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: Q4QIR0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006163 | purine nucleotide metabolic process | 5 | 2 |
GO:0006195 | purine nucleotide catabolic process | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009117 | nucleotide metabolic process | 5 | 2 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 2 |
GO:0009154 | purine ribonucleotide catabolic process | 6 | 2 |
GO:0009166 | nucleotide catabolic process | 6 | 2 |
GO:0009259 | ribonucleotide metabolic process | 5 | 2 |
GO:0009261 | ribonucleotide catabolic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015936 | coenzyme A metabolic process | 6 | 2 |
GO:0015938 | coenzyme A catabolic process | 7 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0019693 | ribose phosphate metabolic process | 4 | 2 |
GO:0033865 | nucleoside bisphosphate metabolic process | 5 | 2 |
GO:0033869 | nucleoside bisphosphate catabolic process | 6 | 2 |
GO:0033875 | ribonucleoside bisphosphate metabolic process | 6 | 2 |
GO:0034031 | ribonucleoside bisphosphate catabolic process | 7 | 2 |
GO:0034032 | purine nucleoside bisphosphate metabolic process | 5 | 2 |
GO:0034034 | purine nucleoside bisphosphate catabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0046434 | organophosphate catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0072521 | purine-containing compound metabolic process | 4 | 2 |
GO:0072523 | purine-containing compound catabolic process | 5 | 2 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 2 |
GO:1901136 | carbohydrate derivative catabolic process | 4 | 2 |
GO:1901292 | nucleoside phosphate catabolic process | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0003986 | acetyl-CoA hydrolase activity | 6 | 2 |
GO:0010945 | CoA pyrophosphatase activity | 6 | 7 |
GO:0016289 | CoA hydrolase activity | 5 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016790 | thiolester hydrolase activity | 4 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 142 | 146 | PF00656 | 0.698 |
CLV_C14_Caspase3-7 | 588 | 592 | PF00656 | 0.693 |
CLV_C14_Caspase3-7 | 598 | 602 | PF00656 | 0.741 |
CLV_MEL_PAP_1 | 39 | 45 | PF00089 | 0.393 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 656 | 658 | PF00675 | 0.572 |
CLV_PCSK_FUR_1 | 466 | 470 | PF00082 | 0.356 |
CLV_PCSK_FUR_1 | 561 | 565 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 655 | 657 | PF00082 | 0.570 |
CLV_PCSK_PC7_1 | 464 | 470 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.380 |
DEG_SCF_FBW7_2 | 495 | 501 | PF00400 | 0.666 |
DEG_SPOP_SBC_1 | 313 | 317 | PF00917 | 0.783 |
DEG_SPOP_SBC_1 | 700 | 704 | PF00917 | 0.691 |
DOC_ANK_TNKS_1 | 113 | 120 | PF00023 | 0.686 |
DOC_CKS1_1 | 495 | 500 | PF01111 | 0.670 |
DOC_MAPK_gen_1 | 165 | 173 | PF00069 | 0.627 |
DOC_MAPK_gen_1 | 33 | 41 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 34 | 43 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 767 | 776 | PF00069 | 0.644 |
DOC_MAPK_RevD_3 | 8 | 24 | PF00069 | 0.552 |
DOC_PP1_RVXF_1 | 121 | 128 | PF00149 | 0.525 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.595 |
DOC_PP4_FxxP_1 | 280 | 283 | PF00568 | 0.699 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.592 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 18 | 27 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 191 | 195 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 261 | 268 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 33 | 41 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 410 | 419 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 452 | 456 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 49 | 58 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 619 | 627 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 632 | 638 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 655 | 665 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 699 | 707 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.667 |
LIG_APCC_ABBAyCdc20_2 | 538 | 544 | PF00400 | 0.582 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.678 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.775 |
LIG_Clathr_ClatBox_1 | 367 | 371 | PF01394 | 0.533 |
LIG_Clathr_ClatBox_1 | 643 | 647 | PF01394 | 0.653 |
LIG_deltaCOP1_diTrp_1 | 118 | 127 | PF00928 | 0.651 |
LIG_deltaCOP1_diTrp_1 | 377 | 380 | PF00928 | 0.633 |
LIG_deltaCOP1_diTrp_1 | 53 | 58 | PF00928 | 0.515 |
LIG_eIF4E_1 | 397 | 403 | PF01652 | 0.467 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.673 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.632 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.587 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.566 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.771 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.750 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.672 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.632 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.585 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.819 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.657 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.496 |
LIG_FHA_2 | 619 | 625 | PF00498 | 0.686 |
LIG_FHA_2 | 658 | 664 | PF00498 | 0.754 |
LIG_FHA_2 | 680 | 686 | PF00498 | 0.760 |
LIG_FHA_2 | 700 | 706 | PF00498 | 0.628 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.669 |
LIG_FHA_2 | 718 | 724 | PF00498 | 0.645 |
LIG_FXI_DFP_1 | 183 | 187 | PF00024 | 0.463 |
LIG_LIR_Apic_2 | 118 | 124 | PF02991 | 0.673 |
LIG_LIR_Apic_2 | 279 | 283 | PF02991 | 0.694 |
LIG_LIR_Apic_2 | 374 | 379 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 206 | 214 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 299 | 308 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 477 | 487 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 52 | 63 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 126 | 130 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 206 | 210 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 377 | 381 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.514 |
LIG_MLH1_MIPbox_1 | 91 | 95 | PF16413 | 0.694 |
LIG_PCNA_PIPBox_1 | 664 | 673 | PF02747 | 0.733 |
LIG_Pex14_2 | 376 | 380 | PF04695 | 0.661 |
LIG_SH2_CRK | 480 | 484 | PF00017 | 0.664 |
LIG_SH2_NCK_1 | 194 | 198 | PF00017 | 0.638 |
LIG_SH2_NCK_1 | 518 | 522 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 67 | 71 | PF00017 | 0.730 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.594 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.728 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 518 | 522 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 779 | 782 | PF00017 | 0.719 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.453 |
LIG_SH3_1 | 492 | 498 | PF00018 | 0.595 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.640 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.588 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.705 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.527 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.576 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.705 |
LIG_SH3_3 | 744 | 750 | PF00018 | 0.736 |
LIG_Sin3_3 | 487 | 494 | PF02671 | 0.544 |
LIG_SUMO_SIM_anti_2 | 9 | 14 | PF11976 | 0.650 |
LIG_SUMO_SIM_par_1 | 366 | 372 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 714 | 720 | PF11976 | 0.722 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.595 |
LIG_TYR_ITSM | 190 | 197 | PF00017 | 0.480 |
LIG_UBA3_1 | 154 | 158 | PF00899 | 0.528 |
LIG_WRC_WIRS_1 | 277 | 282 | PF05994 | 0.678 |
MOD_CDK_SPxxK_3 | 348 | 355 | PF00069 | 0.645 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.646 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.552 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.659 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.681 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.651 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.712 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.709 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.786 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.583 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.713 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.657 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.811 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.663 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.683 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.634 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.585 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.546 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.496 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.581 |
MOD_CK2_1 | 618 | 624 | PF00069 | 0.690 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.681 |
MOD_CK2_1 | 657 | 663 | PF00069 | 0.811 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.668 |
MOD_CK2_1 | 717 | 723 | PF00069 | 0.704 |
MOD_CMANNOS | 354 | 357 | PF00535 | 0.357 |
MOD_CMANNOS | 409 | 412 | PF00535 | 0.352 |
MOD_Cter_Amidation | 175 | 178 | PF01082 | 0.369 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.366 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.482 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.441 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.525 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.337 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.493 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.550 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.483 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.393 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.487 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.554 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.393 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.547 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.595 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.439 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.537 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.457 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.455 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.513 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.484 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.708 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.646 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.618 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.782 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.681 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.587 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.817 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.736 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.797 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.697 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.807 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.726 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.499 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.603 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.558 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.530 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.780 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.627 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.732 |
MOD_NEK2_1 | 707 | 712 | PF00069 | 0.788 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.643 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.548 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.638 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.659 |
MOD_PKA_1 | 165 | 171 | PF00069 | 0.657 |
MOD_PKA_1 | 656 | 662 | PF00069 | 0.673 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.684 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.584 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.638 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.618 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.741 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.718 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.710 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.683 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.689 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.673 |
MOD_PKA_2 | 695 | 701 | PF00069 | 0.699 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.773 |
MOD_PKB_1 | 339 | 347 | PF00069 | 0.699 |
MOD_PKB_1 | 655 | 663 | PF00069 | 0.744 |
MOD_PKB_1 | 778 | 786 | PF00069 | 0.720 |
MOD_Plk_2-3 | 366 | 372 | PF00069 | 0.600 |
MOD_Plk_2-3 | 572 | 578 | PF00069 | 0.728 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.584 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.560 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.636 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.735 |
MOD_Plk_4 | 639 | 645 | PF00069 | 0.650 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.587 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.548 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.765 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.666 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.621 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.735 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.649 |
MOD_SUMO_rev_2 | 765 | 775 | PF00179 | 0.702 |
TRG_DiLeu_BaEn_3 | 770 | 776 | PF01217 | 0.740 |
TRG_DiLeu_BaLyEn_6 | 383 | 388 | PF01217 | 0.645 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.642 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.555 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 270 | 273 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 338 | 341 | PF00400 | 0.726 |
TRG_ER_diArg_1 | 417 | 420 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 468 | 470 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 478 | 480 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 546 | 548 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 655 | 657 | PF00400 | 0.783 |
TRG_Pf-PMV_PEXEL_1 | 18 | 22 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.363 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6E0 | Leptomonas seymouri | 37% | 100% |
A0A3S7WPU2 | Leishmania donovani | 88% | 100% |
A4H4X9 | Leishmania braziliensis | 61% | 95% |
A4HT52 | Leishmania infantum | 87% | 86% |
E9AL44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |