Kinetoplastid proteins, kinteoplast poly(A) polymerase complex 1 subunit Uncharacterized
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4I888
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009895 | negative regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043489 | RNA stabilization | 4 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048255 | mRNA stabilization | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 147 | 151 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.730 |
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.502 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 628 | 632 | PF00656 | 0.675 |
CLV_C14_Caspase3-7 | 669 | 673 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 702 | 706 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 715 | 717 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 763 | 765 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.473 |
CLV_PCSK_FUR_1 | 168 | 172 | PF00082 | 0.544 |
CLV_PCSK_FUR_1 | 226 | 230 | PF00082 | 0.618 |
CLV_PCSK_FUR_1 | 761 | 765 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 720 | 722 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 761 | 763 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 390 | 392 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 408 | 410 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 720 | 722 | PF00082 | 0.526 |
CLV_PCSK_PC7_1 | 214 | 220 | PF00082 | 0.648 |
CLV_PCSK_PC7_1 | 603 | 609 | PF00082 | 0.600 |
CLV_PCSK_PC7_1 | 716 | 722 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 782 | 786 | PF00082 | 0.496 |
DEG_APCC_DBOX_1 | 179 | 187 | PF00400 | 0.469 |
DEG_APCC_DBOX_1 | 678 | 686 | PF00400 | 0.496 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.652 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.591 |
DEG_SPOP_SBC_1 | 540 | 544 | PF00917 | 0.563 |
DOC_CYCLIN_RxL_1 | 299 | 310 | PF00134 | 0.631 |
DOC_MAPK_gen_1 | 113 | 122 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 113 | 122 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 303 | 311 | PF00069 | 0.608 |
DOC_MAPK_NFAT4_5 | 113 | 121 | PF00069 | 0.540 |
DOC_MAPK_RevD_3 | 157 | 171 | PF00069 | 0.505 |
DOC_PP1_RVXF_1 | 734 | 741 | PF00149 | 0.451 |
DOC_PP2B_LxvP_1 | 683 | 686 | PF13499 | 0.502 |
DOC_PP2B_LxvP_1 | 768 | 771 | PF13499 | 0.516 |
DOC_PP4_FxxP_1 | 465 | 468 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.686 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.636 |
DOC_USP7_UBL2_3 | 610 | 614 | PF12436 | 0.678 |
DOC_USP7_UBL2_3 | 69 | 73 | PF12436 | 0.389 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.722 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 219 | 227 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 236 | 241 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 334 | 338 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 358 | 364 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 472 | 477 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 592 | 598 | PF00244 | 0.529 |
LIG_Actin_WH2_2 | 469 | 484 | PF00022 | 0.563 |
LIG_ActinCP_TwfCPI_2 | 465 | 474 | PF01115 | 0.553 |
LIG_AP2alpha_2 | 713 | 715 | PF02296 | 0.597 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.598 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.573 |
LIG_deltaCOP1_diTrp_1 | 387 | 392 | PF00928 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 776 | 781 | PF00928 | 0.480 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.538 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.508 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.320 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.533 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.435 |
LIG_FHA_1 | 743 | 749 | PF00498 | 0.555 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.538 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.559 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.463 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.736 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.691 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.507 |
LIG_GBD_Chelix_1 | 311 | 319 | PF00786 | 0.577 |
LIG_GBD_Chelix_1 | 652 | 660 | PF00786 | 0.549 |
LIG_LIR_Apic_2 | 462 | 468 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 323 | 333 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 53 | 62 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 616 | 625 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 616 | 621 | PF02991 | 0.611 |
LIG_MYND_1 | 680 | 684 | PF01753 | 0.498 |
LIG_NRBOX | 640 | 646 | PF00104 | 0.616 |
LIG_Pex14_2 | 328 | 332 | PF04695 | 0.385 |
LIG_Pex14_2 | 727 | 731 | PF04695 | 0.545 |
LIG_PTAP_UEV_1 | 244 | 249 | PF05743 | 0.630 |
LIG_SH2_CRK | 519 | 523 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 353 | 357 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 393 | 397 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 519 | 523 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 166 | 169 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 691 | 694 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.527 |
LIG_SH3_1 | 764 | 770 | PF00018 | 0.517 |
LIG_SH3_1 | 772 | 778 | PF00018 | 0.459 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.614 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.759 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.506 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.595 |
LIG_SH3_3 | 678 | 684 | PF00018 | 0.495 |
LIG_SH3_3 | 731 | 737 | PF00018 | 0.438 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.510 |
LIG_SH3_3 | 772 | 778 | PF00018 | 0.470 |
LIG_SUMO_SIM_anti_2 | 308 | 314 | PF11976 | 0.593 |
LIG_SUMO_SIM_anti_2 | 369 | 375 | PF11976 | 0.437 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.589 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.535 |
LIG_TRAF2_2 | 119 | 124 | PF00917 | 0.662 |
LIG_UBA3_1 | 315 | 324 | PF00899 | 0.584 |
LIG_UBA3_1 | 656 | 665 | PF00899 | 0.496 |
MOD_CDC14_SPxK_1 | 233 | 236 | PF00782 | 0.670 |
MOD_CDK_SPxK_1 | 230 | 236 | PF00069 | 0.639 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.620 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.759 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.671 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.705 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.601 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.666 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.659 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.443 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.791 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.614 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.552 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.453 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.469 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.644 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.460 |
MOD_GlcNHglycan | 244 | 248 | PF01048 | 0.679 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.689 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.690 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.702 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.545 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.634 |
MOD_GlcNHglycan | 692 | 695 | PF01048 | 0.431 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.466 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.636 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.668 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.734 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.801 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.760 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.717 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.552 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.536 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.755 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.514 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.560 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.452 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.724 |
MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.650 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.583 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.795 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.659 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.592 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.523 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.477 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.578 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.492 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.493 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.503 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.561 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.495 |
MOD_NEK2_2 | 353 | 358 | PF00069 | 0.530 |
MOD_OFUCOSY | 262 | 267 | PF10250 | 0.686 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.580 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.464 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.443 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.623 |
MOD_PIKK_1 | 591 | 597 | PF00454 | 0.526 |
MOD_PK_1 | 359 | 365 | PF00069 | 0.611 |
MOD_PKA_1 | 606 | 612 | PF00069 | 0.671 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.402 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.561 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.604 |
MOD_PKB_1 | 217 | 225 | PF00069 | 0.596 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.490 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.556 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.506 |
MOD_Plk_2-3 | 663 | 669 | PF00069 | 0.460 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.490 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.504 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.532 |
MOD_Plk_4 | 687 | 693 | PF00069 | 0.460 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.704 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.691 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.785 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.792 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.718 |
MOD_SUMO_for_1 | 379 | 382 | PF00179 | 0.572 |
MOD_SUMO_for_1 | 613 | 616 | PF00179 | 0.661 |
MOD_SUMO_rev_2 | 402 | 410 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 661 | 666 | PF00179 | 0.450 |
TRG_DiLeu_BaEn_1 | 640 | 645 | PF01217 | 0.654 |
TRG_DiLeu_BaLyEn_6 | 652 | 657 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 734 | 739 | PF01217 | 0.463 |
TRG_DiLeu_LyEn_5 | 640 | 645 | PF01217 | 0.654 |
TRG_DiLeu_LyEn_5 | 678 | 683 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 226 | 229 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 606 | 608 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 761 | 764 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.481 |
TRG_NLS_MonoExtC_3 | 27 | 32 | PF00514 | 0.665 |
TRG_NLS_MonoExtC_3 | 715 | 720 | PF00514 | 0.591 |
TRG_NLS_MonoExtN_4 | 26 | 32 | PF00514 | 0.672 |
TRG_NLS_MonoExtN_4 | 290 | 296 | PF00514 | 0.667 |
TRG_NLS_MonoExtN_4 | 714 | 720 | PF00514 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 219 | 223 | PF00026 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 474 | 478 | PF00026 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 491 | 495 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 516 | 521 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 73 | 77 | PF00026 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I355 | Leptomonas seymouri | 73% | 93% |
A0A0S4JPP8 | Bodo saltans | 43% | 100% |
A0A1X0NS88 | Trypanosomatidae | 49% | 99% |
A0A3R7LBC9 | Trypanosoma rangeli | 52% | 100% |
A0A3S7X5U8 | Leishmania donovani | 100% | 100% |
A4HKQ8 | Leishmania braziliensis | 85% | 99% |
E9B346 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q508 | Leishmania major | 96% | 100% |
V5AUT0 | Trypanosoma cruzi | 53% | 96% |