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: 0 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9AL44
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006163 | purine nucleotide metabolic process | 5 | 1 |
GO:0006195 | purine nucleotide catabolic process | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009117 | nucleotide metabolic process | 5 | 1 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 1 |
GO:0009154 | purine ribonucleotide catabolic process | 6 | 1 |
GO:0009166 | nucleotide catabolic process | 6 | 1 |
GO:0009259 | ribonucleotide metabolic process | 5 | 1 |
GO:0009261 | ribonucleotide catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015936 | coenzyme A metabolic process | 6 | 1 |
GO:0015938 | coenzyme A catabolic process | 7 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0019693 | ribose phosphate metabolic process | 4 | 1 |
GO:0033865 | nucleoside bisphosphate metabolic process | 5 | 1 |
GO:0033869 | nucleoside bisphosphate catabolic process | 6 | 1 |
GO:0033875 | ribonucleoside bisphosphate metabolic process | 6 | 1 |
GO:0034031 | ribonucleoside bisphosphate catabolic process | 7 | 1 |
GO:0034032 | purine nucleoside bisphosphate metabolic process | 5 | 1 |
GO:0034034 | purine nucleoside bisphosphate catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072521 | purine-containing compound metabolic process | 4 | 1 |
GO:0072523 | purine-containing compound catabolic process | 5 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901136 | carbohydrate derivative catabolic process | 4 | 1 |
GO:1901292 | nucleoside phosphate catabolic process | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0010945 | CoA pyrophosphatase activity | 6 | 8 |
GO:0016462 | pyrophosphatase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 8 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 8 |
GO:0003986 | acetyl-CoA hydrolase activity | 6 | 1 |
GO:0016289 | CoA hydrolase activity | 5 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016790 | thiolester hydrolase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 427 | 431 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 573 | 577 | PF00656 | 0.672 |
CLV_C14_Caspase3-7 | 583 | 587 | PF00656 | 0.689 |
CLV_MEL_PAP_1 | 39 | 45 | PF00089 | 0.343 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 762 | 764 | PF00675 | 0.472 |
CLV_PCSK_FUR_1 | 451 | 455 | PF00082 | 0.308 |
CLV_PCSK_FUR_1 | 546 | 550 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 640 | 642 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 722 | 724 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 762 | 764 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.244 |
CLV_PCSK_PC7_1 | 449 | 455 | PF00082 | 0.311 |
CLV_PCSK_PC7_1 | 528 | 534 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 691 | 695 | PF00082 | 0.488 |
CLV_Separin_Metazoa | 621 | 625 | PF03568 | 0.611 |
DEG_SCF_FBW7_1 | 293 | 300 | PF00400 | 0.569 |
DEG_SCF_FBW7_2 | 479 | 486 | PF00400 | 0.470 |
DEG_SCF_FBW7_2 | 578 | 583 | PF00400 | 0.595 |
DEG_SPOP_SBC_1 | 298 | 302 | PF00917 | 0.764 |
DEG_SPOP_SBC_1 | 685 | 689 | PF00917 | 0.647 |
DEG_SPOP_SBC_1 | 766 | 770 | PF00917 | 0.604 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.626 |
DOC_CKS1_1 | 294 | 299 | PF01111 | 0.574 |
DOC_CKS1_1 | 480 | 485 | PF01111 | 0.482 |
DOC_MAPK_gen_1 | 150 | 158 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 33 | 41 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 34 | 43 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 752 | 761 | PF00069 | 0.617 |
DOC_PP2B_LxvP_1 | 291 | 294 | PF13499 | 0.563 |
DOC_PP2B_LxvP_1 | 477 | 480 | PF13499 | 0.253 |
DOC_PP4_FxxP_1 | 265 | 268 | PF00568 | 0.607 |
DOC_PP4_FxxP_1 | 361 | 364 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.620 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 33 | 41 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 395 | 404 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 437 | 442 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 617 | 623 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 642 | 652 | PF00244 | 0.794 |
LIG_14-3-3_CanoR_1 | 684 | 692 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 84 | 91 | PF00244 | 0.619 |
LIG_Actin_WH2_2 | 609 | 626 | PF00022 | 0.596 |
LIG_Actin_WH2_2 | 744 | 760 | PF00022 | 0.632 |
LIG_BRCT_BRCA1_1 | 81 | 85 | PF00533 | 0.664 |
LIG_Clathr_ClatBox_1 | 352 | 356 | PF01394 | 0.497 |
LIG_deltaCOP1_diTrp_1 | 104 | 113 | PF00928 | 0.557 |
LIG_deltaCOP1_diTrp_1 | 362 | 365 | PF00928 | 0.575 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.581 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.494 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.287 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.631 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.816 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.483 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.481 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.747 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.545 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.504 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.688 |
LIG_FHA_2 | 685 | 691 | PF00498 | 0.627 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.641 |
LIG_FHA_2 | 716 | 722 | PF00498 | 0.610 |
LIG_FXI_DFP_1 | 168 | 172 | PF00024 | 0.317 |
LIG_HCF-1_HBM_1 | 713 | 716 | PF13415 | 0.612 |
LIG_Integrin_RGD_1 | 326 | 328 | PF01839 | 0.418 |
LIG_LIR_Apic_2 | 104 | 109 | PF02991 | 0.576 |
LIG_LIR_Apic_2 | 264 | 268 | PF02991 | 0.612 |
LIG_LIR_Apic_2 | 589 | 594 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 191 | 199 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 462 | 472 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 496 | 505 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 284 | 288 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 462 | 468 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 496 | 500 | PF02991 | 0.252 |
LIG_MAD2 | 758 | 766 | PF02301 | 0.590 |
LIG_NBox_RRM_1 | 491 | 501 | PF00076 | 0.188 |
LIG_Pex14_2 | 361 | 365 | PF04695 | 0.573 |
LIG_SH2_CRK | 375 | 379 | PF00017 | 0.532 |
LIG_SH2_CRK | 465 | 469 | PF00017 | 0.360 |
LIG_SH2_NCK_1 | 179 | 183 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 503 | 507 | PF00017 | 0.376 |
LIG_SH2_NCK_1 | 67 | 71 | PF00017 | 0.682 |
LIG_SH2_SRC | 179 | 182 | PF00017 | 0.483 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.680 |
LIG_SH2_STAP1 | 385 | 389 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.360 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.540 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.550 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.594 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.696 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.571 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.360 |
LIG_SH3_3 | 729 | 735 | PF00018 | 0.757 |
LIG_SUMO_SIM_anti_2 | 9 | 14 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 351 | 357 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 475 | 482 | PF11976 | 0.195 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.483 |
LIG_TYR_ITIM | 373 | 378 | PF00017 | 0.532 |
LIG_UBA3_1 | 139 | 143 | PF00899 | 0.506 |
LIG_WRC_WIRS_1 | 262 | 267 | PF05994 | 0.616 |
LIG_WRC_WIRS_1 | 488 | 493 | PF05994 | 0.274 |
LIG_WRC_WIRS_1 | 55 | 60 | PF05994 | 0.562 |
MOD_CDC14_SPxK_1 | 681 | 684 | PF00782 | 0.650 |
MOD_CDK_SPxK_1 | 576 | 582 | PF00069 | 0.596 |
MOD_CDK_SPxK_1 | 678 | 684 | PF00069 | 0.653 |
MOD_CDK_SPxxK_3 | 333 | 340 | PF00069 | 0.583 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.576 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.680 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.574 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.717 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.700 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.768 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.595 |
MOD_CK1_1 | 683 | 689 | PF00069 | 0.736 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.635 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.761 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.483 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.481 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.504 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.634 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.577 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.691 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.703 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.639 |
MOD_CK2_1 | 715 | 721 | PF00069 | 0.620 |
MOD_CMANNOS | 339 | 342 | PF00535 | 0.354 |
MOD_CMANNOS | 394 | 397 | PF00535 | 0.357 |
MOD_CMANNOS | 590 | 593 | PF00535 | 0.430 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.306 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.378 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.497 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.300 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.360 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.510 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.531 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.461 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.567 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.571 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.408 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.613 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.559 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.432 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.513 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.400 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.730 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.635 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.724 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.691 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.566 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.699 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.615 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.721 |
MOD_GSK3_1 | 692 | 699 | PF00069 | 0.678 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.733 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.483 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.533 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.715 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.556 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.799 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.576 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.440 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.574 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.563 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.547 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.588 |
MOD_PKA_1 | 150 | 156 | PF00069 | 0.505 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.441 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.458 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.517 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.616 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.690 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.654 |
MOD_PKA_2 | 683 | 689 | PF00069 | 0.643 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.689 |
MOD_Plk_2-3 | 351 | 357 | PF00069 | 0.547 |
MOD_Plk_2-3 | 557 | 563 | PF00069 | 0.689 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.552 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.635 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.699 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.686 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.463 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.560 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.677 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.477 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.582 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.609 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.615 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.715 |
MOD_SUMO_rev_2 | 750 | 760 | PF00179 | 0.659 |
TRG_DiLeu_BaLyEn_6 | 368 | 373 | PF01217 | 0.579 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.300 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 449 | 452 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 453 | 455 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 531 | 533 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.737 |
TRG_ER_diArg_1 | 640 | 642 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 761 | 763 | PF00400 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.188 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6E0 | Leptomonas seymouri | 40% | 100% |
A0A1X0NPA0 | Trypanosomatidae | 34% | 100% |
A0A3S7WPU2 | Leishmania donovani | 83% | 99% |
A4H4X9 | Leishmania braziliensis | 63% | 100% |
A4HT52 | Leishmania infantum | 84% | 84% |
Q4QIR0 | Leishmania major | 81% | 100% |