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: E9AIN6
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:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
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_MEL_PAP_1 | 154 | 160 | PF00089 | 0.505 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.273 |
CLV_PCSK_FUR_1 | 448 | 452 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.188 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.489 |
DEG_APCC_DBOX_1 | 521 | 529 | PF00400 | 0.302 |
DEG_APCC_DBOX_1 | 542 | 550 | PF00400 | 0.325 |
DOC_CDC14_PxL_1 | 132 | 140 | PF14671 | 0.510 |
DOC_CDC14_PxL_1 | 186 | 194 | PF14671 | 0.474 |
DOC_CDC14_PxL_1 | 437 | 445 | PF14671 | 0.482 |
DOC_CKS1_1 | 198 | 203 | PF01111 | 0.493 |
DOC_CYCLIN_RxL_1 | 519 | 527 | PF00134 | 0.407 |
DOC_CYCLIN_yClb1_LxF_4 | 543 | 549 | PF00134 | 0.343 |
DOC_CYCLIN_yCln2_LP_2 | 198 | 204 | PF00134 | 0.444 |
DOC_MAPK_DCC_7 | 187 | 195 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 173 | 183 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 469 | 479 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 187 | 195 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 472 | 481 | PF00069 | 0.274 |
DOC_PP1_RVXF_1 | 83 | 90 | PF00149 | 0.269 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.549 |
DOC_PP2B_PxIxI_1 | 190 | 196 | PF00149 | 0.268 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.652 |
DOC_USP7_UBL2_3 | 254 | 258 | PF12436 | 0.401 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 157 | 164 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 261 | 270 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 293 | 301 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 453 | 461 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 487 | 497 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 522 | 532 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 543 | 549 | PF00244 | 0.343 |
LIG_AP2alpha_2 | 473 | 475 | PF02296 | 0.460 |
LIG_BIR_III_4 | 618 | 622 | PF00653 | 0.529 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.616 |
LIG_eIF4E_1 | 100 | 106 | PF01652 | 0.446 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.501 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.547 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.490 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.505 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.451 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.384 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.451 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.461 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.366 |
LIG_Integrin_isoDGR_2 | 248 | 250 | PF01839 | 0.188 |
LIG_LIR_Gen_1 | 314 | 324 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 368 | 377 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 310 | 315 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.459 |
LIG_MYND_1 | 136 | 140 | PF01753 | 0.502 |
LIG_MYND_3 | 135 | 139 | PF01753 | 0.523 |
LIG_NRBOX | 520 | 526 | PF00104 | 0.374 |
LIG_NRBOX | 563 | 569 | PF00104 | 0.408 |
LIG_Rb_pABgroove_1 | 611 | 619 | PF01858 | 0.259 |
LIG_REV1ctd_RIR_1 | 68 | 76 | PF16727 | 0.272 |
LIG_SH2_CRK | 270 | 274 | PF00017 | 0.530 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.549 |
LIG_SH2_NCK_1 | 133 | 137 | PF00017 | 0.514 |
LIG_SH2_PTP2 | 371 | 374 | PF00017 | 0.388 |
LIG_SH2_SRC | 371 | 374 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 37 | 41 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 439 | 442 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.191 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.320 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.549 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.475 |
LIG_SUMO_SIM_anti_2 | 194 | 200 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 611 | 618 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 191 | 197 | PF11976 | 0.409 |
LIG_TYR_ITIM | 315 | 320 | PF00017 | 0.549 |
LIG_TYR_ITSM | 367 | 374 | PF00017 | 0.530 |
LIG_UBA3_1 | 356 | 362 | PF00899 | 0.530 |
LIG_UBA3_1 | 524 | 530 | PF00899 | 0.320 |
LIG_WRC_WIRS_1 | 402 | 407 | PF05994 | 0.549 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.595 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.397 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.388 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.425 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.382 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.398 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.459 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.503 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.382 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.505 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.448 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.425 |
MOD_GlcNHglycan | 386 | 390 | PF01048 | 0.276 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.631 |
MOD_GlcNHglycan | 601 | 605 | PF01048 | 0.475 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.403 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.570 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.337 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.588 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.455 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.255 |
MOD_N-GLC_2 | 23 | 25 | PF02516 | 0.530 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.388 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.479 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.530 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.459 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.457 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.579 |
MOD_NEK2_2 | 501 | 506 | PF00069 | 0.393 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.497 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.382 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.540 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.546 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.552 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.507 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.388 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.388 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.442 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.451 |
MOD_Plk_2-3 | 134 | 140 | PF00069 | 0.298 |
MOD_Plk_2-3 | 229 | 235 | PF00069 | 0.537 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.499 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.520 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.451 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.342 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.607 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.463 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.549 |
MOD_SUMO_for_1 | 253 | 256 | PF00179 | 0.475 |
MOD_SUMO_for_1 | 361 | 364 | PF00179 | 0.530 |
MOD_SUMO_rev_2 | 251 | 260 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 590 | 600 | PF00179 | 0.440 |
TRG_DiLeu_BaEn_1 | 194 | 199 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_2 | 455 | 461 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_4 | 365 | 371 | PF01217 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.385 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.526 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 448 | 451 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.479 |
TRG_NES_CRM1_1 | 558 | 571 | PF08389 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 522 | 527 | PF00026 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDV1 | Leptomonas seymouri | 59% | 100% |
A0A0S4IJK9 | Bodo saltans | 39% | 100% |
A0A1X0NMI4 | Trypanosomatidae | 43% | 100% |
A0A3S7WS98 | Leishmania donovani | 85% | 100% |
A0A422NUZ8 | Trypanosoma rangeli | 45% | 100% |
C9ZI42 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 99% |
E9AGJ2 | Leishmania infantum | 84% | 100% |
E9AP30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QGF9 | Leishmania major | 82% | 100% |
V5DFZ1 | Trypanosoma cruzi | 43% | 100% |