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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H7V0
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 13 |
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
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 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004672 | protein kinase activity | 3 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 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:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
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 | 177 | 181 | PF00656 | 0.320 |
CLV_C14_Caspase3-7 | 568 | 572 | PF00656 | 0.522 |
CLV_C14_Caspase3-7 | 649 | 653 | PF00656 | 0.550 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.654 |
CLV_PCSK_FUR_1 | 457 | 461 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 460 | 466 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.495 |
DEG_APCC_DBOX_1 | 526 | 534 | PF00400 | 0.532 |
DEG_APCC_DBOX_1 | 688 | 696 | PF00400 | 0.496 |
DEG_SCF_FBW7_1 | 488 | 494 | PF00400 | 0.536 |
DEG_SPOP_SBC_1 | 504 | 508 | PF00917 | 0.526 |
DOC_ANK_TNKS_1 | 39 | 46 | PF00023 | 0.506 |
DOC_CKS1_1 | 385 | 390 | PF01111 | 0.540 |
DOC_CKS1_1 | 394 | 399 | PF01111 | 0.515 |
DOC_CKS1_1 | 488 | 493 | PF01111 | 0.539 |
DOC_CYCLIN_yCln2_LP_2 | 395 | 401 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 7 | 13 | PF00134 | 0.546 |
DOC_MAPK_DCC_7 | 575 | 584 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 232 | 241 | PF00069 | 0.272 |
DOC_MAPK_gen_1 | 453 | 463 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 575 | 584 | PF00069 | 0.483 |
DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 620 | 623 | PF13499 | 0.507 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.271 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.476 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.526 |
DOC_USP7_MATH_2 | 127 | 133 | PF00917 | 0.482 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.543 |
LIG_14-3-3_CanoR_1 | 115 | 122 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 25 | 31 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 375 | 385 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 460 | 464 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 511 | 516 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 543 | 552 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 601 | 607 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 689 | 699 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 593 | 609 | PF00022 | 0.662 |
LIG_APCC_ABBA_1 | 183 | 188 | PF00400 | 0.271 |
LIG_APCC_ABBAyCdc20_2 | 227 | 233 | PF00400 | 0.394 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.481 |
LIG_BRCT_BRCA1_1 | 646 | 650 | PF00533 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 338 | 348 | PF00928 | 0.271 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.296 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.227 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.305 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.271 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.541 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.479 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.271 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.571 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.394 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.531 |
LIG_LIR_Apic_2 | 271 | 277 | PF02991 | 0.507 |
LIG_LIR_Apic_2 | 393 | 397 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 201 | 205 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.397 |
LIG_Pex14_2 | 646 | 650 | PF04695 | 0.496 |
LIG_SH2_CRK | 84 | 88 | PF00017 | 0.491 |
LIG_SH2_GRB2like | 173 | 176 | PF00017 | 0.271 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.271 |
LIG_SH2_STAT3 | 550 | 553 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.538 |
LIG_SH3_1 | 394 | 400 | PF00018 | 0.455 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.606 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.271 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.538 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.517 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.490 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 158 | 163 | PF11976 | 0.271 |
LIG_SUMO_SIM_anti_2 | 362 | 368 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 57 | 62 | PF11976 | 0.501 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.271 |
LIG_UBA3_1 | 98 | 102 | PF00899 | 0.347 |
LIG_WRC_WIRS_1 | 202 | 207 | PF05994 | 0.271 |
MOD_CDK_SPK_2 | 35 | 40 | PF00069 | 0.532 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.671 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.271 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.224 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.271 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.679 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.591 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.660 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.591 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.562 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.539 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.525 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.493 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.514 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.605 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.529 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.554 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.532 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.521 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.434 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.527 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.502 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.353 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.406 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.375 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.567 |
MOD_CK2_1 | 608 | 614 | PF00069 | 0.686 |
MOD_Cter_Amidation | 454 | 457 | PF01082 | 0.602 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.360 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.424 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.271 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.555 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.243 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.271 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.672 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.588 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.621 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.562 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.536 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.603 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.596 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.595 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.645 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.555 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.578 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.437 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.530 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.535 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.402 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.319 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.205 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.584 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.590 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.589 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.607 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.583 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.578 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.559 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.528 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.517 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.517 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.637 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.580 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.518 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.549 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.627 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.497 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.514 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.508 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.489 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.512 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.496 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.491 |
MOD_N-GLC_1 | 492 | 497 | PF02516 | 0.532 |
MOD_N-GLC_1 | 584 | 589 | PF02516 | 0.497 |
MOD_N-GLC_2 | 701 | 703 | PF02516 | 0.506 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.531 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.419 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.532 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.317 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.500 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.485 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.633 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.672 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.552 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.515 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.495 |
MOD_NEK2_1 | 699 | 704 | PF00069 | 0.486 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.359 |
MOD_NEK2_2 | 138 | 143 | PF00069 | 0.513 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.480 |
MOD_NEK2_2 | 602 | 607 | PF00069 | 0.560 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.276 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.496 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.271 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.574 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.585 |
MOD_PKA_1 | 459 | 465 | PF00069 | 0.605 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.431 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.497 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.507 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.533 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.586 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.576 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.528 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.584 |
MOD_PKA_2 | 600 | 606 | PF00069 | 0.661 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.406 |
MOD_PKA_2 | 697 | 703 | PF00069 | 0.517 |
MOD_PKA_2 | 706 | 712 | PF00069 | 0.520 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.402 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.542 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.502 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.509 |
MOD_Plk_1 | 548 | 554 | PF00069 | 0.534 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.482 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.552 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.281 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.280 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.271 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.500 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.602 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.586 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.536 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.616 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.616 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.555 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.545 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.545 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.487 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.587 |
MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.543 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.546 |
MOD_SUMO_for_1 | 142 | 145 | PF00179 | 0.501 |
MOD_SUMO_for_1 | 155 | 158 | PF00179 | 0.210 |
MOD_SUMO_for_1 | 74 | 77 | PF00179 | 0.389 |
MOD_SUMO_rev_2 | 332 | 342 | PF00179 | 0.205 |
TRG_DiLeu_BaEn_2 | 343 | 349 | PF01217 | 0.271 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 526 | 528 | PF00400 | 0.542 |
TRG_NLS_MonoExtN_4 | 524 | 529 | PF00514 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 172 | 176 | PF00026 | 0.271 |
TRG_Pf-PMV_PEXEL_1 | 232 | 237 | PF00026 | 0.262 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IND3 | Leishmania donovani | 26% | 100% |
A0A3S7XAX0 | Leishmania donovani | 24% | 100% |
A4HW76 | Leishmania infantum | 76% | 89% |
A4ICP8 | Leishmania infantum | 26% | 100% |
A4IDK3 | Leishmania infantum | 24% | 100% |
E9APX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9ASK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AT06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q1J2 | Leishmania major | 25% | 100% |
Q4Q1Z0 | Leishmania major | 26% | 100% |
Q4QFK4 | Leishmania major | 77% | 100% |
Q8BLF2 | Mus musculus | 23% | 100% |
Q9JM01 | Rattus norvegicus | 24% | 100% |