Uncharacterized Protein, 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) | yes | yes: 3 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4I101
Term | Name | Level | Count |
---|---|---|---|
GO:0006066 | alcohol metabolic process | 3 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0019751 | polyol metabolic process | 4 | 7 |
GO:0032957 | inositol trisphosphate metabolic process | 5 | 7 |
GO:0043647 | inositol phosphate metabolic process | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044281 | small molecule metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 7 |
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006020 | inositol metabolic process | 4 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 1 |
GO:0046835 | carbohydrate phosphorylation | 4 | 1 |
GO:0052746 | obsolete inositol phosphorylation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0000287 | magnesium ion binding | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0047325 | inositol tetrakisphosphate 1-kinase activity | 6 | 7 |
GO:0051765 | inositol tetrakisphosphate kinase activity | 5 | 7 |
GO:0051766 | inositol trisphosphate kinase activity | 5 | 7 |
GO:0052725 | inositol-1,3,4-trisphosphate 6-kinase activity | 6 | 7 |
GO:0052726 | inositol-1,3,4-trisphosphate 5-kinase activity | 6 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.673 |
CLV_PCSK_FUR_1 | 238 | 242 | PF00082 | 0.447 |
CLV_PCSK_FUR_1 | 99 | 103 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.823 |
CLV_PCSK_PC1ET2_1 | 236 | 238 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 705 | 707 | PF00082 | 0.688 |
CLV_PCSK_PC7_1 | 237 | 243 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.487 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.609 |
DEG_APCC_DBOX_1 | 260 | 268 | PF00400 | 0.300 |
DEG_APCC_DBOX_1 | 376 | 384 | PF00400 | 0.347 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.680 |
DEG_SCF_FBW7_1 | 522 | 528 | PF00400 | 0.399 |
DOC_CKS1_1 | 218 | 223 | PF01111 | 0.483 |
DOC_CKS1_1 | 522 | 527 | PF01111 | 0.408 |
DOC_CYCLIN_RxL_1 | 133 | 143 | PF00134 | 0.415 |
DOC_MAPK_gen_1 | 146 | 153 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 236 | 248 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 146 | 153 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 240 | 249 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 404 | 411 | PF00069 | 0.443 |
DOC_MAPK_NFAT4_5 | 146 | 154 | PF00069 | 0.461 |
DOC_PP2B_PxIxI_1 | 244 | 250 | PF00149 | 0.417 |
DOC_PP4_FxxP_1 | 218 | 221 | PF00568 | 0.435 |
DOC_PP4_FxxP_1 | 519 | 522 | PF00568 | 0.419 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.591 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.398 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.591 |
LIG_14-3-3_CanoR_1 | 105 | 114 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 116 | 125 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 136 | 141 | PF00244 | 0.253 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 604 | 614 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 631 | 638 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 706 | 711 | PF00244 | 0.772 |
LIG_BIR_III_2 | 480 | 484 | PF00653 | 0.562 |
LIG_BRCT_BRCA1_1 | 626 | 630 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 632 | 636 | PF00533 | 0.436 |
LIG_Clathr_ClatBox_1 | 246 | 250 | PF01394 | 0.398 |
LIG_deltaCOP1_diTrp_1 | 514 | 519 | PF00928 | 0.424 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.828 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.523 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.404 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.399 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.400 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.634 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.405 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.471 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.703 |
LIG_LIR_Apic_2 | 217 | 221 | PF02991 | 0.431 |
LIG_LIR_Apic_2 | 284 | 290 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 314 | 320 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 39 | 46 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 514 | 522 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 524 | 534 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 514 | 519 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.401 |
LIG_NRBOX | 263 | 269 | PF00104 | 0.392 |
LIG_PTB_Apo_2 | 129 | 136 | PF02174 | 0.398 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.416 |
LIG_SH2_CRK | 527 | 531 | PF00017 | 0.451 |
LIG_SH2_CRK | 663 | 667 | PF00017 | 0.453 |
LIG_SH2_NCK_1 | 527 | 531 | PF00017 | 0.436 |
LIG_SH2_SRC | 384 | 387 | PF00017 | 0.363 |
LIG_SH2_STAT3 | 142 | 145 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 659 | 662 | PF00017 | 0.453 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.410 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.450 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.616 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.427 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.353 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.795 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.575 |
LIG_SUMO_SIM_anti_2 | 206 | 212 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 408 | 413 | PF11976 | 0.417 |
LIG_SUMO_SIM_anti_2 | 551 | 556 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 244 | 250 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 276 | 281 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 649 | 656 | PF11976 | 0.391 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.542 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.644 |
LIG_UBA3_1 | 673 | 680 | PF00899 | 0.501 |
LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.413 |
LIG_WRC_WIRS_1 | 312 | 317 | PF05994 | 0.485 |
MOD_CAAXbox | 708 | 711 | PF01239 | 0.681 |
MOD_CDK_SPK_2 | 177 | 182 | PF00069 | 0.581 |
MOD_CDK_SPK_2 | 278 | 283 | PF00069 | 0.392 |
MOD_CDK_SPxxK_3 | 621 | 628 | PF00069 | 0.490 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.739 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.534 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.691 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.574 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.515 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.475 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.464 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.580 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.668 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.650 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.496 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.578 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.650 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.615 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.465 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.693 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.639 |
MOD_DYRK1A_RPxSP_1 | 3 | 7 | PF00069 | 0.705 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.407 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.737 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.589 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.583 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.786 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.563 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.553 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.710 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.689 |
MOD_GlcNHglycan | 536 | 540 | PF01048 | 0.431 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.624 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.523 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.601 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.380 |
MOD_GlcNHglycan | 70 | 74 | PF01048 | 0.633 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.655 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.653 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.601 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.612 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.683 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.613 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.629 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.464 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.515 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.631 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.526 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.590 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.431 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.510 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.589 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.307 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.567 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.648 |
MOD_LATS_1 | 418 | 424 | PF00433 | 0.535 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.663 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.594 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.579 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.628 |
MOD_N-GLC_2 | 131 | 133 | PF02516 | 0.351 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.825 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.426 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.594 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.397 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.433 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.513 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.630 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.445 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.373 |
MOD_NEK2_2 | 607 | 612 | PF00069 | 0.668 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.579 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.447 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.596 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.669 |
MOD_PKA_1 | 236 | 242 | PF00069 | 0.531 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.671 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.547 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.531 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.677 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.474 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.470 |
MOD_PKB_1 | 116 | 124 | PF00069 | 0.516 |
MOD_PKB_1 | 99 | 107 | PF00069 | 0.714 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.545 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.550 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.463 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.572 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.434 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.443 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.658 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.658 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.418 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.391 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.805 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.457 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.615 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.589 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.410 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.590 |
MOD_SUMO_rev_2 | 154 | 160 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 314 | 324 | PF00179 | 0.449 |
TRG_DiLeu_BaEn_1 | 253 | 258 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_2 | 373 | 379 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 242 | 247 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.469 |
TRG_ER_diArg_1 | 146 | 149 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.675 |
TRG_NES_CRM1_1 | 675 | 686 | PF08389 | 0.497 |
TRG_NLS_MonoCore_2 | 703 | 708 | PF00514 | 0.641 |
TRG_NLS_MonoExtC_3 | 235 | 240 | PF00514 | 0.493 |
TRG_NLS_MonoExtN_4 | 704 | 709 | PF00514 | 0.675 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 377 | 381 | PF00026 | 0.358 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCV4 | Leptomonas seymouri | 49% | 100% |
A0A3S5H7D6 | Leishmania donovani | 100% | 99% |
A4HDQ5 | Leishmania braziliensis | 69% | 98% |
E9AX39 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QAD7 | Leishmania major | 93% | 100% |