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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 7 |
GO:0042995 | cell projection | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 7 |
GO:0000164 | protein phosphatase type 1 complex | 5 | 1 |
GO:0008287 | protein serine/threonine phosphatase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1903293 | phosphatase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HQL1
Term | Name | Level | Count |
---|---|---|---|
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010562 | positive regulation of phosphorus metabolic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 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:0035303 | regulation of dephosphorylation | 7 | 1 |
GO:0035304 | regulation of protein dephosphorylation | 7 | 1 |
GO:0035306 | positive regulation of dephosphorylation | 8 | 1 |
GO:0035307 | positive regulation of protein dephosphorylation | 8 | 1 |
GO:0045937 | positive regulation of phosphate metabolic process | 7 | 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: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:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0004857 | enzyme inhibitor activity | 3 | 1 |
GO:0004864 | protein phosphatase inhibitor activity | 5 | 1 |
GO:0004865 | protein serine/threonine phosphatase inhibitor activity | 6 | 1 |
GO:0019208 | phosphatase regulator activity | 3 | 1 |
GO:0019212 | phosphatase inhibitor activity | 4 | 1 |
GO:0019888 | protein phosphatase regulator activity | 4 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
GO:0140678 | molecular function inhibitor activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 668 | 672 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 703 | 707 | PF00656 | 0.704 |
CLV_MEL_PAP_1 | 692 | 698 | PF00089 | 0.549 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 597 | 599 | PF00675 | 0.708 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.601 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.500 |
CLV_Separin_Metazoa | 711 | 715 | PF03568 | 0.568 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.606 |
DEG_SCF_FBW7_1 | 415 | 420 | PF00400 | 0.703 |
DEG_SCF_FBW7_1 | 605 | 612 | PF00400 | 0.562 |
DEG_SIAH_1 | 216 | 224 | PF03145 | 0.504 |
DEG_SPOP_SBC_1 | 240 | 244 | PF00917 | 0.663 |
DOC_CDC14_PxL_1 | 332 | 340 | PF14671 | 0.587 |
DOC_CYCLIN_RxL_1 | 309 | 322 | PF00134 | 0.610 |
DOC_CYCLIN_yCln2_LP_2 | 224 | 227 | PF00134 | 0.788 |
DOC_CYCLIN_yCln2_LP_2 | 352 | 355 | PF00134 | 0.441 |
DOC_CYCLIN_yCln2_LP_2 | 644 | 650 | PF00134 | 0.568 |
DOC_MAPK_DCC_7 | 479 | 487 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 120 | 126 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.598 |
DOC_MAPK_gen_1 | 297 | 305 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 309 | 318 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 511 | 519 | PF00069 | 0.670 |
DOC_MAPK_gen_1 | 598 | 607 | PF00069 | 0.607 |
DOC_MAPK_MEF2A_6 | 23 | 32 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 297 | 305 | PF00069 | 0.597 |
DOC_MAPK_MEF2A_6 | 88 | 97 | PF00069 | 0.439 |
DOC_PP1_RVXF_1 | 341 | 348 | PF00149 | 0.325 |
DOC_PP2B_LxvP_1 | 224 | 227 | PF13499 | 0.788 |
DOC_PP2B_LxvP_1 | 352 | 355 | PF13499 | 0.441 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.722 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 636 | 641 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 643 | 648 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 158 | 166 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 314 | 319 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 34 | 43 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 405 | 415 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 433 | 438 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 457 | 465 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 472 | 476 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 563 | 568 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 58 | 63 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 689 | 699 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 714 | 718 | PF00244 | 0.761 |
LIG_BIR_III_2 | 629 | 633 | PF00653 | 0.560 |
LIG_BIR_III_4 | 230 | 234 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.671 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.294 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.471 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.627 |
LIG_BRCT_BRCA1_1 | 538 | 542 | PF00533 | 0.567 |
LIG_BRCT_BRCA1_1 | 566 | 570 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_1 | 661 | 665 | PF00533 | 0.653 |
LIG_BRCT_BRCA1_1 | 692 | 696 | PF00533 | 0.762 |
LIG_CaM_IQ_9 | 187 | 203 | PF13499 | 0.663 |
LIG_DLG_GKlike_1 | 58 | 65 | PF00625 | 0.556 |
LIG_eIF4E_1 | 87 | 93 | PF01652 | 0.434 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.525 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.570 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.634 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.554 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.606 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.814 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.452 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.620 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.595 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.544 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.496 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.825 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.650 |
LIG_FHA_2 | 668 | 674 | PF00498 | 0.568 |
LIG_LIR_Apic_2 | 349 | 354 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 139 | 149 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 24 | 32 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 275 | 284 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 329 | 340 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 524 | 535 | PF02991 | 0.735 |
LIG_LIR_Gen_1 | 548 | 559 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 548 | 554 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 693 | 699 | PF02991 | 0.802 |
LIG_LRP6_Inhibitor_1 | 683 | 689 | PF00058 | 0.556 |
LIG_MYND_1 | 223 | 227 | PF01753 | 0.784 |
LIG_NRBOX | 208 | 214 | PF00104 | 0.416 |
LIG_NRBOX | 88 | 94 | PF00104 | 0.534 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.473 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.395 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 543 | 547 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 551 | 555 | PF00017 | 0.516 |
LIG_SH2_SRC | 534 | 537 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.588 |
LIG_SH3_2 | 593 | 598 | PF14604 | 0.568 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.537 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.622 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.346 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.615 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.618 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.577 |
LIG_SUMO_SIM_anti_2 | 251 | 257 | PF11976 | 0.627 |
LIG_SUMO_SIM_par_1 | 164 | 170 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 210 | 216 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 354 | 360 | PF11976 | 0.590 |
LIG_SUMO_SIM_par_1 | 473 | 478 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 483 | 488 | PF11976 | 0.512 |
LIG_TYR_ITIM | 126 | 131 | PF00017 | 0.454 |
LIG_WRC_WIRS_1 | 37 | 42 | PF05994 | 0.431 |
LIG_WRC_WIRS_1 | 59 | 64 | PF05994 | 0.467 |
LIG_WRC_WIRS_1 | 631 | 636 | PF05994 | 0.703 |
LIG_WW_2 | 444 | 447 | PF00397 | 0.709 |
LIG_WW_3 | 595 | 599 | PF00397 | 0.716 |
MOD_CDK_SPK_2 | 506 | 511 | PF00069 | 0.544 |
MOD_CDK_SPxxK_3 | 506 | 513 | PF00069 | 0.548 |
MOD_CDK_SPxxK_3 | 579 | 586 | PF00069 | 0.572 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.625 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.585 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.609 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.826 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.683 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.668 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.640 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.512 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.770 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.679 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.579 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.532 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.821 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.787 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.606 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.460 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.551 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.624 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.604 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.581 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.478 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.546 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.611 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.716 |
MOD_CK2_1 | 702 | 708 | PF00069 | 0.552 |
MOD_Cter_Amidation | 118 | 121 | PF01082 | 0.606 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.647 |
MOD_GlcNHglycan | 273 | 277 | PF01048 | 0.634 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.620 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.719 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.683 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.811 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.788 |
MOD_GlcNHglycan | 681 | 684 | PF01048 | 0.765 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.675 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.734 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.634 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.685 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.831 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.664 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.613 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.689 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.484 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.627 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.703 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.563 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.537 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.777 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.486 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.743 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.759 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.792 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.784 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.654 |
MOD_LATS_1 | 450 | 456 | PF00433 | 0.573 |
MOD_LATS_1 | 56 | 62 | PF00433 | 0.420 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.549 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.536 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.434 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.652 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.370 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.511 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.662 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.481 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.741 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.639 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.674 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.640 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.673 |
MOD_NEK2_1 | 712 | 717 | PF00069 | 0.545 |
MOD_NEK2_2 | 304 | 309 | PF00069 | 0.356 |
MOD_NEK2_2 | 395 | 400 | PF00069 | 0.557 |
MOD_NEK2_2 | 684 | 689 | PF00069 | 0.553 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.663 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.630 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.623 |
MOD_PIKK_1 | 465 | 471 | PF00454 | 0.558 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.449 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.519 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.668 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.784 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.583 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.650 |
MOD_PKA_2 | 713 | 719 | PF00069 | 0.567 |
MOD_PKB_1 | 34 | 42 | PF00069 | 0.425 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.532 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.321 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.567 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.590 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.361 |
MOD_Plk_2-3 | 550 | 556 | PF00069 | 0.544 |
MOD_Plk_2-3 | 702 | 708 | PF00069 | 0.552 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.502 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.568 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.559 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.551 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.573 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.727 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.694 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.541 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.546 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.527 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.538 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.509 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.549 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.485 |
MOD_ProDKin_1 | 636 | 642 | PF00069 | 0.714 |
MOD_ProDKin_1 | 643 | 649 | PF00069 | 0.614 |
TRG_DiLeu_BaEn_1 | 708 | 713 | PF01217 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 220 | 225 | PF01217 | 0.776 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 652 | 655 | PF00400 | 0.563 |
TRG_ER_diLys_1 | 721 | 726 | PF00400 | 0.569 |
TRG_NLS_MonoExtC_3 | 597 | 603 | PF00514 | 0.563 |
TRG_NLS_MonoExtN_4 | 596 | 602 | PF00514 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 150 | 155 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 63 | 68 | PF00026 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4KNZ5 | Bodo saltans | 30% | 100% |
A0A3S7XCG9 | Leishmania donovani | 59% | 100% |
A4ICD1 | Leishmania infantum | 59% | 100% |
E9AUC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
Q4Q064 | Leishmania major | 59% | 100% |