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: Q4QD69
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 | 333 | 337 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 636 | 640 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 756 | 758 | PF00675 | 0.683 |
CLV_PCSK_FUR_1 | 266 | 270 | PF00082 | 0.419 |
CLV_PCSK_FUR_1 | 343 | 347 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 681 | 683 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 756 | 758 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 787 | 789 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 859 | 861 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 597 | 599 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 787 | 789 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 859 | 861 | PF00082 | 0.589 |
CLV_PCSK_PC7_1 | 855 | 861 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 806 | 810 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 899 | 903 | PF00082 | 0.636 |
CLV_Separin_Metazoa | 273 | 277 | PF03568 | 0.614 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.535 |
DEG_MDM2_SWIB_1 | 299 | 307 | PF02201 | 0.489 |
DOC_CDC14_PxL_1 | 886 | 894 | PF14671 | 0.471 |
DOC_CKS1_1 | 592 | 597 | PF01111 | 0.415 |
DOC_CYCLIN_RxL_1 | 319 | 333 | PF00134 | 0.573 |
DOC_CYCLIN_RxL_1 | 745 | 755 | PF00134 | 0.459 |
DOC_CYCLIN_yCln2_LP_2 | 723 | 726 | PF00134 | 0.495 |
DOC_MAPK_gen_1 | 323 | 331 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 432 | 439 | PF00069 | 0.297 |
DOC_MAPK_gen_1 | 859 | 867 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 250 | 258 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 323 | 331 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 522 | 530 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 558 | 566 | PF00069 | 0.312 |
DOC_MAPK_RevD_3 | 254 | 269 | PF00069 | 0.578 |
DOC_MAPK_RevD_3 | 500 | 516 | PF00069 | 0.224 |
DOC_MIT_MIM_1 | 654 | 662 | PF04212 | 0.357 |
DOC_PP1_RVXF_1 | 411 | 417 | PF00149 | 0.473 |
DOC_PP1_RVXF_1 | 514 | 521 | PF00149 | 0.224 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.634 |
DOC_PP2B_LxvP_1 | 329 | 332 | PF13499 | 0.558 |
DOC_PP2B_LxvP_1 | 723 | 726 | PF13499 | 0.477 |
DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.518 |
DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.312 |
DOC_PP4_FxxP_1 | 592 | 595 | PF00568 | 0.391 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 771 | 775 | PF00917 | 0.486 |
DOC_USP7_UBL2_3 | 401 | 405 | PF12436 | 0.510 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 323 | 328 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 606 | 611 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 613 | 621 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 681 | 685 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 806 | 812 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 860 | 866 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 418 | 434 | PF00022 | 0.309 |
LIG_Actin_WH2_2 | 600 | 615 | PF00022 | 0.440 |
LIG_Actin_WH2_2 | 817 | 834 | PF00022 | 0.398 |
LIG_BRCT_BRCA1_1 | 364 | 368 | PF00533 | 0.501 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.330 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.283 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.366 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.532 |
LIG_FHA_1 | 685 | 691 | PF00498 | 0.446 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.495 |
LIG_FHA_1 | 816 | 822 | PF00498 | 0.384 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.273 |
LIG_FHA_2 | 692 | 698 | PF00498 | 0.511 |
LIG_Integrin_RGD_1 | 843 | 845 | PF01839 | 0.620 |
LIG_LIR_Apic_2 | 143 | 149 | PF02991 | 0.511 |
LIG_LIR_Apic_2 | 435 | 441 | PF02991 | 0.311 |
LIG_LIR_Apic_2 | 683 | 689 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 423 | 431 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 532 | 543 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 586 | 595 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 672 | 679 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 697 | 706 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 869 | 879 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 905 | 912 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 586 | 592 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 697 | 701 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 869 | 875 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 905 | 911 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.603 |
LIG_MYND_1 | 275 | 279 | PF01753 | 0.587 |
LIG_MYND_1 | 67 | 71 | PF01753 | 0.554 |
LIG_NRBOX | 109 | 115 | PF00104 | 0.526 |
LIG_NRBOX | 477 | 483 | PF00104 | 0.398 |
LIG_Pex14_2 | 299 | 303 | PF04695 | 0.493 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.501 |
LIG_Pex14_2 | 399 | 403 | PF04695 | 0.496 |
LIG_Rb_pABgroove_1 | 586 | 594 | PF01858 | 0.397 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.653 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.462 |
LIG_SH2_CRK | 686 | 690 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 152 | 156 | PF00017 | 0.653 |
LIG_SH2_PTP2 | 458 | 461 | PF00017 | 0.325 |
LIG_SH2_SRC | 886 | 889 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 544 | 548 | PF00017 | 0.273 |
LIG_SH2_STAP1 | 608 | 612 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 759 | 763 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 872 | 876 | PF00017 | 0.339 |
LIG_SH2_STAT3 | 386 | 389 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 800 | 803 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 648 | 651 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 886 | 889 | PF00017 | 0.456 |
LIG_SH3_1 | 64 | 70 | PF00018 | 0.560 |
LIG_SH3_1 | 686 | 692 | PF00018 | 0.474 |
LIG_SH3_2 | 67 | 72 | PF14604 | 0.579 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.633 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.371 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.379 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.287 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.593 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.474 |
LIG_SH3_3 | 779 | 785 | PF00018 | 0.487 |
LIG_SH3_3 | 864 | 870 | PF00018 | 0.413 |
LIG_SH3_3 | 876 | 882 | PF00018 | 0.482 |
LIG_SH3_3 | 887 | 893 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 252 | 260 | PF11976 | 0.579 |
LIG_SUMO_SIM_anti_2 | 523 | 530 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 827 | 832 | PF11976 | 0.343 |
LIG_TRAF2_1 | 270 | 273 | PF00917 | 0.674 |
LIG_TYR_ITIM | 456 | 461 | PF00017 | 0.382 |
LIG_UBA3_1 | 853 | 859 | PF00899 | 0.441 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.440 |
LIG_WW_2 | 67 | 70 | PF00397 | 0.436 |
LIG_WW_3 | 273 | 277 | PF00397 | 0.437 |
LIG_WW_3 | 69 | 73 | PF00397 | 0.452 |
MOD_CDK_SPK_2 | 591 | 596 | PF00069 | 0.497 |
MOD_CDK_SPxK_1 | 552 | 558 | PF00069 | 0.376 |
MOD_CDK_SPxK_1 | 591 | 597 | PF00069 | 0.501 |
MOD_CDK_SPxxK_3 | 591 | 598 | PF00069 | 0.504 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.551 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.355 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.537 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.312 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.761 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.501 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.658 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.730 |
MOD_Cter_Amidation | 178 | 181 | PF01082 | 0.689 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.621 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.662 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.376 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.352 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.336 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.313 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.592 |
MOD_GlcNHglycan | 916 | 919 | PF01048 | 0.606 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.647 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.552 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.455 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.309 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.311 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.348 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.606 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.612 |
MOD_GSK3_1 | 903 | 910 | PF00069 | 0.547 |
MOD_LATS_1 | 321 | 327 | PF00433 | 0.426 |
MOD_LATS_1 | 604 | 610 | PF00433 | 0.420 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.386 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.386 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.441 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.336 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.488 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.253 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.381 |
MOD_NEK2_1 | 752 | 757 | PF00069 | 0.586 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.600 |
MOD_NEK2_1 | 861 | 866 | PF00069 | 0.505 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.575 |
MOD_NEK2_1 | 907 | 912 | PF00069 | 0.581 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.586 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.640 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.328 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.633 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.648 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.552 |
MOD_PKA_2 | 813 | 819 | PF00069 | 0.536 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.422 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.664 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.382 |
MOD_Plk_2-3 | 188 | 194 | PF00069 | 0.578 |
MOD_Plk_2-3 | 362 | 368 | PF00069 | 0.349 |
MOD_Plk_2-3 | 76 | 82 | PF00069 | 0.452 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.359 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.517 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.462 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.328 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.289 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.311 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.381 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.444 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.430 |
MOD_Plk_4 | 903 | 909 | PF00069 | 0.535 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.483 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.376 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.544 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.420 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.593 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.416 |
TRG_DiLeu_BaEn_1 | 252 | 257 | PF01217 | 0.446 |
TRG_DiLeu_BaEn_1 | 5 | 10 | PF01217 | 0.569 |
TRG_DiLeu_BaEn_4 | 187 | 193 | PF01217 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 109 | 114 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 872 | 875 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 595 | 598 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 928 | 931 | PF00400 | 0.605 |
TRG_NLS_MonoExtN_4 | 343 | 349 | PF00514 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 385 | 389 | PF00026 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 552 | 557 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZT3 | Leptomonas seymouri | 48% | 94% |
A0A3Q8IEM2 | Leishmania donovani | 94% | 100% |
A4HA91 | Leishmania braziliensis | 70% | 100% |
A4HYH1 | Leishmania infantum | 94% | 100% |
E9AS95 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |