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: 10 |
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 | yes | yes: 6, no: 6 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005795 | Golgi stack | 4 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IHJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009987 | cellular process | 1 | 13 |
GO:0015031 | protein transport | 4 | 11 |
GO:0016043 | cellular component organization | 3 | 13 |
GO:0022411 | cellular component disassembly | 4 | 13 |
GO:0032984 | protein-containing complex disassembly | 5 | 13 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0035494 | SNARE complex disassembly | 6 | 13 |
GO:0043933 | protein-containing complex organization | 4 | 13 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 13 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006893 | Golgi to plasma membrane transport | 5 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0043001 | Golgi to plasma membrane protein transport | 5 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0061951 | establishment of protein localization to plasma membrane | 5 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0072659 | protein localization to plasma membrane | 5 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:0098876 | vesicle-mediated transport to the plasma membrane | 4 | 1 |
GO:1990778 | protein localization to cell periphery | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016462 | pyrophosphatase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 13 |
GO:0016887 | ATP hydrolysis activity | 7 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.547 |
CLV_C14_Caspase3-7 | 447 | 451 | PF00656 | 0.322 |
CLV_MEL_PAP_1 | 211 | 217 | PF00089 | 0.446 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 837 | 839 | PF00675 | 0.364 |
CLV_PCSK_FUR_1 | 260 | 264 | PF00082 | 0.500 |
CLV_PCSK_FUR_1 | 546 | 550 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 656 | 658 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 708 | 710 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 837 | 839 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 656 | 658 | PF00082 | 0.455 |
CLV_PCSK_PC7_1 | 190 | 196 | PF00082 | 0.639 |
CLV_PCSK_PC7_1 | 293 | 299 | PF00082 | 0.443 |
CLV_PCSK_PC7_1 | 396 | 402 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 691 | 695 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 724 | 728 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 761 | 765 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 869 | 873 | PF00082 | 0.362 |
DEG_APCC_DBOX_1 | 297 | 305 | PF00400 | 0.357 |
DEG_APCC_DBOX_1 | 454 | 462 | PF00400 | 0.380 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.479 |
DEG_ODPH_VHL_1 | 511 | 522 | PF01847 | 0.365 |
DEG_SPOP_SBC_1 | 812 | 816 | PF00917 | 0.397 |
DOC_CDC14_PxL_1 | 301 | 309 | PF14671 | 0.434 |
DOC_CYCLIN_RxL_1 | 108 | 116 | PF00134 | 0.577 |
DOC_CYCLIN_RxL_1 | 758 | 766 | PF00134 | 0.380 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 334 | 343 | PF00134 | 0.380 |
DOC_CYCLIN_yCln2_LP_2 | 250 | 256 | PF00134 | 0.602 |
DOC_MAPK_gen_1 | 208 | 215 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 406 | 414 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 453 | 461 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 476 | 486 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 667 | 677 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 208 | 215 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 406 | 415 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 455 | 463 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 479 | 486 | PF00069 | 0.296 |
DOC_MAPK_RevD_3 | 409 | 425 | PF00069 | 0.325 |
DOC_PP1_RVXF_1 | 11 | 17 | PF00149 | 0.454 |
DOC_PP1_RVXF_1 | 234 | 240 | PF00149 | 0.559 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.601 |
DOC_PP4_FxxP_1 | 510 | 513 | PF00568 | 0.466 |
DOC_SPAK_OSR1_1 | 479 | 483 | PF12202 | 0.296 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.249 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 852 | 856 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 944 | 948 | PF00917 | 0.576 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 779 | 784 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 202 | 207 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 348 | 352 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 537 | 543 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 639 | 645 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 657 | 665 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 703 | 710 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 873 | 879 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 953 | 957 | PF00244 | 0.407 |
LIG_Actin_WH2_2 | 163 | 181 | PF00022 | 0.411 |
LIG_Actin_WH2_2 | 200 | 216 | PF00022 | 0.589 |
LIG_Actin_WH2_2 | 355 | 372 | PF00022 | 0.380 |
LIG_Actin_WH2_2 | 460 | 478 | PF00022 | 0.284 |
LIG_Actin_WH2_2 | 823 | 839 | PF00022 | 0.500 |
LIG_BIR_III_2 | 39 | 43 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.475 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.426 |
LIG_BRCT_BRCA1_1 | 944 | 948 | PF00533 | 0.628 |
LIG_CtBP_PxDLS_1 | 863 | 867 | PF00389 | 0.398 |
LIG_eIF4E_1 | 547 | 553 | PF01652 | 0.539 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.691 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.422 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.531 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.562 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.465 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.472 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.254 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.284 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.338 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.693 |
LIG_FHA_1 | 657 | 663 | PF00498 | 0.498 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.566 |
LIG_FHA_1 | 812 | 818 | PF00498 | 0.430 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.482 |
LIG_FHA_1 | 905 | 911 | PF00498 | 0.665 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.759 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.269 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.462 |
LIG_FHA_2 | 953 | 959 | PF00498 | 0.492 |
LIG_GBD_Chelix_1 | 335 | 343 | PF00786 | 0.340 |
LIG_GBD_Chelix_1 | 459 | 467 | PF00786 | 0.286 |
LIG_LIR_Apic_2 | 507 | 513 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 15 | 23 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 277 | 288 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 416 | 422 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 541 | 547 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 698 | 705 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 741 | 750 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 870 | 879 | PF02991 | 0.492 |
LIG_LIR_LC3C_4 | 457 | 461 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 541 | 545 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 698 | 702 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 741 | 746 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 865 | 871 | PF02991 | 0.325 |
LIG_MAD2 | 137 | 145 | PF02301 | 0.488 |
LIG_MYND_1 | 305 | 309 | PF01753 | 0.516 |
LIG_NRBOX | 338 | 344 | PF00104 | 0.356 |
LIG_NRBOX | 759 | 765 | PF00104 | 0.424 |
LIG_PCNA_PIPBox_1 | 244 | 253 | PF02747 | 0.571 |
LIG_PCNA_yPIPBox_3 | 106 | 119 | PF02747 | 0.450 |
LIG_PCNA_yPIPBox_3 | 243 | 251 | PF02747 | 0.562 |
LIG_PCNA_yPIPBox_3 | 664 | 676 | PF02747 | 0.359 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.447 |
LIG_Pex14_2 | 418 | 422 | PF04695 | 0.348 |
LIG_Pex14_2 | 613 | 617 | PF04695 | 0.441 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.569 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.610 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.416 |
LIG_SH2_CRK | 438 | 442 | PF00017 | 0.283 |
LIG_SH2_CRK | 542 | 546 | PF00017 | 0.458 |
LIG_SH2_CRK | 743 | 747 | PF00017 | 0.363 |
LIG_SH2_SRC | 376 | 379 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 743 | 747 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.679 |
LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 913 | 916 | PF00017 | 0.569 |
LIG_SH3_2 | 489 | 494 | PF14604 | 0.502 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.624 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.487 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.466 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.556 |
LIG_SH3_3 | 846 | 852 | PF00018 | 0.491 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.504 |
LIG_SUMO_SIM_anti_2 | 17 | 22 | PF11976 | 0.490 |
LIG_SUMO_SIM_anti_2 | 203 | 208 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 347 | 353 | PF11976 | 0.285 |
LIG_SUMO_SIM_anti_2 | 444 | 450 | PF11976 | 0.352 |
LIG_SUMO_SIM_anti_2 | 457 | 462 | PF11976 | 0.269 |
LIG_SUMO_SIM_anti_2 | 733 | 742 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 15 | 22 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 410 | 417 | PF11976 | 0.267 |
LIG_SUMO_SIM_par_1 | 444 | 450 | PF11976 | 0.264 |
LIG_SUMO_SIM_par_1 | 673 | 679 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 733 | 742 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 782 | 789 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 809 | 816 | PF11976 | 0.348 |
LIG_TRAF2_1 | 196 | 199 | PF00917 | 0.493 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.574 |
LIG_TRAF2_1 | 382 | 385 | PF00917 | 0.279 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.249 |
LIG_TYR_ITIM | 540 | 545 | PF00017 | 0.457 |
LIG_UBA3_1 | 445 | 453 | PF00899 | 0.369 |
LIG_WRC_WIRS_1 | 868 | 873 | PF05994 | 0.461 |
MOD_CDK_SPK_2 | 226 | 231 | PF00069 | 0.563 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.382 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.660 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.387 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.334 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.443 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.614 |
MOD_CK1_1 | 628 | 634 | PF00069 | 0.593 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.468 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.677 |
MOD_CK1_1 | 800 | 806 | PF00069 | 0.554 |
MOD_CK1_1 | 815 | 821 | PF00069 | 0.380 |
MOD_CK1_1 | 867 | 873 | PF00069 | 0.458 |
MOD_CK1_1 | 896 | 902 | PF00069 | 0.648 |
MOD_CK1_1 | 903 | 909 | PF00069 | 0.591 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.592 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.687 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.534 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.391 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.286 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.380 |
MOD_CK2_1 | 896 | 902 | PF00069 | 0.644 |
MOD_CK2_1 | 903 | 909 | PF00069 | 0.689 |
MOD_CK2_1 | 970 | 976 | PF00069 | 0.541 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.621 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.632 |
MOD_GlcNHglycan | 395 | 399 | PF01048 | 0.339 |
MOD_GlcNHglycan | 430 | 435 | PF01048 | 0.294 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.308 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.405 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.379 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.361 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.792 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.642 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.623 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.540 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.531 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.555 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.395 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.504 |
MOD_GlcNHglycan | 802 | 805 | PF01048 | 0.567 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.644 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.589 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.653 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.716 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.382 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.465 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.325 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.383 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.625 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.549 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.380 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.424 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.473 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.575 |
MOD_GSK3_1 | 811 | 818 | PF00069 | 0.370 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.688 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.670 |
MOD_N-GLC_1 | 668 | 673 | PF02516 | 0.631 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.477 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.561 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.626 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.551 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.461 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.370 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.562 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.648 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.483 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.532 |
MOD_NEK2_1 | 811 | 816 | PF00069 | 0.298 |
MOD_NEK2_2 | 756 | 761 | PF00069 | 0.279 |
MOD_NEK2_2 | 852 | 857 | PF00069 | 0.456 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.509 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.577 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.592 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.681 |
MOD_PIKK_1 | 628 | 634 | PF00454 | 0.562 |
MOD_PIKK_1 | 893 | 899 | PF00454 | 0.524 |
MOD_PKA_1 | 656 | 662 | PF00069 | 0.479 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.457 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.604 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.711 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.321 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.547 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.709 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.467 |
MOD_PKA_2 | 800 | 806 | PF00069 | 0.547 |
MOD_PKA_2 | 872 | 878 | PF00069 | 0.338 |
MOD_PKA_2 | 952 | 958 | PF00069 | 0.486 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.506 |
MOD_PKB_1 | 423 | 431 | PF00069 | 0.264 |
MOD_Plk_1 | 624 | 630 | PF00069 | 0.591 |
MOD_Plk_1 | 668 | 674 | PF00069 | 0.421 |
MOD_Plk_1 | 697 | 703 | PF00069 | 0.380 |
MOD_Plk_1 | 875 | 881 | PF00069 | 0.359 |
MOD_Plk_1 | 904 | 910 | PF00069 | 0.604 |
MOD_Plk_2-3 | 235 | 241 | PF00069 | 0.521 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.559 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.517 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.597 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.296 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.296 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.287 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.444 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.494 |
MOD_Plk_4 | 816 | 822 | PF00069 | 0.444 |
MOD_Plk_4 | 944 | 950 | PF00069 | 0.497 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.642 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.785 |
MOD_ProDKin_1 | 599 | 605 | PF00069 | 0.623 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.529 |
MOD_ProDKin_1 | 779 | 785 | PF00069 | 0.575 |
MOD_SUMO_for_1 | 221 | 224 | PF00179 | 0.577 |
MOD_SUMO_for_1 | 288 | 291 | PF00179 | 0.470 |
MOD_SUMO_for_1 | 623 | 626 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 971 | 981 | PF00179 | 0.681 |
TRG_AP2beta_CARGO_1 | 416 | 425 | PF09066 | 0.348 |
TRG_DiLeu_BaEn_2 | 494 | 500 | PF01217 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.631 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 160 | 165 | PF01217 | 0.583 |
TRG_DiLeu_BaLyEn_6 | 338 | 343 | PF01217 | 0.356 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.660 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 743 | 746 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 765 | 768 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 868 | 871 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 924 | 927 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 422 | 425 | PF00400 | 0.264 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 708 | 710 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 836 | 838 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 927 | 930 | PF00400 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 518 | 523 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 761 | 766 | PF00026 | 0.365 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6X6 | Leptomonas seymouri | 61% | 98% |
A0A1X0P437 | Trypanosomatidae | 34% | 100% |
A0A422MWC2 | Trypanosoma rangeli | 34% | 100% |
A4HFN1 | Leishmania braziliensis | 79% | 100% |
A4I2Q9 | Leishmania infantum | 100% | 100% |
D0A5W2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AD85 | Leishmania major | 94% | 100% |
E9AID2 | Leishmania braziliensis | 32% | 100% |
E9AUL9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AZ09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5AT58 | Trypanosoma cruzi | 35% | 100% |