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: Q4QD85
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 | 0.753 |
CLV_C14_Caspase3-7 | 566 | 570 | PF00656 | 0.667 |
CLV_C14_Caspase3-7 | 599 | 603 | PF00656 | 0.606 |
CLV_C14_Caspase3-7 | 659 | 663 | PF00656 | 0.593 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.654 |
CLV_PCSK_FUR_1 | 133 | 137 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.521 |
CLV_Separin_Metazoa | 756 | 760 | PF03568 | 0.618 |
DEG_APCC_DBOX_1 | 594 | 602 | PF00400 | 0.600 |
DEG_APCC_DBOX_1 | 707 | 715 | PF00400 | 0.595 |
DEG_APCC_DBOX_1 | 85 | 93 | PF00400 | 0.519 |
DEG_SCF_FBW7_1 | 256 | 262 | PF00400 | 0.609 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.670 |
DOC_CKS1_1 | 176 | 181 | PF01111 | 0.649 |
DOC_CKS1_1 | 256 | 261 | PF01111 | 0.608 |
DOC_CKS1_1 | 308 | 313 | PF01111 | 0.550 |
DOC_CYCLIN_RxL_1 | 367 | 374 | PF00134 | 0.601 |
DOC_CYCLIN_RxL_1 | 681 | 692 | PF00134 | 0.614 |
DOC_CYCLIN_RxL_1 | 697 | 706 | PF00134 | 0.460 |
DOC_CYCLIN_RxL_1 | 707 | 715 | PF00134 | 0.504 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 338 | 347 | PF00134 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 24 | 27 | PF00134 | 0.634 |
DOC_CYCLIN_yCln2_LP_2 | 718 | 724 | PF00134 | 0.585 |
DOC_MAPK_gen_1 | 456 | 465 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 520 | 529 | PF00069 | 0.637 |
DOC_MAPK_gen_1 | 787 | 795 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 749 | 757 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 759 | 766 | PF00069 | 0.569 |
DOC_PP1_RVXF_1 | 585 | 591 | PF00149 | 0.610 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.626 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.641 |
DOC_PP2B_LxvP_1 | 755 | 758 | PF13499 | 0.584 |
DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.580 |
DOC_PP4_FxxP_1 | 308 | 311 | PF00568 | 0.552 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 729 | 733 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 785 | 789 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 828 | 832 | PF00917 | 0.688 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 695 | 700 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 749 | 754 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 810 | 815 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 449 | 458 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 587 | 597 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 614 | 621 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 789 | 794 | PF00244 | 0.590 |
LIG_Actin_WH2_2 | 196 | 212 | PF00022 | 0.633 |
LIG_AP2alpha_1 | 795 | 799 | PF02296 | 0.564 |
LIG_BIR_III_4 | 569 | 573 | PF00653 | 0.667 |
LIG_BRCT_BRCA1_1 | 141 | 145 | PF00533 | 0.639 |
LIG_BRCT_BRCA1_1 | 660 | 664 | PF00533 | 0.627 |
LIG_BRCT_BRCA1_1 | 791 | 795 | PF00533 | 0.517 |
LIG_CaM_IQ_9 | 735 | 751 | PF13499 | 0.583 |
LIG_Clathr_ClatBox_1 | 711 | 715 | PF01394 | 0.594 |
LIG_CtBP_PxDLS_1 | 126 | 130 | PF00389 | 0.569 |
LIG_CtBP_PxDLS_1 | 557 | 563 | PF00389 | 0.625 |
LIG_deltaCOP1_diTrp_1 | 471 | 479 | PF00928 | 0.565 |
LIG_deltaCOP1_diTrp_1 | 658 | 664 | PF00928 | 0.623 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.535 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.567 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.543 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.625 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.603 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.554 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.591 |
LIG_FHA_1 | 761 | 767 | PF00498 | 0.484 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.573 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.551 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.639 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.583 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.717 |
LIG_Integrin_RGD_1 | 66 | 68 | PF01839 | 0.581 |
LIG_LIR_Gen_1 | 596 | 605 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 698 | 709 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 726 | 736 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 29 | 33 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 596 | 600 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 650 | 655 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 726 | 731 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 797 | 802 | PF02991 | 0.561 |
LIG_NRBOX | 713 | 719 | PF00104 | 0.593 |
LIG_PCNA_yPIPBox_3 | 395 | 405 | PF02747 | 0.603 |
LIG_Pex14_1 | 473 | 477 | PF04695 | 0.541 |
LIG_Pex14_1 | 660 | 664 | PF04695 | 0.627 |
LIG_Pex14_2 | 795 | 799 | PF04695 | 0.564 |
LIG_PTB_Apo_2 | 471 | 478 | PF02174 | 0.532 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.608 |
LIG_SH2_STAT3 | 781 | 784 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 655 | 658 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 848 | 851 | PF00017 | 0.632 |
LIG_SH3_1 | 187 | 193 | PF00018 | 0.654 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.664 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.541 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.629 |
LIG_SH3_3 | 638 | 644 | PF00018 | 0.597 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.662 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.637 |
LIG_SH3_3 | 809 | 815 | PF00018 | 0.742 |
LIG_SH3_CIN85_PxpxPR_1 | 156 | 161 | PF14604 | 0.540 |
LIG_SUMO_SIM_anti_2 | 35 | 43 | PF11976 | 0.588 |
LIG_SUMO_SIM_anti_2 | 596 | 602 | PF11976 | 0.600 |
LIG_SUMO_SIM_anti_2 | 761 | 766 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 125 | 130 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 710 | 715 | PF11976 | 0.623 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.656 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.567 |
LIG_TRAF2_1 | 780 | 783 | PF00917 | 0.626 |
LIG_TRAF2_2 | 537 | 542 | PF00917 | 0.658 |
LIG_UBA3_1 | 711 | 719 | PF00899 | 0.481 |
MOD_CDK_SPK_2 | 211 | 216 | PF00069 | 0.730 |
MOD_CDK_SPK_2 | 695 | 700 | PF00069 | 0.509 |
MOD_CDK_SPxK_1 | 117 | 123 | PF00069 | 0.668 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.674 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.702 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.647 |
MOD_CK1_1 | 788 | 794 | PF00069 | 0.619 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.564 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.559 |
MOD_CK2_1 | 613 | 619 | PF00069 | 0.721 |
MOD_Cter_Amidation | 223 | 226 | PF01082 | 0.676 |
MOD_DYRK1A_RPxSP_1 | 749 | 753 | PF00069 | 0.506 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.681 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.673 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.520 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.670 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.453 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.489 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.502 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.728 |
MOD_GlcNHglycan | 569 | 573 | PF01048 | 0.593 |
MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.626 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.561 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.492 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.724 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.670 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.560 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.626 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.700 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.628 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.618 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.685 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.521 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.563 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.604 |
MOD_N-GLC_1 | 695 | 700 | PF02516 | 0.509 |
MOD_N-GLC_2 | 547 | 549 | PF02516 | 0.572 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.610 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.570 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.533 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.539 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.592 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.563 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.547 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.626 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.681 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.657 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.517 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.573 |
MOD_NEK2_1 | 766 | 771 | PF00069 | 0.576 |
MOD_NEK2_2 | 447 | 452 | PF00069 | 0.704 |
MOD_NEK2_2 | 617 | 622 | PF00069 | 0.516 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.657 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.657 |
MOD_PIKK_1 | 743 | 749 | PF00454 | 0.588 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.638 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.578 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.574 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.637 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.506 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.599 |
MOD_PKA_2 | 788 | 794 | PF00069 | 0.591 |
MOD_PKB_1 | 787 | 795 | PF00069 | 0.591 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.594 |
MOD_Plk_1 | 760 | 766 | PF00069 | 0.579 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.522 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.736 |
MOD_Plk_4 | 760 | 766 | PF00069 | 0.572 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.780 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.673 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.554 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.732 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.613 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.642 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.560 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.691 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.542 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.599 |
MOD_ProDKin_1 | 695 | 701 | PF00069 | 0.508 |
MOD_ProDKin_1 | 749 | 755 | PF00069 | 0.519 |
MOD_ProDKin_1 | 810 | 816 | PF00069 | 0.647 |
TRG_DiLeu_BaEn_1 | 202 | 207 | PF01217 | 0.622 |
TRG_DiLeu_BaEn_1 | 406 | 411 | PF01217 | 0.569 |
TRG_DiLeu_BaEn_1 | 619 | 624 | PF01217 | 0.625 |
TRG_DiLeu_BaEn_1 | 713 | 718 | PF01217 | 0.591 |
TRG_DiLeu_BaLyEn_6 | 584 | 589 | PF01217 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 707 | 712 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 813 | 818 | PF01217 | 0.606 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.657 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 132 | 135 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 525 | 528 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 707 | 710 | PF00400 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 102 | 107 | PF00026 | 0.648 |
TRG_Pf-PMV_PEXEL_1 | 370 | 374 | PF00026 | 0.686 |
TRG_Pf-PMV_PEXEL_1 | 449 | 454 | PF00026 | 0.804 |
TRG_Pf-PMV_PEXEL_1 | 676 | 680 | PF00026 | 0.676 |
TRG_Pf-PMV_PEXEL_1 | 710 | 715 | PF00026 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 772 | 776 | PF00026 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WVK3 | Leishmania donovani | 90% | 100% |
A4HYE8 | Leishmania infantum | 89% | 100% |
E9AS81 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |