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: 10 |
NetGPI | no | yes: 0, no: 10 |
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: A4HDN5
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 | 461 | 465 | PF00656 | 0.653 |
CLV_C14_Caspase3-7 | 63 | 67 | PF00656 | 0.591 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.458 |
CLV_PCSK_FUR_1 | 591 | 595 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.562 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.388 |
DEG_APCC_DBOX_1 | 179 | 187 | PF00400 | 0.489 |
DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.458 |
DEG_APCC_DBOX_1 | 317 | 325 | PF00400 | 0.552 |
DEG_SCF_FBW7_1 | 95 | 102 | PF00400 | 0.451 |
DEG_SPOP_SBC_1 | 294 | 298 | PF00917 | 0.597 |
DOC_ANK_TNKS_1 | 325 | 332 | PF00023 | 0.400 |
DOC_CDC14_PxL_1 | 385 | 393 | PF14671 | 0.427 |
DOC_CKS1_1 | 164 | 169 | PF01111 | 0.664 |
DOC_CYCLIN_RxL_1 | 280 | 291 | PF00134 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 383 | 389 | PF00134 | 0.405 |
DOC_MAPK_gen_1 | 158 | 164 | PF00069 | 0.523 |
DOC_MAPK_gen_1 | 268 | 276 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 273 | 281 | PF00069 | 0.408 |
DOC_PP1_RVXF_1 | 281 | 288 | PF00149 | 0.488 |
DOC_PP2B_LxvP_1 | 128 | 131 | PF13499 | 0.554 |
DOC_PP4_FxxP_1 | 164 | 167 | PF00568 | 0.629 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.535 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.807 |
LIG_14-3-3_CanoR_1 | 147 | 155 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 286 | 290 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 345 | 349 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 493 | 498 | PF00244 | 0.347 |
LIG_Actin_WH2_1 | 273 | 288 | PF00022 | 0.444 |
LIG_Actin_WH2_2 | 270 | 288 | PF00022 | 0.482 |
LIG_Actin_WH2_2 | 329 | 347 | PF00022 | 0.558 |
LIG_BIR_III_4 | 464 | 468 | PF00653 | 0.726 |
LIG_EVH1_1 | 128 | 132 | PF00568 | 0.552 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.709 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.430 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.547 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.538 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.502 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.533 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.340 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.371 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.500 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.537 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.444 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.296 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.572 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.696 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.503 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.574 |
LIG_GBD_Chelix_1 | 281 | 289 | PF00786 | 0.396 |
LIG_HP1_1 | 223 | 227 | PF01393 | 0.497 |
LIG_LIR_Apic_2 | 3 | 9 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 102 | 112 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 347 | 356 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 361 | 370 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 492 | 503 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 573 | 581 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 347 | 351 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 361 | 366 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 492 | 498 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 599 | 603 | PF02991 | 0.555 |
LIG_LYPXL_S_1 | 387 | 391 | PF13949 | 0.417 |
LIG_LYPXL_yS_3 | 388 | 391 | PF13949 | 0.428 |
LIG_NRBOX | 275 | 281 | PF00104 | 0.511 |
LIG_Rb_LxCxE_1 | 352 | 371 | PF01857 | 0.463 |
LIG_SH2_CRK | 363 | 367 | PF00017 | 0.458 |
LIG_SH2_NCK_1 | 363 | 367 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 532 | 536 | PF00017 | 0.482 |
LIG_SH2_PTP2 | 575 | 578 | PF00017 | 0.409 |
LIG_SH2_SRC | 328 | 331 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 363 | 367 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.461 |
LIG_SH3_2 | 129 | 134 | PF14604 | 0.548 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.543 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.560 |
LIG_SUMO_SIM_anti_2 | 376 | 385 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 487 | 492 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 364 | 369 | PF11976 | 0.354 |
LIG_TRAF2_1 | 36 | 39 | PF00917 | 0.551 |
LIG_TRFH_1 | 385 | 389 | PF08558 | 0.584 |
LIG_TYR_ITSM | 571 | 578 | PF00017 | 0.531 |
LIG_UBA3_1 | 276 | 283 | PF00899 | 0.510 |
MOD_CDK_SPK_2 | 142 | 147 | PF00069 | 0.739 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.425 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.775 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.562 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.507 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.581 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.682 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.615 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.550 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.680 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.356 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.669 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.502 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.488 |
MOD_CMANNOS | 452 | 455 | PF00535 | 0.571 |
MOD_Cter_Amidation | 156 | 159 | PF01082 | 0.385 |
MOD_Cter_Amidation | 177 | 180 | PF01082 | 0.602 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.720 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.691 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.657 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.452 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.715 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.329 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.506 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.425 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.490 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.431 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.501 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.691 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.711 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.488 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.695 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.662 |
MOD_N-GLC_1 | 538 | 543 | PF02516 | 0.282 |
MOD_N-GLC_2 | 27 | 29 | PF02516 | 0.539 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.517 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.598 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.353 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.474 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.440 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.370 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.531 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.579 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.579 |
MOD_NEK2_2 | 259 | 264 | PF00069 | 0.536 |
MOD_NEK2_2 | 520 | 525 | PF00069 | 0.227 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.592 |
MOD_PK_1 | 79 | 85 | PF00069 | 0.520 |
MOD_PKA_1 | 134 | 140 | PF00069 | 0.540 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.505 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.455 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.367 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.457 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.586 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.453 |
MOD_Plk_2-3 | 170 | 176 | PF00069 | 0.615 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.323 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.338 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.411 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.664 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.457 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.604 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.458 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.539 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.403 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.425 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.716 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.615 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.614 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.714 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.503 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.376 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.774 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.805 |
MOD_SUMO_rev_2 | 173 | 181 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 32 | 41 | PF00179 | 0.602 |
TRG_DiLeu_BaEn_1 | 272 | 277 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_1 | 339 | 344 | PF01217 | 0.559 |
TRG_DiLeu_BaEn_3 | 176 | 182 | PF01217 | 0.641 |
TRG_DiLeu_BaEn_4 | 60 | 66 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 50 | 55 | PF01217 | 0.623 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.501 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 591 | 594 | PF00400 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 595 | 599 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I099 | Leptomonas seymouri | 43% | 86% |
A0A1X0NVU7 | Trypanosomatidae | 28% | 100% |
A0A3R7RB97 | Trypanosoma rangeli | 29% | 100% |
A0A3S7WYH5 | Leishmania donovani | 73% | 84% |
C9ZWC8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AH82 | Leishmania infantum | 73% | 84% |
E9AX20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 83% |
Q4QAF6 | Leishmania major | 72% | 100% |
V5CZP8 | Trypanosoma cruzi | 28% | 100% |