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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HKC4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006370 | 7-methylguanosine mRNA capping | 8 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006397 | mRNA processing | 7 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009452 | 7-methylguanosine RNA capping | 8 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0016071 | mRNA metabolic process | 6 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0036260 | RNA capping | 7 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004484 | mRNA guanylyltransferase activity | 5 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0005525 | GTP binding | 5 | 5 |
GO:0008192 | RNA guanylyltransferase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016779 | nucleotidyltransferase activity | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0019001 | guanyl nucleotide binding | 5 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 5 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0070568 | guanylyltransferase activity | 5 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0019002 | GMP binding | 4 | 1 |
GO:0003909 | DNA ligase activity | 4 | 1 |
GO:0003910 | DNA ligase (ATP) activity | 5 | 1 |
GO:0016874 | ligase activity | 2 | 1 |
GO:0016886 | ligase activity, forming phosphoric ester bonds | 3 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.512 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 308 | 310 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.462 |
CLV_PCSK_PC7_1 | 374 | 380 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.509 |
CLV_Separin_Metazoa | 488 | 492 | PF03568 | 0.462 |
DEG_APCC_DBOX_1 | 159 | 167 | PF00400 | 0.571 |
DEG_APCC_KENBOX_2 | 186 | 190 | PF00400 | 0.336 |
DEG_SCF_FBW7_1 | 67 | 72 | PF00400 | 0.583 |
DOC_CDC14_PxL_1 | 518 | 526 | PF14671 | 0.462 |
DOC_CKS1_1 | 317 | 322 | PF01111 | 0.543 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.731 |
DOC_CYCLIN_RxL_1 | 552 | 566 | PF00134 | 0.512 |
DOC_CYCLIN_RxL_1 | 673 | 681 | PF00134 | 0.552 |
DOC_CYCLIN_yCln2_LP_2 | 227 | 233 | PF00134 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 405 | 411 | PF00134 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 420 | 426 | PF00134 | 0.223 |
DOC_MAPK_DCC_7 | 225 | 233 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 195 | 204 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 276 | 283 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 308 | 317 | PF00069 | 0.596 |
DOC_MAPK_gen_1 | 378 | 385 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 225 | 233 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 308 | 317 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 378 | 387 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 613 | 622 | PF00069 | 0.462 |
DOC_MAPK_RevD_3 | 278 | 293 | PF00069 | 0.552 |
DOC_PP1_RVXF_1 | 674 | 681 | PF00149 | 0.553 |
DOC_PP2B_LxvP_1 | 227 | 230 | PF13499 | 0.371 |
DOC_PP4_FxxP_1 | 680 | 683 | PF00568 | 0.556 |
DOC_SPAK_OSR1_1 | 393 | 397 | PF12202 | 0.301 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.738 |
DOC_USP7_UBL2_3 | 552 | 556 | PF12436 | 0.346 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.798 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.698 |
LIG_14-3-3_CanoR_1 | 379 | 384 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 613 | 617 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 650 | 660 | PF00244 | 0.423 |
LIG_Actin_WH2_2 | 228 | 246 | PF00022 | 0.549 |
LIG_Actin_WH2_2 | 598 | 615 | PF00022 | 0.462 |
LIG_Actin_WH2_2 | 92 | 110 | PF00022 | 0.537 |
LIG_APCC_ABBA_1 | 599 | 604 | PF00400 | 0.462 |
LIG_APCC_Cbox_2 | 205 | 211 | PF00515 | 0.467 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.730 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.752 |
LIG_EH1_1 | 532 | 540 | PF00400 | 0.462 |
LIG_eIF4E_1 | 324 | 330 | PF01652 | 0.528 |
LIG_eIF4E_1 | 415 | 421 | PF01652 | 0.346 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.547 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.378 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.449 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.321 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.550 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.512 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.565 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.479 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.564 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.547 |
LIG_FHA_2 | 665 | 671 | PF00498 | 0.498 |
LIG_HCF-1_HBM_1 | 272 | 275 | PF13415 | 0.313 |
LIG_Integrin_RGD_1 | 249 | 251 | PF01839 | 0.591 |
LIG_LIR_Gen_1 | 159 | 166 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 296 | 307 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 325 | 333 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 334 | 343 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 381 | 389 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 392 | 402 | PF02991 | 0.144 |
LIG_LIR_Gen_1 | 416 | 424 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 469 | 478 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 485 | 494 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 580 | 588 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 667 | 672 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 331 | 336 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.144 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 416 | 420 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 469 | 473 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 481 | 487 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 492 | 496 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 580 | 585 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 667 | 671 | PF02991 | 0.501 |
LIG_MYND_1 | 522 | 526 | PF01753 | 0.462 |
LIG_PCNA_APIM_2 | 550 | 556 | PF02747 | 0.462 |
LIG_PCNA_TLS_4 | 547 | 554 | PF02747 | 0.462 |
LIG_PDZ_Class_1 | 683 | 688 | PF00595 | 0.433 |
LIG_Pex14_2 | 407 | 411 | PF04695 | 0.326 |
LIG_Pex14_2 | 417 | 421 | PF04695 | 0.326 |
LIG_Pex14_2 | 553 | 557 | PF04695 | 0.346 |
LIG_Rb_LxCxE_1 | 520 | 536 | PF01857 | 0.303 |
LIG_REV1ctd_RIR_1 | 481 | 490 | PF16727 | 0.440 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.488 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.403 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 299 | 303 | PF00017 | 0.458 |
LIG_SH2_PTP2 | 384 | 387 | PF00017 | 0.462 |
LIG_SH2_PTP2 | 515 | 518 | PF00017 | 0.346 |
LIG_SH2_SRC | 365 | 368 | PF00017 | 0.530 |
LIG_SH2_SRC | 515 | 518 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.753 |
LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 216 | 219 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 261 | 264 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.326 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.766 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.239 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.536 |
LIG_SH3_3 | 643 | 649 | PF00018 | 0.462 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.622 |
LIG_SUMO_SIM_anti_2 | 135 | 142 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 615 | 621 | PF11976 | 0.441 |
LIG_TRAF2_1 | 667 | 670 | PF00917 | 0.441 |
LIG_TYR_ITIM | 666 | 671 | PF00017 | 0.496 |
LIG_UBA3_1 | 301 | 308 | PF00899 | 0.514 |
LIG_UBA3_1 | 420 | 425 | PF00899 | 0.239 |
MOD_CDK_SPK_2 | 89 | 94 | PF00069 | 0.531 |
MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.570 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.513 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.596 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.527 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.462 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.468 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.547 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.426 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.346 |
MOD_Cter_Amidation | 126 | 129 | PF01082 | 0.736 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.744 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.369 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.689 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.144 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.549 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.417 |
MOD_GlcNHglycan | 438 | 443 | PF01048 | 0.263 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.444 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.751 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.239 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.624 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.561 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.701 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.747 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.529 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.517 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.364 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.764 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.787 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.482 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.508 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.712 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.358 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.511 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.566 |
MOD_N-GLC_1 | 651 | 656 | PF02516 | 0.398 |
MOD_N-GLC_1 | 683 | 688 | PF02516 | 0.656 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.479 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.398 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.490 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.462 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.462 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.558 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.474 |
MOD_PIKK_1 | 634 | 640 | PF00454 | 0.490 |
MOD_PK_1 | 297 | 303 | PF00069 | 0.522 |
MOD_PK_1 | 309 | 315 | PF00069 | 0.274 |
MOD_PKA_1 | 378 | 384 | PF00069 | 0.462 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.555 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.462 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.475 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.565 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.571 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.505 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.430 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.461 |
MOD_Plk_2-3 | 577 | 583 | PF00069 | 0.574 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.509 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.462 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.462 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.560 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.384 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.363 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.545 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.739 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.462 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.798 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.701 |
MOD_SUMO_rev_2 | 168 | 178 | PF00179 | 0.507 |
MOD_SUMO_rev_2 | 248 | 254 | PF00179 | 0.593 |
MOD_SUMO_rev_2 | 370 | 380 | PF00179 | 0.547 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.571 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.430 |
TRG_DiLeu_BaEn_1 | 485 | 490 | PF01217 | 0.462 |
TRG_DiLeu_BaEn_1 | 492 | 497 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 134 | 139 | PF01217 | 0.549 |
TRG_DiLeu_BaLyEn_6 | 460 | 465 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.468 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 643 | 646 | PF00400 | 0.462 |
TRG_NES_CRM1_1 | 226 | 241 | PF08389 | 0.531 |
TRG_NES_CRM1_1 | 611 | 624 | PF08389 | 0.398 |
TRG_NLS_Bipartite_1 | 292 | 312 | PF00514 | 0.550 |
TRG_NLS_MonoExtN_4 | 307 | 312 | PF00514 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IM27 | Bodo saltans | 34% | 96% |
A0A1X0NUI5 | Trypanosomatidae | 40% | 100% |
A0A3S7X5E2 | Leishmania donovani | 85% | 99% |
A0A422P1D1 | Trypanosoma rangeli | 41% | 100% |
D0AA12 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9B2R1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q5E6 | Leishmania major | 85% | 100% |
V5DHN7 | Trypanosoma cruzi | 42% | 100% |