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: A0A3S7XCG9
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 | 0.477 |
CLV_C14_Caspase3-7 | 435 | 439 | PF00656 | 0.741 |
CLV_C14_Caspase3-7 | 681 | 685 | PF00656 | 0.726 |
CLV_C14_Caspase3-7 | 701 | 705 | PF00656 | 0.601 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.771 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.696 |
CLV_PCSK_FUR_1 | 151 | 155 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.696 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.594 |
CLV_PCSK_PC7_1 | 154 | 160 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 695 | 699 | PF00082 | 0.622 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.521 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.479 |
DEG_SPOP_SBC_1 | 240 | 244 | PF00917 | 0.654 |
DEG_SPOP_SBC_1 | 377 | 381 | PF00917 | 0.603 |
DEG_SPOP_SBC_1 | 414 | 418 | PF00917 | 0.738 |
DOC_CDC14_PxL_1 | 332 | 340 | PF14671 | 0.488 |
DOC_CDC14_PxL_1 | 567 | 575 | PF14671 | 0.691 |
DOC_CKS1_1 | 106 | 111 | PF01111 | 0.406 |
DOC_CYCLIN_RxL_1 | 309 | 322 | PF00134 | 0.521 |
DOC_CYCLIN_RxL_1 | 340 | 349 | PF00134 | 0.452 |
DOC_CYCLIN_RxL_1 | 692 | 702 | PF00134 | 0.686 |
DOC_CYCLIN_yCln2_LP_2 | 224 | 227 | PF00134 | 0.784 |
DOC_MAPK_DCC_7 | 309 | 318 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 120 | 126 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 297 | 305 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 309 | 318 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 652 | 663 | PF00069 | 0.703 |
DOC_MAPK_MEF2A_6 | 23 | 32 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 297 | 305 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 351 | 358 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 88 | 97 | PF00069 | 0.438 |
DOC_PP2B_LxvP_1 | 224 | 227 | PF13499 | 0.784 |
DOC_PP2B_LxvP_1 | 591 | 594 | PF13499 | 0.763 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.835 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.802 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.793 |
DOC_USP7_UBL2_3 | 116 | 120 | PF12436 | 0.496 |
DOC_USP7_UBL2_3 | 466 | 470 | PF12436 | 0.738 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 623 | 628 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 159 | 168 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 177 | 184 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 239 | 247 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 314 | 319 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 34 | 43 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 469 | 477 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 549 | 557 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 601 | 609 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 693 | 698 | PF00244 | 0.711 |
LIG_BIR_III_4 | 230 | 234 | PF00653 | 0.656 |
LIG_BIR_III_4 | 322 | 326 | PF00653 | 0.581 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.620 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.687 |
LIG_BRCT_BRCA1_1 | 490 | 494 | PF00533 | 0.722 |
LIG_BRCT_BRCA1_1 | 526 | 530 | PF00533 | 0.715 |
LIG_BRCT_BRCA1_1 | 536 | 540 | PF00533 | 0.606 |
LIG_BRCT_BRCA1_1 | 645 | 649 | PF00533 | 0.772 |
LIG_BRCT_BRCA1_1 | 659 | 663 | PF00533 | 0.653 |
LIG_BRCT_BRCA1_1 | 690 | 694 | PF00533 | 0.762 |
LIG_CaM_IQ_9 | 187 | 203 | PF13499 | 0.675 |
LIG_DLG_GKlike_1 | 58 | 65 | PF00625 | 0.549 |
LIG_DLG_GKlike_1 | 67 | 74 | PF00625 | 0.451 |
LIG_eIF4E_1 | 3 | 9 | PF01652 | 0.469 |
LIG_eIF4E_1 | 342 | 348 | PF01652 | 0.497 |
LIG_eIF4E_1 | 87 | 93 | PF01652 | 0.432 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.587 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.538 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.661 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.787 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.826 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.608 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.515 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.496 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.648 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.506 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.674 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.565 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.814 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.645 |
LIG_LIR_Gen_1 | 139 | 149 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 2 | 9 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 24 | 32 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 276 | 284 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 276 | 280 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 691 | 697 | PF02991 | 0.781 |
LIG_MYND_1 | 223 | 227 | PF01753 | 0.681 |
LIG_MYND_1 | 571 | 575 | PF01753 | 0.726 |
LIG_NRBOX | 88 | 94 | PF00104 | 0.430 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.477 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 184 | 188 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 463 | 467 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.454 |
LIG_SH3_1 | 569 | 575 | PF00018 | 0.728 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.405 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.672 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.539 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.674 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.712 |
LIG_SH3_3 | 621 | 627 | PF00018 | 0.694 |
LIG_SUMO_SIM_anti_2 | 250 | 256 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 354 | 360 | PF11976 | 0.632 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.504 |
LIG_TRAF2_1 | 550 | 553 | PF00917 | 0.720 |
LIG_TYR_ITIM | 126 | 131 | PF00017 | 0.454 |
LIG_TYR_ITIM | 54 | 59 | PF00017 | 0.347 |
LIG_WRC_WIRS_1 | 13 | 18 | PF05994 | 0.412 |
LIG_WRC_WIRS_1 | 37 | 42 | PF05994 | 0.430 |
LIG_WRC_WIRS_1 | 385 | 390 | PF05994 | 0.728 |
LIG_WRC_WIRS_1 | 59 | 64 | PF05994 | 0.460 |
LIG_WRC_WIRS_1 | 632 | 637 | PF05994 | 0.703 |
LIG_WW_2 | 444 | 447 | PF00397 | 0.670 |
LIG_WW_3 | 593 | 597 | PF00397 | 0.732 |
MOD_CDK_SPxxK_3 | 105 | 112 | PF00069 | 0.405 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.637 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.640 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.639 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.774 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.642 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.748 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.693 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.769 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.733 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.733 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.688 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.547 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.547 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.520 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.505 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.650 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.511 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.577 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.557 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.672 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.692 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.748 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.667 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.613 |
MOD_Cter_Amidation | 118 | 121 | PF01082 | 0.504 |
MOD_Cter_Amidation | 650 | 653 | PF01082 | 0.703 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.526 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.679 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.625 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.585 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.524 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.744 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.715 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.699 |
MOD_GlcNHglycan | 561 | 565 | PF01048 | 0.724 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.758 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.671 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.592 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.628 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.760 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.699 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.628 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.580 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.666 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.824 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.708 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.590 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.712 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.693 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.653 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.751 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.814 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.429 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.720 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.586 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.686 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.667 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.648 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.679 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.575 |
MOD_LATS_1 | 312 | 318 | PF00433 | 0.503 |
MOD_N-GLC_1 | 438 | 443 | PF02516 | 0.733 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.449 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.662 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.425 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.543 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.748 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.731 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.592 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.572 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.633 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.725 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.654 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.751 |
MOD_NEK2_1 | 663 | 668 | PF00069 | 0.780 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.682 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.675 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.639 |
MOD_PIKK_1 | 595 | 601 | PF00454 | 0.728 |
MOD_PIKK_1 | 639 | 645 | PF00454 | 0.731 |
MOD_PK_1 | 164 | 170 | PF00069 | 0.510 |
MOD_PKA_1 | 601 | 607 | PF00069 | 0.624 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.421 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.572 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.611 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.445 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.794 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.747 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.719 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.713 |
MOD_PKB_1 | 34 | 42 | PF00069 | 0.432 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.549 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.661 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.519 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.536 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.387 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.624 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.535 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.745 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.408 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.592 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.790 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.679 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.700 |
MOD_ProDKin_1 | 623 | 629 | PF00069 | 0.637 |
MOD_SUMO_rev_2 | 155 | 160 | PF00179 | 0.580 |
TRG_DiLeu_BaEn_1 | 524 | 529 | PF01217 | 0.586 |
TRG_DiLeu_BaLyEn_6 | 220 | 225 | PF01217 | 0.737 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.603 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.716 |
TRG_NES_CRM1_1 | 689 | 702 | PF08389 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 150 | 155 | PF00026 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 63 | 68 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 695 | 700 | PF00026 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 72 | 77 | PF00026 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0K7 | Leptomonas seymouri | 45% | 100% |
A4HQL1 | Leishmania braziliensis | 59% | 100% |
A4ICD1 | Leishmania infantum | 99% | 100% |
E9AUC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q064 | Leishmania major | 87% | 100% |