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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: E9AS81
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 5 |
GO:0006793 | phosphorus metabolic process | 3 | 5 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016310 | phosphorylation | 5 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0036211 | protein modification process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043412 | macromolecule modification | 4 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 5 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004672 | protein kinase activity | 3 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0005524 | ATP binding | 5 | 5 |
GO:0016301 | kinase activity | 4 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 5 |
GO:0032553 | ribonucleotide binding | 3 | 5 |
GO:0032555 | purine ribonucleotide binding | 4 | 5 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 5 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 5 |
GO:0036094 | small molecule binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043168 | anion binding | 3 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:0097367 | carbohydrate derivative binding | 2 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
GO:1901265 | nucleoside phosphate binding | 3 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 217 | 221 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 569 | 573 | PF00656 | 0.674 |
CLV_C14_Caspase3-7 | 602 | 606 | PF00656 | 0.517 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 774 | 776 | PF00675 | 0.416 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 838 | 842 | PF00082 | 0.475 |
CLV_Separin_Metazoa | 759 | 763 | PF03568 | 0.609 |
DEG_APCC_DBOX_1 | 597 | 605 | PF00400 | 0.501 |
DEG_APCC_DBOX_1 | 710 | 718 | PF00400 | 0.581 |
DEG_APCC_DBOX_1 | 773 | 781 | PF00400 | 0.414 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.689 |
DOC_CKS1_1 | 308 | 313 | PF01111 | 0.477 |
DOC_CYCLIN_RxL_1 | 367 | 374 | PF00134 | 0.562 |
DOC_CYCLIN_RxL_1 | 684 | 695 | PF00134 | 0.627 |
DOC_CYCLIN_RxL_1 | 700 | 709 | PF00134 | 0.464 |
DOC_CYCLIN_RxL_1 | 710 | 718 | PF00134 | 0.493 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 338 | 347 | PF00134 | 0.496 |
DOC_CYCLIN_yCln2_LP_2 | 24 | 27 | PF00134 | 0.629 |
DOC_CYCLIN_yCln2_LP_2 | 721 | 727 | PF00134 | 0.564 |
DOC_MAPK_gen_1 | 12 | 20 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 523 | 532 | PF00069 | 0.617 |
DOC_MAPK_gen_1 | 774 | 782 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 762 | 769 | PF00069 | 0.565 |
DOC_PP1_RVXF_1 | 588 | 594 | PF00149 | 0.579 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.622 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.607 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.526 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.634 |
DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.628 |
DOC_PP4_FxxP_1 | 308 | 311 | PF00568 | 0.486 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 732 | 736 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 831 | 835 | PF00917 | 0.576 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 451 | 455 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 526 | 531 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 590 | 600 | PF00244 | 0.535 |
LIG_Actin_WH2_2 | 196 | 212 | PF00022 | 0.592 |
LIG_AP2alpha_1 | 798 | 802 | PF02296 | 0.548 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.487 |
LIG_BIR_III_4 | 464 | 468 | PF00653 | 0.542 |
LIG_BIR_III_4 | 572 | 576 | PF00653 | 0.679 |
LIG_BRCT_BRCA1_1 | 141 | 145 | PF00533 | 0.646 |
LIG_BRCT_BRCA1_1 | 329 | 333 | PF00533 | 0.358 |
LIG_BRCT_BRCA1_1 | 528 | 532 | PF00533 | 0.562 |
LIG_BRCT_BRCA1_1 | 663 | 667 | PF00533 | 0.630 |
LIG_BRCT_BRCA1_1 | 794 | 798 | PF00533 | 0.499 |
LIG_CaM_IQ_9 | 738 | 754 | PF13499 | 0.571 |
LIG_Clathr_ClatBox_1 | 714 | 718 | PF01394 | 0.575 |
LIG_deltaCOP1_diTrp_1 | 474 | 482 | PF00928 | 0.470 |
LIG_deltaCOP1_diTrp_1 | 661 | 667 | PF00928 | 0.628 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.527 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.622 |
LIG_FHA_1 | 710 | 716 | PF00498 | 0.446 |
LIG_FHA_1 | 827 | 833 | PF00498 | 0.411 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.562 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.642 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.417 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.570 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.547 |
LIG_Integrin_RGD_1 | 66 | 68 | PF01839 | 0.572 |
LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 599 | 608 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 729 | 739 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 29 | 33 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 599 | 603 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 729 | 734 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 800 | 805 | PF02991 | 0.546 |
LIG_MYND_1 | 130 | 134 | PF01753 | 0.609 |
LIG_NRBOX | 716 | 722 | PF00104 | 0.576 |
LIG_PCNA_yPIPBox_3 | 395 | 405 | PF02747 | 0.531 |
LIG_PCNA_yPIPBox_3 | 682 | 692 | PF02747 | 0.476 |
LIG_Pex14_1 | 476 | 480 | PF04695 | 0.477 |
LIG_Pex14_1 | 663 | 667 | PF04695 | 0.630 |
LIG_Pex14_2 | 798 | 802 | PF04695 | 0.548 |
LIG_PTB_Apo_2 | 474 | 481 | PF02174 | 0.473 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 558 | 562 | PF00017 | 0.517 |
LIG_SH2_SRC | 62 | 65 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 784 | 788 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 658 | 661 | PF00017 | 0.720 |
LIG_SH2_STAT5 | 851 | 854 | PF00017 | 0.638 |
LIG_SH3_1 | 187 | 193 | PF00018 | 0.673 |
LIG_SH3_1 | 812 | 818 | PF00018 | 0.467 |
LIG_SH3_2 | 130 | 135 | PF14604 | 0.610 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.616 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.660 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.564 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.518 |
LIG_SH3_3 | 642 | 648 | PF00018 | 0.591 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.652 |
LIG_SH3_3 | 665 | 671 | PF00018 | 0.640 |
LIG_SH3_3 | 694 | 700 | PF00018 | 0.480 |
LIG_SH3_3 | 812 | 818 | PF00018 | 0.615 |
LIG_SUMO_SIM_anti_2 | 35 | 44 | PF11976 | 0.653 |
LIG_SUMO_SIM_anti_2 | 599 | 605 | PF11976 | 0.499 |
LIG_SUMO_SIM_anti_2 | 764 | 770 | PF11976 | 0.591 |
LIG_SUMO_SIM_par_1 | 125 | 131 | PF11976 | 0.605 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.631 |
LIG_SUMO_SIM_par_1 | 712 | 718 | PF11976 | 0.570 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.655 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.559 |
LIG_TRAF2_1 | 783 | 786 | PF00917 | 0.596 |
LIG_WW_3 | 132 | 136 | PF00397 | 0.634 |
MOD_CDK_SPK_2 | 211 | 216 | PF00069 | 0.646 |
MOD_CDK_SPxK_1 | 117 | 123 | PF00069 | 0.686 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.532 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.676 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.678 |
MOD_CK1_1 | 709 | 715 | PF00069 | 0.433 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.600 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.611 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.693 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.620 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.473 |
MOD_Cter_Amidation | 223 | 226 | PF01082 | 0.664 |
MOD_Cter_Amidation | 449 | 452 | PF01082 | 0.609 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.672 |
MOD_GlcNHglycan | 175 | 179 | PF01048 | 0.641 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.499 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.689 |
MOD_GlcNHglycan | 389 | 393 | PF01048 | 0.628 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.444 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.384 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.658 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.608 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.393 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.436 |
MOD_GlcNHglycan | 572 | 576 | PF01048 | 0.622 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.629 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.684 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.492 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.652 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.580 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.620 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.668 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.445 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.519 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.609 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.621 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.616 |
MOD_LATS_1 | 10 | 16 | PF00433 | 0.472 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.505 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.508 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.520 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.490 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.596 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.433 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.737 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.546 |
MOD_NEK2_1 | 659 | 664 | PF00069 | 0.616 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.553 |
MOD_NEK2_1 | 769 | 774 | PF00069 | 0.571 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.453 |
MOD_NEK2_1 | 826 | 831 | PF00069 | 0.412 |
MOD_NEK2_2 | 450 | 455 | PF00069 | 0.684 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.674 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.474 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.642 |
MOD_PIKK_1 | 746 | 752 | PF00454 | 0.576 |
MOD_PIKK_1 | 831 | 837 | PF00454 | 0.436 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.475 |
MOD_PKA_1 | 566 | 572 | PF00069 | 0.525 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.623 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.695 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.547 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.604 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.618 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.614 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.642 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.474 |
MOD_Plk_1 | 778 | 784 | PF00069 | 0.471 |
MOD_Plk_1 | 788 | 794 | PF00069 | 0.495 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.498 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.633 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.686 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.648 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.581 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.648 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.488 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.506 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.640 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.521 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.526 |
MOD_SUMO_rev_2 | 68 | 75 | PF00179 | 0.512 |
TRG_DiLeu_BaEn_1 | 202 | 207 | PF01217 | 0.564 |
TRG_DiLeu_BaEn_1 | 622 | 627 | PF01217 | 0.522 |
TRG_DiLeu_BaEn_1 | 716 | 721 | PF01217 | 0.573 |
TRG_DiLeu_BaLyEn_6 | 368 | 373 | PF01217 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 587 | 592 | PF01217 | 0.581 |
TRG_DiLeu_BaLyEn_6 | 710 | 715 | PF01217 | 0.584 |
TRG_DiLeu_BaLyEn_6 | 816 | 821 | PF01217 | 0.606 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.668 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.532 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 710 | 713 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 773 | 775 | PF00400 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 102 | 107 | PF00026 | 0.649 |
TRG_Pf-PMV_PEXEL_1 | 370 | 374 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 452 | 457 | PF00026 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 713 | 718 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 775 | 779 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WVK3 | Leishmania donovani | 86% | 100% |
A4HYE8 | Leishmania infantum | 86% | 100% |
Q4QD85 | Leishmania major | 84% | 100% |