tRNA synthetase, Multisite-specific tRNA:(cytosine-C(5))-methyltransferase methyltransferase
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:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HXY5
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 13 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 13 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009451 | RNA modification | 5 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016070 | RNA metabolic process | 5 | 13 |
GO:0032259 | methylation | 2 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0043414 | macromolecule methylation | 3 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 13 |
GO:0046483 | heterocycle metabolic process | 3 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0090304 | nucleic acid metabolic process | 4 | 13 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0003723 | RNA binding | 4 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0008168 | methyltransferase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 687 | 693 | PF00089 | 0.460 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 685 | 687 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.476 |
CLV_PCSK_FUR_1 | 355 | 359 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 685 | 687 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 269 | 271 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.286 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.604 |
CLV_PCSK_PC7_1 | 681 | 687 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 695 | 699 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 714 | 718 | PF00082 | 0.450 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.668 |
DEG_ODPH_VHL_1 | 678 | 691 | PF01847 | 0.480 |
DEG_SIAH_1 | 729 | 737 | PF03145 | 0.520 |
DEG_SPOP_SBC_1 | 596 | 600 | PF00917 | 0.538 |
DOC_CKS1_1 | 211 | 216 | PF01111 | 0.501 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.560 |
DOC_CKS1_1 | 623 | 628 | PF01111 | 0.488 |
DOC_CYCLIN_RxL_1 | 432 | 444 | PF00134 | 0.504 |
DOC_CYCLIN_RxL_1 | 681 | 692 | PF00134 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 563 | 569 | PF00134 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 623 | 629 | PF00134 | 0.489 |
DOC_MAPK_gen_1 | 560 | 569 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 636 | 645 | PF00069 | 0.423 |
DOC_MAPK_HePTP_8 | 633 | 645 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 636 | 645 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 683 | 690 | PF00149 | 0.518 |
DOC_PP2B_LxvP_1 | 50 | 53 | PF13499 | 0.569 |
DOC_PP2B_LxvP_1 | 563 | 566 | PF13499 | 0.482 |
DOC_PP4_FxxP_1 | 677 | 680 | PF00568 | 0.521 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.580 |
DOC_USP7_UBL2_3 | 343 | 347 | PF12436 | 0.480 |
DOC_USP7_UBL2_3 | 731 | 735 | PF12436 | 0.556 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 100 | 109 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 220 | 228 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 234 | 239 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 345 | 353 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 413 | 423 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 620 | 626 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 681 | 689 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 823 | 827 | PF00244 | 0.604 |
LIG_APCC_ABBA_1 | 522 | 527 | PF00400 | 0.480 |
LIG_BRCT_BRCA1_1 | 673 | 677 | PF00533 | 0.494 |
LIG_deltaCOP1_diTrp_1 | 201 | 207 | PF00928 | 0.436 |
LIG_deltaCOP1_diTrp_1 | 570 | 580 | PF00928 | 0.397 |
LIG_Dynein_DLC8_1 | 345 | 351 | PF01221 | 0.520 |
LIG_FAT_LD_1 | 75 | 83 | PF03623 | 0.527 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.563 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.540 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.399 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.420 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.516 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.489 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.547 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.446 |
LIG_FHA_1 | 761 | 767 | PF00498 | 0.424 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.563 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.545 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.539 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.491 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.688 |
LIG_FHA_2 | 750 | 756 | PF00498 | 0.617 |
LIG_LIR_Apic_2 | 544 | 548 | PF02991 | 0.483 |
LIG_LIR_Apic_2 | 635 | 641 | PF02991 | 0.432 |
LIG_LIR_Apic_2 | 674 | 680 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 156 | 162 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 285 | 294 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 391 | 402 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 571 | 581 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 89 | 97 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 285 | 289 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 571 | 577 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 578 | 583 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 588 | 594 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 711 | 716 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 814 | 818 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.564 |
LIG_MYND_1 | 508 | 512 | PF01753 | 0.577 |
LIG_NRBOX | 697 | 703 | PF00104 | 0.521 |
LIG_NRBOX | 739 | 745 | PF00104 | 0.557 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.521 |
LIG_Pex14_1 | 374 | 378 | PF04695 | 0.504 |
LIG_Pex14_1 | 419 | 423 | PF04695 | 0.480 |
LIG_Pex14_2 | 533 | 537 | PF04695 | 0.475 |
LIG_SH2_CRK | 359 | 363 | PF00017 | 0.504 |
LIG_SH2_CRK | 638 | 642 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.579 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.461 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.502 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.532 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 473 | 479 | PF11976 | 0.480 |
LIG_SUMO_SIM_anti_2 | 754 | 764 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 124 | 131 | PF11976 | 0.557 |
LIG_TRAF2_1 | 285 | 288 | PF00917 | 0.370 |
LIG_TRAF2_1 | 754 | 757 | PF00917 | 0.589 |
LIG_TRAF2_1 | 839 | 842 | PF00917 | 0.795 |
LIG_TRFH_1 | 609 | 613 | PF08558 | 0.447 |
LIG_WRC_WIRS_1 | 577 | 582 | PF05994 | 0.497 |
LIG_WRC_WIRS_1 | 812 | 817 | PF05994 | 0.500 |
LIG_WW_1 | 511 | 514 | PF00397 | 0.472 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.430 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.460 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.490 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.474 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.382 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.373 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.323 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.585 |
MOD_CK1_1 | 748 | 754 | PF00069 | 0.620 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.725 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.374 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.315 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.649 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.537 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.575 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.483 |
MOD_CK2_1 | 761 | 767 | PF00069 | 0.424 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.564 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.547 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.597 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.760 |
MOD_GlcNHglycan | 203 | 207 | PF01048 | 0.455 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.524 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.405 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.362 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.415 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.383 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.323 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.323 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.396 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.756 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.718 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.569 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.376 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.357 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.398 |
MOD_GlcNHglycan | 790 | 793 | PF01048 | 0.398 |
MOD_GlcNHglycan | 794 | 797 | PF01048 | 0.410 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.741 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.665 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.517 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.532 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.510 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.411 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.452 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.323 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.323 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.323 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.753 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.543 |
MOD_GSK3_1 | 745 | 752 | PF00069 | 0.587 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.500 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.367 |
MOD_LATS_1 | 130 | 136 | PF00433 | 0.674 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.677 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.503 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.258 |
MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.418 |
MOD_N-GLC_1 | 828 | 833 | PF02516 | 0.731 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.537 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.579 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.482 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.379 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.299 |
MOD_NEK2_1 | 689 | 694 | PF00069 | 0.524 |
MOD_NEK2_1 | 761 | 766 | PF00069 | 0.453 |
MOD_NEK2_1 | 790 | 795 | PF00069 | 0.382 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.323 |
MOD_NEK2_2 | 811 | 816 | PF00069 | 0.542 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.476 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.464 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.336 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.636 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.336 |
MOD_PIKK_1 | 761 | 767 | PF00454 | 0.490 |
MOD_PK_1 | 411 | 417 | PF00069 | 0.418 |
MOD_PK_1 | 77 | 83 | PF00069 | 0.517 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.690 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.684 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.560 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.506 |
MOD_PKA_2 | 689 | 695 | PF00069 | 0.456 |
MOD_PKA_2 | 822 | 828 | PF00069 | 0.695 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.550 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.561 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.438 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.418 |
MOD_Plk_1 | 575 | 581 | PF00069 | 0.430 |
MOD_Plk_1 | 749 | 755 | PF00069 | 0.560 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.534 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.344 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.370 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.352 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.570 |
MOD_Plk_4 | 576 | 582 | PF00069 | 0.461 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.409 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.509 |
MOD_Plk_4 | 811 | 817 | PF00069 | 0.520 |
MOD_Plk_4 | 822 | 828 | PF00069 | 0.648 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.420 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.529 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.335 |
MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.489 |
MOD_SUMO_rev_2 | 654 | 661 | PF00179 | 0.438 |
TRG_DiLeu_BaEn_1 | 757 | 762 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_1 | 822 | 827 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_2 | 202 | 208 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_2 | 672 | 678 | PF01217 | 0.494 |
TRG_DiLeu_LyEn_5 | 145 | 150 | PF01217 | 0.456 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 633 | 636 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 685 | 687 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.495 |
TRG_NES_CRM1_1 | 13 | 29 | PF08389 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 695 | 699 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8H1 | Leptomonas seymouri | 71% | 98% |
A0A0S4KJ12 | Bodo saltans | 43% | 100% |
A0A1X0P6Y3 | Trypanosomatidae | 54% | 100% |
A0A3R7M922 | Trypanosoma rangeli | 52% | 100% |
A0A3S7WV22 | Leishmania donovani | 99% | 100% |
A4H9M1 | Leishmania braziliensis | 84% | 99% |
D0A386 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A5C2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9ARP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QDT1 | Leishmania major | 94% | 100% |
V5DFH6 | Trypanosoma cruzi | 52% | 100% |