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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QC33
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 13 |
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004672 | protein kinase activity | 3 | 13 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.740 |
CLV_C14_Caspase3-7 | 696 | 700 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.751 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 661 | 663 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 680 | 682 | PF00675 | 0.458 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 245 | 247 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.179 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.727 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 683 | 687 | PF00082 | 0.734 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 729 | 733 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 258 | 266 | PF00400 | 0.390 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.452 |
DEG_SCF_FBW7_1 | 480 | 487 | PF00400 | 0.769 |
DEG_SCF_FBW7_2 | 633 | 638 | PF00400 | 0.738 |
DEG_SPOP_SBC_1 | 484 | 488 | PF00917 | 0.739 |
DEG_SPOP_SBC_1 | 571 | 575 | PF00917 | 0.552 |
DOC_CKS1_1 | 481 | 486 | PF01111 | 0.771 |
DOC_MAPK_gen_1 | 127 | 136 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 273 | 282 | PF00069 | 0.646 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 724 | 732 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 73 | 80 | PF00069 | 0.325 |
DOC_PP2B_LxvP_1 | 569 | 572 | PF13499 | 0.750 |
DOC_PP4_FxxP_1 | 710 | 713 | PF00568 | 0.607 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 697 | 701 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 792 | 796 | PF00917 | 0.584 |
DOC_USP7_MATH_2 | 42 | 48 | PF00917 | 0.307 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.643 |
DOC_USP7_UBL2_3 | 581 | 585 | PF12436 | 0.737 |
DOC_USP7_UBL2_3 | 678 | 682 | PF12436 | 0.702 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.366 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.293 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 650 | 655 | PF00397 | 0.745 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 233 | 239 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 246 | 255 | PF00244 | 0.247 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 681 | 686 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 789 | 799 | PF00244 | 0.621 |
LIG_Actin_WH2_2 | 145 | 162 | PF00022 | 0.307 |
LIG_Actin_WH2_2 | 204 | 219 | PF00022 | 0.323 |
LIG_Actin_WH2_2 | 28 | 43 | PF00022 | 0.397 |
LIG_AP2alpha_1 | 685 | 689 | PF02296 | 0.698 |
LIG_APCC_ABBA_1 | 728 | 733 | PF00400 | 0.412 |
LIG_APCC_ABBAyCdc20_2 | 122 | 128 | PF00400 | 0.284 |
LIG_BRCT_BRCA1_1 | 504 | 508 | PF00533 | 0.713 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.323 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.310 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.715 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.307 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.496 |
LIG_FHA_1 | 716 | 722 | PF00498 | 0.471 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.674 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.762 |
LIG_FHA_2 | 653 | 659 | PF00498 | 0.696 |
LIG_LIR_Apic_2 | 166 | 172 | PF02991 | 0.293 |
LIG_LIR_Apic_2 | 709 | 713 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 663 | 673 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 75 | 83 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 663 | 669 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.307 |
LIG_LYPXL_S_1 | 219 | 223 | PF13949 | 0.323 |
LIG_LYPXL_yS_3 | 220 | 223 | PF13949 | 0.307 |
LIG_MAD2 | 214 | 222 | PF02301 | 0.293 |
LIG_PCNA_yPIPBox_3 | 209 | 220 | PF02747 | 0.326 |
LIG_PDZ_Class_2 | 796 | 801 | PF00595 | 0.674 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.293 |
LIG_Pex14_2 | 685 | 689 | PF04695 | 0.698 |
LIG_PTB_Apo_2 | 251 | 258 | PF02174 | 0.221 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.366 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.307 |
LIG_SH2_GRB2like | 82 | 85 | PF00017 | 0.342 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.307 |
LIG_SH2_SRC | 82 | 85 | PF00017 | 0.307 |
LIG_SH2_STAP1 | 227 | 231 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.293 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.342 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.654 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.702 |
LIG_SH3_3 | 608 | 614 | PF00018 | 0.755 |
LIG_SH3_4 | 581 | 588 | PF00018 | 0.678 |
LIG_SUMO_SIM_par_1 | 278 | 284 | PF11976 | 0.618 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.551 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.471 |
LIG_TRAF2_1 | 496 | 499 | PF00917 | 0.663 |
LIG_UBA3_1 | 238 | 245 | PF00899 | 0.374 |
LIG_WW_3 | 479 | 483 | PF00397 | 0.770 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.301 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.337 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.624 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.424 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.639 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.628 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.614 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.681 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.765 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.653 |
MOD_CK2_1 | 650 | 656 | PF00069 | 0.681 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.650 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.307 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.645 |
MOD_GlcNHglycan | 428 | 432 | PF01048 | 0.601 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.307 |
MOD_GlcNHglycan | 468 | 473 | PF01048 | 0.720 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.690 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.645 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.623 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.637 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.605 |
MOD_GlcNHglycan | 794 | 797 | PF01048 | 0.691 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.293 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.328 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.749 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.753 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.693 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.760 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.759 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.740 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.581 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.293 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.342 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.342 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.342 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.307 |
MOD_N-GLC_1 | 713 | 718 | PF02516 | 0.594 |
MOD_N-GLC_1 | 749 | 754 | PF02516 | 0.595 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.461 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.293 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.293 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.405 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.374 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.331 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.440 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.436 |
MOD_NEK2_2 | 450 | 455 | PF00069 | 0.626 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.323 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.293 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.388 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.342 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.704 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.702 |
MOD_PKA_1 | 681 | 687 | PF00069 | 0.619 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.293 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.644 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.314 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.704 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.307 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.390 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.210 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.315 |
MOD_Plk_1 | 698 | 704 | PF00069 | 0.584 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.461 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.307 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.351 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.363 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.692 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.615 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.342 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.293 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.661 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.638 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.723 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.723 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.614 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.705 |
MOD_ProDKin_1 | 650 | 656 | PF00069 | 0.742 |
MOD_SUMO_rev_2 | 347 | 356 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 372 | 378 | PF00179 | 0.516 |
MOD_SUMO_rev_2 | 573 | 583 | PF00179 | 0.682 |
MOD_SUMO_rev_2 | 675 | 684 | PF00179 | 0.599 |
MOD_SUMO_rev_2 | 68 | 75 | PF00179 | 0.411 |
MOD_SUMO_rev_2 | 700 | 710 | PF00179 | 0.668 |
TRG_DiLeu_BaEn_4 | 283 | 289 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 230 | 235 | PF01217 | 0.436 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 666 | 669 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 745 | 748 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.338 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 438 | 440 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 511 | 513 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 660 | 662 | PF00400 | 0.704 |
TRG_NES_CRM1_1 | 260 | 275 | PF08389 | 0.508 |
TRG_NES_CRM1_1 | 719 | 733 | PF08389 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 123 | 128 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 333 | 337 | PF00026 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 340 | 345 | PF00026 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 365 | 370 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9W7 | Leptomonas seymouri | 65% | 100% |
A0A0S4IQV2 | Bodo saltans | 35% | 91% |
A0A0S4JKY4 | Bodo saltans | 44% | 100% |
A0A1X0NHD4 | Trypanosomatidae | 49% | 100% |
A0A3Q8IBZ9 | Leishmania donovani | 96% | 100% |
A0A3R7M6Z7 | Trypanosoma rangeli | 47% | 100% |
A4HC09 | Leishmania braziliensis | 84% | 99% |
A4HZM2 | Leishmania infantum | 95% | 100% |
D0A118 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AVE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BLW4 | Trypanosoma cruzi | 49% | 100% |