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 591 | 596 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 765 | 769 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 792 | 797 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 884 | 890 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 892 | 897 | PF02991 | 0.424 |
LIG_LYPXL_yS_3 | 887 | 890 | PF13949 | 0.547 |
LIG_NRBOX | 340 | 346 | PF00104 | 0.413 |
LIG_NRBOX | 450 | 456 | PF00104 | 0.328 |
LIG_NRBOX | 545 | 551 | PF00104 | 0.417 |
LIG_PDZ_Class_2 | 895 | 900 | PF00595 | 0.463 |
LIG_Pex14_1 | 194 | 198 | PF04695 | 0.651 |
LIG_Pex14_1 | 283 | 287 | PF04695 | 0.372 |
LIG_Pex14_1 | 381 | 385 | PF04695 | 0.344 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.640 |
LIG_RPA_C_Fungi | 261 | 273 | PF08784 | 0.453 |
LIG_RPA_C_Fungi | 69 | 81 | PF08784 | 0.691 |
LIG_SH2_CRK | 593 | 597 | PF00017 | 0.344 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 393 | 397 | PF00017 | 0.351 |
LIG_SH2_NCK_1 | 94 | 98 | PF00017 | 0.706 |
LIG_SH2_PTP2 | 198 | 201 | PF00017 | 0.675 |
LIG_SH2_SRC | 278 | 281 | PF00017 | 0.547 |
LIG_SH2_SRC | 436 | 439 | PF00017 | 0.449 |
LIG_SH2_SRC | 814 | 817 | PF00017 | 0.449 |
LIG_SH2_SRC | 94 | 97 | PF00017 | 0.717 |
LIG_SH2_STAP1 | 779 | 783 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.648 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 814 | 817 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 818 | 821 | PF00017 | 0.449 |
LIG_SH3_3 | 795 | 801 | PF00018 | 0.344 |
LIG_SH3_3 | 882 | 888 | PF00018 | 0.550 |
LIG_SUMO_SIM_anti_2 | 247 | 256 | PF11976 | 0.587 |
LIG_SUMO_SIM_anti_2 | 301 | 306 | PF11976 | 0.421 |
LIG_SUMO_SIM_anti_2 | 595 | 600 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 520 | 525 | PF11976 | 0.390 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.659 |
LIG_TYR_ITIM | 885 | 890 | PF00017 | 0.564 |
LIG_WRC_WIRS_1 | 382 | 387 | PF05994 | 0.262 |
LIG_WRC_WIRS_1 | 532 | 537 | PF05994 | 0.449 |
LIG_WRC_WIRS_1 | 766 | 771 | PF05994 | 0.475 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.690 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.643 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.671 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.524 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.738 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.614 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.449 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.449 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.449 |
MOD_CK1_1 | 730 | 736 | PF00069 | 0.367 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.393 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.722 |
MOD_CK2_1 | 868 | 874 | PF00069 | 0.475 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.709 |
MOD_GlcNHglycan | 145 | 149 | PF01048 | 0.645 |
MOD_GlcNHglycan | 21 | 26 | PF01048 | 0.659 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.680 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.716 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.530 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.425 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.475 |
MOD_GlcNHglycan | 496 | 500 | PF01048 | 0.482 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.472 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.425 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.428 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.440 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.437 |
MOD_GlcNHglycan | 829 | 832 | PF01048 | 0.445 |
MOD_GlcNHglycan | 837 | 840 | PF01048 | 0.452 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.670 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.656 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.460 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.413 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.425 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.437 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.423 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.353 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.440 |
MOD_LATS_1 | 175 | 181 | PF00433 | 0.641 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.475 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.367 |
MOD_N-GLC_1 | 781 | 786 | PF02516 | 0.421 |
MOD_N-GLC_2 | 528 | 530 | PF02516 | 0.398 |
MOD_N-GLC_2 | 85 | 87 | PF02516 | 0.709 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.711 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.539 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.338 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.403 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.372 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.374 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.357 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.363 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.306 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.387 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.447 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.652 |
MOD_NEK2_1 | 781 | 786 | PF00069 | 0.458 |
MOD_NEK2_1 | 827 | 832 | PF00069 | 0.393 |
MOD_NEK2_2 | 404 | 409 | PF00069 | 0.475 |
MOD_NEK2_2 | 503 | 508 | PF00069 | 0.475 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.556 |
MOD_PIKK_1 | 522 | 528 | PF00454 | 0.449 |
MOD_PIKK_1 | 696 | 702 | PF00454 | 0.411 |
MOD_PIKK_1 | 737 | 743 | PF00454 | 0.433 |
MOD_PK_1 | 177 | 183 | PF00069 | 0.672 |
MOD_PK_1 | 592 | 598 | PF00069 | 0.449 |
MOD_PKA_1 | 176 | 182 | PF00069 | 0.611 |
MOD_PKA_1 | 318 | 324 | PF00069 | 0.475 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.589 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.449 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.443 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.580 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.388 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.353 |
MOD_PKA_2 | 730 | 736 | PF00069 | 0.451 |
MOD_PKA_2 | 848 | 854 | PF00069 | 0.417 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.794 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.572 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.438 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.344 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.605 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.551 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.619 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.503 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.378 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.467 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.328 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.344 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.303 |
MOD_Plk_4 | 730 | 736 | PF00069 | 0.449 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.393 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.389 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.398 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.475 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.449 |
MOD_SUMO_rev_2 | 331 | 341 | PF00179 | 0.329 |
MOD_SUMO_rev_2 | 857 | 863 | PF00179 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.644 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 544 | 549 | PF01217 | 0.328 |
TRG_DiLeu_BaLyEn_6 | 637 | 642 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 861 | 866 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.648 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.673 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 766 | 769 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 887 | 890 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.774 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 603 | 605 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 711 | 713 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 862 | 865 | PF00400 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 347 | 352 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 547 | 551 | PF00026 | 0.328 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6C7 | Leptomonas seymouri | 73% | 100% |
A0A0S4JS37 | Bodo saltans | 32% | 100% |
A0A1X0P8L0 | Trypanosomatidae | 35% | 100% |
A0A422NCE5 | Trypanosoma rangeli | 37% | 100% |
A4HPB7 | Leishmania braziliensis | 89% | 100% |
A4ICF7 | Leishmania infantum | 100% | 100% |
D0A3C7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AT28 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q1H0 | Leishmania major | 95% | 100% |
V5BCK1 | Trypanosoma cruzi | 37% | 100% |