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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9AS95
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0031123 | RNA 3'-end processing | 7 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071076 | RNA 3' uridylation | 8 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016779 | nucleotidyltransferase activity | 4 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 7 |
GO:0070569 | uridylyltransferase activity | 5 | 7 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.550 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 756 | 758 | PF00675 | 0.703 |
CLV_PCSK_FUR_1 | 266 | 270 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 681 | 683 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 756 | 758 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 859 | 861 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 597 | 599 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 859 | 861 | PF00082 | 0.578 |
CLV_PCSK_PC7_1 | 855 | 861 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 855 | 859 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 899 | 903 | PF00082 | 0.629 |
CLV_Separin_Metazoa | 273 | 277 | PF03568 | 0.615 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.527 |
DOC_CKS1_1 | 592 | 597 | PF01111 | 0.411 |
DOC_CYCLIN_RxL_1 | 319 | 333 | PF00134 | 0.583 |
DOC_CYCLIN_RxL_1 | 745 | 755 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 723 | 726 | PF00134 | 0.496 |
DOC_MAPK_DCC_7 | 899 | 909 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 323 | 331 | PF00069 | 0.554 |
DOC_MAPK_gen_1 | 432 | 438 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 858 | 867 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 283 | 290 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 323 | 331 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 522 | 530 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 558 | 566 | PF00069 | 0.304 |
DOC_MIT_MIM_1 | 654 | 662 | PF04212 | 0.353 |
DOC_PP1_RVXF_1 | 411 | 417 | PF00149 | 0.469 |
DOC_PP1_RVXF_1 | 561 | 567 | PF00149 | 0.293 |
DOC_PP2B_LxvP_1 | 329 | 332 | PF13499 | 0.559 |
DOC_PP2B_LxvP_1 | 723 | 726 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 879 | 882 | PF13499 | 0.324 |
DOC_PP2B_LxvP_1 | 890 | 893 | PF13499 | 0.382 |
DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.513 |
DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.308 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.269 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 771 | 775 | PF00917 | 0.473 |
DOC_USP7_UBL2_3 | 401 | 405 | PF12436 | 0.508 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.315 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 902 | 907 | PF00397 | 0.407 |
LIG_14-3-3_CanoR_1 | 276 | 281 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 306 | 312 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 323 | 328 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 681 | 685 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 814 | 818 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 850 | 854 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 860 | 866 | PF00244 | 0.447 |
LIG_Actin_WH2_2 | 194 | 209 | PF00022 | 0.658 |
LIG_Actin_WH2_2 | 418 | 434 | PF00022 | 0.304 |
LIG_Actin_WH2_2 | 817 | 834 | PF00022 | 0.387 |
LIG_BRCT_BRCA1_1 | 364 | 368 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 389 | 393 | PF00533 | 0.469 |
LIG_DLG_GKlike_1 | 323 | 331 | PF00625 | 0.512 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.297 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.279 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.511 |
LIG_FHA_1 | 816 | 822 | PF00498 | 0.373 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.663 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.269 |
LIG_FHA_2 | 692 | 698 | PF00498 | 0.490 |
LIG_LIR_Apic_2 | 143 | 149 | PF02991 | 0.508 |
LIG_LIR_Apic_2 | 435 | 441 | PF02991 | 0.306 |
LIG_LIR_Apic_2 | 683 | 689 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 423 | 431 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 586 | 595 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 672 | 679 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 697 | 706 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 869 | 879 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 905 | 912 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 586 | 592 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 697 | 701 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 869 | 875 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 905 | 911 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.595 |
LIG_MYND_1 | 900 | 904 | PF01753 | 0.458 |
LIG_NRBOX | 109 | 115 | PF00104 | 0.517 |
LIG_NRBOX | 477 | 483 | PF00104 | 0.316 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.498 |
LIG_Pex14_2 | 399 | 403 | PF04695 | 0.493 |
LIG_PTB_Apo_2 | 529 | 536 | PF02174 | 0.198 |
LIG_PTB_Phospho_1 | 529 | 535 | PF10480 | 0.198 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.653 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.455 |
LIG_SH2_CRK | 686 | 690 | PF00017 | 0.459 |
LIG_SH2_NCK_1 | 152 | 156 | PF00017 | 0.653 |
LIG_SH2_NCK_1 | 686 | 690 | PF00017 | 0.481 |
LIG_SH2_PTP2 | 458 | 461 | PF00017 | 0.314 |
LIG_SH2_SRC | 886 | 889 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 544 | 548 | PF00017 | 0.269 |
LIG_SH2_STAP1 | 608 | 612 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 759 | 763 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 811 | 815 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 872 | 876 | PF00017 | 0.329 |
LIG_SH2_STAT3 | 386 | 389 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 800 | 803 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 648 | 651 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 856 | 859 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 886 | 889 | PF00017 | 0.442 |
LIG_SH3_1 | 64 | 70 | PF00018 | 0.541 |
LIG_SH3_1 | 686 | 692 | PF00018 | 0.469 |
LIG_SH3_2 | 67 | 72 | PF14604 | 0.563 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.349 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.341 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.575 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.481 |
LIG_SH3_3 | 879 | 885 | PF00018 | 0.434 |
LIG_SUMO_SIM_anti_2 | 523 | 530 | PF11976 | 0.316 |
LIG_SUMO_SIM_anti_2 | 827 | 833 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 326 | 336 | PF11976 | 0.473 |
LIG_TRAF2_1 | 270 | 273 | PF00917 | 0.667 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.466 |
LIG_TYR_ITIM | 456 | 461 | PF00017 | 0.373 |
LIG_UBA3_1 | 853 | 859 | PF00899 | 0.422 |
LIG_WW_2 | 67 | 70 | PF00397 | 0.411 |
LIG_WW_3 | 273 | 277 | PF00397 | 0.442 |
MOD_CDC14_SPxK_1 | 210 | 213 | PF00782 | 0.581 |
MOD_CDK_SPK_2 | 591 | 596 | PF00069 | 0.487 |
MOD_CDK_SPxK_1 | 207 | 213 | PF00069 | 0.575 |
MOD_CDK_SPxK_1 | 552 | 558 | PF00069 | 0.364 |
MOD_CDK_SPxK_1 | 591 | 597 | PF00069 | 0.495 |
MOD_CDK_SPxxK_3 | 591 | 598 | PF00069 | 0.496 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.537 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.352 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.467 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.758 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.506 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.647 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.712 |
MOD_DYRK1A_RPxSP_1 | 581 | 585 | PF00069 | 0.422 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.603 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.612 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.581 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.413 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.365 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.328 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.308 |
MOD_GlcNHglycan | 633 | 637 | PF01048 | 0.515 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.560 |
MOD_GlcNHglycan | 916 | 919 | PF01048 | 0.603 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.643 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.567 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.534 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.564 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.468 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.347 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.304 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.303 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.295 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.603 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.499 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.594 |
MOD_LATS_1 | 321 | 327 | PF00433 | 0.446 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.425 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.381 |
MOD_N-GLC_2 | 532 | 534 | PF02516 | 0.205 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.377 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.314 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.335 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.473 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.237 |
MOD_NEK2_1 | 752 | 757 | PF00069 | 0.567 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.569 |
MOD_NEK2_1 | 861 | 866 | PF00069 | 0.469 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.560 |
MOD_NEK2_1 | 907 | 912 | PF00069 | 0.563 |
MOD_NEK2_2 | 790 | 795 | PF00069 | 0.516 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.357 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.621 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.387 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.330 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.641 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.529 |
MOD_PKA_2 | 813 | 819 | PF00069 | 0.516 |
MOD_PKA_2 | 849 | 855 | PF00069 | 0.360 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.413 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.663 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.378 |
MOD_Plk_1 | 868 | 874 | PF00069 | 0.343 |
MOD_Plk_2-3 | 188 | 194 | PF00069 | 0.579 |
MOD_Plk_2-3 | 362 | 368 | PF00069 | 0.344 |
MOD_Plk_2-3 | 76 | 82 | PF00069 | 0.427 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.355 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.330 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.284 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.369 |
MOD_Plk_4 | 790 | 796 | PF00069 | 0.555 |
MOD_Plk_4 | 849 | 855 | PF00069 | 0.380 |
MOD_Plk_4 | 861 | 867 | PF00069 | 0.411 |
MOD_Plk_4 | 907 | 913 | PF00069 | 0.513 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.575 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.464 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.364 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.547 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.419 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.590 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.490 |
MOD_ProDKin_1 | 902 | 908 | PF00069 | 0.490 |
MOD_SUMO_rev_2 | 173 | 183 | PF00179 | 0.530 |
MOD_SUMO_rev_2 | 463 | 470 | PF00179 | 0.315 |
TRG_DiLeu_BaEn_1 | 5 | 10 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 109 | 114 | PF01217 | 0.363 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 872 | 875 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 530 | 533 | PF00400 | 0.205 |
TRG_ER_diArg_1 | 595 | 598 | PF00400 | 0.448 |
TRG_NLS_MonoExtN_4 | 855 | 862 | PF00514 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 385 | 389 | PF00026 | 0.373 |
TRG_Pf-PMV_PEXEL_1 | 552 | 557 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZT3 | Leptomonas seymouri | 47% | 95% |
A0A3Q8IEM2 | Leishmania donovani | 91% | 100% |
A4HA91 | Leishmania braziliensis | 71% | 100% |
A4HYH1 | Leishmania infantum | 92% | 100% |
Q4QD69 | Leishmania major | 90% | 100% |