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: A0A3S7WP32
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 | 4 |
GO:0003713 | transcription coactivator activity | 3 | 4 |
GO:0140110 | transcription regulator activity | 1 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 190 | 194 | PF00656 | 0.287 |
CLV_C14_Caspase3-7 | 757 | 761 | PF00656 | 0.720 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.504 |
CLV_PCSK_FUR_1 | 679 | 683 | PF00082 | 0.531 |
CLV_PCSK_FUR_1 | 729 | 733 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 681 | 683 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 727 | 729 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 731 | 733 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 491 | 493 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 523 | 525 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 639 | 641 | PF00082 | 0.560 |
CLV_PCSK_PC7_1 | 487 | 493 | PF00082 | 0.380 |
CLV_PCSK_PC7_1 | 636 | 642 | PF00082 | 0.559 |
CLV_PCSK_PC7_1 | 677 | 683 | PF00082 | 0.556 |
CLV_PCSK_PC7_1 | 727 | 733 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.507 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.269 |
DEG_APCC_KENBOX_2 | 671 | 675 | PF00400 | 0.756 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.754 |
DOC_AGCK_PIF_1 | 425 | 430 | PF00069 | 0.359 |
DOC_CKS1_1 | 395 | 400 | PF01111 | 0.578 |
DOC_CKS1_1 | 99 | 104 | PF01111 | 0.687 |
DOC_CYCLIN_RxL_1 | 255 | 265 | PF00134 | 0.380 |
DOC_CYCLIN_yCln2_LP_2 | 479 | 485 | PF00134 | 0.369 |
DOC_MAPK_gen_1 | 449 | 457 | PF00069 | 0.325 |
DOC_PP1_RVXF_1 | 388 | 395 | PF00149 | 0.638 |
DOC_PP1_RVXF_1 | 521 | 528 | PF00149 | 0.575 |
DOC_PP2B_LxvP_1 | 479 | 482 | PF13499 | 0.369 |
DOC_PP2B_PxIxI_1 | 206 | 212 | PF00149 | 0.421 |
DOC_PP4_FxxP_1 | 331 | 334 | PF00568 | 0.649 |
DOC_PP4_MxPP_1 | 574 | 577 | PF00568 | 0.623 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.716 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.842 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 25 | 34 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 315 | 323 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 327 | 332 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 487 | 491 | PF00244 | 0.593 |
LIG_AP2alpha_2 | 127 | 129 | PF02296 | 0.641 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.655 |
LIG_deltaCOP1_diTrp_1 | 151 | 155 | PF00928 | 0.304 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.304 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.434 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.408 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.326 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.269 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.735 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.340 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.230 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.207 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.409 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.458 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.599 |
LIG_LIR_Apic_2 | 329 | 334 | PF02991 | 0.650 |
LIG_LIR_Apic_2 | 393 | 398 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 151 | 160 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 178 | 189 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 302 | 311 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 342 | 349 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 397 | 408 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 427 | 433 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 513 | 522 | PF02991 | 0.576 |
LIG_LIR_LC3C_4 | 472 | 475 | PF02991 | 0.270 |
LIG_LIR_LC3C_4 | 748 | 752 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 265 | 269 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 302 | 306 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 424 | 428 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 429 | 433 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 513 | 519 | PF02991 | 0.577 |
LIG_MYND_1 | 249 | 253 | PF01753 | 0.394 |
LIG_MYND_1 | 499 | 503 | PF01753 | 0.619 |
LIG_Pex14_1 | 143 | 147 | PF04695 | 0.630 |
LIG_Pex14_1 | 426 | 430 | PF04695 | 0.329 |
LIG_Pex14_2 | 150 | 154 | PF04695 | 0.469 |
LIG_Pex14_2 | 355 | 359 | PF04695 | 0.620 |
LIG_Pex14_2 | 405 | 409 | PF04695 | 0.495 |
LIG_Pex14_2 | 422 | 426 | PF04695 | 0.227 |
LIG_Pex14_2 | 515 | 519 | PF04695 | 0.578 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.304 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.304 |
LIG_SH2_GRB2like | 276 | 279 | PF00017 | 0.331 |
LIG_SH2_NCK_1 | 395 | 399 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 447 | 451 | PF00017 | 0.305 |
LIG_SH2_STAT3 | 100 | 103 | PF00017 | 0.686 |
LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.746 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.686 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.580 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.638 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.658 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.636 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.690 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.641 |
LIG_SH3_3 | 701 | 707 | PF00018 | 0.709 |
LIG_SH3_3 | 749 | 755 | PF00018 | 0.751 |
LIG_SUMO_SIM_anti_2 | 302 | 308 | PF11976 | 0.304 |
LIG_SUMO_SIM_anti_2 | 454 | 459 | PF11976 | 0.316 |
LIG_SUMO_SIM_anti_2 | 472 | 478 | PF11976 | 0.201 |
LIG_SUMO_SIM_par_1 | 169 | 174 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 207 | 212 | PF11976 | 0.405 |
LIG_TYR_ITIM | 306 | 311 | PF00017 | 0.304 |
LIG_WRC_WIRS_1 | 263 | 268 | PF05994 | 0.396 |
LIG_WRC_WIRS_1 | 300 | 305 | PF05994 | 0.272 |
LIG_WRC_WIRS_1 | 412 | 417 | PF05994 | 0.362 |
LIG_WRC_WIRS_1 | 422 | 427 | PF05994 | 0.269 |
MOD_CDK_SPK_2 | 129 | 134 | PF00069 | 0.707 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.707 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.444 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.435 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.663 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.738 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.741 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.304 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.362 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.657 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.675 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.615 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.622 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.430 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.404 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.609 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.546 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.589 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.564 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.575 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.584 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.352 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.526 |
MOD_GlcNHglycan | 609 | 613 | PF01048 | 0.511 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.551 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.534 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.430 |
MOD_GlcNHglycan | 745 | 750 | PF01048 | 0.522 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.411 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.665 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.423 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.455 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.737 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.741 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.303 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.753 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.648 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.698 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.790 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.768 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.692 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.728 |
MOD_LATS_1 | 685 | 691 | PF00433 | 0.759 |
MOD_LATS_1 | 730 | 736 | PF00433 | 0.716 |
MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.657 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.512 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.517 |
MOD_N-GLC_1 | 673 | 678 | PF02516 | 0.554 |
MOD_N-GLC_2 | 76 | 78 | PF02516 | 0.488 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.746 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.469 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.394 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.307 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.304 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.304 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.341 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.586 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.666 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.726 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.693 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.742 |
MOD_NEK2_2 | 142 | 147 | PF00069 | 0.589 |
MOD_NEK2_2 | 442 | 447 | PF00069 | 0.318 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.688 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.622 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.714 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.662 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.580 |
MOD_PIKK_1 | 555 | 561 | PF00454 | 0.640 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.654 |
MOD_PIKK_1 | 702 | 708 | PF00454 | 0.712 |
MOD_PKA_1 | 681 | 687 | PF00069 | 0.757 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.269 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.696 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.365 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.573 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.757 |
MOD_PKA_2 | 730 | 736 | PF00069 | 0.729 |
MOD_PKA_2 | 755 | 761 | PF00069 | 0.716 |
MOD_PKB_1 | 640 | 648 | PF00069 | 0.714 |
MOD_PKB_1 | 679 | 687 | PF00069 | 0.742 |
MOD_PKB_1 | 691 | 699 | PF00069 | 0.675 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.744 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.665 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.469 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.433 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.559 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.361 |
MOD_Plk_2-3 | 547 | 553 | PF00069 | 0.654 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.591 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.304 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.386 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.346 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.238 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.249 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.658 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.299 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.618 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.669 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.681 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.686 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.707 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.718 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.602 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.604 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.697 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.576 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.677 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.743 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.788 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.843 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.645 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.641 |
MOD_SUMO_rev_2 | 518 | 525 | PF00179 | 0.579 |
TRG_DiLeu_BaEn_1 | 472 | 477 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.326 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.367 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 640 | 642 | PF00400 | 0.716 |
TRG_ER_diArg_1 | 679 | 682 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 727 | 729 | PF00400 | 0.703 |
TRG_NLS_MonoCore_2 | 638 | 643 | PF00514 | 0.758 |
TRG_NLS_MonoExtN_4 | 636 | 643 | PF00514 | 0.757 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I288 | Leptomonas seymouri | 50% | 90% |
A4H4A9 | Leishmania braziliensis | 67% | 98% |
A4HSI0 | Leishmania infantum | 100% | 100% |
E9AKG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QJE4 | Leishmania major | 93% | 100% |