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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: E9B124
Term | Name | Level | Count |
---|---|---|---|
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0042254 | ribosome biogenesis | 5 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0044085 | cellular component biogenesis | 3 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051052 | regulation of DNA metabolic process | 5 | 1 |
GO:0051054 | positive regulation of DNA metabolic process | 6 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 1 |
GO:0051972 | regulation of telomerase activity | 5 | 1 |
GO:0051973 | positive regulation of telomerase activity | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:2000278 | regulation of DNA biosynthetic process | 6 | 1 |
GO:2000573 | positive regulation of DNA biosynthetic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016462 | pyrophosphatase activity | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 16 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 16 |
GO:0016887 | ATP hydrolysis activity | 7 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:1990275 | preribosome binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.608 |
CLV_C14_Caspase3-7 | 617 | 621 | PF00656 | 0.324 |
CLV_C14_Caspase3-7 | 641 | 645 | PF00656 | 0.324 |
CLV_C14_Caspase3-7 | 667 | 671 | PF00656 | 0.397 |
CLV_C14_Caspase3-7 | 717 | 721 | PF00656 | 0.422 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 778 | 780 | PF00675 | 0.422 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 681 | 683 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.194 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 654 | 658 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.458 |
DEG_APCC_DBOX_1 | 178 | 186 | PF00400 | 0.411 |
DEG_APCC_DBOX_1 | 428 | 436 | PF00400 | 0.462 |
DEG_SCF_TRCP1_1 | 249 | 254 | PF00400 | 0.471 |
DOC_CDC14_PxL_1 | 684 | 692 | PF14671 | 0.472 |
DOC_CYCLIN_yClb1_LxF_4 | 654 | 660 | PF00134 | 0.369 |
DOC_MAPK_DCC_7 | 23 | 32 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 23 | 32 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 301 | 311 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 382 | 388 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 504 | 510 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 653 | 660 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 675 | 685 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 163 | 171 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 25 | 34 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 607 | 615 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 678 | 687 | PF00069 | 0.324 |
DOC_PP1_RVXF_1 | 302 | 309 | PF00149 | 0.509 |
DOC_PP1_RVXF_1 | 765 | 772 | PF00149 | 0.386 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 548 | 551 | PF13499 | 0.358 |
DOC_SPAK_OSR1_1 | 505 | 509 | PF12202 | 0.543 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 743 | 747 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.513 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.392 |
LIG_14-3-3_CanoR_1 | 121 | 126 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 157 | 161 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 170 | 176 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 234 | 238 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 276 | 282 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 362 | 368 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 387 | 393 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 481 | 486 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 499 | 504 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 628 | 636 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 693 | 701 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 779 | 786 | PF00244 | 0.556 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.422 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.425 |
LIG_deltaCOP1_diTrp_1 | 151 | 156 | PF00928 | 0.520 |
LIG_deltaCOP1_diTrp_1 | 533 | 541 | PF00928 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 768 | 775 | PF00928 | 0.380 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.520 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.527 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.464 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.487 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.395 |
LIG_FHA_2 | 460 | 466 | PF00498 | 0.344 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.551 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.377 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.305 |
LIG_FHA_2 | 639 | 645 | PF00498 | 0.324 |
LIG_FHA_2 | 687 | 693 | PF00498 | 0.559 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.331 |
LIG_FHA_2 | 747 | 753 | PF00498 | 0.278 |
LIG_Integrin_RGD_1 | 14 | 16 | PF01839 | 0.454 |
LIG_LIR_Gen_1 | 149 | 160 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 307 | 315 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 514 | 522 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 540 | 551 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 698 | 708 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 733 | 743 | PF02991 | 0.260 |
LIG_LIR_LC3C_4 | 260 | 263 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 514 | 518 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 733 | 739 | PF02991 | 0.260 |
LIG_MYND_1 | 109 | 113 | PF01753 | 0.440 |
LIG_PCNA_yPIPBox_3 | 457 | 470 | PF02747 | 0.379 |
LIG_Pex14_1 | 152 | 156 | PF04695 | 0.513 |
LIG_SH2_CRK | 557 | 561 | PF00017 | 0.324 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.410 |
LIG_SH2_PTP2 | 166 | 169 | PF00017 | 0.510 |
LIG_SH2_PTP2 | 684 | 687 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 684 | 687 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.260 |
LIG_SH3_2 | 688 | 693 | PF14604 | 0.370 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.395 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.411 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.260 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.290 |
LIG_SH3_3 | 682 | 688 | PF00018 | 0.373 |
LIG_SUMO_SIM_anti_2 | 726 | 733 | PF11976 | 0.260 |
LIG_SUMO_SIM_par_1 | 183 | 188 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 259 | 266 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 375 | 381 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 411 | 416 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 447 | 456 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.532 |
LIG_TRAF2_1 | 420 | 423 | PF00917 | 0.283 |
LIG_TRFH_1 | 546 | 550 | PF08558 | 0.360 |
LIG_TYR_ITIM | 164 | 169 | PF00017 | 0.491 |
LIG_TYR_ITSM | 65 | 72 | PF00017 | 0.529 |
MOD_CDK_SPxK_1 | 546 | 552 | PF00069 | 0.417 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.617 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.544 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.469 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.501 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.328 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.369 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.336 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.407 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.620 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.414 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.388 |
MOD_CK2_1 | 686 | 692 | PF00069 | 0.475 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.266 |
MOD_DYRK1A_RPxSP_1 | 234 | 238 | PF00069 | 0.551 |
MOD_DYRK1A_RPxSP_1 | 607 | 611 | PF00069 | 0.392 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.576 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.407 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.645 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.691 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.638 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.517 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.524 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.330 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.318 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.506 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.390 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.394 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.390 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.455 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.662 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.496 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.667 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.687 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.438 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.380 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.309 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.272 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.522 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.270 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.260 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.444 |
MOD_LATS_1 | 777 | 783 | PF00433 | 0.492 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.449 |
MOD_N-GLC_1 | 546 | 551 | PF02516 | 0.509 |
MOD_N-GLC_1 | 572 | 577 | PF02516 | 0.324 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.572 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.334 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.586 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.504 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.506 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.537 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.550 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.357 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.395 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.428 |
MOD_OFUCOSY | 431 | 437 | PF10250 | 0.373 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.447 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.361 |
MOD_PIKK_1 | 634 | 640 | PF00454 | 0.260 |
MOD_PKA_1 | 779 | 785 | PF00069 | 0.684 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.421 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.275 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.750 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.380 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.501 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.501 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.298 |
MOD_PKA_2 | 778 | 784 | PF00069 | 0.590 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.601 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.473 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.537 |
MOD_Plk_1 | 506 | 512 | PF00069 | 0.482 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.392 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.426 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.506 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.420 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.443 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.472 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.324 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.608 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.759 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.716 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.393 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.392 |
MOD_SUMO_rev_2 | 517 | 527 | PF00179 | 0.398 |
MOD_SUMO_rev_2 | 651 | 656 | PF00179 | 0.251 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 684 | 687 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 681 | 683 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 760 | 763 | PF00400 | 0.399 |
TRG_NLS_MonoExtC_3 | 757 | 762 | PF00514 | 0.272 |
TRG_Pf-PMV_PEXEL_1 | 600 | 604 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 634 | 638 | PF00026 | 0.260 |
TRG_PTS1 | 783 | 786 | PF00515 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H1 | Leptomonas seymouri | 66% | 85% |
A0A1X0P1J4 | Trypanosomatidae | 48% | 100% |
A0A3Q8IS46 | Leishmania donovani | 91% | 81% |
A0A3R7M308 | Trypanosoma rangeli | 49% | 100% |
A0A3S7X0L3 | Leishmania donovani | 32% | 100% |
A4HFM9 | Leishmania braziliensis | 33% | 100% |
A4HII5 | Leishmania braziliensis | 81% | 100% |
A4I2Q7 | Leishmania infantum | 32% | 100% |
A4I5S8 | Leishmania infantum | 91% | 75% |
C9ZR48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 99% |
E9AD83 | Leishmania major | 33% | 100% |
E9AZ07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
Q07844 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 94% |
Q4Q741 | Leishmania major | 91% | 100% |
Q8RY16 | Arabidopsis thaliana | 31% | 84% |
V5AUZ1 | Trypanosoma cruzi | 49% | 100% |