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 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A0A3S7WPU2
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 | 109 | 113 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 582 | 586 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 592 | 596 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 676 | 680 | PF00656 | 0.643 |
CLV_MEL_PAP_1 | 39 | 45 | PF00089 | 0.336 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 771 | 773 | PF00675 | 0.455 |
CLV_PCSK_FUR_1 | 555 | 559 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 771 | 773 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.239 |
CLV_PCSK_PC7_1 | 29 | 35 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.338 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.544 |
DEG_SCF_FBW7_2 | 489 | 495 | PF00400 | 0.470 |
DEG_SPOP_SBC_1 | 101 | 105 | PF00917 | 0.606 |
DEG_SPOP_SBC_1 | 307 | 311 | PF00917 | 0.711 |
DOC_ANK_TNKS_1 | 107 | 114 | PF00023 | 0.637 |
DOC_CKS1_1 | 489 | 494 | PF01111 | 0.474 |
DOC_MAPK_gen_1 | 159 | 167 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 33 | 41 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 34 | 43 | PF00069 | 0.498 |
DOC_MAPK_RevD_3 | 8 | 24 | PF00069 | 0.547 |
DOC_PP2B_LxvP_1 | 300 | 303 | PF13499 | 0.540 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.604 |
DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.596 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.236 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.606 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.708 |
LIG_14-3-3_CanoR_1 | 255 | 262 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 33 | 41 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 404 | 413 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 446 | 450 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 613 | 621 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 626 | 632 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 651 | 661 | PF00244 | 0.758 |
LIG_14-3-3_CanoR_1 | 674 | 684 | PF00244 | 0.720 |
LIG_Actin_WH2_2 | 753 | 769 | PF00022 | 0.615 |
LIG_BIR_III_2 | 337 | 341 | PF00653 | 0.648 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.488 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.699 |
LIG_Clathr_ClatBox_1 | 361 | 365 | PF01394 | 0.504 |
LIG_deltaCOP1_diTrp_1 | 112 | 122 | PF00928 | 0.560 |
LIG_deltaCOP1_diTrp_1 | 371 | 374 | PF00928 | 0.568 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.570 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.553 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.514 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.629 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.813 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.755 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.632 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.472 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.471 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.742 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.547 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.685 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.694 |
LIG_FHA_2 | 674 | 680 | PF00498 | 0.797 |
LIG_FXI_DFP_1 | 177 | 181 | PF00024 | 0.304 |
LIG_Integrin_RGD_1 | 731 | 733 | PF01839 | 0.436 |
LIG_LIR_Apic_2 | 112 | 118 | PF02991 | 0.583 |
LIG_LIR_Apic_2 | 273 | 277 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 120 | 126 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 178 | 188 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 293 | 302 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 471 | 481 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.476 |
LIG_PCNA_PIPBox_1 | 658 | 667 | PF02747 | 0.683 |
LIG_Pex14_2 | 370 | 374 | PF04695 | 0.566 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.523 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.351 |
LIG_SH2_NCK_1 | 188 | 192 | PF00017 | 0.504 |
LIG_SH2_NCK_1 | 512 | 516 | PF00017 | 0.357 |
LIG_SH2_NCK_1 | 67 | 71 | PF00017 | 0.666 |
LIG_SH2_SRC | 188 | 191 | PF00017 | 0.472 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.664 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 394 | 398 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 512 | 516 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 545 | 549 | PF00017 | 0.566 |
LIG_SH2_STAT3 | 773 | 776 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.351 |
LIG_SH3_1 | 486 | 492 | PF00018 | 0.291 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.604 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.549 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.630 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.758 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.533 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.351 |
LIG_SH3_3 | 680 | 686 | PF00018 | 0.665 |
LIG_SH3_3 | 738 | 744 | PF00018 | 0.741 |
LIG_Sin3_3 | 481 | 488 | PF02671 | 0.313 |
LIG_SUMO_SIM_anti_2 | 9 | 14 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 360 | 366 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 685 | 690 | PF11976 | 0.643 |
LIG_SUMO_SIM_par_1 | 708 | 713 | PF11976 | 0.664 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.472 |
LIG_TYR_ITIM | 382 | 387 | PF00017 | 0.381 |
LIG_UBA3_1 | 148 | 152 | PF00899 | 0.351 |
LIG_WRC_WIRS_1 | 271 | 276 | PF05994 | 0.499 |
LIG_WRC_WIRS_1 | 55 | 60 | PF05994 | 0.427 |
MOD_CDC14_SPxK_1 | 690 | 693 | PF00782 | 0.569 |
MOD_CDK_SPK_2 | 328 | 333 | PF00069 | 0.545 |
MOD_CDK_SPxK_1 | 687 | 693 | PF00069 | 0.573 |
MOD_CDK_SPxxK_3 | 328 | 335 | PF00069 | 0.546 |
MOD_CDK_SPxxK_3 | 342 | 349 | PF00069 | 0.511 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.514 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.424 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.658 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.443 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.668 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.537 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.744 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.459 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.647 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.671 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.530 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.788 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.313 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.311 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.359 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.473 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.615 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.628 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.681 |
MOD_CMANNOS | 348 | 351 | PF00535 | 0.384 |
MOD_CMANNOS | 403 | 406 | PF00535 | 0.429 |
MOD_Cter_Amidation | 169 | 172 | PF01082 | 0.283 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.454 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.351 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.438 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.699 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.347 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.700 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.612 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.351 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.578 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.641 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.720 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.722 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.620 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.654 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.507 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.658 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.788 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.496 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.513 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.779 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.641 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.534 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.437 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.748 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.695 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.663 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.567 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.673 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.783 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.727 |
MOD_N-GLC_1 | 571 | 576 | PF02516 | 0.575 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.313 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.395 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.615 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.435 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.584 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.653 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.258 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.447 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.425 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.429 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.459 |
MOD_PKA_1 | 159 | 165 | PF00069 | 0.341 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.553 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.285 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.357 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.515 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.583 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.569 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.564 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.537 |
MOD_PKA_2 | 625 | 631 | PF00069 | 0.559 |
MOD_PKA_2 | 673 | 679 | PF00069 | 0.672 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.630 |
MOD_PKB_1 | 649 | 657 | PF00069 | 0.614 |
MOD_PKB_1 | 772 | 780 | PF00069 | 0.581 |
MOD_Plk_2-3 | 360 | 366 | PF00069 | 0.425 |
MOD_Plk_2-3 | 566 | 572 | PF00069 | 0.608 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.371 |
MOD_Plk_4 | 576 | 582 | PF00069 | 0.601 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.292 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.546 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.615 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.470 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.645 |
MOD_SUMO_rev_2 | 69 | 78 | PF00179 | 0.563 |
MOD_SUMO_rev_2 | 763 | 769 | PF00179 | 0.536 |
TRG_AP2beta_CARGO_1 | 120 | 129 | PF09066 | 0.319 |
TRG_DiLeu_BaEn_3 | 764 | 770 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 377 | 382 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 633 | 638 | PF01217 | 0.543 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.292 |
TRG_ER_diArg_1 | 159 | 161 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 264 | 267 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 458 | 461 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 540 | 542 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 554 | 557 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 649 | 651 | PF00400 | 0.754 |
TRG_ER_diArg_1 | 770 | 772 | PF00400 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 18 | 22 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6E0 | Leptomonas seymouri | 39% | 100% |
A0A1X0NPA0 | Trypanosomatidae | 31% | 100% |
A4H4X9 | Leishmania braziliensis | 64% | 100% |
A4HT52 | Leishmania infantum | 99% | 100% |
E9AL44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4QIR0 | Leishmania major | 88% | 100% |