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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4QET5
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008213 | protein alkylation | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0018022 | peptidyl-lysine methylation | 5 | 2 |
GO:0018026 | peptidyl-lysine monomethylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018205 | peptidyl-lysine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032259 | methylation | 2 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0008170 | N-methyltransferase activity | 5 | 2 |
GO:0008276 | protein methyltransferase activity | 3 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 2 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 334 | 338 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 546 | 550 | PF00656 | 0.601 |
CLV_C14_Caspase3-7 | 592 | 596 | PF00656 | 0.545 |
CLV_C14_Caspase3-7 | 783 | 787 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.688 |
CLV_MEL_PAP_1 | 274 | 280 | PF00089 | 0.663 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.513 |
CLV_PCSK_FUR_1 | 128 | 132 | PF00082 | 0.538 |
CLV_PCSK_FUR_1 | 172 | 176 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 670 | 672 | PF00082 | 0.513 |
CLV_PCSK_PC7_1 | 126 | 132 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.566 |
DEG_APCC_DBOX_1 | 559 | 567 | PF00400 | 0.622 |
DEG_APCC_DBOX_1 | 611 | 619 | PF00400 | 0.632 |
DEG_SCF_FBW7_1 | 626 | 633 | PF00400 | 0.710 |
DEG_SCF_FBW7_1 | 714 | 719 | PF00400 | 0.499 |
DOC_CDC14_PxL_1 | 520 | 528 | PF14671 | 0.682 |
DOC_CKS1_1 | 711 | 716 | PF01111 | 0.675 |
DOC_CYCLIN_RxL_1 | 775 | 786 | PF00134 | 0.619 |
DOC_MAPK_FxFP_2 | 390 | 393 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 467 | 475 | PF00069 | 0.674 |
DOC_MAPK_gen_1 | 533 | 540 | PF00069 | 0.774 |
DOC_PP1_RVXF_1 | 729 | 736 | PF00149 | 0.440 |
DOC_PP2B_LxvP_1 | 521 | 524 | PF13499 | 0.736 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.529 |
DOC_PP4_FxxP_1 | 711 | 714 | PF00568 | 0.627 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 716 | 720 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 781 | 785 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.703 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 697 | 702 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 710 | 715 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 116 | 123 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 296 | 302 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 348 | 357 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 57 | 67 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 718 | 728 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 767 | 772 | PF00244 | 0.678 |
LIG_Actin_WH2_2 | 160 | 176 | PF00022 | 0.573 |
LIG_Actin_WH2_2 | 502 | 519 | PF00022 | 0.559 |
LIG_Actin_WH2_2 | 690 | 706 | PF00022 | 0.592 |
LIG_AP2alpha_1 | 402 | 406 | PF02296 | 0.482 |
LIG_APCC_ABBA_1 | 399 | 404 | PF00400 | 0.476 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.645 |
LIG_BIR_III_4 | 547 | 551 | PF00653 | 0.719 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.433 |
LIG_CaM_NSCaTE_8 | 634 | 641 | PF13499 | 0.536 |
LIG_CSL_BTD_1 | 711 | 714 | PF09270 | 0.627 |
LIG_deltaCOP1_diTrp_1 | 212 | 219 | PF00928 | 0.504 |
LIG_deltaCOP1_diTrp_1 | 394 | 402 | PF00928 | 0.447 |
LIG_deltaCOP1_diTrp_1 | 666 | 672 | PF00928 | 0.515 |
LIG_deltaCOP1_diTrp_1 | 675 | 680 | PF00928 | 0.558 |
LIG_deltaCOP1_diTrp_1 | 772 | 779 | PF00928 | 0.565 |
LIG_eIF4E_1 | 503 | 509 | PF01652 | 0.490 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.569 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.456 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.569 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.473 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.452 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.758 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.637 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.758 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.592 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.535 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.683 |
LIG_FHA_1 | 766 | 772 | PF00498 | 0.608 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.680 |
LIG_FHA_2 | 631 | 637 | PF00498 | 0.643 |
LIG_LIR_Apic_2 | 387 | 393 | PF02991 | 0.510 |
LIG_LIR_Apic_2 | 709 | 714 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 394 | 405 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 480 | 491 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 737 | 746 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 772 | 782 | PF02991 | 0.553 |
LIG_LIR_LC3C_4 | 725 | 730 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 674 | 680 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 772 | 777 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 790 | 795 | PF02991 | 0.604 |
LIG_MYND_1 | 518 | 522 | PF01753 | 0.583 |
LIG_MYND_1 | 539 | 543 | PF01753 | 0.698 |
LIG_NRBOX | 634 | 640 | PF00104 | 0.615 |
LIG_NRBOX | 9 | 15 | PF00104 | 0.462 |
LIG_PCNA_PIPBox_1 | 773 | 782 | PF02747 | 0.548 |
LIG_PCNA_yPIPBox_3 | 767 | 780 | PF02747 | 0.649 |
LIG_Pex14_1 | 287 | 291 | PF04695 | 0.614 |
LIG_Pex14_1 | 735 | 739 | PF04695 | 0.503 |
LIG_Pex14_2 | 378 | 382 | PF04695 | 0.462 |
LIG_Pex14_2 | 402 | 406 | PF04695 | 0.482 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.501 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.506 |
LIG_SH2_CRK | 611 | 615 | PF00017 | 0.609 |
LIG_SH2_GRB2like | 227 | 230 | PF00017 | 0.508 |
LIG_SH2_GRB2like | 405 | 408 | PF00017 | 0.432 |
LIG_SH2_GRB2like | 739 | 742 | PF00017 | 0.545 |
LIG_SH2_NCK_1 | 503 | 507 | PF00017 | 0.626 |
LIG_SH2_PTP2 | 156 | 159 | PF00017 | 0.444 |
LIG_SH2_PTP2 | 291 | 294 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 227 | 231 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 481 | 485 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 481 | 484 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 739 | 742 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 792 | 795 | PF00017 | 0.553 |
LIG_SH3_1 | 611 | 617 | PF00018 | 0.601 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.599 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.703 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.742 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.523 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.711 |
LIG_SH3_3 | 611 | 617 | PF00018 | 0.601 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.555 |
LIG_SH3_5 | 401 | 405 | PF00018 | 0.431 |
LIG_SUMO_SIM_anti_2 | 504 | 510 | PF11976 | 0.576 |
LIG_SUMO_SIM_anti_2 | 725 | 731 | PF11976 | 0.598 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.793 |
LIG_TRAF2_1 | 788 | 791 | PF00917 | 0.524 |
LIG_TRFH_1 | 514 | 518 | PF08558 | 0.528 |
LIG_TYR_ITIM | 154 | 159 | PF00017 | 0.444 |
LIG_Vh1_VBS_1 | 552 | 570 | PF01044 | 0.612 |
MOD_CDK_SPxK_1 | 712 | 718 | PF00069 | 0.608 |
MOD_CDK_SPxxK_3 | 697 | 704 | PF00069 | 0.598 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.541 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.594 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.661 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.511 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.558 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.747 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.497 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.670 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.423 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.648 |
MOD_CK1_1 | 719 | 725 | PF00069 | 0.579 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.587 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.643 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.602 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.493 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.610 |
MOD_CK2_1 | 719 | 725 | PF00069 | 0.617 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.700 |
MOD_Cter_Amidation | 531 | 534 | PF01082 | 0.711 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.684 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.778 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.713 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.522 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.754 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.663 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.603 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.681 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.599 |
MOD_GlcNHglycan | 682 | 685 | PF01048 | 0.683 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.569 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.603 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.598 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.518 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.500 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.736 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.586 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.710 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.738 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.702 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.577 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.549 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.616 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.641 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.586 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.612 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.681 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.706 |
MOD_N-GLC_1 | 263 | 268 | PF02516 | 0.807 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.490 |
MOD_N-GLC_1 | 686 | 691 | PF02516 | 0.632 |
MOD_N-GLC_1 | 740 | 745 | PF02516 | 0.631 |
MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.720 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.684 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.716 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.605 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.599 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.652 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.594 |
MOD_NEK2_2 | 512 | 517 | PF00069 | 0.558 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.789 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.622 |
MOD_PK_1 | 256 | 262 | PF00069 | 0.731 |
MOD_PK_1 | 767 | 773 | PF00069 | 0.671 |
MOD_PKA_1 | 534 | 540 | PF00069 | 0.659 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.524 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.644 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.783 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.539 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.624 |
MOD_PKA_2 | 717 | 723 | PF00069 | 0.614 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.745 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.515 |
MOD_Plk_1 | 716 | 722 | PF00069 | 0.576 |
MOD_Plk_2-3 | 654 | 660 | PF00069 | 0.593 |
MOD_Plk_2-3 | 794 | 800 | PF00069 | 0.657 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.369 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.755 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.410 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.550 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.571 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.709 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.591 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.590 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.568 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.785 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.728 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.720 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.545 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.596 |
MOD_ProDKin_1 | 642 | 648 | PF00069 | 0.413 |
MOD_ProDKin_1 | 697 | 703 | PF00069 | 0.565 |
MOD_ProDKin_1 | 710 | 716 | PF00069 | 0.592 |
MOD_SUMO_for_1 | 138 | 141 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 616 | 626 | PF00179 | 0.614 |
TRG_DiLeu_BaLyEn_6 | 270 | 275 | PF01217 | 0.755 |
TRG_DiLeu_BaLyEn_6 | 723 | 728 | PF01217 | 0.632 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.508 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 739 | 742 | PF00928 | 0.621 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.771 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 669 | 671 | PF00400 | 0.512 |
TRG_NLS_MonoExtN_4 | 530 | 537 | PF00514 | 0.670 |
TRG_Pf-PMV_PEXEL_1 | 12 | 17 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 778 | 783 | PF00026 | 0.611 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I059 | Leptomonas seymouri | 52% | 99% |
A0A1X0NQD9 | Trypanosomatidae | 26% | 100% |
A0A3S7WTX8 | Leishmania donovani | 92% | 100% |
A4H8K8 | Leishmania braziliensis | 74% | 100% |
E9AGN5 | Leishmania infantum | 92% | 100% |
E9AQP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |