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: 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: A4HIG0
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 | 7 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016874 | ligase activity | 2 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 4 |
GO:0016881 | acid-amino acid ligase activity | 4 | 4 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 2 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 433 | 437 | PF00656 | 0.436 |
CLV_C14_Caspase3-7 | 460 | 464 | PF00656 | 0.428 |
CLV_C14_Caspase3-7 | 609 | 613 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 703 | 707 | PF00656 | 0.405 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.394 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.453 |
CLV_PCSK_PC7_1 | 477 | 483 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.443 |
CLV_Separin_Metazoa | 133 | 137 | PF03568 | 0.600 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.598 |
DEG_SCF_FBW7_1 | 577 | 582 | PF00400 | 0.361 |
DOC_CYCLIN_yCln2_LP_2 | 43 | 49 | PF00134 | 0.280 |
DOC_CYCLIN_yCln2_LP_2 | 593 | 599 | PF00134 | 0.507 |
DOC_MAPK_DCC_7 | 136 | 146 | PF00069 | 0.391 |
DOC_MAPK_FxFP_2 | 61 | 64 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 136 | 143 | PF00069 | 0.395 |
DOC_MAPK_gen_1 | 307 | 315 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 623 | 630 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 138 | 146 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 307 | 315 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 623 | 632 | PF00069 | 0.452 |
DOC_MAPK_NFAT4_5 | 308 | 316 | PF00069 | 0.472 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.324 |
DOC_PP2B_LxvP_1 | 426 | 429 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 43 | 46 | PF13499 | 0.490 |
DOC_PP2B_LxvP_1 | 670 | 673 | PF13499 | 0.573 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.433 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 679 | 683 | PF00917 | 0.531 |
DOC_USP7_MATH_2 | 224 | 230 | PF00917 | 0.444 |
DOC_USP7_UBL2_3 | 279 | 283 | PF12436 | 0.557 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 575 | 580 | PF00397 | 0.497 |
LIG_14-3-3_CanoR_1 | 136 | 142 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 388 | 396 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 423 | 429 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 57 | 62 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 595 | 604 | PF00244 | 0.437 |
LIG_Actin_WH2_2 | 35 | 52 | PF00022 | 0.592 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 548 | 552 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 59 | 63 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 663 | 667 | PF00533 | 0.736 |
LIG_Clathr_ClatBox_1 | 567 | 571 | PF01394 | 0.351 |
LIG_deltaCOP1_diTrp_1 | 450 | 459 | PF00928 | 0.345 |
LIG_EH_1 | 533 | 537 | PF12763 | 0.444 |
LIG_eIF4E_1 | 297 | 303 | PF01652 | 0.431 |
LIG_eIF4E_1 | 696 | 702 | PF01652 | 0.384 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.568 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.506 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.523 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.465 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.441 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.429 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.481 |
LIG_FHA_2 | 622 | 628 | PF00498 | 0.526 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.298 |
LIG_FXI_DFP_1 | 143 | 147 | PF00024 | 0.443 |
LIG_GBD_Chelix_1 | 491 | 499 | PF00786 | 0.252 |
LIG_LIR_Apic_2 | 220 | 224 | PF02991 | 0.463 |
LIG_LIR_Apic_2 | 60 | 64 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 128 | 135 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 268 | 276 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 338 | 347 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 401 | 406 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 664 | 670 | PF02991 | 0.676 |
LIG_LIR_Nem_3 | 706 | 711 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.350 |
LIG_MLH1_MIPbox_1 | 59 | 63 | PF16413 | 0.474 |
LIG_MYND_3 | 543 | 547 | PF01753 | 0.504 |
LIG_Pex14_2 | 642 | 646 | PF04695 | 0.338 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.484 |
LIG_SH2_PTP2 | 314 | 317 | PF00017 | 0.443 |
LIG_SH2_SRC | 461 | 464 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 98 | 102 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 216 | 219 | PF00017 | 0.351 |
LIG_SH2_STAT3 | 292 | 295 | PF00017 | 0.481 |
LIG_SH2_STAT3 | 696 | 699 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 689 | 692 | PF00017 | 0.516 |
LIG_SH3_1 | 644 | 650 | PF00018 | 0.341 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.507 |
LIG_SH3_3 | 644 | 650 | PF00018 | 0.296 |
LIG_SUMO_SIM_par_1 | 424 | 433 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 536 | 542 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 566 | 571 | PF11976 | 0.351 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.672 |
LIG_UBA3_1 | 272 | 279 | PF00899 | 0.533 |
LIG_WW_1 | 71 | 74 | PF00397 | 0.468 |
MOD_CDC14_SPxK_1 | 54 | 57 | PF00782 | 0.487 |
MOD_CDK_SPxK_1 | 475 | 481 | PF00069 | 0.447 |
MOD_CDK_SPxK_1 | 51 | 57 | PF00069 | 0.515 |
MOD_CDK_SPxxK_3 | 200 | 207 | PF00069 | 0.430 |
MOD_CDK_SPxxK_3 | 343 | 350 | PF00069 | 0.561 |
MOD_CDK_SPxxK_3 | 475 | 482 | PF00069 | 0.434 |
MOD_CDK_SPxxK_3 | 51 | 58 | PF00069 | 0.517 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.541 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.529 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.649 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.659 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.655 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.453 |
MOD_CK1_1 | 652 | 658 | PF00069 | 0.619 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.664 |
MOD_CK1_1 | 671 | 677 | PF00069 | 0.676 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.453 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.468 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.435 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.554 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.547 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.481 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.348 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.604 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.399 |
MOD_Cter_Amidation | 305 | 308 | PF01082 | 0.288 |
MOD_Cter_Amidation | 411 | 414 | PF01082 | 0.385 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.511 |
MOD_GlcNHglycan | 352 | 356 | PF01048 | 0.652 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.684 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.679 |
MOD_GlcNHglycan | 430 | 435 | PF01048 | 0.442 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.303 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.661 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.677 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.733 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.736 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.627 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.549 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.649 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.507 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.414 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.479 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.566 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.476 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.547 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.646 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.463 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.516 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.446 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.477 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.378 |
MOD_N-GLC_1 | 558 | 563 | PF02516 | 0.151 |
MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.602 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.562 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.498 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.498 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.639 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.373 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.441 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.556 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.632 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.401 |
MOD_OFUCOSY | 374 | 380 | PF10250 | 0.451 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.566 |
MOD_PIKK_1 | 584 | 590 | PF00454 | 0.453 |
MOD_PKA_1 | 481 | 487 | PF00069 | 0.347 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.353 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.536 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.568 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.449 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.384 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.324 |
MOD_PKB_1 | 402 | 410 | PF00069 | 0.496 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.447 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.401 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.589 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.634 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.482 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.562 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.534 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.452 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.447 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.689 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.533 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.382 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.601 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.564 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.450 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.430 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.745 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.663 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.495 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.605 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.449 |
MOD_ProDKin_1 | 575 | 581 | PF00069 | 0.499 |
MOD_SUMO_for_1 | 632 | 635 | PF00179 | 0.251 |
MOD_SUMO_rev_2 | 275 | 281 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.323 |
TRG_DiLeu_BaEn_1 | 226 | 231 | PF01217 | 0.483 |
TRG_DiLeu_BaEn_1 | 299 | 304 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_1 | 490 | 495 | PF01217 | 0.550 |
TRG_DiLeu_BaLyEn_6 | 100 | 105 | PF01217 | 0.328 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.549 |
TRG_DiLeu_BaLyEn_6 | 298 | 303 | PF01217 | 0.431 |
TRG_DiLeu_LyEn_5 | 159 | 164 | PF01217 | 0.323 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 135 | 138 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 481 | 483 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 64 | 67 | PF00400 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Q6 | Leptomonas seymouri | 58% | 99% |
A0A0S4ISF0 | Bodo saltans | 37% | 100% |
A0A0S4KQK8 | Bodo saltans | 30% | 100% |
A0A1X0P1M0 | Trypanosomatidae | 41% | 100% |
A0A3Q8IDL7 | Leishmania donovani | 27% | 98% |
A0A3Q8IEC1 | Leishmania donovani | 76% | 100% |
A0A3S5IS28 | Trypanosoma rangeli | 44% | 100% |
A4HYN9 | Leishmania infantum | 27% | 98% |
A4I5Q6 | Leishmania infantum | 76% | 100% |
A8CVX7 | Danio rerio | 24% | 92% |
C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZR25 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZYH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AID0 | Leishmania braziliensis | 25% | 95% |
E9B101 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q765 | Leishmania major | 76% | 99% |
Q4QCW7 | Leishmania major | 27% | 100% |
V5B4U2 | Trypanosoma cruzi | 25% | 100% |
V5BLC0 | Trypanosoma cruzi | 42% | 100% |