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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4H4X9
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 | 7 |
GO:0010945 | CoA pyrophosphatase activity | 6 | 7 |
GO:0016462 | pyrophosphatase activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 7 |
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 | 323 | 327 | PF00656 | 0.455 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.617 |
CLV_PCSK_FUR_1 | 422 | 426 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.456 |
CLV_PCSK_PC7_1 | 547 | 553 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.439 |
DEG_APCC_DBOX_1 | 284 | 292 | PF00400 | 0.300 |
DEG_COP1_1 | 607 | 616 | PF00400 | 0.637 |
DEG_SCF_FBW7_1 | 304 | 311 | PF00400 | 0.377 |
DEG_SCF_FBW7_1 | 689 | 695 | PF00400 | 0.653 |
DEG_SCF_FBW7_2 | 498 | 505 | PF00400 | 0.485 |
DEG_SPOP_SBC_1 | 309 | 313 | PF00917 | 0.570 |
DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.428 |
DOC_CKS1_1 | 305 | 310 | PF01111 | 0.383 |
DOC_CKS1_1 | 499 | 504 | PF01111 | 0.495 |
DOC_CKS1_1 | 689 | 694 | PF01111 | 0.653 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 122 | PF00134 | 0.290 |
DOC_CYCLIN_yCln2_LP_2 | 457 | 463 | PF00134 | 0.583 |
DOC_MAPK_DCC_7 | 722 | 732 | PF00069 | 0.640 |
DOC_MAPK_gen_1 | 796 | 803 | PF00069 | 0.631 |
DOC_MAPK_MEF2A_6 | 34 | 43 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 728 | 736 | PF00069 | 0.636 |
DOC_PP1_RVXF_1 | 190 | 196 | PF00149 | 0.217 |
DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.304 |
DOC_PP4_FxxP_1 | 276 | 279 | PF00568 | 0.432 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.384 |
DOC_PP4_FxxP_1 | 496 | 499 | PF00568 | 0.225 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 804 | 808 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.415 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.275 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 680 | 685 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 809 | 814 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 257 | 264 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 377 | 381 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 619 | 625 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 728 | 733 | PF00244 | 0.649 |
LIG_BIR_III_2 | 579 | 583 | PF00653 | 0.607 |
LIG_BRCT_BRCA1_1 | 220 | 224 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 774 | 778 | PF00533 | 0.623 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.515 |
LIG_CtBP_PxDLS_1 | 638 | 642 | PF00389 | 0.611 |
LIG_deltaCOP1_diTrp_1 | 159 | 169 | PF00928 | 0.217 |
LIG_EH1_1 | 521 | 529 | PF00400 | 0.231 |
LIG_eIF4E_1 | 522 | 528 | PF01652 | 0.231 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.478 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.404 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.371 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.275 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.287 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.374 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.597 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.362 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.297 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.742 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.695 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.714 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.670 |
LIG_FHA_1 | 729 | 735 | PF00498 | 0.647 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.453 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.562 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.372 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.621 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.696 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.655 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.751 |
LIG_FHA_2 | 705 | 711 | PF00498 | 0.651 |
LIG_FHA_2 | 718 | 724 | PF00498 | 0.645 |
LIG_FXI_DFP_1 | 179 | 183 | PF00024 | 0.529 |
LIG_Integrin_RGD_1 | 426 | 428 | PF01839 | 0.354 |
LIG_IRF3_LxIS_1 | 582 | 589 | PF10401 | 0.603 |
LIG_LIR_Apic_2 | 275 | 279 | PF02991 | 0.433 |
LIG_LIR_Apic_2 | 379 | 383 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 180 | 190 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 202 | 210 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 295 | 304 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 481 | 491 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 509 | 518 | PF02991 | 0.229 |
LIG_LIR_Gen_1 | 643 | 652 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.228 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 481 | 487 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 643 | 647 | PF02991 | 0.624 |
LIG_MLH1_MIPbox_1 | 90 | 94 | PF16413 | 0.454 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.304 |
LIG_REV1ctd_RIR_1 | 120 | 128 | PF16727 | 0.280 |
LIG_RPA_C_Fungi | 641 | 653 | PF08784 | 0.523 |
LIG_RPA_C_Fungi | 793 | 805 | PF08784 | 0.531 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.327 |
LIG_SH2_CRK | 484 | 488 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 190 | 194 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 522 | 526 | PF00017 | 0.388 |
LIG_SH2_SRC | 125 | 128 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 522 | 526 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 755 | 759 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.388 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.441 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.427 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.588 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.462 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.312 |
LIG_SH3_3 | 731 | 737 | PF00018 | 0.675 |
LIG_SUMO_SIM_anti_2 | 515 | 521 | PF11976 | 0.231 |
LIG_SUMO_SIM_anti_2 | 9 | 14 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 517 | 523 | PF11976 | 0.231 |
LIG_TRAF2_1 | 608 | 611 | PF00917 | 0.544 |
LIG_TRAF2_1 | 822 | 825 | PF00917 | 0.551 |
LIG_TYR_ITIM | 392 | 397 | PF00017 | 0.403 |
LIG_UBA3_1 | 150 | 154 | PF00899 | 0.312 |
LIG_WRC_WIRS_1 | 273 | 278 | PF05994 | 0.527 |
LIG_WRC_WIRS_1 | 507 | 512 | PF05994 | 0.326 |
LIG_WRC_WIRS_1 | 55 | 60 | PF05994 | 0.392 |
LIG_WRC_WIRS_1 | 694 | 699 | PF05994 | 0.573 |
MOD_CDK_SPxxK_3 | 459 | 466 | PF00069 | 0.433 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.560 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.279 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.534 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.541 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.646 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.472 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.616 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.703 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.458 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.552 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.715 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.574 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.503 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.482 |
MOD_CK1_1 | 790 | 796 | PF00069 | 0.528 |
MOD_CK1_1 | 809 | 815 | PF00069 | 0.491 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.706 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.580 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.373 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.514 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.440 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.620 |
MOD_CK2_1 | 617 | 623 | PF00069 | 0.618 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.560 |
MOD_CK2_1 | 704 | 710 | PF00069 | 0.615 |
MOD_CK2_1 | 717 | 723 | PF00069 | 0.550 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.484 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.526 |
MOD_CK2_1 | 819 | 825 | PF00069 | 0.557 |
MOD_CMANNOS | 358 | 361 | PF00535 | 0.437 |
MOD_CMANNOS | 413 | 416 | PF00535 | 0.402 |
MOD_CMANNOS | 593 | 596 | PF00535 | 0.526 |
MOD_Cter_Amidation | 171 | 174 | PF01082 | 0.302 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.488 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.388 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.318 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.373 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.584 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.522 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.312 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.300 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.573 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.646 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.617 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.686 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.496 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.824 |
MOD_GlcNHglycan | 748 | 753 | PF01048 | 0.559 |
MOD_GlcNHglycan | 769 | 773 | PF01048 | 0.636 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.657 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.776 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.503 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.528 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.471 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.398 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.394 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.642 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.653 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.562 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.596 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.452 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.587 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.710 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.664 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.656 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.657 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.602 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.526 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.504 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.773 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.656 |
MOD_LATS_1 | 215 | 221 | PF00433 | 0.231 |
MOD_N-GLC_2 | 333 | 335 | PF02516 | 0.557 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.234 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.533 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.428 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.234 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.550 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.805 |
MOD_NEK2_1 | 794 | 799 | PF00069 | 0.558 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.507 |
MOD_NEK2_2 | 361 | 366 | PF00069 | 0.469 |
MOD_NEK2_2 | 447 | 452 | PF00069 | 0.507 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.441 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.489 |
MOD_PIKK_1 | 682 | 688 | PF00454 | 0.554 |
MOD_PIKK_1 | 770 | 776 | PF00454 | 0.515 |
MOD_PK_1 | 426 | 432 | PF00069 | 0.447 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.333 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.322 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.388 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.485 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.607 |
MOD_PKA_2 | 710 | 716 | PF00069 | 0.623 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.644 |
MOD_PKB_1 | 339 | 347 | PF00069 | 0.597 |
MOD_PKB_1 | 424 | 432 | PF00069 | 0.439 |
MOD_PKB_1 | 550 | 558 | PF00069 | 0.437 |
MOD_Plk_1 | 476 | 482 | PF00069 | 0.363 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.364 |
MOD_Plk_1 | 748 | 754 | PF00069 | 0.504 |
MOD_Plk_2-3 | 710 | 716 | PF00069 | 0.550 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.461 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.394 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.418 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.569 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.231 |
MOD_Plk_4 | 790 | 796 | PF00069 | 0.582 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.507 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.312 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.442 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.530 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.621 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.435 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.492 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.503 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.659 |
MOD_ProDKin_1 | 680 | 686 | PF00069 | 0.670 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.618 |
MOD_ProDKin_1 | 809 | 815 | PF00069 | 0.537 |
MOD_SUMO_rev_2 | 70 | 78 | PF00179 | 0.560 |
TRG_DiLeu_BaEn_3 | 757 | 763 | PF01217 | 0.608 |
TRG_DiLeu_BaLyEn_6 | 282 | 287 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 387 | 392 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 421 | 424 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 482 | 484 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 550 | 552 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 795 | 798 | PF00400 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 109 | 114 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 285 | 290 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 49 | 54 | PF00026 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 595 | 599 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6E0 | Leptomonas seymouri | 42% | 100% |
A0A3S7WPU2 | Leishmania donovani | 64% | 100% |
A4HT52 | Leishmania infantum | 64% | 90% |
E9AL44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4QIR0 | Leishmania major | 61% | 99% |