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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HDQ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006066 | alcohol metabolic process | 3 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0019751 | polyol metabolic process | 4 | 8 |
GO:0032957 | inositol trisphosphate metabolic process | 5 | 8 |
GO:0043647 | inositol phosphate metabolic process | 4 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044281 | small molecule metabolic process | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 8 |
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 | 8 |
GO:0000287 | magnesium ion binding | 5 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016301 | kinase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0047325 | inositol tetrakisphosphate 1-kinase activity | 6 | 8 |
GO:0051765 | inositol tetrakisphosphate kinase activity | 5 | 8 |
GO:0051766 | inositol trisphosphate kinase activity | 5 | 8 |
GO:0052725 | inositol-1,3,4-trisphosphate 6-kinase activity | 6 | 8 |
GO:0052726 | inositol-1,3,4-trisphosphate 5-kinase activity | 6 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 119 | 123 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.291 |
CLV_C14_Caspase3-7 | 152 | 156 | PF00656 | 0.401 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.702 |
CLV_PCSK_FUR_1 | 97 | 101 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 675 | 677 | PF00082 | 0.629 |
CLV_PCSK_PC7_1 | 95 | 101 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.531 |
DEG_APCC_DBOX_1 | 239 | 247 | PF00400 | 0.437 |
DEG_COP1_1 | 354 | 362 | PF00400 | 0.381 |
DEG_SCF_FBW7_1 | 472 | 478 | PF00400 | 0.392 |
DEG_SCF_FBW7_1 | 492 | 498 | PF00400 | 0.426 |
DEG_SCF_FBW7_1 | 569 | 576 | PF00400 | 0.544 |
DEG_SCF_TRCP1_1 | 152 | 157 | PF00400 | 0.413 |
DEG_SPOP_SBC_1 | 554 | 558 | PF00917 | 0.489 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.433 |
DOC_CKS1_1 | 303 | 308 | PF01111 | 0.345 |
DOC_CKS1_1 | 472 | 477 | PF01111 | 0.403 |
DOC_CKS1_1 | 492 | 497 | PF01111 | 0.423 |
DOC_CYCLIN_RxL_1 | 132 | 142 | PF00134 | 0.373 |
DOC_MAPK_DCC_7 | 237 | 246 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 171 | 180 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 233 | 243 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 237 | 246 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 400 | 407 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 416 | 425 | PF00069 | 0.502 |
DOC_PP1_RVXF_1 | 430 | 436 | PF00149 | 0.335 |
DOC_PP4_FxxP_1 | 215 | 218 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 489 | 492 | PF00568 | 0.444 |
DOC_SPAK_OSR1_1 | 373 | 377 | PF12202 | 0.248 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.628 |
DOC_USP7_UBL2_3 | 229 | 233 | PF12436 | 0.349 |
DOC_USP7_UBL2_3 | 671 | 675 | PF12436 | 0.482 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 416 | 425 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 447 | 455 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 464 | 472 | PF00244 | 0.525 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.710 |
LIG_BIR_III_4 | 65 | 69 | PF00653 | 0.499 |
LIG_BRCT_BRCA1_1 | 288 | 292 | PF00533 | 0.439 |
LIG_BRCT_BRCA1_1 | 310 | 314 | PF00533 | 0.363 |
LIG_BRCT_BRCA1_1 | 602 | 606 | PF00533 | 0.398 |
LIG_Clathr_ClatBox_1 | 243 | 247 | PF01394 | 0.404 |
LIG_deltaCOP1_diTrp_1 | 225 | 230 | PF00928 | 0.288 |
LIG_deltaCOP1_diTrp_1 | 484 | 490 | PF00928 | 0.414 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.672 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.459 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.306 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.326 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.426 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.367 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.617 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.545 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.356 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.334 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.619 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.473 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.638 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.371 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.519 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.614 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.433 |
LIG_LIR_Apic_2 | 214 | 218 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 281 | 287 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 487 | 492 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 142 | 150 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 225 | 231 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 311 | 320 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 34 | 41 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 473 | 483 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 484 | 492 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 603 | 613 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 34 | 38 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 484 | 489 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 508 | 513 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 548 | 554 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 603 | 609 | PF02991 | 0.325 |
LIG_MYND_1 | 569 | 573 | PF01753 | 0.539 |
LIG_MYND_1 | 593 | 597 | PF01753 | 0.455 |
LIG_Pex14_1 | 486 | 490 | PF04695 | 0.330 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.302 |
LIG_PTB_Apo_2 | 128 | 135 | PF02174 | 0.419 |
LIG_PTB_Phospho_1 | 135 | 141 | PF10480 | 0.304 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.380 |
LIG_SH2_CRK | 510 | 514 | PF00017 | 0.352 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.462 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.476 |
LIG_SH2_SRC | 380 | 383 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.298 |
LIG_SH2_STAT3 | 141 | 144 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 629 | 632 | PF00017 | 0.366 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.511 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.415 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.394 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.427 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.436 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.445 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.382 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.557 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.686 |
LIG_SUMO_SIM_anti_2 | 202 | 209 | PF11976 | 0.397 |
LIG_SUMO_SIM_anti_2 | 521 | 526 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 176 | 182 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 241 | 247 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 273 | 278 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 422 | 429 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 619 | 626 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 645 | 651 | PF11976 | 0.415 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.500 |
LIG_TYR_ITIM | 549 | 554 | PF00017 | 0.537 |
LIG_UBA3_1 | 264 | 272 | PF00899 | 0.353 |
LIG_UBA3_1 | 643 | 650 | PF00899 | 0.421 |
LIG_WRC_WIRS_1 | 212 | 217 | PF05994 | 0.418 |
LIG_WRC_WIRS_1 | 309 | 314 | PF05994 | 0.440 |
MOD_CAAXbox | 678 | 681 | PF01239 | 0.630 |
MOD_CDK_SPK_2 | 275 | 280 | PF00069 | 0.358 |
MOD_CDK_SPK_2 | 569 | 574 | PF00069 | 0.542 |
MOD_CDK_SPK_2 | 90 | 95 | PF00069 | 0.535 |
MOD_CDK_SPxxK_3 | 90 | 97 | PF00069 | 0.540 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.792 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.480 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.448 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.781 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.514 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.432 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.634 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.577 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.627 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.678 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.795 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.590 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.734 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.427 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.662 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.533 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.372 |
MOD_DYRK1A_RPxSP_1 | 90 | 94 | PF00069 | 0.531 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.542 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.618 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.532 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.738 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.608 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.639 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.452 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.694 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.742 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.651 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.320 |
MOD_GlcNHglycan | 65 | 69 | PF01048 | 0.636 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.746 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.671 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.688 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.601 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.515 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.597 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.517 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.514 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.629 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.651 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.437 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.385 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.531 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.674 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.611 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.625 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.271 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.667 |
MOD_LATS_1 | 414 | 420 | PF00433 | 0.535 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.539 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.315 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.323 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.548 |
MOD_N-GLC_1 | 655 | 660 | PF02516 | 0.442 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.590 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.687 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.441 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.373 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.343 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.660 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.522 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.554 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.359 |
MOD_NEK2_2 | 577 | 582 | PF00069 | 0.668 |
MOD_NEK2_2 | 648 | 653 | PF00069 | 0.395 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.538 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.396 |
MOD_PK_1 | 176 | 182 | PF00069 | 0.502 |
MOD_PK_1 | 286 | 292 | PF00069 | 0.411 |
MOD_PKA_1 | 233 | 239 | PF00069 | 0.457 |
MOD_PKA_1 | 99 | 105 | PF00069 | 0.693 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.457 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.479 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.630 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.545 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.508 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.529 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.629 |
MOD_PKA_2 | 607 | 613 | PF00069 | 0.412 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.690 |
MOD_PKB_1 | 97 | 105 | PF00069 | 0.682 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.545 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.551 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.546 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.532 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.337 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.407 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.386 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.511 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.537 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.429 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.356 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.678 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.464 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.416 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.424 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.617 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.577 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.576 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.609 |
MOD_SUMO_rev_2 | 168 | 172 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 266 | 274 | PF00179 | 0.362 |
TRG_DiLeu_BaEn_1 | 250 | 255 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_2 | 369 | 375 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.472 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 234 | 237 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.684 |
TRG_NES_CRM1_1 | 645 | 657 | PF08389 | 0.458 |
TRG_NLS_MonoExtC_3 | 232 | 237 | PF00514 | 0.424 |
TRG_NLS_MonoExtN_4 | 671 | 678 | PF00514 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 176 | 181 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 373 | 377 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 48 | 53 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCV4 | Leptomonas seymouri | 48% | 100% |
A0A1X0NVY7 | Trypanosomatidae | 30% | 100% |
A0A3S5H7D6 | Leishmania donovani | 68% | 95% |
A4I101 | Leishmania infantum | 69% | 96% |
E9AX39 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 98% |
Q4QAD7 | Leishmania major | 69% | 99% |