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: E9AKG4
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_C14_Caspase3-7 | 762 | 766 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 684 | 686 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.513 |
CLV_PCSK_FUR_1 | 682 | 686 | PF00082 | 0.536 |
CLV_PCSK_FUR_1 | 728 | 732 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 684 | 686 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 731 | 733 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 492 | 494 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 524 | 526 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 642 | 644 | PF00082 | 0.554 |
CLV_PCSK_PC7_1 | 488 | 494 | PF00082 | 0.378 |
CLV_PCSK_PC7_1 | 639 | 645 | PF00082 | 0.553 |
CLV_PCSK_PC7_1 | 680 | 686 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.507 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.269 |
DEG_APCC_KENBOX_2 | 674 | 678 | PF00400 | 0.750 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.752 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.670 |
DOC_CKS1_1 | 396 | 401 | PF01111 | 0.576 |
DOC_CYCLIN_RxL_1 | 257 | 266 | PF00134 | 0.360 |
DOC_CYCLIN_yCln2_LP_2 | 480 | 486 | PF00134 | 0.369 |
DOC_MAPK_gen_1 | 203 | 212 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 450 | 458 | PF00069 | 0.319 |
DOC_PP1_RVXF_1 | 389 | 396 | PF00149 | 0.647 |
DOC_PP1_RVXF_1 | 522 | 529 | PF00149 | 0.574 |
DOC_PP2B_LxvP_1 | 480 | 483 | PF13499 | 0.369 |
DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.357 |
DOC_PP4_FxxP_1 | 332 | 335 | PF00568 | 0.636 |
DOC_PP4_MxPP_1 | 575 | 578 | PF00568 | 0.624 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.704 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 26 | 35 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 328 | 333 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 488 | 492 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 653 | 657 | PF00244 | 0.628 |
LIG_AP2alpha_2 | 129 | 131 | PF02296 | 0.623 |
LIG_BIR_III_4 | 236 | 240 | PF00653 | 0.359 |
LIG_BRCT_BRCA1_1 | 372 | 376 | PF00533 | 0.644 |
LIG_deltaCOP1_diTrp_1 | 153 | 157 | PF00928 | 0.304 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.304 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.396 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.327 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.269 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.799 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.367 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.223 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.207 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.632 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.580 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.403 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.574 |
LIG_FHA_2 | 671 | 677 | PF00498 | 0.681 |
LIG_LIR_Apic_2 | 244 | 250 | PF02991 | 0.361 |
LIG_LIR_Apic_2 | 330 | 335 | PF02991 | 0.639 |
LIG_LIR_Apic_2 | 394 | 399 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 153 | 162 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 306 | 315 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 343 | 350 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 398 | 409 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 428 | 434 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 514 | 523 | PF02991 | 0.578 |
LIG_LIR_LC3C_4 | 473 | 476 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 425 | 429 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 443 | 448 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.576 |
LIG_MYND_1 | 500 | 504 | PF01753 | 0.610 |
LIG_Pex14_1 | 145 | 149 | PF04695 | 0.635 |
LIG_Pex14_1 | 427 | 431 | PF04695 | 0.324 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.469 |
LIG_Pex14_2 | 356 | 360 | PF04695 | 0.604 |
LIG_Pex14_2 | 406 | 410 | PF04695 | 0.441 |
LIG_Pex14_2 | 423 | 427 | PF04695 | 0.237 |
LIG_Pex14_2 | 516 | 520 | PF04695 | 0.586 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.304 |
LIG_SH2_CRK | 309 | 313 | PF00017 | 0.304 |
LIG_SH2_NCK_1 | 396 | 400 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.297 |
LIG_SH2_STAT3 | 102 | 105 | PF00017 | 0.669 |
LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.729 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.669 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.570 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.620 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.644 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.601 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.691 |
LIG_SH3_3 | 702 | 708 | PF00018 | 0.706 |
LIG_SH3_3 | 754 | 760 | PF00018 | 0.750 |
LIG_SUMO_SIM_anti_2 | 303 | 309 | PF11976 | 0.304 |
LIG_SUMO_SIM_anti_2 | 455 | 460 | PF11976 | 0.316 |
LIG_SUMO_SIM_anti_2 | 473 | 479 | PF11976 | 0.201 |
LIG_SUMO_SIM_par_1 | 171 | 176 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 453 | 460 | PF11976 | 0.251 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.623 |
LIG_TYR_ITIM | 307 | 312 | PF00017 | 0.304 |
LIG_WRC_WIRS_1 | 264 | 269 | PF05994 | 0.378 |
LIG_WRC_WIRS_1 | 423 | 428 | PF05994 | 0.275 |
LIG_WRC_WIRS_1 | 441 | 446 | PF05994 | 0.302 |
MOD_CDK_SPK_2 | 131 | 136 | PF00069 | 0.692 |
MOD_CDK_SPxK_1 | 131 | 137 | PF00069 | 0.692 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.604 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.357 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.287 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.472 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.674 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.730 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.792 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.304 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.356 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.661 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.690 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.611 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.386 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.585 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.654 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.604 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.392 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.545 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.570 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.304 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.473 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.554 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.533 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.573 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.458 |
MOD_GlcNHglycan | 750 | 755 | PF01048 | 0.516 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.432 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.399 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.524 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.801 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.765 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.674 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.784 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.721 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.769 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.731 |
MOD_LATS_1 | 688 | 694 | PF00433 | 0.757 |
MOD_LATS_1 | 735 | 741 | PF00433 | 0.706 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.650 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.586 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.500 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.423 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.314 |
MOD_N-GLC_1 | 676 | 681 | PF02516 | 0.554 |
MOD_N-GLC_2 | 78 | 80 | PF02516 | 0.487 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.742 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.469 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.344 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.364 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.373 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.304 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.304 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.304 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.336 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.581 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.653 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.718 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.684 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.694 |
MOD_NEK2_2 | 144 | 149 | PF00069 | 0.593 |
MOD_NEK2_2 | 256 | 261 | PF00069 | 0.290 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.662 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.601 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.701 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.656 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.569 |
MOD_PIKK_1 | 556 | 562 | PF00454 | 0.634 |
MOD_PIKK_1 | 703 | 709 | PF00454 | 0.705 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.302 |
MOD_PKA_1 | 684 | 690 | PF00069 | 0.757 |
MOD_PKA_1 | 731 | 737 | PF00069 | 0.647 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.615 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.269 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.722 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.357 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.574 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.664 |
MOD_PKA_2 | 684 | 690 | PF00069 | 0.757 |
MOD_PKA_2 | 731 | 737 | PF00069 | 0.732 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.709 |
MOD_PKB_1 | 643 | 651 | PF00069 | 0.708 |
MOD_PKB_1 | 682 | 690 | PF00069 | 0.743 |
MOD_PKB_1 | 729 | 737 | PF00069 | 0.662 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.740 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.504 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.378 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.547 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.356 |
MOD_Plk_2-3 | 548 | 554 | PF00069 | 0.646 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.597 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.343 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.366 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.332 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.346 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.238 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.249 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.644 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.334 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.294 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.608 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.672 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.668 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.673 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.624 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.692 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.705 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.598 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.581 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.562 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.696 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.681 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.736 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.785 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 519 | 526 | PF00179 | 0.573 |
TRG_DiLeu_BaEn_1 | 473 | 478 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 135 | 137 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 643 | 645 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 682 | 685 | PF00400 | 0.737 |
TRG_ER_diArg_1 | 727 | 730 | PF00400 | 0.704 |
TRG_NLS_MonoCore_2 | 641 | 646 | PF00514 | 0.753 |
TRG_NLS_MonoExtN_4 | 639 | 646 | PF00514 | 0.753 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I288 | Leptomonas seymouri | 52% | 91% |
A0A3S7WP32 | Leishmania donovani | 87% | 100% |
A4H4A9 | Leishmania braziliensis | 65% | 99% |
A4HSI0 | Leishmania infantum | 87% | 100% |
Q4QJE4 | Leishmania major | 85% | 100% |