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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0016020 | membrane | 2 | 4 |
Related structures:
AlphaFold database: E9AEP8
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008213 | protein alkylation | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016570 | histone modification | 5 | 2 |
GO:0016571 | histone methylation | 5 | 2 |
GO:0018022 | peptidyl-lysine methylation | 5 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018205 | peptidyl-lysine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032259 | methylation | 2 | 2 |
GO:0034968 | histone lysine methylation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0008170 | N-methyltransferase activity | 5 | 2 |
GO:0008276 | protein methyltransferase activity | 3 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 2 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 2 |
GO:0042054 | histone methyltransferase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 529 | 533 | PF00656 | 0.798 |
CLV_C14_Caspase3-7 | 557 | 561 | PF00656 | 0.661 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 686 | 688 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 690 | 692 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.567 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.552 |
CLV_PCSK_PC7_1 | 686 | 692 | PF00082 | 0.643 |
CLV_PCSK_PC7_1 | 89 | 95 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.593 |
DEG_APCC_DBOX_1 | 690 | 698 | PF00400 | 0.463 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.668 |
DEG_SPOP_SBC_1 | 49 | 53 | PF00917 | 0.766 |
DEG_SPOP_SBC_1 | 500 | 504 | PF00917 | 0.763 |
DOC_CDC14_PxL_1 | 550 | 558 | PF14671 | 0.681 |
DOC_CYCLIN_yClb3_PxF_3 | 217 | 225 | PF00134 | 0.688 |
DOC_MAPK_DCC_7 | 406 | 415 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 181 | 190 | PF00069 | 0.695 |
DOC_MAPK_gen_1 | 202 | 212 | PF00069 | 0.657 |
DOC_MAPK_gen_1 | 224 | 231 | PF00069 | 0.688 |
DOC_MAPK_gen_1 | 322 | 333 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 617 | 627 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 686 | 694 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 89 | 99 | PF00069 | 0.769 |
DOC_MAPK_MEF2A_6 | 205 | 214 | PF00069 | 0.706 |
DOC_MAPK_MEF2A_6 | 621 | 629 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 74 | 82 | PF00069 | 0.772 |
DOC_MAPK_RevD_3 | 674 | 688 | PF00069 | 0.469 |
DOC_PIKK_1 | 662 | 669 | PF02985 | 0.432 |
DOC_PP1_RVXF_1 | 200 | 207 | PF00149 | 0.592 |
DOC_PP1_RVXF_1 | 537 | 544 | PF00149 | 0.656 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.832 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.790 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.678 |
DOC_USP7_MATH_2 | 111 | 117 | PF00917 | 0.752 |
DOC_USP7_MATH_2 | 29 | 35 | PF00917 | 0.737 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.707 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.817 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 287 | 291 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 642 | 647 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 83 | 91 | PF00244 | 0.708 |
LIG_Actin_WH2_2 | 631 | 649 | PF00022 | 0.405 |
LIG_APCC_ABBA_1 | 249 | 254 | PF00400 | 0.701 |
LIG_APCC_ABBA_1 | 463 | 468 | PF00400 | 0.484 |
LIG_BIR_III_4 | 397 | 401 | PF00653 | 0.548 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.710 |
LIG_CaM_IQ_9 | 330 | 345 | PF13499 | 0.544 |
LIG_DLG_GKlike_1 | 642 | 650 | PF00625 | 0.364 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.686 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.464 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.464 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.544 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.477 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.465 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.780 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.760 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.718 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.665 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.762 |
LIG_Integrin_isoDGR_2 | 298 | 300 | PF01839 | 0.426 |
LIG_KLC1_Yacidic_2 | 470 | 474 | PF13176 | 0.573 |
LIG_LIR_Apic_2 | 583 | 587 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 457 | 466 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 616 | 627 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 651 | 660 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 280 | 284 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 616 | 622 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 651 | 657 | PF02991 | 0.434 |
LIG_LYPXL_yS_3 | 553 | 556 | PF13949 | 0.676 |
LIG_NRP_CendR_1 | 726 | 729 | PF00754 | 0.684 |
LIG_PTB_Apo_2 | 590 | 597 | PF02174 | 0.527 |
LIG_PTB_Phospho_1 | 590 | 596 | PF10480 | 0.529 |
LIG_REV1ctd_RIR_1 | 541 | 550 | PF16727 | 0.575 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.701 |
LIG_SH2_CRK | 619 | 623 | PF00017 | 0.616 |
LIG_SH2_NCK_1 | 619 | 623 | PF00017 | 0.616 |
LIG_SH2_PTP2 | 584 | 587 | PF00017 | 0.526 |
LIG_SH2_SRC | 584 | 587 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 654 | 658 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.520 |
LIG_SH3_1 | 242 | 248 | PF00018 | 0.671 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.753 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.648 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.666 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.741 |
LIG_SH3_5 | 215 | 219 | PF00018 | 0.699 |
LIG_SUMO_SIM_anti_2 | 328 | 336 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 420 | 426 | PF11976 | 0.550 |
LIG_SUMO_SIM_par_1 | 628 | 633 | PF11976 | 0.419 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.704 |
LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.658 |
LIG_TRAF2_1 | 484 | 487 | PF00917 | 0.719 |
LIG_TRAF2_1 | 576 | 579 | PF00917 | 0.587 |
LIG_TRAF2_1 | 661 | 664 | PF00917 | 0.410 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.809 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.633 |
LIG_ULM_U2AF65_1 | 202 | 207 | PF00076 | 0.598 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.751 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.464 |
MOD_CDC14_SPxK_1 | 32 | 35 | PF00782 | 0.794 |
MOD_CDK_SPxK_1 | 29 | 35 | PF00069 | 0.762 |
MOD_CDK_SPxxK_3 | 195 | 202 | PF00069 | 0.675 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.770 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.548 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.734 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.785 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.707 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.703 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.482 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.509 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.677 |
MOD_CK2_1 | 658 | 664 | PF00069 | 0.422 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.771 |
MOD_GlcNHglycan | 113 | 118 | PF01048 | 0.551 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.448 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.561 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.574 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.687 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.785 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.561 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.475 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.483 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.708 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.784 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.679 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.675 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.771 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.270 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.266 |
MOD_N-GLC_1 | 521 | 526 | PF02516 | 0.466 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.734 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.581 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.485 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.487 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.753 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.770 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.705 |
MOD_PIKK_1 | 523 | 529 | PF00454 | 0.740 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.762 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.665 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.705 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.619 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.701 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.739 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.715 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.468 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.468 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.510 |
MOD_Plk_2-3 | 269 | 275 | PF00069 | 0.720 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.519 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.475 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.464 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.409 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.673 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.817 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.672 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.749 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.653 |
MOD_SUMO_for_1 | 210 | 213 | PF00179 | 0.748 |
MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.548 |
MOD_SUMO_for_1 | 342 | 345 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 430 | 439 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 612 | 620 | PF00179 | 0.668 |
TRG_DiLeu_BaEn_2 | 164 | 170 | PF01217 | 0.604 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.686 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.695 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.648 |
TRG_ENDOCYTIC_2 | 619 | 622 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 641 | 644 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 690 | 692 | PF00400 | 0.429 |
TRG_NLS_MonoExtC_3 | 686 | 691 | PF00514 | 0.421 |
TRG_NLS_MonoExtN_4 | 686 | 691 | PF00514 | 0.419 |
TRG_NLS_MonoExtN_4 | 89 | 96 | PF00514 | 0.755 |
TRG_Pf-PMV_PEXEL_1 | 292 | 296 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.358 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5D5 | Leptomonas seymouri | 61% | 99% |
A0A0S4JG56 | Bodo saltans | 46% | 100% |
A0A3S5H7Y5 | Leishmania donovani | 93% | 100% |
A4HMA5 | Leishmania braziliensis | 79% | 100% |
A4IAX0 | Leishmania infantum | 93% | 100% |
D0A284 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9B5V3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
V5B354 | Trypanosoma cruzi | 51% | 100% |