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 | 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 | 2 |
Related structures:
AlphaFold database: Q4QGF9
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:0005488 | binding | 1 | 6 |
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:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.757 |
CLV_C14_Caspase3-7 | 513 | 517 | PF00656 | 0.412 |
CLV_MEL_PAP_1 | 154 | 160 | PF00089 | 0.494 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.553 |
CLV_PCSK_FUR_1 | 447 | 451 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.375 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 580 | 582 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.482 |
DEG_APCC_DBOX_1 | 541 | 549 | PF00400 | 0.317 |
DOC_CDC14_PxL_1 | 132 | 140 | PF14671 | 0.501 |
DOC_CDC14_PxL_1 | 186 | 194 | PF14671 | 0.456 |
DOC_CDC14_PxL_1 | 436 | 444 | PF14671 | 0.482 |
DOC_CKS1_1 | 198 | 203 | PF01111 | 0.480 |
DOC_CYCLIN_RxL_1 | 328 | 339 | PF00134 | 0.434 |
DOC_CYCLIN_yClb1_LxF_4 | 542 | 548 | PF00134 | 0.333 |
DOC_CYCLIN_yCln2_LP_2 | 198 | 204 | PF00134 | 0.430 |
DOC_MAPK_DCC_7 | 187 | 195 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 173 | 183 | PF00069 | 0.541 |
DOC_MAPK_JIP1_4 | 221 | 227 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 187 | 195 | PF00069 | 0.453 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.537 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.476 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 157 | 161 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 292 | 300 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 334 | 339 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 452 | 460 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 476 | 481 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 542 | 548 | PF00244 | 0.333 |
LIG_AP2alpha_2 | 472 | 474 | PF02296 | 0.466 |
LIG_APCC_ABBA_1 | 41 | 46 | PF00400 | 0.521 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.518 |
LIG_BIR_III_4 | 617 | 621 | PF00653 | 0.514 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.469 |
LIG_BRCT_BRCA1_1 | 455 | 459 | PF00533 | 0.407 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.658 |
LIG_eIF4E_1 | 100 | 106 | PF01652 | 0.433 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.494 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.519 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.498 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.448 |
LIG_LIR_Gen_1 | 313 | 323 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 368 | 376 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 454 | 460 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.329 |
LIG_MLH1_MIPbox_1 | 455 | 459 | PF16413 | 0.277 |
LIG_MYND_1 | 136 | 140 | PF01753 | 0.483 |
LIG_MYND_3 | 135 | 139 | PF01753 | 0.514 |
LIG_NRBOX | 519 | 525 | PF00104 | 0.375 |
LIG_NRBOX | 562 | 568 | PF00104 | 0.402 |
LIG_SH2_CRK | 269 | 273 | PF00017 | 0.393 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.444 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.480 |
LIG_SH2_CRK | 549 | 553 | PF00017 | 0.392 |
LIG_SH2_NCK_1 | 133 | 137 | PF00017 | 0.507 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 37 | 41 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 36 | 39 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 438 | 441 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.193 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.315 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.497 |
LIG_SUMO_SIM_anti_2 | 194 | 200 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 610 | 617 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 191 | 197 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 333 | 339 | PF11976 | 0.544 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.788 |
LIG_TYR_ITIM | 314 | 319 | PF00017 | 0.442 |
LIG_TYR_ITSM | 366 | 373 | PF00017 | 0.522 |
LIG_UBA3_1 | 296 | 304 | PF00899 | 0.554 |
LIG_UBA3_1 | 355 | 361 | PF00899 | 0.452 |
LIG_WRC_WIRS_1 | 401 | 406 | PF05994 | 0.549 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.588 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.384 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.406 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.478 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.430 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.454 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.512 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.696 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.470 |
MOD_GlcNHglycan | 385 | 389 | PF01048 | 0.274 |
MOD_GlcNHglycan | 600 | 604 | PF01048 | 0.472 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.400 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.557 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.455 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.455 |
MOD_LATS_1 | 332 | 338 | PF00433 | 0.433 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.252 |
MOD_N-GLC_1 | 596 | 601 | PF02516 | 0.400 |
MOD_N-GLC_2 | 23 | 25 | PF02516 | 0.525 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.488 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.457 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.346 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.456 |
MOD_NEK2_2 | 414 | 419 | PF00069 | 0.578 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.403 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.489 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.536 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.510 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.504 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.448 |
MOD_Plk_2-3 | 11 | 17 | PF00069 | 0.348 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.573 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.489 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.518 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.448 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.271 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.334 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.592 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.451 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.428 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.526 |
MOD_SUMO_for_1 | 360 | 363 | PF00179 | 0.477 |
MOD_SUMO_for_1 | 582 | 585 | PF00179 | 0.381 |
TRG_DiLeu_BaEn_1 | 194 | 199 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_1 | 519 | 524 | PF01217 | 0.474 |
TRG_DiLeu_BaEn_2 | 454 | 460 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.432 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 447 | 450 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.475 |
TRG_NES_CRM1_1 | 148 | 162 | PF08389 | 0.432 |
TRG_NES_CRM1_1 | 557 | 570 | PF08389 | 0.453 |
TRG_NLS_MonoExtC_3 | 579 | 585 | PF00514 | 0.379 |
TRG_NLS_MonoExtN_4 | 578 | 584 | PF00514 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 476 | 481 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 522 | 526 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDV1 | Leptomonas seymouri | 61% | 100% |
A0A0S4IJK9 | Bodo saltans | 39% | 100% |
A0A1X0NMI4 | Trypanosomatidae | 42% | 100% |
A0A3S7WS98 | Leishmania donovani | 93% | 100% |
A0A422NUZ8 | Trypanosoma rangeli | 46% | 100% |
C9ZI42 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 99% |
E9AGJ2 | Leishmania infantum | 93% | 100% |
E9AIN6 | Leishmania braziliensis | 82% | 100% |
E9AP30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5DFZ1 | Trypanosoma cruzi | 44% | 100% |