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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IKU3
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008213 | protein alkylation | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016571 | histone methylation | 5 | 1 |
GO:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034968 | histone lysine methylation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008276 | protein methyltransferase activity | 3 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 1 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 1 |
GO:0042054 | histone methyltransferase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.785 |
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.645 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.510 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.412 |
CLV_Separin_Metazoa | 661 | 665 | PF03568 | 0.478 |
DEG_APCC_DBOX_1 | 508 | 516 | PF00400 | 0.560 |
DEG_SPOP_SBC_1 | 430 | 434 | PF00917 | 0.561 |
DOC_CDC14_PxL_1 | 333 | 341 | PF14671 | 0.562 |
DOC_CKS1_1 | 688 | 693 | PF01111 | 0.717 |
DOC_MAPK_gen_1 | 164 | 174 | PF00069 | 0.523 |
DOC_MAPK_gen_1 | 404 | 412 | PF00069 | 0.539 |
DOC_MAPK_HePTP_8 | 162 | 174 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 165 | 174 | PF00069 | 0.525 |
DOC_PP1_RVXF_1 | 639 | 645 | PF00149 | 0.444 |
DOC_PP4_FxxP_1 | 293 | 296 | PF00568 | 0.580 |
DOC_PP4_FxxP_1 | 666 | 669 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.513 |
DOC_USP7_MATH_2 | 427 | 433 | PF00917 | 0.521 |
DOC_USP7_UBL2_3 | 90 | 94 | PF12436 | 0.491 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 645 | 650 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.728 |
LIG_14-3-3_CanoR_1 | 131 | 135 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 164 | 170 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 241 | 248 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 511 | 516 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 561 | 571 | PF00244 | 0.373 |
LIG_Actin_WH2_2 | 388 | 406 | PF00022 | 0.500 |
LIG_APCC_ABBAyCdc20_2 | 131 | 137 | PF00400 | 0.489 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.749 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.351 |
LIG_BRCT_BRCA1_1 | 288 | 292 | PF00533 | 0.555 |
LIG_DLG_GKlike_1 | 165 | 172 | PF00625 | 0.502 |
LIG_eIF4E_1 | 450 | 456 | PF01652 | 0.537 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.442 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.434 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.642 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.526 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.503 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.464 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.540 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.562 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.552 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.510 |
LIG_HCF-1_HBM_1 | 138 | 141 | PF13415 | 0.563 |
LIG_LIR_Gen_1 | 171 | 182 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 250 | 261 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 504 | 512 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 573 | 581 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 494 | 500 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 517 | 522 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 573 | 577 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.531 |
LIG_LYPXL_S_1 | 32 | 36 | PF13949 | 0.538 |
LIG_LYPXL_yS_3 | 33 | 36 | PF13949 | 0.544 |
LIG_LYPXL_yS_3 | 336 | 339 | PF13949 | 0.562 |
LIG_MYND_1 | 346 | 350 | PF01753 | 0.580 |
LIG_NRBOX | 123 | 129 | PF00104 | 0.399 |
LIG_NRBOX | 54 | 60 | PF00104 | 0.543 |
LIG_Rb_LxCxE_1 | 110 | 133 | PF01857 | 0.504 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.558 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.562 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.579 |
LIG_SH2_GRB2like | 111 | 114 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.562 |
LIG_SH2_PTP2 | 580 | 583 | PF00017 | 0.507 |
LIG_SH2_SRC | 141 | 144 | PF00017 | 0.525 |
LIG_SH2_SRC | 253 | 256 | PF00017 | 0.574 |
LIG_SH2_SRC | 450 | 453 | PF00017 | 0.492 |
LIG_SH2_SRC | 574 | 577 | PF00017 | 0.440 |
LIG_SH2_SRC | 667 | 670 | PF00017 | 0.421 |
LIG_SH2_SRC | 679 | 682 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 563 | 567 | PF00017 | 0.403 |
LIG_SH2_STAP1 | 574 | 578 | PF00017 | 0.357 |
LIG_SH2_STAT3 | 268 | 271 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 603 | 606 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.516 |
LIG_SH3_1 | 685 | 691 | PF00018 | 0.681 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.604 |
LIG_SH3_3 | 581 | 587 | PF00018 | 0.437 |
LIG_SH3_3 | 685 | 691 | PF00018 | 0.700 |
LIG_SUMO_SIM_anti_2 | 122 | 128 | PF11976 | 0.468 |
LIG_SUMO_SIM_anti_2 | 54 | 60 | PF11976 | 0.553 |
LIG_SUMO_SIM_anti_2 | 565 | 571 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 259 | 267 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 54 | 60 | PF11976 | 0.569 |
LIG_SUMO_SIM_par_1 | 567 | 573 | PF11976 | 0.431 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.556 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.449 |
LIG_TYR_ITIM | 495 | 500 | PF00017 | 0.413 |
LIG_UBA3_1 | 55 | 63 | PF00899 | 0.514 |
LIG_WRC_WIRS_1 | 465 | 470 | PF05994 | 0.344 |
LIG_WW_3 | 215 | 219 | PF00397 | 0.577 |
MOD_CDK_SPxxK_3 | 645 | 652 | PF00069 | 0.532 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.724 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.519 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.406 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.449 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.514 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.447 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.456 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.403 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.478 |
MOD_Cter_Amidation | 553 | 556 | PF01082 | 0.502 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.745 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.550 |
MOD_GlcNHglycan | 228 | 232 | PF01048 | 0.547 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.376 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.597 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.762 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.487 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.546 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.757 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.607 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.573 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.680 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.457 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.145 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.413 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.358 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.744 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.423 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.474 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.783 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.481 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.344 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.441 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.487 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.325 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.449 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.486 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.465 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.524 |
MOD_NEK2_2 | 498 | 503 | PF00069 | 0.545 |
MOD_NEK2_2 | 524 | 529 | PF00069 | 0.481 |
MOD_OFUCOSY | 523 | 528 | PF10250 | 0.528 |
MOD_PKA_1 | 78 | 84 | PF00069 | 0.566 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.388 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.392 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.488 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.488 |
MOD_PKB_1 | 509 | 517 | PF00069 | 0.499 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.417 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.274 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.400 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.443 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.342 |
MOD_Plk_1 | 637 | 643 | PF00069 | 0.463 |
MOD_Plk_1 | 680 | 686 | PF00069 | 0.570 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.489 |
MOD_Plk_2-3 | 349 | 355 | PF00069 | 0.392 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.393 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.490 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.366 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.428 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.390 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.474 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.601 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.474 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.451 |
MOD_ProDKin_1 | 645 | 651 | PF00069 | 0.536 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.731 |
MOD_SUMO_for_1 | 684 | 687 | PF00179 | 0.583 |
MOD_SUMO_rev_2 | 13 | 23 | PF00179 | 0.774 |
MOD_SUMO_rev_2 | 648 | 654 | PF00179 | 0.496 |
TRG_DiLeu_BaEn_1 | 54 | 59 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 475 | 480 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 508 | 511 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 555 | 557 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 663 | 665 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 555 | 560 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKN8 | Leptomonas seymouri | 75% | 99% |
A0A0S4JQY2 | Bodo saltans | 42% | 100% |
A0A1X0P998 | Trypanosomatidae | 36% | 100% |
A0A422N693 | Trypanosoma rangeli | 37% | 100% |
A4HAL8 | Leishmania braziliensis | 87% | 100% |
A4I9Q7 | Leishmania infantum | 100% | 100% |
C9ZMX7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B4S7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q3A0 | Leishmania major | 97% | 100% |
V5BJB7 | Trypanosoma cruzi | 36% | 100% |