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. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | 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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0000123 | histone acetyltransferase complex | 4 | 1 |
GO:0000124 | SAGA complex | 4 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0031248 | protein acetyltransferase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0070461 | SAGA-type complex | 5 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902493 | acetyltransferase complex | 4 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905368 | peptidase complex | 3 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4H4A9
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic 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:0031326 | regulation of cellular biosynthetic process | 5 | 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:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003712 | transcription coregulator activity | 2 | 3 |
GO:0003713 | transcription coactivator activity | 3 | 3 |
GO:0140110 | transcription regulator activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.805 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.607 |
CLV_PCSK_FUR_1 | 676 | 680 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.805 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 520 | 522 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 637 | 639 | PF00082 | 0.663 |
CLV_PCSK_PC7_1 | 484 | 490 | PF00082 | 0.474 |
CLV_PCSK_PC7_1 | 634 | 640 | PF00082 | 0.663 |
CLV_PCSK_PC7_1 | 674 | 680 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 696 | 700 | PF00082 | 0.588 |
DEG_APCC_DBOX_1 | 286 | 294 | PF00400 | 0.546 |
DEG_APCC_KENBOX_2 | 668 | 672 | PF00400 | 0.862 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.661 |
DEG_SCF_FBW7_1 | 653 | 660 | PF00400 | 0.668 |
DOC_CKS1_1 | 392 | 397 | PF01111 | 0.458 |
DOC_CKS1_1 | 598 | 603 | PF01111 | 0.659 |
DOC_CKS1_1 | 84 | 89 | PF01111 | 0.568 |
DOC_CYCLIN_RxL_1 | 252 | 261 | PF00134 | 0.652 |
DOC_CYCLIN_yCln2_LP_2 | 476 | 482 | PF00134 | 0.513 |
DOC_CYCLIN_yCln2_LP_2 | 620 | 626 | PF00134 | 0.680 |
DOC_MAPK_gen_1 | 446 | 454 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 645 | 655 | PF00069 | 0.679 |
DOC_MAPK_RevD_3 | 145 | 161 | PF00069 | 0.261 |
DOC_PP1_RVXF_1 | 518 | 525 | PF00149 | 0.665 |
DOC_PP1_RVXF_1 | 559 | 565 | PF00149 | 0.657 |
DOC_PP2B_LxvP_1 | 476 | 479 | PF13499 | 0.513 |
DOC_PP2B_PxIxI_1 | 185 | 191 | PF00149 | 0.605 |
DOC_PP4_MxPP_1 | 571 | 574 | PF00568 | 0.710 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 711 | 715 | PF00917 | 0.786 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 597 | 602 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.858 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 312 | 316 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 447 | 453 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 484 | 491 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 561 | 571 | PF00244 | 0.590 |
LIG_BIR_III_4 | 630 | 634 | PF00653 | 0.687 |
LIG_BRCT_BRCA1_1 | 53 | 57 | PF00533 | 0.437 |
LIG_deltaCOP1_diTrp_1 | 136 | 139 | PF00928 | 0.411 |
LIG_EH_1 | 111 | 115 | PF12763 | 0.431 |
LIG_EVH1_1 | 703 | 707 | PF00568 | 0.668 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.411 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.550 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.695 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.650 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.606 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.510 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.482 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.400 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.493 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.235 |
LIG_FHA_1 | 746 | 752 | PF00498 | 0.675 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.682 |
LIG_FHA_2 | 654 | 660 | PF00498 | 0.691 |
LIG_HP1_1 | 30 | 34 | PF01393 | 0.471 |
LIG_LIR_Apic_2 | 390 | 395 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 136 | 145 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 163 | 171 | PF02991 | 0.684 |
LIG_LIR_Gen_1 | 301 | 310 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 338 | 345 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 394 | 405 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 424 | 430 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 510 | 519 | PF02991 | 0.669 |
LIG_LIR_LC3C_4 | 275 | 278 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.666 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 421 | 425 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.666 |
LIG_PCNA_yPIPBox_3 | 160 | 169 | PF02747 | 0.508 |
LIG_Pex14_1 | 128 | 132 | PF04695 | 0.540 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.346 |
LIG_Pex14_2 | 351 | 355 | PF04695 | 0.532 |
LIG_Pex14_2 | 419 | 423 | PF04695 | 0.322 |
LIG_Pex14_2 | 512 | 516 | PF04695 | 0.671 |
LIG_RPA_C_Fungi | 442 | 454 | PF08784 | 0.261 |
LIG_SH2_CRK | 297 | 301 | PF00017 | 0.411 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 392 | 396 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.463 |
LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.838 |
LIG_SH2_STAT3 | 85 | 88 | PF00017 | 0.720 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.720 |
LIG_SH3_2 | 235 | 240 | PF14604 | 0.509 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.672 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.682 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.374 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.484 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.560 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.620 |
LIG_SH3_3 | 701 | 707 | PF00018 | 0.746 |
LIG_SH3_3 | 748 | 754 | PF00018 | 0.849 |
LIG_SUMO_SIM_anti_2 | 298 | 304 | PF11976 | 0.355 |
LIG_SUMO_SIM_anti_2 | 451 | 456 | PF11976 | 0.513 |
LIG_SUMO_SIM_anti_2 | 469 | 475 | PF11976 | 0.216 |
LIG_SUMO_SIM_par_1 | 450 | 456 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 651 | 656 | PF11976 | 0.588 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.616 |
LIG_TYR_ITIM | 302 | 307 | PF00017 | 0.411 |
LIG_WRC_WIRS_1 | 259 | 264 | PF05994 | 0.584 |
LIG_WRC_WIRS_1 | 419 | 424 | PF05994 | 0.379 |
LIG_WRC_WIRS_1 | 437 | 442 | PF05994 | 0.474 |
MOD_CDK_SPK_2 | 114 | 119 | PF00069 | 0.788 |
MOD_CDK_SPK_2 | 374 | 379 | PF00069 | 0.528 |
MOD_CDK_SPxK_1 | 114 | 120 | PF00069 | 0.752 |
MOD_CDK_SPxxK_3 | 597 | 604 | PF00069 | 0.568 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.828 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.495 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.390 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.679 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.830 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.411 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.468 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.796 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.700 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.523 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.452 |
MOD_CK2_1 | 653 | 659 | PF00069 | 0.686 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.682 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.835 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.348 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.674 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.810 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.489 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.436 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.739 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.759 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.728 |
MOD_GlcNHglycan | 766 | 769 | PF01048 | 0.611 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.771 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.830 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.530 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.608 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.537 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.831 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.726 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.809 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.722 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.763 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.656 |
MOD_LATS_1 | 682 | 688 | PF00433 | 0.856 |
MOD_LATS_1 | 734 | 740 | PF00433 | 0.752 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.618 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.423 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.290 |
MOD_N-GLC_1 | 670 | 675 | PF02516 | 0.822 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.841 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.411 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.723 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.580 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.411 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.411 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.411 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.448 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.594 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.731 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.704 |
MOD_NEK2_1 | 658 | 663 | PF00069 | 0.818 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.708 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.557 |
MOD_NEK2_2 | 127 | 132 | PF00069 | 0.589 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.409 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.651 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.613 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.727 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.616 |
MOD_PK_1 | 199 | 205 | PF00069 | 0.512 |
MOD_PKA_1 | 678 | 684 | PF00069 | 0.848 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.408 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.609 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.590 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.581 |
MOD_PKA_2 | 641 | 647 | PF00069 | 0.668 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.848 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.589 |
MOD_PKA_2 | 732 | 738 | PF00069 | 0.763 |
MOD_PKA_2 | 754 | 760 | PF00069 | 0.766 |
MOD_PKB_1 | 638 | 646 | PF00069 | 0.759 |
MOD_PKB_1 | 676 | 684 | PF00069 | 0.783 |
MOD_PKB_1 | 686 | 694 | PF00069 | 0.704 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.838 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.353 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.602 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.408 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.551 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.513 |
MOD_Plk_1 | 658 | 664 | PF00069 | 0.597 |
MOD_Plk_1 | 744 | 750 | PF00069 | 0.622 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.731 |
MOD_Plk_2-3 | 544 | 550 | PF00069 | 0.682 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.593 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.411 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.474 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.353 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.342 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.388 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.629 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.738 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.752 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.609 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.748 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.744 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.628 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.619 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.733 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.545 |
MOD_ProDKin_1 | 597 | 603 | PF00069 | 0.609 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.832 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.851 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.583 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.677 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.627 |
MOD_SUMO_rev_2 | 515 | 522 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_1 | 469 | 474 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_1 | 771 | 776 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_2 | 218 | 224 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.531 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.786 |
TRG_ER_diArg_1 | 220 | 223 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 638 | 640 | PF00400 | 0.757 |
TRG_ER_diArg_1 | 676 | 679 | PF00400 | 0.773 |
TRG_NLS_MonoCore_2 | 636 | 641 | PF00514 | 0.856 |
TRG_NLS_MonoExtN_4 | 634 | 641 | PF00514 | 0.856 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I288 | Leptomonas seymouri | 49% | 90% |
A0A3S7WP32 | Leishmania donovani | 67% | 100% |
A4HSI0 | Leishmania infantum | 67% | 100% |
E9AKG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 99% |
Q4QJE4 | Leishmania major | 66% | 98% |