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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q0Y9
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |
GO:0018107 | peptidyl-threonine phosphorylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018209 | peptidyl-serine modification | 6 | 2 |
GO:0018210 | peptidyl-threonine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0004713 | protein tyrosine kinase activity | 4 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.624 |
CLV_C14_Caspase3-7 | 363 | 367 | PF00656 | 0.389 |
CLV_C14_Caspase3-7 | 494 | 498 | PF00656 | 0.411 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.411 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.411 |
CLV_Separin_Metazoa | 99 | 103 | PF03568 | 0.411 |
DEG_APCC_DBOX_1 | 54 | 62 | PF00400 | 0.411 |
DEG_APCC_KENBOX_2 | 67 | 71 | PF00400 | 0.513 |
DEG_SCF_FBW7_2 | 486 | 493 | PF00400 | 0.436 |
DEG_SIAH_1 | 751 | 759 | PF03145 | 0.699 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 92 | 101 | PF00134 | 0.411 |
DOC_MAPK_gen_1 | 102 | 111 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 112 | 121 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 324 | 331 | PF00069 | 0.445 |
DOC_MAPK_HePTP_8 | 109 | 121 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 112 | 121 | PF00069 | 0.436 |
DOC_PP2B_LxvP_1 | 585 | 588 | PF13499 | 0.779 |
DOC_PP4_FxxP_1 | 276 | 279 | PF00568 | 0.666 |
DOC_PP4_FxxP_1 | 417 | 420 | PF00568 | 0.513 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.705 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 717 | 722 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 736 | 741 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 785 | 790 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 120 | 128 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 146 | 150 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 267 | 273 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 324 | 331 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 521 | 531 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 54 | 61 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.486 |
LIG_Actin_WH2_2 | 131 | 148 | PF00022 | 0.411 |
LIG_BIR_III_2 | 319 | 323 | PF00653 | 0.577 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.551 |
LIG_BRCT_BRCA1_1 | 220 | 224 | PF00533 | 0.688 |
LIG_BRCT_BRCA1_1 | 719 | 723 | PF00533 | 0.699 |
LIG_CtBP_PxDLS_1 | 108 | 112 | PF00389 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 366 | 375 | PF00928 | 0.411 |
LIG_eIF4E_1 | 323 | 329 | PF01652 | 0.473 |
LIG_EVH1_2 | 7 | 11 | PF00568 | 0.534 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.745 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.824 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.475 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.411 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.436 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.418 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.728 |
LIG_FHA_1 | 657 | 663 | PF00498 | 0.724 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.633 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.697 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.411 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.372 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.389 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.380 |
LIG_IBAR_NPY_1 | 321 | 323 | PF08397 | 0.607 |
LIG_LIR_Apic_2 | 273 | 279 | PF02991 | 0.665 |
LIG_LIR_Apic_2 | 347 | 353 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 4 | 8 | PF02991 | 0.548 |
LIG_LIR_Apic_2 | 415 | 420 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 699 | 703 | PF02991 | 0.702 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 643 | 648 | PF02991 | 0.771 |
LIG_LYPXL_yS_3 | 645 | 648 | PF13949 | 0.779 |
LIG_PTB_Apo_2 | 127 | 134 | PF02174 | 0.513 |
LIG_PTB_Phospho_1 | 127 | 133 | PF10480 | 0.513 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.411 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.411 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.535 |
LIG_SH2_CRK | 700 | 704 | PF00017 | 0.717 |
LIG_SH2_GRB2like | 34 | 37 | PF00017 | 0.280 |
LIG_SH2_NCK_1 | 34 | 38 | PF00017 | 0.280 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 268 | 272 | PF00017 | 0.775 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.353 |
LIG_SH2_STAT3 | 244 | 247 | PF00017 | 0.845 |
LIG_SH2_STAT3 | 343 | 346 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 654 | 657 | PF00017 | 0.720 |
LIG_SH2_STAT5 | 700 | 703 | PF00017 | 0.818 |
LIG_SH2_STAT5 | 764 | 767 | PF00017 | 0.725 |
LIG_SH2_STAT5 | 790 | 793 | PF00017 | 0.758 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.411 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.411 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.675 |
LIG_SH3_3 | 746 | 752 | PF00018 | 0.712 |
LIG_SH3_3 | 801 | 807 | PF00018 | 0.663 |
LIG_SUMO_SIM_anti_2 | 500 | 508 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 107 | 113 | PF11976 | 0.411 |
LIG_TRAF2_1 | 499 | 502 | PF00917 | 0.411 |
LIG_TRFH_1 | 158 | 162 | PF08558 | 0.565 |
LIG_UBA3_1 | 374 | 381 | PF00899 | 0.411 |
LIG_UBA3_1 | 64 | 68 | PF00899 | 0.411 |
LIG_WRC_WIRS_1 | 77 | 82 | PF05994 | 0.411 |
MOD_CDK_SPK_2 | 231 | 236 | PF00069 | 0.690 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.694 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.559 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.808 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.663 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.566 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.682 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.674 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.639 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.747 |
MOD_CK1_1 | 715 | 721 | PF00069 | 0.685 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.759 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.411 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.369 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.397 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.399 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.428 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.692 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.657 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.685 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.832 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.679 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.643 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.657 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.400 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.561 |
MOD_GlcNHglycan | 60 | 64 | PF01048 | 0.411 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.694 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.774 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.760 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.500 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.490 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.593 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.713 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.790 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.737 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.726 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.360 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.362 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.606 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.684 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.774 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.758 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.795 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.706 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.794 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.728 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.717 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.734 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.280 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.592 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.741 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.663 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.513 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.389 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.681 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.389 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.683 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.725 |
MOD_NEK2_1 | 663 | 668 | PF00069 | 0.641 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.800 |
MOD_NEK2_1 | 759 | 764 | PF00069 | 0.687 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.513 |
MOD_NEK2_2 | 649 | 654 | PF00069 | 0.640 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.739 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.389 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.389 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.411 |
MOD_PIKK_1 | 631 | 637 | PF00454 | 0.742 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.699 |
MOD_PIKK_1 | 705 | 711 | PF00454 | 0.744 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.584 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.684 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.767 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.540 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.420 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.411 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.513 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.552 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.736 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.411 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.411 |
MOD_Plk_1 | 625 | 631 | PF00069 | 0.726 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.411 |
MOD_Plk_2-3 | 497 | 503 | PF00069 | 0.411 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.557 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.731 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.411 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.411 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.785 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.753 |
MOD_Plk_4 | 760 | 766 | PF00069 | 0.667 |
MOD_Plk_4 | 800 | 806 | PF00069 | 0.678 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.640 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.691 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.513 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.683 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.692 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.683 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.707 |
MOD_ProDKin_1 | 717 | 723 | PF00069 | 0.703 |
MOD_ProDKin_1 | 736 | 742 | PF00069 | 0.558 |
MOD_ProDKin_1 | 785 | 791 | PF00069 | 0.632 |
MOD_SUMO_for_1 | 138 | 141 | PF00179 | 0.411 |
MOD_SUMO_rev_2 | 131 | 140 | PF00179 | 0.513 |
TRG_DiLeu_BaEn_1 | 481 | 486 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_1 | 501 | 506 | PF01217 | 0.183 |
TRG_DiLeu_BaEn_1 | 60 | 65 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_4 | 481 | 487 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 645 | 648 | PF00928 | 0.779 |
TRG_ER_diArg_1 | 101 | 104 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCR0 | Leptomonas seymouri | 57% | 100% |
A0A3S7XBF4 | Leishmania donovani | 94% | 100% |
A4HPU4 | Leishmania braziliensis | 79% | 94% |
A4IE49 | Leishmania infantum | 94% | 99% |
E9ATK9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |