This Kinetoplastid-unique protein has a 4TM central helical bundle and long cytoplasmic termini with strikingly low complexity. Its function is unknown.
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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000123 | histone acetyltransferase complex | 4 | 2 |
GO:0000124 | SAGA complex | 4 | 2 |
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0016020 | membrane | 2 | 7 |
GO:0031248 | protein acetyltransferase complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0070461 | SAGA-type complex | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902493 | acetyltransferase complex | 4 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905368 | peptidase complex | 3 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4QJE4
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003712 | transcription coregulator activity | 2 | 4 |
GO:0003713 | transcription coactivator activity | 3 | 4 |
GO:0140110 | transcription regulator activity | 1 | 4 |
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 | 762 | 766 | PF00656 | 0.775 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.755 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 686 | 688 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 733 | 735 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.564 |
CLV_PCSK_FUR_1 | 652 | 656 | PF00082 | 0.551 |
CLV_PCSK_FUR_1 | 684 | 688 | PF00082 | 0.589 |
CLV_PCSK_FUR_1 | 734 | 738 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 732 | 734 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 736 | 738 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 527 | 529 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 644 | 646 | PF00082 | 0.615 |
CLV_PCSK_PC7_1 | 491 | 497 | PF00082 | 0.472 |
CLV_PCSK_PC7_1 | 641 | 647 | PF00082 | 0.614 |
CLV_PCSK_PC7_1 | 682 | 688 | PF00082 | 0.657 |
CLV_PCSK_PC7_1 | 732 | 738 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.601 |
DEG_APCC_DBOX_1 | 294 | 302 | PF00400 | 0.324 |
DEG_APCC_KENBOX_2 | 676 | 680 | PF00400 | 0.816 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.809 |
DEG_SPOP_SBC_1 | 232 | 236 | PF00917 | 0.440 |
DOC_AGCK_PIF_1 | 429 | 434 | PF00069 | 0.407 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.734 |
DOC_CKS1_1 | 399 | 404 | PF01111 | 0.642 |
DOC_CYCLIN_RxL_1 | 259 | 269 | PF00134 | 0.472 |
DOC_CYCLIN_yCln2_LP_2 | 483 | 489 | PF00134 | 0.423 |
DOC_PP1_RVXF_1 | 392 | 399 | PF00149 | 0.712 |
DOC_PP1_RVXF_1 | 525 | 532 | PF00149 | 0.695 |
DOC_PP1_RVXF_1 | 566 | 572 | PF00149 | 0.649 |
DOC_PP2B_LxvP_1 | 483 | 486 | PF13499 | 0.423 |
DOC_PP4_FxxP_1 | 335 | 338 | PF00568 | 0.694 |
DOC_PP4_MxPP_1 | 578 | 581 | PF00568 | 0.730 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.788 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.875 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.913 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.738 |
LIG_14-3-3_CanoR_1 | 227 | 237 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 28 | 38 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 331 | 336 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 491 | 495 | PF00244 | 0.662 |
LIG_AP2alpha_2 | 131 | 133 | PF02296 | 0.721 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.698 |
LIG_deltaCOP1_diTrp_1 | 155 | 159 | PF00928 | 0.418 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.359 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.492 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.393 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.360 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.437 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.286 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.794 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.275 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.492 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.496 |
LIG_FHA_2 | 538 | 544 | PF00498 | 0.705 |
LIG_FHA_2 | 673 | 679 | PF00498 | 0.744 |
LIG_LIR_Apic_2 | 333 | 338 | PF02991 | 0.698 |
LIG_LIR_Apic_2 | 397 | 402 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 306 | 315 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 346 | 353 | PF02991 | 0.686 |
LIG_LIR_Gen_1 | 401 | 412 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 431 | 437 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 517 | 526 | PF02991 | 0.639 |
LIG_LIR_LC3C_4 | 753 | 757 | PF02991 | 0.758 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 155 | 159 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 428 | 432 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 433 | 437 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.628 |
LIG_MYND_1 | 503 | 507 | PF01753 | 0.662 |
LIG_Pex14_1 | 147 | 151 | PF04695 | 0.691 |
LIG_Pex14_1 | 430 | 434 | PF04695 | 0.379 |
LIG_Pex14_2 | 154 | 158 | PF04695 | 0.566 |
LIG_Pex14_2 | 359 | 363 | PF04695 | 0.660 |
LIG_Pex14_2 | 409 | 413 | PF04695 | 0.535 |
LIG_Pex14_2 | 426 | 430 | PF04695 | 0.332 |
LIG_Pex14_2 | 519 | 523 | PF04695 | 0.624 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.395 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.306 |
LIG_SH2_GRB2like | 280 | 283 | PF00017 | 0.381 |
LIG_SH2_NCK_1 | 399 | 403 | PF00017 | 0.692 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 280 | 284 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 451 | 455 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 104 | 107 | PF00017 | 0.751 |
LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.792 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.760 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.688 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.685 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.689 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.419 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.660 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.785 |
LIG_SH3_3 | 706 | 712 | PF00018 | 0.818 |
LIG_SH3_3 | 754 | 760 | PF00018 | 0.803 |
LIG_SUMO_SIM_anti_2 | 306 | 312 | PF11976 | 0.368 |
LIG_SUMO_SIM_anti_2 | 458 | 463 | PF11976 | 0.441 |
LIG_SUMO_SIM_anti_2 | 476 | 482 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 173 | 178 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 456 | 463 | PF11976 | 0.345 |
LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.693 |
LIG_TRAF2_1 | 664 | 667 | PF00917 | 0.713 |
LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.359 |
LIG_WRC_WIRS_1 | 267 | 272 | PF05994 | 0.487 |
LIG_WRC_WIRS_1 | 304 | 309 | PF05994 | 0.380 |
LIG_WRC_WIRS_1 | 416 | 421 | PF05994 | 0.401 |
LIG_WRC_WIRS_1 | 426 | 431 | PF05994 | 0.330 |
LIG_WRC_WIRS_1 | 444 | 449 | PF05994 | 0.359 |
MOD_CDK_SPK_2 | 133 | 138 | PF00069 | 0.747 |
MOD_CDK_SPxK_1 | 133 | 139 | PF00069 | 0.747 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.668 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.485 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.408 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.733 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.786 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.790 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.418 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.470 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.748 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.767 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.698 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.608 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.456 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.674 |
MOD_CK2_1 | 661 | 667 | PF00069 | 0.852 |
MOD_CK2_1 | 672 | 678 | PF00069 | 0.718 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.597 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.478 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.615 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.661 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.380 |
MOD_GlcNHglycan | 614 | 618 | PF01048 | 0.567 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.625 |
MOD_GlcNHglycan | 666 | 671 | PF01048 | 0.711 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.515 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.494 |
MOD_GlcNHglycan | 750 | 755 | PF01048 | 0.595 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.486 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.703 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.623 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.829 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.792 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.464 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.850 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.780 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.870 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.772 |
MOD_GSK3_1 | 692 | 699 | PF00069 | 0.866 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.836 |
MOD_LATS_1 | 690 | 696 | PF00433 | 0.809 |
MOD_LATS_1 | 735 | 741 | PF00433 | 0.812 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.626 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.564 |
MOD_N-GLC_1 | 623 | 628 | PF02516 | 0.517 |
MOD_N-GLC_1 | 678 | 683 | PF02516 | 0.688 |
MOD_N-GLC_1 | 692 | 697 | PF02516 | 0.548 |
MOD_N-GLC_2 | 80 | 82 | PF02516 | 0.539 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.800 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.566 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.485 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.359 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.372 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.344 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.402 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.701 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.803 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.779 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.799 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.756 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.745 |
MOD_NEK2_2 | 146 | 151 | PF00069 | 0.690 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.731 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.658 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.785 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.714 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.661 |
MOD_PIKK_1 | 559 | 565 | PF00454 | 0.737 |
MOD_PIKK_1 | 707 | 713 | PF00454 | 0.766 |
MOD_PKA_1 | 686 | 692 | PF00069 | 0.837 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.324 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.763 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.410 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.669 |
MOD_PKA_2 | 686 | 692 | PF00069 | 0.874 |
MOD_PKA_2 | 735 | 741 | PF00069 | 0.825 |
MOD_PKB_1 | 645 | 653 | PF00069 | 0.765 |
MOD_PKB_1 | 684 | 692 | PF00069 | 0.802 |
MOD_PKB_1 | 696 | 704 | PF00069 | 0.722 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.797 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.708 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.524 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.634 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.421 |
MOD_Plk_1 | 623 | 629 | PF00069 | 0.718 |
MOD_Plk_2-3 | 551 | 557 | PF00069 | 0.743 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.693 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.418 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.430 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.353 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.335 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.702 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.420 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.349 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.715 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.783 |
MOD_Plk_4 | 777 | 783 | PF00069 | 0.675 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.731 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.730 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.757 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.471 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.701 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.683 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.779 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.627 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.757 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.751 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.793 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.876 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.915 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.735 |
MOD_SUMO_rev_2 | 522 | 529 | PF00179 | 0.708 |
TRG_DiLeu_BaEn_1 | 476 | 481 | PF01217 | 0.423 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.671 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.748 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 27 | 29 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 645 | 647 | PF00400 | 0.815 |
TRG_ER_diArg_1 | 684 | 687 | PF00400 | 0.788 |
TRG_ER_diArg_1 | 732 | 734 | PF00400 | 0.871 |
TRG_NLS_MonoCore_2 | 643 | 648 | PF00514 | 0.812 |
TRG_NLS_MonoExtN_4 | 641 | 648 | PF00514 | 0.812 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I288 | Leptomonas seymouri | 49% | 91% |
A0A3S7WP32 | Leishmania donovani | 93% | 100% |
A4H4A9 | Leishmania braziliensis | 66% | 100% |
A4HSI0 | Leishmania infantum | 93% | 100% |
E9AKG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5BAT7 | Trypanosoma cruzi | 33% | 100% |