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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AJD0
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007264 | small GTPase mediated signal transduction | 4 | 1 |
GO:0007265 | Ras protein signal transduction | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 147 | 151 | PF00656 | 0.525 |
CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.606 |
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.763 |
CLV_C14_Caspase3-7 | 563 | 567 | PF00656 | 0.775 |
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.615 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.801 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.837 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.601 |
CLV_PCSK_FUR_1 | 464 | 468 | PF00082 | 0.346 |
CLV_PCSK_FUR_1 | 611 | 615 | PF00082 | 0.570 |
CLV_PCSK_FUR_1 | 656 | 660 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.801 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 655 | 657 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 658 | 660 | PF00082 | 0.604 |
CLV_PCSK_PC7_1 | 611 | 617 | PF00082 | 0.564 |
CLV_PCSK_PC7_1 | 655 | 661 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.606 |
CLV_Separin_Metazoa | 158 | 162 | PF03568 | 0.511 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.626 |
DEG_SCF_FBW7_1 | 62 | 69 | PF00400 | 0.471 |
DEG_SPOP_SBC_1 | 535 | 539 | PF00917 | 0.810 |
DOC_CKS1_1 | 323 | 328 | PF01111 | 0.826 |
DOC_CYCLIN_yCln2_LP_2 | 199 | 205 | PF00134 | 0.677 |
DOC_CYCLIN_yCln2_LP_2 | 21 | 24 | PF00134 | 0.648 |
DOC_MAPK_gen_1 | 222 | 228 | PF00069 | 0.505 |
DOC_PP2B_LxvP_1 | 199 | 202 | PF13499 | 0.695 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.648 |
DOC_PP2B_LxvP_1 | 371 | 374 | PF13499 | 0.559 |
DOC_SPAK_OSR1_1 | 430 | 434 | PF12202 | 0.550 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.825 |
DOC_USP7_MATH_1 | 747 | 751 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.662 |
DOC_USP7_MATH_2 | 66 | 72 | PF00917 | 0.519 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.836 |
LIG_14-3-3_CanoR_1 | 365 | 373 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 430 | 434 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 491 | 499 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 560 | 565 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 649 | 653 | PF00244 | 0.427 |
LIG_APCC_ABBA_1 | 497 | 502 | PF00400 | 0.546 |
LIG_APCC_ABBAyCdc20_2 | 496 | 502 | PF00400 | 0.546 |
LIG_BIR_III_2 | 208 | 212 | PF00653 | 0.628 |
LIG_BRCT_BRCA1_1 | 385 | 389 | PF00533 | 0.574 |
LIG_BRCT_BRCA1_1 | 494 | 498 | PF00533 | 0.546 |
LIG_Clathr_ClatBox_1 | 54 | 58 | PF01394 | 0.524 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.620 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.563 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.567 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.566 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.450 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.645 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.475 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.543 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.666 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.661 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.527 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.545 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.546 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.585 |
LIG_FHA_2 | 649 | 655 | PF00498 | 0.421 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.727 |
LIG_LIR_Gen_1 | 386 | 397 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 414 | 424 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 432 | 440 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 447 | 456 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 414 | 419 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.546 |
LIG_PCNA_PIPBox_1 | 697 | 706 | PF02747 | 0.537 |
LIG_PDZ_Class_1 | 746 | 751 | PF00595 | 0.544 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.492 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.411 |
LIG_SH2_CRK | 434 | 438 | PF00017 | 0.572 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 589 | 593 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 604 | 608 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 110 | 113 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 588 | 591 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.661 |
LIG_SH3_2 | 84 | 89 | PF14604 | 0.525 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.832 |
LIG_SH3_3 | 620 | 626 | PF00018 | 0.452 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.527 |
LIG_SUMO_SIM_anti_2 | 154 | 161 | PF11976 | 0.524 |
LIG_SUMO_SIM_anti_2 | 502 | 510 | PF11976 | 0.553 |
LIG_SUMO_SIM_anti_2 | 669 | 674 | PF11976 | 0.653 |
LIG_SUMO_SIM_par_1 | 210 | 215 | PF11976 | 0.627 |
LIG_SUMO_SIM_par_1 | 252 | 259 | PF11976 | 0.660 |
LIG_SUMO_SIM_par_1 | 52 | 58 | PF11976 | 0.533 |
LIG_TRAF2_1 | 190 | 193 | PF00917 | 0.551 |
LIG_TRAF2_1 | 538 | 541 | PF00917 | 0.664 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.572 |
LIG_TRAF2_1 | 734 | 737 | PF00917 | 0.594 |
LIG_WW_3 | 240 | 244 | PF00397 | 0.642 |
MOD_CDK_SPK_2 | 312 | 317 | PF00069 | 0.560 |
MOD_CDK_SPxK_1 | 359 | 365 | PF00069 | 0.573 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.753 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.791 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.512 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.773 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.691 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.572 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.411 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.748 |
MOD_CK1_1 | 633 | 639 | PF00069 | 0.651 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.724 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.623 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.574 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.578 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.590 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.402 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.716 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.806 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.678 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.527 |
MOD_CK2_1 | 648 | 654 | PF00069 | 0.428 |
MOD_CMANNOS | 35 | 38 | PF00535 | 0.544 |
MOD_Cter_Amidation | 627 | 630 | PF01082 | 0.735 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.653 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.637 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.338 |
MOD_GlcNHglycan | 232 | 237 | PF01048 | 0.546 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.694 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.837 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.769 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.767 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.640 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.569 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.394 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.411 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.411 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.747 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.691 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.616 |
MOD_GlcNHglycan | 705 | 708 | PF01048 | 0.520 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.590 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.760 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.697 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.776 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.729 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.772 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.709 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.635 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.610 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.512 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.347 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.543 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.392 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.793 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.752 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.609 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.641 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.461 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.636 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.576 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.601 |
MOD_N-GLC_1 | 491 | 496 | PF02516 | 0.411 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.584 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.629 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.592 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.635 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.500 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.512 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.282 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.545 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.781 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.485 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.514 |
MOD_NEK2_1 | 699 | 704 | PF00069 | 0.607 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.394 |
MOD_NEK2_2 | 429 | 434 | PF00069 | 0.547 |
MOD_NEK2_2 | 643 | 648 | PF00069 | 0.442 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.506 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.644 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.523 |
MOD_PIKK_1 | 716 | 722 | PF00454 | 0.525 |
MOD_PK_1 | 53 | 59 | PF00069 | 0.534 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.726 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.635 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.724 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.637 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.526 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.495 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.428 |
MOD_PKB_1 | 489 | 497 | PF00069 | 0.512 |
MOD_PKB_1 | 558 | 566 | PF00069 | 0.726 |
MOD_PKB_1 | 658 | 666 | PF00069 | 0.698 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.615 |
MOD_Plk_2-3 | 152 | 158 | PF00069 | 0.681 |
MOD_Plk_2-3 | 283 | 289 | PF00069 | 0.835 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.681 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.641 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.588 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.756 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.469 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.646 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.778 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.615 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.753 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.714 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.676 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.741 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.739 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.566 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.630 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.506 |
MOD_SUMO_rev_2 | 108 | 117 | PF00179 | 0.698 |
MOD_SUMO_rev_2 | 599 | 609 | PF00179 | 0.422 |
TRG_DiLeu_BaEn_1 | 502 | 507 | PF01217 | 0.525 |
TRG_DiLeu_BaEn_1 | 739 | 744 | PF01217 | 0.570 |
TRG_DiLeu_BaEn_4 | 192 | 198 | PF01217 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.625 |
TRG_DiLeu_BaLyEn_6 | 380 | 385 | PF01217 | 0.461 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.646 |
TRG_ENDOCYTIC_2 | 680 | 683 | PF00928 | 0.554 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 558 | 561 | PF00400 | 0.735 |
TRG_ER_diArg_1 | 611 | 614 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 655 | 658 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 659 | 661 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 715 | 718 | PF00400 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 594 | 598 | PF00026 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 660 | 664 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2L0 | Leptomonas seymouri | 47% | 88% |
A0A3S5H4V1 | Leishmania donovani | 82% | 100% |
A4H369 | Leishmania braziliensis | 70% | 99% |
A4HRG6 | Leishmania infantum | 82% | 100% |
E9AC34 | Leishmania major | 79% | 96% |