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: E9B0E1
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 | 158 | 162 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 169 | 173 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.471 |
CLV_MEL_PAP_1 | 602 | 608 | PF00089 | 0.344 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.326 |
CLV_PCSK_FUR_1 | 264 | 268 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.273 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.358 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 609 | 611 | PF00082 | 0.288 |
CLV_PCSK_PC7_1 | 262 | 268 | PF00082 | 0.388 |
CLV_PCSK_PC7_1 | 605 | 611 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.378 |
DEG_APCC_DBOX_1 | 202 | 210 | PF00400 | 0.389 |
DEG_APCC_DBOX_1 | 604 | 612 | PF00400 | 0.469 |
DEG_APCC_DBOX_1 | 67 | 75 | PF00400 | 0.446 |
DOC_CYCLIN_RxL_1 | 262 | 270 | PF00134 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 448 | 454 | PF00134 | 0.441 |
DOC_MAPK_gen_1 | 493 | 499 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 593 | 602 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 596 | 604 | PF00069 | 0.494 |
DOC_MAPK_RevD_3 | 289 | 304 | PF00069 | 0.406 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.417 |
DOC_PP1_RVXF_1 | 175 | 181 | PF00149 | 0.481 |
DOC_PP1_RVXF_1 | 27 | 34 | PF00149 | 0.381 |
DOC_PP1_RVXF_1 | 612 | 619 | PF00149 | 0.335 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.382 |
DOC_PP2B_LxvP_1 | 452 | 455 | PF13499 | 0.580 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.509 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.564 |
LIG_14-3-3_CanoR_1 | 156 | 160 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 166 | 171 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 266 | 276 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.545 |
LIG_14-3-3_CterR_2 | 621 | 623 | PF00244 | 0.424 |
LIG_Actin_WH2_2 | 595 | 611 | PF00022 | 0.521 |
LIG_AP2alpha_2 | 97 | 99 | PF02296 | 0.430 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.561 |
LIG_BRCT_BRCA1_1 | 211 | 215 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.360 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 359 | 363 | PF00533 | 0.215 |
LIG_Clathr_ClatBox_1 | 71 | 75 | PF01394 | 0.449 |
LIG_deltaCOP1_diTrp_1 | 172 | 180 | PF00928 | 0.419 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.407 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.402 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.486 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.484 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.596 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.545 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.702 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.631 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.481 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.441 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.484 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.456 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.545 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.464 |
LIG_GBD_Chelix_1 | 310 | 318 | PF00786 | 0.321 |
LIG_LIR_Apic_2 | 58 | 63 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 527 | 537 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.366 |
LIG_LYPXL_yS_3 | 276 | 279 | PF13949 | 0.339 |
LIG_NRBOX | 216 | 222 | PF00104 | 0.280 |
LIG_NRBOX | 235 | 241 | PF00104 | 0.392 |
LIG_NRBOX | 514 | 520 | PF00104 | 0.486 |
LIG_SH2_CRK | 423 | 427 | PF00017 | 0.326 |
LIG_SH2_CRK | 435 | 439 | PF00017 | 0.338 |
LIG_SH2_NCK_1 | 136 | 140 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.404 |
LIG_SH3_1 | 274 | 280 | PF00018 | 0.316 |
LIG_SH3_1 | 536 | 542 | PF00018 | 0.508 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.344 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.508 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.455 |
LIG_SUMO_SIM_par_1 | 70 | 75 | PF11976 | 0.425 |
LIG_TRFH_1 | 437 | 441 | PF08558 | 0.447 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.550 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.684 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.504 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.469 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.732 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.437 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.462 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.540 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.658 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.535 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.494 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.459 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.494 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.269 |
MOD_Cter_Amidation | 533 | 536 | PF01082 | 0.222 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.716 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.509 |
MOD_GlcNHglycan | 151 | 155 | PF01048 | 0.663 |
MOD_GlcNHglycan | 341 | 345 | PF01048 | 0.469 |
MOD_GlcNHglycan | 463 | 467 | PF01048 | 0.694 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.692 |
MOD_GlcNHglycan | 477 | 481 | PF01048 | 0.589 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.615 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.485 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.641 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.539 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.457 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.694 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.618 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.466 |
MOD_LATS_1 | 164 | 170 | PF00433 | 0.564 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.614 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.449 |
MOD_N-GLC_1 | 385 | 390 | PF02516 | 0.370 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.700 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.329 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.465 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.345 |
MOD_NEK2_2 | 137 | 142 | PF00069 | 0.481 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.469 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.476 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.442 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.574 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.456 |
MOD_Plk_1 | 480 | 486 | PF00069 | 0.480 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.534 |
MOD_Plk_2-3 | 573 | 579 | PF00069 | 0.524 |
MOD_Plk_2-3 | 75 | 81 | PF00069 | 0.466 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.430 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.292 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.393 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.546 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.526 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.564 |
MOD_SUMO_rev_2 | 587 | 595 | PF00179 | 0.496 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_2 | 44 | 50 | PF01217 | 0.528 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.486 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.532 |
TRG_ER_diArg_1 | 262 | 265 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 487 | 489 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 492 | 494 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 535 | 537 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.415 |
TRG_NES_CRM1_1 | 287 | 299 | PF08389 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 286 | 290 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8B9 | Leptomonas seymouri | 60% | 99% |
A0A0S4JJX6 | Bodo saltans | 35% | 90% |
A0A1X0P2C3 | Trypanosomatidae | 42% | 100% |
A0A3Q8IFL1 | Leishmania donovani | 93% | 100% |
A0A422N122 | Trypanosoma rangeli | 44% | 100% |
A4HHW1 | Leishmania braziliensis | 80% | 100% |
A4I511 | Leishmania infantum | 92% | 100% |
C9ZQG5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q4Q7U0 | Leishmania major | 92% | 100% |
V5AWY0 | Trypanosoma cruzi | 44% | 100% |