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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q4F8
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:0016570 | histone modification | 5 | 2 |
GO:0016571 | histone methylation | 5 | 2 |
GO:0018022 | peptidyl-lysine methylation | 5 | 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:0034968 | histone lysine methylation | 6 | 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:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 2 |
GO:0042054 | histone methyltransferase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 485 | 489 | PF00656 | 0.439 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 821 | 823 | PF00675 | 0.411 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 821 | 823 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 632 | 634 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 676 | 680 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.421 |
DEG_APCC_DBOX_1 | 216 | 224 | PF00400 | 0.498 |
DEG_APCC_DBOX_1 | 56 | 64 | PF00400 | 0.578 |
DEG_APCC_DBOX_1 | 76 | 84 | PF00400 | 0.389 |
DEG_SPOP_SBC_1 | 228 | 232 | PF00917 | 0.492 |
DOC_CDC14_PxL_1 | 443 | 451 | PF14671 | 0.631 |
DOC_CYCLIN_RxL_1 | 583 | 591 | PF00134 | 0.396 |
DOC_CYCLIN_RxL_1 | 707 | 715 | PF00134 | 0.466 |
DOC_CYCLIN_yCln2_LP_2 | 158 | 164 | PF00134 | 0.402 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 215 | 223 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 127 | 134 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 215 | 223 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 668 | 677 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 77 | 85 | PF00069 | 0.553 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.600 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 160 | 168 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 197 | 207 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 215 | 220 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 316 | 326 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 57 | 66 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 633 | 637 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 858 | 862 | PF00244 | 0.442 |
LIG_Actin_WH2_2 | 357 | 375 | PF00022 | 0.572 |
LIG_Actin_WH2_2 | 521 | 538 | PF00022 | 0.439 |
LIG_APCC_ABBA_1 | 14 | 19 | PF00400 | 0.631 |
LIG_APCC_ABBA_1 | 143 | 148 | PF00400 | 0.485 |
LIG_APCC_ABBA_1 | 238 | 243 | PF00400 | 0.429 |
LIG_BIR_III_4 | 100 | 104 | PF00653 | 0.599 |
LIG_Clathr_ClatBox_1 | 701 | 705 | PF01394 | 0.426 |
LIG_EVH1_1 | 48 | 52 | PF00568 | 0.623 |
LIG_EVH1_2 | 10 | 14 | PF00568 | 0.550 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.482 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.574 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.641 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.489 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.408 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.597 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.446 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.530 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.389 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.434 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.439 |
LIG_FHA_2 | 749 | 755 | PF00498 | 0.443 |
LIG_FHA_2 | 792 | 798 | PF00498 | 0.406 |
LIG_FHA_2 | 867 | 873 | PF00498 | 0.450 |
LIG_Integrin_RGD_1 | 288 | 290 | PF01839 | 0.491 |
LIG_Integrin_RGD_1 | 486 | 488 | PF01839 | 0.301 |
LIG_LIR_Gen_1 | 715 | 724 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 830 | 840 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 715 | 720 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 830 | 835 | PF02991 | 0.447 |
LIG_LYPXL_SIV_4 | 728 | 736 | PF13949 | 0.456 |
LIG_NRBOX | 219 | 225 | PF00104 | 0.499 |
LIG_NRBOX | 360 | 366 | PF00104 | 0.587 |
LIG_PCNA_yPIPBox_3 | 667 | 679 | PF02747 | 0.420 |
LIG_PDZ_Class_3 | 882 | 887 | PF00595 | 0.507 |
LIG_PTAP_UEV_1 | 1 | 6 | PF05743 | 0.628 |
LIG_PTAP_UEV_1 | 443 | 448 | PF05743 | 0.586 |
LIG_Rb_LxCxE_1 | 872 | 887 | PF01857 | 0.505 |
LIG_SH2_CRK | 729 | 733 | PF00017 | 0.439 |
LIG_SH2_NCK_1 | 146 | 150 | PF00017 | 0.481 |
LIG_SH2_NCK_1 | 729 | 733 | PF00017 | 0.439 |
LIG_SH2_PTP2 | 832 | 835 | PF00017 | 0.462 |
LIG_SH2_SRC | 146 | 149 | PF00017 | 0.481 |
LIG_SH2_SRC | 237 | 240 | PF00017 | 0.578 |
LIG_SH2_SRC | 563 | 566 | PF00017 | 0.484 |
LIG_SH2_SRC | 610 | 613 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 729 | 733 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 859 | 863 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 772 | 775 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 832 | 835 | PF00017 | 0.462 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.656 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.629 |
LIG_SH3_3 | 687 | 693 | PF00018 | 0.427 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.632 |
LIG_SH3_3 | 812 | 818 | PF00018 | 0.430 |
LIG_SUMO_SIM_anti_2 | 155 | 160 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 256 | 262 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 35 | 41 | PF11976 | 0.643 |
LIG_SUMO_SIM_par_1 | 524 | 529 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 61 | 67 | PF11976 | 0.572 |
LIG_SUMO_SIM_par_1 | 700 | 705 | PF11976 | 0.430 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.605 |
LIG_TRAF2_1 | 555 | 558 | PF00917 | 0.532 |
LIG_TRAF2_1 | 751 | 754 | PF00917 | 0.444 |
LIG_TRFH_1 | 236 | 240 | PF08558 | 0.432 |
LIG_WRC_WIRS_1 | 852 | 857 | PF05994 | 0.452 |
LIG_WW_3 | 463 | 467 | PF00397 | 0.624 |
MOD_CDK_SPxxK_3 | 305 | 312 | PF00069 | 0.635 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.516 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.578 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.564 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.287 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.554 |
MOD_CK1_1 | 738 | 744 | PF00069 | 0.454 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.434 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.420 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.456 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.585 |
MOD_CK2_1 | 747 | 753 | PF00069 | 0.432 |
MOD_CK2_1 | 791 | 797 | PF00069 | 0.400 |
MOD_CK2_1 | 866 | 872 | PF00069 | 0.445 |
MOD_CK2_1 | 875 | 881 | PF00069 | 0.403 |
MOD_GlcNHglycan | 106 | 110 | PF01048 | 0.474 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.667 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.608 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.627 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.746 |
MOD_GlcNHglycan | 354 | 358 | PF01048 | 0.587 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.585 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.580 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.368 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.382 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.407 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.569 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.579 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.462 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.447 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.581 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.508 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.556 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.315 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.466 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.496 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.666 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.533 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.317 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.485 |
MOD_GSK3_1 | 628 | 635 | PF00069 | 0.589 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.528 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.463 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.650 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.499 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.533 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.545 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.612 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.558 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.499 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.407 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.317 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.435 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.371 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.238 |
MOD_NEK2_1 | 773 | 778 | PF00069 | 0.414 |
MOD_PIKK_1 | 570 | 576 | PF00454 | 0.487 |
MOD_PIKK_1 | 588 | 594 | PF00454 | 0.437 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.597 |
MOD_PKA_1 | 632 | 638 | PF00069 | 0.546 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.484 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.643 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.553 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.254 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.546 |
MOD_PKA_2 | 857 | 863 | PF00069 | 0.443 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.537 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.480 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.447 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.484 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.654 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.476 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.385 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.392 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.601 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.641 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.385 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.385 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.609 |
MOD_Plk_4 | 848 | 854 | PF00069 | 0.446 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.648 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.551 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.491 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.635 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.636 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.496 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.254 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.385 |
MOD_SUMO_for_1 | 678 | 681 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 114 | 122 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 651 | 661 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_1 | 604 | 609 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_1 | 754 | 759 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_1 | 805 | 810 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_1 | 848 | 853 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_1 | 872 | 877 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_4 | 27 | 33 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 344 | 349 | PF01217 | 0.602 |
TRG_DiLeu_BaLyEn_6 | 761 | 766 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 729 | 732 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 832 | 835 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 468 | 470 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 535 | 537 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 646 | 648 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 718 | 721 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 820 | 822 | PF00400 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 668 | 672 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 699 | 703 | PF00026 | 0.441 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X6B7 | Leishmania donovani | 90% | 88% |
A4HL86 | Leishmania braziliensis | 70% | 100% |
A4I8R4 | Leishmania infantum | 89% | 88% |
E9B3M9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |