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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HBU3
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 5 |
GO:0006793 | phosphorus metabolic process | 3 | 5 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016310 | phosphorylation | 5 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0036211 | protein modification process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043412 | macromolecule modification | 4 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 5 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004672 | protein kinase activity | 3 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0005524 | ATP binding | 5 | 5 |
GO:0016301 | kinase activity | 4 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 5 |
GO:0032553 | ribonucleotide binding | 3 | 5 |
GO:0032555 | purine ribonucleotide binding | 4 | 5 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 5 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 5 |
GO:0036094 | small molecule binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043168 | anion binding | 3 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:0097367 | carbohydrate derivative binding | 2 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
GO:1901265 | nucleoside phosphate binding | 3 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 708 | 712 | PF00656 | 0.506 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 719 | 721 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 837 | 839 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.357 |
CLV_Separin_Metazoa | 367 | 371 | PF03568 | 0.344 |
DEG_APCC_DBOX_1 | 354 | 362 | PF00400 | 0.428 |
DEG_SCF_FBW7_1 | 677 | 684 | PF00400 | 0.638 |
DEG_SCF_FBW7_1 | 685 | 692 | PF00400 | 0.473 |
DEG_SPOP_SBC_1 | 59 | 63 | PF00917 | 0.430 |
DEG_SPOP_SBC_1 | 620 | 624 | PF00917 | 0.669 |
DEG_SPOP_SBC_1 | 633 | 637 | PF00917 | 0.455 |
DEG_SPOP_SBC_1 | 752 | 756 | PF00917 | 0.474 |
DOC_CDC14_PxL_1 | 774 | 782 | PF14671 | 0.478 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.463 |
DOC_CKS1_1 | 409 | 414 | PF01111 | 0.401 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.377 |
DOC_CKS1_1 | 686 | 691 | PF01111 | 0.633 |
DOC_CKS1_1 | 739 | 744 | PF01111 | 0.473 |
DOC_CYCLIN_RxL_1 | 3 | 13 | PF00134 | 0.509 |
DOC_CYCLIN_yCln2_LP_2 | 625 | 631 | PF00134 | 0.456 |
DOC_CYCLIN_yCln2_LP_2 | 739 | 745 | PF00134 | 0.472 |
DOC_MAPK_gen_1 | 207 | 213 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 84 | 91 | PF00069 | 0.338 |
DOC_MAPK_MEF2A_6 | 504 | 513 | PF00069 | 0.305 |
DOC_PP2B_LxvP_1 | 294 | 297 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 566 | 569 | PF13499 | 0.326 |
DOC_PP2B_LxvP_1 | 625 | 628 | PF13499 | 0.454 |
DOC_PP2B_LxvP_1 | 89 | 92 | PF13499 | 0.346 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.368 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.263 |
DOC_PP4_FxxP_1 | 56 | 59 | PF00568 | 0.267 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.260 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.239 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.310 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 614 | 618 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 790 | 794 | PF00917 | 0.704 |
DOC_USP7_MATH_2 | 218 | 224 | PF00917 | 0.483 |
DOC_USP7_UBL2_3 | 836 | 840 | PF12436 | 0.576 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 649 | 654 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 664 | 669 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 672 | 677 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 685 | 690 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 812 | 817 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 280 | 284 | PF00244 | 0.242 |
LIG_14-3-3_CanoR_1 | 419 | 427 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 84 | 90 | PF00244 | 0.355 |
LIG_Actin_WH2_2 | 263 | 278 | PF00022 | 0.474 |
LIG_Actin_WH2_2 | 522 | 539 | PF00022 | 0.411 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.458 |
LIG_BIR_III_4 | 239 | 243 | PF00653 | 0.357 |
LIG_BIR_III_4 | 498 | 502 | PF00653 | 0.260 |
LIG_BRCT_BRCA1_1 | 727 | 731 | PF00533 | 0.601 |
LIG_BRCT_BRCA1_2 | 727 | 733 | PF00533 | 0.600 |
LIG_Clathr_ClatBox_1 | 182 | 186 | PF01394 | 0.276 |
LIG_Clathr_ClatBox_1 | 330 | 334 | PF01394 | 0.415 |
LIG_CtBP_PxDLS_1 | 218 | 222 | PF00389 | 0.500 |
LIG_DLG_GKlike_1 | 262 | 270 | PF00625 | 0.263 |
LIG_eIF4E_1 | 409 | 415 | PF01652 | 0.341 |
LIG_eIF4E_1 | 467 | 473 | PF01652 | 0.350 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.327 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.402 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.248 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.409 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.452 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.331 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.416 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.434 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.316 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.417 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.539 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.633 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.621 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.709 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.527 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.454 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.442 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.503 |
LIG_Integrin_isoDGR_2 | 260 | 262 | PF01839 | 0.446 |
LIG_LIR_Apic_2 | 39 | 45 | PF02991 | 0.433 |
LIG_LIR_Apic_2 | 407 | 412 | PF02991 | 0.368 |
LIG_LIR_Apic_2 | 530 | 534 | PF02991 | 0.251 |
LIG_LIR_Apic_2 | 54 | 59 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 448 | 453 | PF02991 | 0.226 |
LIG_LIR_Nem_3 | 637 | 643 | PF02991 | 0.647 |
LIG_LRP6_Inhibitor_1 | 78 | 84 | PF00058 | 0.241 |
LIG_NRBOX | 326 | 332 | PF00104 | 0.404 |
LIG_Pex14_1 | 38 | 42 | PF04695 | 0.346 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.358 |
LIG_REV1ctd_RIR_1 | 1 | 10 | PF16727 | 0.516 |
LIG_SH2_CRK | 215 | 219 | PF00017 | 0.361 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.444 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.327 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.460 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.402 |
LIG_SH2_NCK_1 | 248 | 252 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 31 | 35 | PF00017 | 0.383 |
LIG_SH2_NCK_1 | 459 | 463 | PF00017 | 0.429 |
LIG_SH2_PTP2 | 409 | 412 | PF00017 | 0.316 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 436 | 440 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 467 | 471 | PF00017 | 0.347 |
LIG_SH2_STAT3 | 130 | 133 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.408 |
LIG_SH3_2 | 113 | 118 | PF14604 | 0.316 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.230 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.404 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.244 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.613 |
LIG_SH3_3 | 739 | 745 | PF00018 | 0.758 |
LIG_Sin3_3 | 469 | 476 | PF02671 | 0.387 |
LIG_SUMO_SIM_anti_2 | 328 | 334 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 525 | 530 | PF11976 | 0.242 |
LIG_SUMO_SIM_par_1 | 572 | 577 | PF11976 | 0.378 |
LIG_TRAF2_1 | 134 | 137 | PF00917 | 0.299 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.482 |
LIG_TYR_ITIM | 246 | 251 | PF00017 | 0.267 |
LIG_TYR_ITIM | 425 | 430 | PF00017 | 0.362 |
LIG_WRC_WIRS_1 | 305 | 310 | PF05994 | 0.256 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.367 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.481 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.301 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.360 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.439 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.470 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.444 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.593 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.659 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.628 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.539 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.724 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.540 |
MOD_CK1_1 | 747 | 753 | PF00069 | 0.638 |
MOD_CK1_1 | 759 | 765 | PF00069 | 0.578 |
MOD_CK1_1 | 783 | 789 | PF00069 | 0.742 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.656 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.404 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.457 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.488 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.369 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.388 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.465 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.254 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.371 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.334 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.526 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.337 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.379 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.456 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.306 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.379 |
MOD_GlcNHglycan | 466 | 470 | PF01048 | 0.374 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.450 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.552 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.697 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.550 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.715 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.629 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.550 |
MOD_GlcNHglycan | 764 | 767 | PF01048 | 0.502 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.720 |
MOD_GlcNHglycan | 831 | 834 | PF01048 | 0.573 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.421 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.413 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.394 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.390 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.369 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.500 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.278 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.436 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.421 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.368 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.520 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.503 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.582 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.583 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.540 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.654 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.669 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.563 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.493 |
MOD_GSK3_1 | 734 | 741 | PF00069 | 0.488 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.693 |
MOD_GSK3_1 | 755 | 762 | PF00069 | 0.757 |
MOD_GSK3_1 | 779 | 786 | PF00069 | 0.702 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.668 |
MOD_GSK3_1 | 799 | 806 | PF00069 | 0.703 |
MOD_GSK3_1 | 820 | 827 | PF00069 | 0.727 |
MOD_LATS_1 | 601 | 607 | PF00433 | 0.438 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.526 |
MOD_N-GLC_1 | 445 | 450 | PF02516 | 0.390 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.297 |
MOD_N-GLC_1 | 614 | 619 | PF02516 | 0.576 |
MOD_N-GLC_1 | 824 | 829 | PF02516 | 0.592 |
MOD_N-GLC_2 | 277 | 279 | PF02516 | 0.439 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.423 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.504 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.458 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.376 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.466 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.448 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.370 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.402 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.301 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.417 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.478 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.572 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.655 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.640 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.650 |
MOD_NEK2_1 | 785 | 790 | PF00069 | 0.610 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.261 |
MOD_NEK2_2 | 547 | 552 | PF00069 | 0.360 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.455 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.407 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.479 |
MOD_PIKK_1 | 747 | 753 | PF00454 | 0.479 |
MOD_PIKK_1 | 783 | 789 | PF00454 | 0.615 |
MOD_PK_1 | 603 | 609 | PF00069 | 0.320 |
MOD_PKA_1 | 316 | 322 | PF00069 | 0.285 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.429 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.421 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.415 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.558 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.221 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.308 |
MOD_Plk_1 | 689 | 695 | PF00069 | 0.483 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.320 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.274 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.348 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.298 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.459 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.334 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.419 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.702 |
MOD_Plk_4 | 726 | 732 | PF00069 | 0.462 |
MOD_Plk_4 | 734 | 740 | PF00069 | 0.440 |
MOD_Plk_4 | 803 | 809 | PF00069 | 0.728 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.334 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.454 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.392 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.415 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.400 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.487 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.437 |
MOD_ProDKin_1 | 649 | 655 | PF00069 | 0.588 |
MOD_ProDKin_1 | 664 | 670 | PF00069 | 0.746 |
MOD_ProDKin_1 | 672 | 678 | PF00069 | 0.676 |
MOD_ProDKin_1 | 685 | 691 | PF00069 | 0.668 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.648 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.740 |
MOD_ProDKin_1 | 812 | 818 | PF00069 | 0.512 |
MOD_SUMO_for_1 | 596 | 599 | PF00179 | 0.339 |
MOD_SUMO_rev_2 | 713 | 722 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_2 | 309 | 315 | PF01217 | 0.406 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.449 |
TRG_NES_CRM1_1 | 322 | 334 | PF08389 | 0.399 |
TRG_NLS_MonoExtN_4 | 836 | 842 | PF00514 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 561 | 565 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PER2 | Leptomonas seymouri | 53% | 95% |
A0A0S4KHN7 | Bodo saltans | 34% | 100% |
A0A1X0NY37 | Trypanosomatidae | 38% | 100% |
A0A3S5IS35 | Trypanosoma rangeli | 37% | 100% |
A0A3S7WWH4 | Leishmania donovani | 78% | 99% |
D0A1C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AGU9 | Leishmania infantum | 78% | 99% |
E9AV65 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
O13733 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
Q4QCB6 | Leishmania major | 76% | 100% |
Q55GS2 | Dictyostelium discoideum | 26% | 100% |