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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9APX7
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 14 |
GO:0006793 | phosphorus metabolic process | 3 | 14 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 14 |
GO:0006807 | nitrogen compound metabolic process | 2 | 14 |
GO:0008152 | metabolic process | 1 | 14 |
GO:0009987 | cellular process | 1 | 14 |
GO:0016310 | phosphorylation | 5 | 14 |
GO:0019538 | protein metabolic process | 3 | 14 |
GO:0036211 | protein modification process | 4 | 14 |
GO:0043170 | macromolecule metabolic process | 3 | 14 |
GO:0043412 | macromolecule modification | 4 | 14 |
GO:0044237 | cellular metabolic process | 2 | 14 |
GO:0044238 | primary metabolic process | 2 | 14 |
GO:0071704 | organic substance metabolic process | 2 | 14 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 14 |
GO:0000165 | MAPK cascade | 4 | 1 |
GO:0001932 | regulation of protein phosphorylation | 7 | 1 |
GO:0001934 | positive regulation of protein phosphorylation | 8 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009966 | regulation of signal transduction | 4 | 1 |
GO:0009967 | positive regulation of signal transduction | 5 | 1 |
GO:0010562 | positive regulation of phosphorus metabolic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010646 | regulation of cell communication | 4 | 1 |
GO:0010647 | positive regulation of cell communication | 5 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0023051 | regulation of signaling | 3 | 1 |
GO:0023056 | positive regulation of signaling | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031399 | regulation of protein modification process | 6 | 1 |
GO:0031401 | positive regulation of protein modification process | 7 | 1 |
GO:0033674 | positive regulation of kinase activity | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0042325 | regulation of phosphorylation | 7 | 1 |
GO:0042327 | positive regulation of phosphorylation | 8 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0043405 | regulation of MAP kinase activity | 8 | 1 |
GO:0043406 | positive regulation of MAP kinase activity | 8 | 1 |
GO:0043408 | regulation of MAPK cascade | 6 | 1 |
GO:0043410 | positive regulation of MAPK cascade | 7 | 1 |
GO:0043549 | regulation of kinase activity | 5 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045859 | regulation of protein kinase activity | 6 | 1 |
GO:0045860 | positive regulation of protein kinase activity | 7 | 1 |
GO:0045937 | positive regulation of phosphate metabolic process | 7 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0048584 | positive regulation of response to stimulus | 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:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 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:0071900 | regulation of protein serine/threonine kinase activity | 7 | 1 |
GO:0071902 | positive regulation of protein serine/threonine kinase activity | 8 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
GO:1902533 | positive regulation of intracellular signal transduction | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0003824 | catalytic activity | 1 | 14 |
GO:0004672 | protein kinase activity | 3 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0016301 | kinase activity | 4 | 14 |
GO:0016740 | transferase activity | 2 | 14 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 14 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 14 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
GO:0004708 | MAP kinase kinase activity | 5 | 1 |
GO:0004712 | protein serine/threonine/tyrosine kinase activity | 4 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0019900 | kinase binding | 4 | 1 |
GO:0019901 | protein kinase binding | 5 | 1 |
GO:0051019 | mitogen-activated protein kinase binding | 6 | 1 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.303 |
CLV_C14_Caspase3-7 | 652 | 656 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.593 |
CLV_PCSK_FUR_1 | 461 | 465 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.264 |
CLV_PCSK_PC1ET2_1 | 460 | 462 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 463 | 465 | PF00082 | 0.597 |
CLV_PCSK_PC7_1 | 464 | 470 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.442 |
DOC_CKS1_1 | 385 | 390 | PF01111 | 0.547 |
DOC_CKS1_1 | 394 | 399 | PF01111 | 0.549 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 418 | 427 | PF00134 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 8 | 14 | PF00134 | 0.551 |
DOC_MAPK_gen_1 | 233 | 242 | PF00069 | 0.258 |
DOC_MAPK_gen_1 | 631 | 638 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 17 | 23 | PF00149 | 0.509 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.245 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.264 |
DOC_PP4_FxxP_1 | 394 | 397 | PF00568 | 0.524 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.264 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.541 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 404 | 409 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 515 | 520 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 547 | 556 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 604 | 610 | PF00244 | 0.651 |
LIG_14-3-3_CterR_2 | 710 | 713 | PF00244 | 0.521 |
LIG_Actin_WH2_2 | 596 | 612 | PF00022 | 0.549 |
LIG_APCC_ABBA_1 | 184 | 189 | PF00400 | 0.264 |
LIG_APCC_ABBAyCdc20_2 | 228 | 234 | PF00400 | 0.439 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.492 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.492 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.492 |
LIG_deltaCOP1_diTrp_1 | 339 | 349 | PF00928 | 0.264 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.475 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.284 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.235 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.286 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.264 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.625 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.525 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.264 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.593 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.361 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.639 |
LIG_FHA_2 | 624 | 630 | PF00498 | 0.513 |
LIG_LIR_Apic_2 | 205 | 209 | PF02991 | 0.245 |
LIG_LIR_Apic_2 | 272 | 278 | PF02991 | 0.530 |
LIG_LIR_Apic_2 | 392 | 397 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 371 | 379 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 657 | 663 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.379 |
LIG_PALB2_WD40_1 | 368 | 376 | PF16756 | 0.212 |
LIG_PTAP_UEV_1 | 396 | 401 | PF05743 | 0.511 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.552 |
LIG_SH2_CRK | 533 | 537 | PF00017 | 0.531 |
LIG_SH2_CRK | 660 | 664 | PF00017 | 0.509 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.436 |
LIG_SH2_GRB2like | 174 | 177 | PF00017 | 0.264 |
LIG_SH2_NCK_1 | 533 | 537 | PF00017 | 0.531 |
LIG_SH2_SRC | 335 | 338 | PF00017 | 0.264 |
LIG_SH2_STAP1 | 598 | 602 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 624 | 628 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 554 | 557 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.504 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.580 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.264 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.659 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.528 |
LIG_SUMO_SIM_anti_2 | 159 | 164 | PF11976 | 0.282 |
LIG_SUMO_SIM_anti_2 | 363 | 369 | PF11976 | 0.264 |
LIG_SUMO_SIM_anti_2 | 599 | 605 | PF11976 | 0.495 |
LIG_TRAF2_1 | 205 | 208 | PF00917 | 0.264 |
LIG_TYR_ITIM | 658 | 663 | PF00017 | 0.510 |
LIG_UBA3_1 | 99 | 103 | PF00899 | 0.331 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.264 |
LIG_WRC_WIRS_1 | 391 | 396 | PF05994 | 0.527 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.264 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.232 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.516 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.270 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.256 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.626 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.586 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.650 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.592 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.592 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.571 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.579 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.622 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.566 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.603 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.562 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.558 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.499 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.456 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.533 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.426 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.342 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.638 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.568 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.648 |
MOD_CK2_1 | 623 | 629 | PF00069 | 0.528 |
MOD_Cter_Amidation | 458 | 461 | PF01082 | 0.597 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.572 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.458 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.293 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.576 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.304 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.244 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.268 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.610 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.620 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.582 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.552 |
MOD_GlcNHglycan | 505 | 509 | PF01048 | 0.604 |
MOD_GlcNHglycan | 52 | 57 | PF01048 | 0.564 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.601 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.533 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.589 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.524 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.539 |
MOD_GlcNHglycan | 687 | 691 | PF01048 | 0.511 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.531 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.568 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.384 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.554 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.573 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.702 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.597 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.580 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.617 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.569 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.541 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.571 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.592 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.565 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.585 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.644 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.639 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.603 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.517 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.520 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.422 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.515 |
MOD_N-GLC_1 | 444 | 449 | PF02516 | 0.546 |
MOD_N-GLC_1 | 576 | 581 | PF02516 | 0.568 |
MOD_N-GLC_1 | 605 | 610 | PF02516 | 0.527 |
MOD_N-GLC_1 | 696 | 701 | PF02516 | 0.506 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.482 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.614 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.368 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.555 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.306 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.495 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.609 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.568 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.637 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.552 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.538 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.353 |
MOD_NEK2_2 | 702 | 707 | PF00069 | 0.531 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.266 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.299 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.586 |
MOD_PKA_1 | 46 | 52 | PF00069 | 0.524 |
MOD_PKA_1 | 463 | 469 | PF00069 | 0.594 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.490 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.530 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.607 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.575 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.538 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.575 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.568 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.632 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.661 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.412 |
MOD_PKB_1 | 502 | 510 | PF00069 | 0.567 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.284 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.247 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.476 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.544 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.539 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.537 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.552 |
MOD_Plk_1 | 696 | 702 | PF00069 | 0.501 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.284 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.254 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.587 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.577 |
MOD_Plk_4 | 678 | 684 | PF00069 | 0.546 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.577 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.561 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.603 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.662 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.496 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.514 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.546 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.587 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.544 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.553 |
MOD_SUMO_for_1 | 143 | 146 | PF00179 | 0.516 |
MOD_SUMO_for_1 | 156 | 159 | PF00179 | 0.222 |
MOD_SUMO_for_1 | 75 | 78 | PF00179 | 0.379 |
TRG_DiLeu_BaEn_2 | 344 | 350 | PF01217 | 0.264 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 660 | 663 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.520 |
TRG_NES_CRM1_1 | 345 | 360 | PF08389 | 0.212 |
TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.264 |
TRG_Pf-PMV_PEXEL_1 | 233 | 238 | PF00026 | 0.258 |
TRG_Pf-PMV_PEXEL_1 | 651 | 655 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAX0 | Leishmania donovani | 25% | 100% |
A4H7V0 | Leishmania braziliensis | 76% | 100% |
A4HNU6 | Leishmania braziliensis | 26% | 100% |
A4HW76 | Leishmania infantum | 86% | 89% |
A4IDK3 | Leishmania infantum | 25% | 100% |
E9AH34 | Leishmania infantum | 22% | 100% |
E9ASK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AT06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AWL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
Q4Q1J2 | Leishmania major | 25% | 100% |
Q4Q1Z0 | Leishmania major | 26% | 100% |
Q4QFK4 | Leishmania major | 86% | 99% |