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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
Related structures:
AlphaFold database: E9AID0
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 20 |
GO:0008152 | metabolic process | 1 | 20 |
GO:0019538 | protein metabolic process | 3 | 20 |
GO:0036211 | protein modification process | 4 | 20 |
GO:0043170 | macromolecule metabolic process | 3 | 20 |
GO:0043412 | macromolecule modification | 4 | 20 |
GO:0044238 | primary metabolic process | 2 | 20 |
GO:0071704 | organic substance metabolic process | 2 | 20 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 20 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0018095 | protein polyglutamylation | 7 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0005488 | binding | 1 | 4 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0016874 | ligase activity | 2 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 7 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 7 |
GO:0016881 | acid-amino acid ligase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 2 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 478 | 482 | PF00656 | 0.423 |
CLV_C14_Caspase3-7 | 734 | 738 | PF00656 | 0.360 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.157 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.400 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 698 | 700 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 654 | 658 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.533 |
CLV_Separin_Metazoa | 521 | 525 | PF03568 | 0.507 |
DEG_APCC_DBOX_1 | 425 | 433 | PF00400 | 0.507 |
DEG_APCC_DBOX_1 | 608 | 616 | PF00400 | 0.507 |
DEG_SPOP_SBC_1 | 353 | 357 | PF00917 | 0.357 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 646 | 649 | PF00134 | 0.303 |
DOC_MAPK_gen_1 | 240 | 248 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 404 | 412 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 715 | 722 | PF00069 | 0.592 |
DOC_MAPK_gen_1 | 81 | 88 | PF00069 | 0.375 |
DOC_MAPK_JIP1_4 | 609 | 615 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 404 | 412 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 518 | 527 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 609 | 617 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 81 | 88 | PF00069 | 0.435 |
DOC_MAPK_NFAT4_5 | 241 | 249 | PF00069 | 0.357 |
DOC_MAPK_NFAT4_5 | 405 | 413 | PF00069 | 0.429 |
DOC_PP1_RVXF_1 | 522 | 528 | PF00149 | 0.416 |
DOC_PP1_RVXF_1 | 652 | 658 | PF00149 | 0.421 |
DOC_PP2B_LxvP_1 | 646 | 649 | PF13499 | 0.303 |
DOC_PP4_MxPP_1 | 647 | 650 | PF00568 | 0.326 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 731 | 735 | PF00917 | 0.550 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 725 | 730 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.337 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 164 | 168 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 332 | 340 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 35 | 45 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 431 | 436 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 439 | 448 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 539 | 546 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 710 | 716 | PF00244 | 0.302 |
LIG_Actin_WH2_2 | 454 | 469 | PF00022 | 0.357 |
LIG_Actin_WH2_2 | 523 | 541 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 594 | 611 | PF00022 | 0.374 |
LIG_APCC_ABBA_1 | 112 | 117 | PF00400 | 0.439 |
LIG_APCC_ABBA_1 | 422 | 427 | PF00400 | 0.466 |
LIG_APCC_ABBAyCdc20_2 | 421 | 427 | PF00400 | 0.431 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.490 |
LIG_BRCT_BRCA1_1 | 311 | 315 | PF00533 | 0.357 |
LIG_BRCT_BRCA1_1 | 572 | 576 | PF00533 | 0.507 |
LIG_EH_1 | 396 | 400 | PF12763 | 0.412 |
LIG_EH1_1 | 578 | 586 | PF00400 | 0.412 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.353 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.388 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.441 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.426 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.525 |
LIG_FHA_1 | 657 | 663 | PF00498 | 0.683 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.460 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.450 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.507 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.382 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.621 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.402 |
LIG_FHA_2 | 691 | 697 | PF00498 | 0.349 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.521 |
LIG_LIR_Apic_2 | 287 | 292 | PF02991 | 0.457 |
LIG_LIR_Apic_2 | 507 | 513 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 174 | 183 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 573 | 584 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 622 | 632 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 701 | 708 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 622 | 628 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 701 | 706 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 714 | 719 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.430 |
LIG_MLH1_MIPbox_1 | 572 | 576 | PF16413 | 0.412 |
LIG_NRBOX | 243 | 249 | PF00104 | 0.412 |
LIG_PCNA_PIPBox_1 | 618 | 627 | PF02747 | 0.424 |
LIG_PCNA_yPIPBox_3 | 386 | 395 | PF02747 | 0.387 |
LIG_Pex14_2 | 575 | 579 | PF04695 | 0.507 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.337 |
LIG_SH2_CRK | 226 | 230 | PF00017 | 0.540 |
LIG_SH2_CRK | 417 | 421 | PF00017 | 0.546 |
LIG_SH2_CRK | 716 | 720 | PF00017 | 0.376 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.465 |
LIG_SH2_NCK_1 | 673 | 677 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 91 | 95 | PF00017 | 0.486 |
LIG_SH2_PTP2 | 411 | 414 | PF00017 | 0.406 |
LIG_SH2_SRC | 417 | 420 | PF00017 | 0.452 |
LIG_SH2_STAT3 | 389 | 392 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.436 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.481 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.657 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.313 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.441 |
LIG_SUMO_SIM_anti_2 | 582 | 592 | PF11976 | 0.507 |
LIG_SUMO_SIM_anti_2 | 639 | 645 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 582 | 592 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 597 | 602 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 609 | 614 | PF11976 | 0.526 |
LIG_TRAF2_1 | 692 | 695 | PF00917 | 0.286 |
LIG_TYR_ITSM | 413 | 420 | PF00017 | 0.412 |
LIG_WW_2 | 650 | 653 | PF00397 | 0.345 |
MOD_CDK_SPxxK_3 | 528 | 535 | PF00069 | 0.507 |
MOD_CDK_SPxxK_3 | 74 | 81 | PF00069 | 0.477 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.705 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.391 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.453 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.441 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.471 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.439 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.421 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.452 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.731 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.528 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.462 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.443 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.358 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.583 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.409 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.372 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.603 |
MOD_CK2_1 | 690 | 696 | PF00069 | 0.305 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.655 |
MOD_Cter_Amidation | 238 | 241 | PF01082 | 0.231 |
MOD_Cter_Amidation | 402 | 405 | PF01082 | 0.331 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.639 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.728 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.784 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.650 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.470 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.293 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.354 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.349 |
MOD_GlcNHglycan | 367 | 371 | PF01048 | 0.205 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.370 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.289 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.314 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.208 |
MOD_GlcNHglycan | 62 | 66 | PF01048 | 0.523 |
MOD_GlcNHglycan | 711 | 714 | PF01048 | 0.508 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.683 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.497 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.445 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.446 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.486 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.634 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.447 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.539 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.504 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.450 |
MOD_GSK3_1 | 727 | 734 | PF00069 | 0.635 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.473 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.264 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.233 |
MOD_N-GLC_1 | 462 | 467 | PF02516 | 0.259 |
MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.157 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.187 |
MOD_N-GLC_1 | 663 | 668 | PF02516 | 0.708 |
MOD_N-GLC_1 | 701 | 706 | PF02516 | 0.346 |
MOD_N-GLC_1 | 725 | 730 | PF02516 | 0.437 |
MOD_N-GLC_2 | 688 | 690 | PF02516 | 0.300 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.519 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.353 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.254 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.366 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.404 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.513 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.416 |
MOD_NEK2_2 | 381 | 386 | PF00069 | 0.357 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.506 |
MOD_PIKK_1 | 665 | 671 | PF00454 | 0.526 |
MOD_PKA_1 | 82 | 88 | PF00069 | 0.365 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.530 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.583 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.320 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.520 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.412 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.382 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.564 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.508 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.409 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.627 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.375 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.480 |
MOD_Plk_1 | 701 | 707 | PF00069 | 0.466 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.393 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.400 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.523 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.576 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.426 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.629 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.423 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.411 |
MOD_Plk_4 | 639 | 645 | PF00069 | 0.477 |
MOD_Plk_4 | 739 | 745 | PF00069 | 0.357 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.539 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.507 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.514 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.459 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.507 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.381 |
MOD_ProDKin_1 | 725 | 731 | PF00069 | 0.650 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.347 |
MOD_SUMO_rev_2 | 492 | 497 | PF00179 | 0.410 |
TRG_DiLeu_BaEn_1 | 521 | 526 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 206 | 211 | PF01217 | 0.271 |
TRG_DiLeu_BaLyEn_6 | 702 | 707 | PF01217 | 0.465 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.411 |
TRG_NES_CRM1_1 | 521 | 533 | PF08389 | 0.412 |
TRG_NES_CRM1_1 | 577 | 589 | PF08389 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.212 |
TRG_Pf-PMV_PEXEL_1 | 717 | 721 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7G7 | Leptomonas seymouri | 44% | 91% |
A0A0S4IZZ2 | Bodo saltans | 28% | 84% |
A0A0S4JH38 | Bodo saltans | 22% | 100% |
A0A0S4KQK8 | Bodo saltans | 28% | 100% |
A0A1X0NXX8 | Trypanosomatidae | 31% | 100% |
A0A3Q8IDL7 | Leishmania donovani | 75% | 100% |
A0A3Q8IEC1 | Leishmania donovani | 28% | 100% |
A0A3Q8III2 | Leishmania donovani | 28% | 100% |
A0A3S5H6X0 | Leishmania donovani | 24% | 92% |
A0A3S7X261 | Leishmania donovani | 25% | 100% |
A0A422NPL9 | Trypanosoma rangeli | 34% | 100% |
A4H8G3 | Leishmania braziliensis | 25% | 100% |
A4HG29 | Leishmania braziliensis | 24% | 100% |
A4HIG0 | Leishmania braziliensis | 25% | 100% |
A4HNF6 | Leishmania braziliensis | 28% | 100% |
A4HWT7 | Leishmania infantum | 24% | 92% |
A4HYN9 | Leishmania infantum | 76% | 100% |
A4I479 | Leishmania infantum | 24% | 100% |
A4I5Q6 | Leishmania infantum | 27% | 100% |
A4IC28 | Leishmania infantum | 28% | 100% |
A4Q9F0 | Mus musculus | 22% | 82% |
A8X9V4 | Caenorhabditis briggsae | 23% | 100% |
C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9ADM8 | Leishmania major | 24% | 100% |
E9AFW7 | Leishmania major | 28% | 100% |
E9AM52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AUL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9B720 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9P886 | Caenorhabditis elegans | 27% | 100% |
Q09647 | Caenorhabditis elegans | 24% | 100% |
Q4QCW7 | Leishmania major | 76% | 100% |
Q6ZT98 | Homo sapiens | 24% | 84% |
V5BVF5 | Trypanosoma cruzi | 33% | 100% |
V5C123 | Trypanosoma cruzi | 22% | 79% |