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 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q5E6
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:0019002 | GMP binding | 4 | 2 |
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: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 | 304 | 308 | PF00656 | 0.460 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.400 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 483 | 485 | PF00082 | 0.423 |
CLV_PCSK_PC7_1 | 378 | 384 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.459 |
CLV_Separin_Metazoa | 492 | 496 | PF03568 | 0.296 |
DEG_APCC_DBOX_1 | 163 | 171 | PF00400 | 0.452 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.580 |
DOC_CDC14_PxL_1 | 522 | 530 | PF14671 | 0.296 |
DOC_CKS1_1 | 321 | 326 | PF01111 | 0.396 |
DOC_CYCLIN_RxL_1 | 556 | 570 | PF00134 | 0.366 |
DOC_CYCLIN_RxL_1 | 677 | 685 | PF00134 | 0.395 |
DOC_CYCLIN_yCln2_LP_2 | 231 | 237 | PF00134 | 0.289 |
DOC_CYCLIN_yCln2_LP_2 | 409 | 415 | PF00134 | 0.296 |
DOC_CYCLIN_yCln2_LP_2 | 424 | 430 | PF00134 | 0.265 |
DOC_MAPK_gen_1 | 199 | 208 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 277 | 287 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 312 | 319 | PF00069 | 0.587 |
DOC_MAPK_gen_1 | 382 | 389 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 382 | 391 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 617 | 626 | PF00069 | 0.296 |
DOC_MAPK_RevD_3 | 282 | 297 | PF00069 | 0.390 |
DOC_PP1_RVXF_1 | 678 | 685 | PF00149 | 0.424 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.291 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.509 |
DOC_PP4_FxxP_1 | 532 | 535 | PF00568 | 0.174 |
DOC_PP4_FxxP_1 | 684 | 687 | PF00568 | 0.412 |
DOC_PP4_MxPP_1 | 35 | 38 | PF00568 | 0.523 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.250 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.218 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.573 |
DOC_USP7_UBL2_3 | 556 | 560 | PF12436 | 0.267 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 383 | 388 | PF00244 | 0.259 |
LIG_14-3-3_CanoR_1 | 617 | 621 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 654 | 664 | PF00244 | 0.374 |
LIG_Actin_WH2_2 | 232 | 250 | PF00022 | 0.382 |
LIG_Actin_WH2_2 | 602 | 619 | PF00022 | 0.296 |
LIG_APCC_ABBA_1 | 603 | 608 | PF00400 | 0.296 |
LIG_APCC_Cbox_2 | 209 | 215 | PF00515 | 0.392 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.689 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.601 |
LIG_BRCT_BRCA1_1 | 430 | 434 | PF00533 | 0.256 |
LIG_EH1_1 | 536 | 544 | PF00400 | 0.296 |
LIG_eIF4E_1 | 328 | 334 | PF01652 | 0.379 |
LIG_eIF4E_1 | 419 | 425 | PF01652 | 0.267 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.334 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.278 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.399 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.245 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.502 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.204 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.554 |
LIG_FHA_2 | 589 | 595 | PF00498 | 0.396 |
LIG_FHA_2 | 669 | 675 | PF00498 | 0.448 |
LIG_Integrin_RGD_1 | 253 | 255 | PF01839 | 0.522 |
LIG_LIR_Apic_2 | 123 | 128 | PF02991 | 0.708 |
LIG_LIR_Apic_2 | 26 | 31 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 163 | 170 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 300 | 311 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 329 | 336 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 338 | 347 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 385 | 393 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 420 | 429 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 431 | 439 | PF02991 | 0.204 |
LIG_LIR_Gen_1 | 473 | 482 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 489 | 498 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 584 | 592 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 671 | 676 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.172 |
LIG_LIR_Nem_3 | 420 | 424 | PF02991 | 0.188 |
LIG_LIR_Nem_3 | 431 | 437 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 496 | 500 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 584 | 589 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 671 | 675 | PF02991 | 0.448 |
LIG_LRP6_Inhibitor_1 | 36 | 49 | PF00058 | 0.500 |
LIG_MYND_1 | 526 | 530 | PF01753 | 0.296 |
LIG_PCNA_APIM_2 | 554 | 560 | PF02747 | 0.296 |
LIG_PCNA_TLS_4 | 551 | 558 | PF02747 | 0.296 |
LIG_Pex14_2 | 411 | 415 | PF04695 | 0.250 |
LIG_Pex14_2 | 421 | 425 | PF04695 | 0.250 |
LIG_Pex14_2 | 430 | 434 | PF04695 | 0.144 |
LIG_Pex14_2 | 557 | 561 | PF04695 | 0.267 |
LIG_Rb_LxCxE_1 | 524 | 540 | PF01857 | 0.220 |
LIG_REV1ctd_RIR_1 | 485 | 494 | PF16727 | 0.383 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.432 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.329 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.340 |
LIG_SH2_CRK | 511 | 515 | PF00017 | 0.250 |
LIG_SH2_NCK_1 | 303 | 307 | PF00017 | 0.328 |
LIG_SH2_PTP2 | 388 | 391 | PF00017 | 0.296 |
LIG_SH2_PTP2 | 519 | 522 | PF00017 | 0.267 |
LIG_SH2_SRC | 369 | 372 | PF00017 | 0.363 |
LIG_SH2_SRC | 519 | 522 | PF00017 | 0.250 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.726 |
LIG_SH2_STAP1 | 419 | 423 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 511 | 515 | PF00017 | 0.250 |
LIG_SH2_STAT3 | 220 | 223 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 265 | 268 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.250 |
LIG_SH3_1 | 318 | 324 | PF00018 | 0.352 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.422 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.702 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.369 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.342 |
LIG_SUMO_SIM_par_1 | 619 | 625 | PF11976 | 0.386 |
LIG_TRAF2_1 | 671 | 674 | PF00917 | 0.367 |
LIG_TYR_ITIM | 670 | 675 | PF00017 | 0.444 |
LIG_UBA3_1 | 305 | 312 | PF00899 | 0.490 |
MOD_CDK_SPxxK_3 | 105 | 112 | PF00069 | 0.554 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.733 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.523 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.593 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.723 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.505 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.435 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.523 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.369 |
MOD_CK2_1 | 668 | 674 | PF00069 | 0.370 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.577 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.624 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.739 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.390 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.583 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.251 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.507 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.407 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.391 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.614 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.367 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.607 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.707 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.641 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.455 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.505 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.285 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.300 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.699 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.484 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.694 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.494 |
MOD_N-GLC_1 | 655 | 660 | PF02516 | 0.265 |
MOD_N-GLC_1 | 687 | 692 | PF02516 | 0.524 |
MOD_N-GLC_2 | 227 | 229 | PF02516 | 0.316 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.730 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.423 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.280 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.296 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.199 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.363 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.296 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.412 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.420 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.430 |
MOD_PK_1 | 301 | 307 | PF00069 | 0.359 |
MOD_PKA_1 | 382 | 388 | PF00069 | 0.296 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.515 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.296 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.296 |
MOD_PKA_2 | 682 | 688 | PF00069 | 0.424 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.597 |
MOD_Plk_1 | 655 | 661 | PF00069 | 0.422 |
MOD_Plk_2-3 | 581 | 587 | PF00069 | 0.556 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.466 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.296 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.296 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.400 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.338 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.284 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.641 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.586 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.397 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.296 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.669 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.556 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.510 |
MOD_SUMO_rev_2 | 172 | 182 | PF00179 | 0.451 |
MOD_SUMO_rev_2 | 252 | 258 | PF00179 | 0.523 |
MOD_SUMO_rev_2 | 374 | 384 | PF00179 | 0.388 |
TRG_DiLeu_BaEn_1 | 163 | 168 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_1 | 489 | 494 | PF01217 | 0.296 |
TRG_DiLeu_BaEn_1 | 496 | 501 | PF01217 | 0.243 |
TRG_DiLeu_BaEn_1 | 524 | 529 | PF01217 | 0.250 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 464 | 469 | PF01217 | 0.296 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.235 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.144 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 672 | 675 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 647 | 650 | PF00400 | 0.296 |
TRG_NES_CRM1_1 | 230 | 245 | PF08389 | 0.364 |
TRG_NES_CRM1_1 | 615 | 628 | PF08389 | 0.265 |
TRG_NLS_Bipartite_1 | 296 | 316 | PF00514 | 0.393 |
TRG_NLS_MonoExtN_4 | 311 | 316 | PF00514 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IM27 | Bodo saltans | 33% | 96% |
A0A1X0NUI5 | Trypanosomatidae | 39% | 100% |
A0A3S7X5E2 | Leishmania donovani | 97% | 100% |
A0A422P1D1 | Trypanosoma rangeli | 40% | 100% |
A4HKC4 | Leishmania braziliensis | 85% | 100% |
D0AA12 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9B2R1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5DHN7 | Trypanosoma cruzi | 42% | 100% |