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: A4HHW1
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 11 |
GO:0032259 | methylation | 2 | 11 |
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008213 | protein alkylation | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018026 | peptidyl-lysine monomethylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 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 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
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:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 169 | 173 | PF00656 | 0.505 |
CLV_MEL_PAP_1 | 602 | 608 | PF00089 | 0.339 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.291 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 609 | 611 | PF00082 | 0.324 |
CLV_PCSK_PC7_1 | 605 | 611 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.341 |
DEG_APCC_DBOX_1 | 604 | 612 | PF00400 | 0.462 |
DEG_APCC_DBOX_1 | 67 | 75 | PF00400 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 448 | 454 | PF00134 | 0.416 |
DOC_MAPK_gen_1 | 493 | 499 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 596 | 604 | PF00069 | 0.487 |
DOC_MAPK_RevD_3 | 289 | 304 | PF00069 | 0.389 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.384 |
DOC_PP1_RVXF_1 | 612 | 619 | PF00149 | 0.323 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.367 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.479 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.575 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.561 |
LIG_14-3-3_CanoR_1 | 166 | 171 | PF00244 | 0.535 |
LIG_Actin_WH2_2 | 595 | 611 | PF00022 | 0.515 |
LIG_AP2alpha_2 | 97 | 99 | PF02296 | 0.418 |
LIG_BIR_III_2 | 161 | 165 | PF00653 | 0.441 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 359 | 363 | PF00533 | 0.212 |
LIG_Clathr_ClatBox_1 | 180 | 184 | PF01394 | 0.286 |
LIG_Clathr_ClatBox_1 | 71 | 75 | PF01394 | 0.440 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.516 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.417 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.416 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.343 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.457 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.473 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.506 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.517 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.529 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.594 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.412 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.449 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.551 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.447 |
LIG_LIR_Apic_2 | 58 | 63 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 527 | 534 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.346 |
LIG_LYPXL_yS_3 | 276 | 279 | PF13949 | 0.314 |
LIG_NRBOX | 216 | 222 | PF00104 | 0.267 |
LIG_NRBOX | 235 | 241 | PF00104 | 0.369 |
LIG_NRBOX | 514 | 520 | PF00104 | 0.480 |
LIG_PCNA_yPIPBox_3 | 556 | 564 | PF02747 | 0.379 |
LIG_RPA_C_Fungi | 65 | 77 | PF08784 | 0.217 |
LIG_SH2_CRK | 223 | 227 | PF00017 | 0.349 |
LIG_SH2_CRK | 423 | 427 | PF00017 | 0.311 |
LIG_SH2_CRK | 435 | 439 | PF00017 | 0.330 |
LIG_SH2_NCK_1 | 136 | 140 | PF00017 | 0.422 |
LIG_SH2_SRC | 498 | 501 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.303 |
LIG_SH3_1 | 536 | 542 | PF00018 | 0.350 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.318 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.253 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.303 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.350 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.438 |
LIG_Sin3_3 | 69 | 76 | PF02671 | 0.217 |
LIG_SUMO_SIM_anti_2 | 175 | 182 | PF11976 | 0.263 |
LIG_SUMO_SIM_anti_2 | 468 | 477 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 450 | 455 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 468 | 477 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 70 | 75 | PF11976 | 0.414 |
LIG_TRFH_1 | 437 | 441 | PF08558 | 0.417 |
LIG_TYR_ITIM | 221 | 226 | PF00017 | 0.400 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.520 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.678 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.493 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.475 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.260 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.634 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.309 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.424 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.318 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.368 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.309 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.498 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.251 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.648 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.548 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.680 |
MOD_GlcNHglycan | 341 | 345 | PF01048 | 0.409 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.603 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.664 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.461 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.585 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.401 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.450 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.431 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.346 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.341 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.428 |
MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.445 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.347 |
MOD_N-GLC_1 | 555 | 560 | PF02516 | 0.259 |
MOD_N-GLC_2 | 613 | 615 | PF02516 | 0.339 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.633 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.453 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.473 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.307 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.473 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.354 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.364 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.233 |
MOD_NEK2_2 | 137 | 142 | PF00069 | 0.459 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.402 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.451 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.450 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.433 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.403 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.453 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.402 |
MOD_Plk_2-3 | 573 | 579 | PF00069 | 0.388 |
MOD_Plk_2-3 | 75 | 81 | PF00069 | 0.449 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.566 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.332 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.417 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.294 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.383 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.456 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.444 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.333 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.447 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.370 |
TRG_DiLeu_BaEn_1 | 45 | 50 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 317 | 322 | PF01217 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 44 | 49 | PF01217 | 0.523 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.323 |
TRG_ER_diArg_1 | 487 | 489 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 492 | 494 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.404 |
TRG_NES_CRM1_1 | 287 | 299 | PF08389 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 237 | 241 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.344 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8B9 | Leptomonas seymouri | 60% | 99% |
A0A0S4JJX6 | Bodo saltans | 33% | 90% |
A0A1X0P2C3 | Trypanosomatidae | 42% | 100% |
A0A3Q8IFL1 | Leishmania donovani | 81% | 100% |
A0A422N122 | Trypanosoma rangeli | 45% | 100% |
A4I511 | Leishmania infantum | 81% | 100% |
C9ZQG5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B0E1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q7U0 | Leishmania major | 79% | 100% |
V5AWY0 | Trypanosoma cruzi | 45% | 100% |