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. | yes | yes: 30 |
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 2 |
GO:0005929 | cilium | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0020016 | ciliary pocket | 2 | 2 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 2 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0099080 | supramolecular complex | 2 | 2 |
GO:0099081 | supramolecular polymer | 3 | 2 |
GO:0099512 | supramolecular fiber | 4 | 2 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 8 |
GO:0007018 | microtubule-based movement | 3 | 8 |
GO:0009987 | cellular process | 1 | 9 |
GO:0000281 | mitotic cytokinesis | 4 | 1 |
GO:0000910 | cytokinesis | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003774 | cytoskeletal motor activity | 1 | 8 |
GO:0003777 | microtubule motor activity | 2 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005515 | protein binding | 2 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0008017 | microtubule binding | 5 | 8 |
GO:0008092 | cytoskeletal protein binding | 3 | 8 |
GO:0015631 | tubulin binding | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 36 | 40 | PF00656 | 0.501 |
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.332 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 2302 | 2304 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.636 |
CLV_PCSK_FUR_1 | 440 | 444 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 2302 | 2304 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 653 | 655 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.575 |
DEG_APCC_DBOX_1 | 321 | 329 | PF00400 | 0.435 |
DEG_APCC_DBOX_1 | 550 | 558 | PF00400 | 0.595 |
DEG_SPOP_SBC_1 | 18 | 22 | PF00917 | 0.590 |
DEG_SPOP_SBC_1 | 34 | 38 | PF00917 | 0.505 |
DOC_CKS1_1 | 119 | 124 | PF01111 | 0.435 |
DOC_CYCLIN_RxL_1 | 468 | 479 | PF00134 | 0.475 |
DOC_CYCLIN_RxL_1 | 548 | 556 | PF00134 | 0.592 |
DOC_MAPK_gen_1 | 1894 | 1902 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 1971 | 1979 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 2216 | 2224 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 288 | 298 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 425 | 432 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 470 | 476 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 627 | 634 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 683 | 691 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 746 | 754 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 291 | 300 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 345 | 354 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 534 | 542 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 627 | 634 | PF00069 | 0.463 |
DOC_PP1_RVXF_1 | 383 | 389 | PF00149 | 0.496 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.337 |
DOC_USP7_UBL2_3 | 1816 | 1820 | PF12436 | 0.553 |
DOC_USP7_UBL2_3 | 1886 | 1890 | PF12436 | 0.555 |
DOC_USP7_UBL2_3 | 1963 | 1967 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 2040 | 2044 | PF12436 | 0.601 |
DOC_USP7_UBL2_3 | 2145 | 2149 | PF12436 | 0.564 |
DOC_USP7_UBL2_3 | 2208 | 2212 | PF12436 | 0.566 |
DOC_USP7_UBL2_3 | 229 | 233 | PF12436 | 0.435 |
DOC_USP7_UBL2_3 | 555 | 559 | PF12436 | 0.547 |
DOC_USP7_UBL2_3 | 679 | 683 | PF12436 | 0.535 |
DOC_USP7_UBL2_3 | 738 | 742 | PF12436 | 0.580 |
DOC_USP7_UBL2_3 | 857 | 861 | PF12436 | 0.593 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 1850 | 1860 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 1927 | 1937 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 195 | 200 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 2004 | 2014 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 2081 | 2091 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 2186 | 2196 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 2249 | 2259 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 278 | 285 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 288 | 298 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 589 | 596 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 620 | 630 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 716 | 726 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 76 | 82 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 779 | 789 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 898 | 908 | PF00244 | 0.515 |
LIG_APCC_ABBA_1 | 214 | 219 | PF00400 | 0.517 |
LIG_APCC_ABBA_1 | 378 | 383 | PF00400 | 0.461 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.699 |
LIG_BIR_III_4 | 123 | 127 | PF00653 | 0.435 |
LIG_BRCT_BRCA1_1 | 152 | 156 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 397 | 401 | PF00533 | 0.455 |
LIG_CaM_IQ_9 | 484 | 500 | PF13499 | 0.602 |
LIG_Clathr_ClatBox_1 | 1857 | 1861 | PF01394 | 0.518 |
LIG_Clathr_ClatBox_1 | 1934 | 1938 | PF01394 | 0.506 |
LIG_Clathr_ClatBox_1 | 2011 | 2015 | PF01394 | 0.507 |
LIG_Clathr_ClatBox_1 | 2088 | 2092 | PF01394 | 0.515 |
LIG_Clathr_ClatBox_1 | 2193 | 2197 | PF01394 | 0.520 |
LIG_Clathr_ClatBox_1 | 2256 | 2260 | PF01394 | 0.514 |
LIG_Clathr_ClatBox_1 | 473 | 477 | PF01394 | 0.456 |
LIG_Clathr_ClatBox_1 | 723 | 727 | PF01394 | 0.497 |
LIG_Clathr_ClatBox_1 | 786 | 790 | PF01394 | 0.520 |
LIG_Clathr_ClatBox_1 | 905 | 909 | PF01394 | 0.549 |
LIG_EH1_1 | 292 | 300 | PF00400 | 0.435 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.435 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.534 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.538 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.350 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.397 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.292 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.443 |
LIG_FHA_2 | 1822 | 1828 | PF00498 | 0.549 |
LIG_FHA_2 | 1899 | 1905 | PF00498 | 0.497 |
LIG_FHA_2 | 1976 | 1982 | PF00498 | 0.500 |
LIG_FHA_2 | 2053 | 2059 | PF00498 | 0.530 |
LIG_FHA_2 | 2158 | 2164 | PF00498 | 0.519 |
LIG_FHA_2 | 2221 | 2227 | PF00498 | 0.539 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.545 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.656 |
LIG_FHA_2 | 653 | 659 | PF00498 | 0.465 |
LIG_FHA_2 | 688 | 694 | PF00498 | 0.544 |
LIG_FHA_2 | 751 | 757 | PF00498 | 0.549 |
LIG_FHA_2 | 870 | 876 | PF00498 | 0.574 |
LIG_KLC1_Yacidic_2 | 237 | 242 | PF13176 | 0.352 |
LIG_LIR_Gen_1 | 166 | 174 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 210 | 221 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 237 | 247 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 655 | 665 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 655 | 660 | PF02991 | 0.425 |
LIG_LYPXL_yS_3 | 141 | 144 | PF13949 | 0.435 |
LIG_PCNA_yPIPBox_3 | 218 | 230 | PF02747 | 0.435 |
LIG_Pex14_2 | 112 | 116 | PF04695 | 0.500 |
LIG_RPA_C_Fungi | 422 | 434 | PF08784 | 0.455 |
LIG_SH2_CRK | 376 | 380 | PF00017 | 0.290 |
LIG_SH2_NCK_1 | 376 | 380 | PF00017 | 0.455 |
LIG_SH2_PTP2 | 213 | 216 | PF00017 | 0.435 |
LIG_SH2_PTP2 | 240 | 243 | PF00017 | 0.352 |
LIG_SH2_SRC | 213 | 216 | PF00017 | 0.435 |
LIG_SH2_SRC | 240 | 243 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 413 | 417 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 422 | 426 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.500 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.635 |
LIG_SH3_2 | 5 | 10 | PF14604 | 0.629 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.635 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.658 |
LIG_SH3_3 | 2295 | 2301 | PF00018 | 0.594 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.548 |
LIG_SUMO_SIM_par_1 | 257 | 263 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 296 | 303 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 472 | 479 | PF11976 | 0.454 |
LIG_TRAF2_1 | 601 | 604 | PF00917 | 0.553 |
LIG_TYR_ITIM | 139 | 144 | PF00017 | 0.435 |
LIG_TYR_ITIM | 211 | 216 | PF00017 | 0.435 |
LIG_TYR_ITSM | 653 | 660 | PF00017 | 0.419 |
LIG_UBA3_1 | 553 | 560 | PF00899 | 0.617 |
LIG_UBA3_1 | 606 | 613 | PF00899 | 0.570 |
LIG_UBA3_1 | 648 | 653 | PF00899 | 0.449 |
MOD_CDC14_SPxK_1 | 7 | 10 | PF00782 | 0.629 |
MOD_CDK_SPK_2 | 182 | 187 | PF00069 | 0.435 |
MOD_CDK_SPxK_1 | 4 | 10 | PF00069 | 0.629 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.627 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.286 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.376 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.521 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.385 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.426 |
MOD_CK1_1 | 1821 | 1827 | PF00069 | 0.539 |
MOD_CK1_1 | 1898 | 1904 | PF00069 | 0.500 |
MOD_CK1_1 | 1975 | 1981 | PF00069 | 0.505 |
MOD_CK1_1 | 2052 | 2058 | PF00069 | 0.534 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.572 |
MOD_CK1_1 | 2157 | 2163 | PF00069 | 0.523 |
MOD_CK1_1 | 2220 | 2226 | PF00069 | 0.520 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.472 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.437 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.505 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.538 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.683 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.520 |
MOD_CK1_1 | 750 | 756 | PF00069 | 0.517 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.321 |
MOD_CK1_1 | 869 | 875 | PF00069 | 0.553 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.273 |
MOD_CK2_1 | 1821 | 1827 | PF00069 | 0.592 |
MOD_CK2_1 | 1898 | 1904 | PF00069 | 0.561 |
MOD_CK2_1 | 1975 | 1981 | PF00069 | 0.548 |
MOD_CK2_1 | 2052 | 2058 | PF00069 | 0.586 |
MOD_CK2_1 | 2157 | 2163 | PF00069 | 0.612 |
MOD_CK2_1 | 2220 | 2226 | PF00069 | 0.602 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.451 |
MOD_CK2_1 | 504 | 510 | PF00069 | 0.664 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.480 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.613 |
MOD_CK2_1 | 750 | 756 | PF00069 | 0.555 |
MOD_CK2_1 | 869 | 875 | PF00069 | 0.616 |
MOD_Cter_Amidation | 225 | 228 | PF01082 | 0.435 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.521 |
MOD_GlcNHglycan | 173 | 177 | PF01048 | 0.397 |
MOD_GlcNHglycan | 180 | 184 | PF01048 | 0.369 |
MOD_GlcNHglycan | 1827 | 1831 | PF01048 | 0.525 |
MOD_GlcNHglycan | 1904 | 1908 | PF01048 | 0.495 |
MOD_GlcNHglycan | 1981 | 1985 | PF01048 | 0.522 |
MOD_GlcNHglycan | 2058 | 2062 | PF01048 | 0.541 |
MOD_GlcNHglycan | 2163 | 2167 | PF01048 | 0.544 |
MOD_GlcNHglycan | 2226 | 2230 | PF01048 | 0.547 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.455 |
MOD_GlcNHglycan | 54 | 58 | PF01048 | 0.406 |
MOD_GlcNHglycan | 693 | 697 | PF01048 | 0.576 |
MOD_GlcNHglycan | 756 | 760 | PF01048 | 0.551 |
MOD_GlcNHglycan | 875 | 879 | PF01048 | 0.610 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.425 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.662 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.389 |
MOD_GSK3_1 | 1821 | 1828 | PF00069 | 0.538 |
MOD_GSK3_1 | 1838 | 1845 | PF00069 | 0.454 |
MOD_GSK3_1 | 1898 | 1905 | PF00069 | 0.500 |
MOD_GSK3_1 | 1915 | 1922 | PF00069 | 0.458 |
MOD_GSK3_1 | 1975 | 1982 | PF00069 | 0.505 |
MOD_GSK3_1 | 1992 | 1999 | PF00069 | 0.454 |
MOD_GSK3_1 | 2052 | 2059 | PF00069 | 0.535 |
MOD_GSK3_1 | 2069 | 2076 | PF00069 | 0.464 |
MOD_GSK3_1 | 2157 | 2164 | PF00069 | 0.524 |
MOD_GSK3_1 | 2174 | 2181 | PF00069 | 0.493 |
MOD_GSK3_1 | 2220 | 2227 | PF00069 | 0.559 |
MOD_GSK3_1 | 2237 | 2244 | PF00069 | 0.480 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.387 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.420 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.555 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.521 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.290 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.552 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.301 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.532 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.591 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.589 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.327 |
MOD_GSK3_1 | 767 | 774 | PF00069 | 0.475 |
MOD_GSK3_1 | 869 | 876 | PF00069 | 0.586 |
MOD_GSK3_1 | 886 | 893 | PF00069 | 0.481 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.365 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.297 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.517 |
MOD_N-GLC_2 | 152 | 154 | PF02516 | 0.435 |
MOD_NEK2_1 | 1818 | 1823 | PF00069 | 0.586 |
MOD_NEK2_1 | 1825 | 1830 | PF00069 | 0.528 |
MOD_NEK2_1 | 1895 | 1900 | PF00069 | 0.526 |
MOD_NEK2_1 | 1902 | 1907 | PF00069 | 0.489 |
MOD_NEK2_1 | 1972 | 1977 | PF00069 | 0.577 |
MOD_NEK2_1 | 1979 | 1984 | PF00069 | 0.533 |
MOD_NEK2_1 | 2049 | 2054 | PF00069 | 0.597 |
MOD_NEK2_1 | 2056 | 2061 | PF00069 | 0.590 |
MOD_NEK2_1 | 2154 | 2159 | PF00069 | 0.553 |
MOD_NEK2_1 | 2161 | 2166 | PF00069 | 0.519 |
MOD_NEK2_1 | 2217 | 2222 | PF00069 | 0.605 |
MOD_NEK2_1 | 2224 | 2229 | PF00069 | 0.586 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.581 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.435 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.538 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.408 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.414 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.611 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.621 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.618 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.633 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.533 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.377 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.682 |
MOD_NEK2_1 | 873 | 878 | PF00069 | 0.620 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.303 |
MOD_NEK2_2 | 273 | 278 | PF00069 | 0.328 |
MOD_NEK2_2 | 310 | 315 | PF00069 | 0.290 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.517 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.451 |
MOD_PK_1 | 195 | 201 | PF00069 | 0.435 |
MOD_PKA_1 | 195 | 201 | PF00069 | 0.435 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.605 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.406 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.435 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.342 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.538 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.602 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.544 |
MOD_Plk_1 | 1151 | 1157 | PF00069 | 0.613 |
MOD_Plk_1 | 1641 | 1647 | PF00069 | 0.597 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.393 |
MOD_Plk_1 | 1739 | 1745 | PF00069 | 0.612 |
MOD_Plk_1 | 1895 | 1901 | PF00069 | 0.511 |
MOD_Plk_1 | 1972 | 1978 | PF00069 | 0.516 |
MOD_Plk_1 | 2217 | 2223 | PF00069 | 0.528 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.435 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.496 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.538 |
MOD_Plk_1 | 684 | 690 | PF00069 | 0.548 |
MOD_Plk_1 | 747 | 753 | PF00069 | 0.570 |
MOD_Plk_2-3 | 260 | 266 | PF00069 | 0.393 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.290 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.435 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.480 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.400 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.486 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.621 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.463 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.409 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.435 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.546 |
MOD_SUMO_for_1 | 1893 | 1896 | PF00179 | 0.533 |
MOD_SUMO_for_1 | 1970 | 1973 | PF00179 | 0.547 |
MOD_SUMO_for_1 | 2047 | 2050 | PF00179 | 0.579 |
MOD_SUMO_for_1 | 2152 | 2155 | PF00179 | 0.559 |
MOD_SUMO_for_1 | 2215 | 2218 | PF00179 | 0.585 |
MOD_SUMO_for_1 | 542 | 545 | PF00179 | 0.583 |
MOD_SUMO_for_1 | 682 | 685 | PF00179 | 0.508 |
MOD_SUMO_for_1 | 745 | 748 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 1833 | 1841 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 1910 | 1918 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 1987 | 1995 | PF00179 | 0.563 |
MOD_SUMO_rev_2 | 2064 | 2072 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 2169 | 2177 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 2232 | 2240 | PF00179 | 0.527 |
MOD_SUMO_rev_2 | 377 | 387 | PF00179 | 0.414 |
MOD_SUMO_rev_2 | 584 | 591 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 699 | 707 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 762 | 770 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 881 | 889 | PF00179 | 0.576 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_1 | 566 | 571 | PF01217 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 266 | 271 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 499 | 504 | PF01217 | 0.625 |
TRG_DiLeu_BaLyEn_6 | 644 | 649 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 73 | 78 | PF01217 | 0.332 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 2301 | 2303 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 439 | 442 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.419 |
TRG_NLS_MonoCore_2 | 226 | 231 | PF00514 | 0.435 |
TRG_NLS_MonoExtN_4 | 227 | 232 | PF00514 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 442 | 446 | PF00026 | 0.690 |
TRG_Pf-PMV_PEXEL_1 | 551 | 556 | PF00026 | 0.630 |
TRG_Pf-PMV_PEXEL_1 | 647 | 651 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I9Y0 | Leishmania donovani | 54% | 68% |
A4H7R4 | Leishmania braziliensis | 49% | 96% |
A4HW58 | Leishmania infantum | 27% | 79% |
E8NHK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 97% |
Q4Q3D8 | Leishmania major | 30% | 73% |
Q4QEL9 | Leishmania major | 22% | 100% |
Q4QFM2 | Leishmania major | 31% | 78% |