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: 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: A0A3S5H7D6
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 | 106 | 108 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.775 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 711 | 713 | PF00675 | 0.600 |
CLV_PCSK_FUR_1 | 104 | 108 | PF00082 | 0.706 |
CLV_PCSK_FUR_1 | 243 | 247 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.775 |
CLV_PCSK_KEX2_1 | 710 | 712 | PF00082 | 0.669 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 710 | 712 | PF00082 | 0.669 |
CLV_PCSK_PC7_1 | 242 | 248 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.466 |
DEG_APCC_DBOX_1 | 247 | 255 | PF00400 | 0.612 |
DEG_APCC_DBOX_1 | 265 | 273 | PF00400 | 0.271 |
DEG_APCC_DBOX_1 | 381 | 389 | PF00400 | 0.326 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.669 |
DEG_SCF_FBW7_1 | 527 | 533 | PF00400 | 0.378 |
DOC_CKS1_1 | 223 | 228 | PF01111 | 0.462 |
DOC_CKS1_1 | 527 | 532 | PF01111 | 0.373 |
DOC_CYCLIN_RxL_1 | 138 | 148 | PF00134 | 0.393 |
DOC_MAPK_gen_1 | 151 | 158 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 241 | 253 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 151 | 158 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 245 | 254 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 409 | 416 | PF00069 | 0.381 |
DOC_MAPK_NFAT4_5 | 151 | 159 | PF00069 | 0.440 |
DOC_PP2B_PxIxI_1 | 249 | 255 | PF00149 | 0.395 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.415 |
DOC_PP4_FxxP_1 | 524 | 527 | PF00568 | 0.395 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.294 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.570 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.395 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 110 | 119 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 121 | 130 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.232 |
LIG_14-3-3_CanoR_1 | 425 | 430 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 609 | 619 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 636 | 643 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 711 | 716 | PF00244 | 0.625 |
LIG_BIR_III_2 | 485 | 489 | PF00653 | 0.553 |
LIG_BRCT_BRCA1_1 | 631 | 635 | PF00533 | 0.510 |
LIG_BRCT_BRCA1_1 | 637 | 641 | PF00533 | 0.409 |
LIG_Clathr_ClatBox_1 | 251 | 255 | PF01394 | 0.377 |
LIG_deltaCOP1_diTrp_1 | 519 | 524 | PF00928 | 0.401 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.809 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.493 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.389 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.378 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.381 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.511 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.617 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.428 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.480 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.708 |
LIG_LIR_Apic_2 | 222 | 226 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 289 | 295 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 319 | 325 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 44 | 51 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 519 | 527 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 529 | 539 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 319 | 323 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 519 | 524 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.381 |
LIG_NRBOX | 268 | 274 | PF00104 | 0.417 |
LIG_PTB_Apo_2 | 134 | 141 | PF02174 | 0.375 |
LIG_SH2_CRK | 391 | 395 | PF00017 | 0.393 |
LIG_SH2_CRK | 532 | 536 | PF00017 | 0.431 |
LIG_SH2_CRK | 668 | 672 | PF00017 | 0.459 |
LIG_SH2_NCK_1 | 532 | 536 | PF00017 | 0.416 |
LIG_SH2_SRC | 389 | 392 | PF00017 | 0.341 |
LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 664 | 667 | PF00017 | 0.401 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.607 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.391 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.413 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.599 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.394 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.330 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.716 |
LIG_SH3_3 | 624 | 630 | PF00018 | 0.574 |
LIG_SUMO_SIM_anti_2 | 211 | 217 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 413 | 418 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 556 | 561 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 249 | 255 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 281 | 286 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 654 | 661 | PF11976 | 0.367 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.527 |
LIG_TRAF2_1 | 87 | 90 | PF00917 | 0.633 |
LIG_UBA3_1 | 678 | 685 | PF00899 | 0.431 |
LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.394 |
LIG_WRC_WIRS_1 | 317 | 322 | PF05994 | 0.464 |
MOD_CAAXbox | 713 | 716 | PF01239 | 0.667 |
MOD_CDK_SPK_2 | 182 | 187 | PF00069 | 0.568 |
MOD_CDK_SPK_2 | 283 | 288 | PF00069 | 0.369 |
MOD_CDK_SPxxK_3 | 626 | 633 | PF00069 | 0.488 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.688 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.614 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.604 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.637 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.489 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.458 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.467 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.571 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.644 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.644 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.484 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.540 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.626 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.598 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.473 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.753 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.648 |
MOD_DYRK1A_RPxSP_1 | 3 | 7 | PF00069 | 0.679 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.444 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.704 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.548 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.441 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.657 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.664 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.539 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.692 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.777 |
MOD_GlcNHglycan | 541 | 545 | PF01048 | 0.418 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.616 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.586 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.364 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.494 |
MOD_GlcNHglycan | 75 | 79 | PF01048 | 0.600 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.538 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.630 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.579 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.662 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.544 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.589 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.580 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.472 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.494 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.616 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.529 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.570 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.378 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.498 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.578 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.287 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.498 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.616 |
MOD_LATS_1 | 423 | 429 | PF00433 | 0.544 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.661 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.564 |
MOD_N-GLC_1 | 331 | 336 | PF02516 | 0.583 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.629 |
MOD_N-GLC_2 | 136 | 138 | PF02516 | 0.329 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.682 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.413 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.505 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.377 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.415 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.490 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.632 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.430 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.350 |
MOD_NEK2_2 | 612 | 617 | PF00069 | 0.649 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.566 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.427 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.582 |
MOD_PKA_1 | 106 | 112 | PF00069 | 0.658 |
MOD_PKA_1 | 241 | 247 | PF00069 | 0.503 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.663 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.523 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.507 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.620 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.480 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.442 |
MOD_PKB_1 | 104 | 112 | PF00069 | 0.704 |
MOD_PKB_1 | 121 | 129 | PF00069 | 0.492 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.569 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.517 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.528 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.495 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.549 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.535 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.423 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.633 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.737 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.534 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.397 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.367 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.746 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.431 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.612 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.672 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.414 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.595 |
MOD_SUMO_rev_2 | 159 | 165 | PF00179 | 0.571 |
MOD_SUMO_rev_2 | 319 | 329 | PF00179 | 0.438 |
TRG_DiLeu_BaEn_1 | 258 | 263 | PF01217 | 0.395 |
TRG_DiLeu_BaEn_2 | 378 | 384 | PF01217 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 247 | 252 | PF01217 | 0.417 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 242 | 245 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.460 |
TRG_NES_CRM1_1 | 680 | 691 | PF08389 | 0.478 |
TRG_NLS_MonoCore_2 | 708 | 713 | PF00514 | 0.623 |
TRG_NLS_MonoExtC_3 | 240 | 245 | PF00514 | 0.465 |
TRG_NLS_MonoExtN_4 | 709 | 714 | PF00514 | 0.661 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCV4 | Leptomonas seymouri | 49% | 100% |
A4HDQ5 | Leishmania braziliensis | 68% | 98% |
A4I101 | Leishmania infantum | 100% | 100% |
E9AX39 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QAD7 | Leishmania major | 93% | 100% |