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:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HY02
Term | Name | Level | Count |
---|---|---|---|
GO:0007059 | chromosome segregation | 2 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0006473 | protein acetylation | 6 | 1 |
GO:0006474 | N-terminal protein amino acid acetylation | 5 | 1 |
GO:0006475 | internal protein amino acid acetylation | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016573 | histone acetylation | 6 | 1 |
GO:0017196 | N-terminal peptidyl-methionine acetylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0018206 | peptidyl-methionine modification | 6 | 1 |
GO:0018393 | internal peptidyl-lysine acetylation | 8 | 1 |
GO:0018394 | peptidyl-lysine acetylation | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0031365 | N-terminal protein amino acid modification | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0043966 | histone H3 acetylation | 7 | 1 |
GO:0043967 | histone H4 acetylation | 7 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004596 | peptide alpha-N-acetyltransferase activity | 8 | 7 |
GO:0008080 | N-acetyltransferase activity | 6 | 7 |
GO:0016407 | acetyltransferase activity | 5 | 7 |
GO:0016410 | N-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 7 |
GO:0004402 | histone acetyltransferase activity | 4 | 1 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.652 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.630 |
CLV_C14_Caspase3-7 | 513 | 517 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 644 | 648 | PF00656 | 0.609 |
CLV_C14_Caspase3-7 | 710 | 714 | PF00656 | 0.677 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 758 | 760 | PF00675 | 0.418 |
CLV_PCSK_FUR_1 | 671 | 675 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 757 | 759 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 419 | 421 | PF00082 | 0.314 |
CLV_PCSK_PC7_1 | 538 | 544 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.351 |
DEG_SPOP_SBC_1 | 144 | 148 | PF00917 | 0.610 |
DEG_SPOP_SBC_1 | 159 | 163 | PF00917 | 0.651 |
DEG_SPOP_SBC_1 | 176 | 180 | PF00917 | 0.549 |
DEG_SPOP_SBC_1 | 261 | 265 | PF00917 | 0.657 |
DOC_CDC14_PxL_1 | 486 | 494 | PF14671 | 0.569 |
DOC_CKS1_1 | 705 | 710 | PF01111 | 0.680 |
DOC_CYCLIN_RxL_1 | 44 | 55 | PF00134 | 0.519 |
DOC_MAPK_gen_1 | 34 | 41 | PF00069 | 0.559 |
DOC_MAPK_gen_1 | 405 | 411 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 80 | 89 | PF00069 | 0.608 |
DOC_MAPK_RevD_3 | 658 | 674 | PF00069 | 0.647 |
DOC_PP1_RVXF_1 | 183 | 189 | PF00149 | 0.544 |
DOC_PP1_RVXF_1 | 32 | 39 | PF00149 | 0.566 |
DOC_PP1_RVXF_1 | 778 | 785 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 459 | 462 | PF13499 | 0.608 |
DOC_PP2B_LxvP_1 | 660 | 663 | PF13499 | 0.649 |
DOC_SPAK_OSR1_1 | 543 | 547 | PF12202 | 0.539 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 712 | 716 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.669 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 674 | 679 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 701 | 706 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 717 | 722 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 731 | 736 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 28 | 38 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 384 | 389 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 448 | 453 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 697 | 703 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 757 | 762 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 97 | 106 | PF00244 | 0.606 |
LIG_BIR_III_2 | 204 | 208 | PF00653 | 0.509 |
LIG_BRCT_BRCA1_1 | 478 | 482 | PF00533 | 0.618 |
LIG_CaM_IQ_9 | 229 | 244 | PF13499 | 0.508 |
LIG_deltaCOP1_diTrp_1 | 238 | 243 | PF00928 | 0.551 |
LIG_eIF4E_1 | 403 | 409 | PF01652 | 0.547 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.651 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.573 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.718 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.467 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.487 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.569 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.511 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.708 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.535 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.648 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.647 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.610 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.610 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.612 |
LIG_FHA_2 | 691 | 697 | PF00498 | 0.659 |
LIG_FHA_2 | 708 | 714 | PF00498 | 0.605 |
LIG_LIR_Apic_2 | 729 | 735 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 213 | 223 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 479 | 490 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 37 | 41 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 399 | 403 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 737 | 741 | PF02991 | 0.559 |
LIG_LYPXL_yS_3 | 738 | 741 | PF13949 | 0.560 |
LIG_NRBOX | 407 | 413 | PF00104 | 0.570 |
LIG_PCNA_yPIPBox_3 | 542 | 554 | PF02747 | 0.523 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.559 |
LIG_Rb_LxCxE_1 | 768 | 781 | PF01857 | 0.536 |
LIG_RPA_C_Fungi | 344 | 356 | PF08784 | 0.334 |
LIG_RPA_C_Fungi | 566 | 578 | PF08784 | 0.361 |
LIG_SH2_CRK | 590 | 594 | PF00017 | 0.407 |
LIG_SH2_CRK | 800 | 804 | PF00017 | 0.334 |
LIG_SH2_SRC | 452 | 455 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.320 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 590 | 594 | PF00017 | 0.382 |
LIG_SH2_STAT3 | 388 | 391 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.416 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.447 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.516 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.324 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.539 |
LIG_SH3_3 | 672 | 678 | PF00018 | 0.503 |
LIG_SH3_3 | 702 | 708 | PF00018 | 0.557 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.473 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.440 |
LIG_TRAF2_1 | 302 | 305 | PF00917 | 0.369 |
LIG_TRAF2_1 | 511 | 514 | PF00917 | 0.391 |
LIG_TRAF2_1 | 530 | 533 | PF00917 | 0.465 |
LIG_TRAF2_1 | 638 | 641 | PF00917 | 0.562 |
LIG_TYR_ITIM | 798 | 803 | PF00017 | 0.334 |
LIG_WRC_WIRS_1 | 363 | 368 | PF05994 | 0.290 |
MOD_CDC14_SPxK_1 | 677 | 680 | PF00782 | 0.509 |
MOD_CDK_SPK_2 | 247 | 252 | PF00069 | 0.499 |
MOD_CDK_SPK_2 | 731 | 736 | PF00069 | 0.481 |
MOD_CDK_SPK_2 | 92 | 97 | PF00069 | 0.465 |
MOD_CDK_SPxK_1 | 674 | 680 | PF00069 | 0.514 |
MOD_CDK_SPxK_1 | 717 | 723 | PF00069 | 0.571 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.520 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.539 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.546 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.435 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.571 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.538 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.557 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.542 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.334 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.567 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.459 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.515 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.581 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.648 |
MOD_CK1_1 | 726 | 732 | PF00069 | 0.541 |
MOD_CK1_1 | 734 | 740 | PF00069 | 0.441 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.490 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.583 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.401 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.397 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.406 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.447 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.489 |
MOD_CK2_1 | 762 | 768 | PF00069 | 0.558 |
MOD_DYRK1A_RPxSP_1 | 674 | 678 | PF00069 | 0.500 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.541 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.579 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.544 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.469 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.536 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.618 |
MOD_GlcNHglycan | 602 | 606 | PF01048 | 0.515 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.595 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.533 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.513 |
MOD_GlcNHglycan | 713 | 717 | PF01048 | 0.597 |
MOD_GlcNHglycan | 764 | 767 | PF01048 | 0.539 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.489 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.528 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.527 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.580 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.461 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.520 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.421 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.471 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.540 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.546 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.436 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.503 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.552 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.650 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.502 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.650 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.571 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.598 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.556 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.303 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.557 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.395 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.601 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.509 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.630 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.522 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.506 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.545 |
MOD_NEK2_2 | 477 | 482 | PF00069 | 0.516 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.348 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.569 |
MOD_PIKK_1 | 387 | 393 | PF00454 | 0.334 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.633 |
MOD_PKA_1 | 34 | 40 | PF00069 | 0.434 |
MOD_PKA_1 | 757 | 763 | PF00069 | 0.564 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.455 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.458 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.471 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.512 |
MOD_PKA_2 | 757 | 763 | PF00069 | 0.647 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.499 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.401 |
MOD_Plk_2-3 | 491 | 497 | PF00069 | 0.406 |
MOD_Plk_2-3 | 527 | 533 | PF00069 | 0.472 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.401 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.370 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.460 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.444 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.315 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.531 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.348 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.422 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.319 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.504 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.556 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.704 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.507 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.570 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.447 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.490 |
MOD_ProDKin_1 | 674 | 680 | PF00069 | 0.514 |
MOD_ProDKin_1 | 701 | 707 | PF00069 | 0.755 |
MOD_ProDKin_1 | 717 | 723 | PF00069 | 0.552 |
MOD_ProDKin_1 | 731 | 737 | PF00069 | 0.497 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.520 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.504 |
MOD_SUMO_rev_2 | 755 | 765 | PF00179 | 0.524 |
TRG_DiLeu_BaEn_2 | 539 | 545 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 94 | 99 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 738 | 741 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 800 | 803 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 502 | 505 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 518 | 520 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 537 | 539 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 542 | 544 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 670 | 673 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 756 | 759 | PF00400 | 0.535 |
TRG_NLS_Bipartite_1 | 405 | 423 | PF00514 | 0.395 |
TRG_NLS_MonoCore_2 | 417 | 422 | PF00514 | 0.425 |
TRG_NLS_MonoExtN_4 | 418 | 423 | PF00514 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 196 | 200 | PF00026 | 0.379 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4M7 | Leptomonas seymouri | 45% | 98% |
A0A3S7WV24 | Leishmania donovani | 100% | 100% |
A4H9N7 | Leishmania braziliensis | 70% | 100% |
E9ARR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4QDQ8 | Leishmania major | 86% | 99% |