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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0020023 | kinetoplast | 2 | 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 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q6F7
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:0018022 | peptidyl-lysine methylation | 5 | 2 |
GO:0018026 | peptidyl-lysine monomethylation | 6 | 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: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: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:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.480 |
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.488 |
CLV_C14_Caspase3-7 | 297 | 301 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 352 | 356 | PF00656 | 0.582 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.273 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.280 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.273 |
CLV_PCSK_PC7_1 | 214 | 220 | PF00082 | 0.180 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.269 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.550 |
DOC_ANK_TNKS_1 | 261 | 268 | PF00023 | 0.380 |
DOC_MAPK_DCC_7 | 327 | 336 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 327 | 336 | PF00069 | 0.580 |
DOC_MAPK_gen_1 | 76 | 86 | PF00069 | 0.522 |
DOC_MAPK_HePTP_8 | 324 | 336 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 327 | 336 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 80 | 88 | PF00069 | 0.482 |
DOC_MAPK_RevD_3 | 63 | 77 | PF00069 | 0.382 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.480 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 359 | 363 | PF12436 | 0.510 |
DOC_USP7_UBL2_3 | 76 | 80 | PF12436 | 0.464 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 327 | 332 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 66 | 74 | PF00244 | 0.438 |
LIG_Actin_WH2_2 | 50 | 68 | PF00022 | 0.459 |
LIG_BIR_III_4 | 242 | 246 | PF00653 | 0.380 |
LIG_BIR_III_4 | 25 | 29 | PF00653 | 0.492 |
LIG_BIR_III_4 | 355 | 359 | PF00653 | 0.480 |
LIG_eIF4E_1 | 173 | 179 | PF01652 | 0.461 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.509 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.430 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.446 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.523 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.480 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.507 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.423 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.495 |
LIG_Integrin_RGD_1 | 437 | 439 | PF01839 | 0.230 |
LIG_LIR_Gen_1 | 102 | 112 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 127 | 135 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 18 | 29 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 449 | 458 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.367 |
LIG_LYPXL_S_1 | 172 | 176 | PF13949 | 0.261 |
LIG_LYPXL_yS_3 | 173 | 176 | PF13949 | 0.461 |
LIG_Pex14_1 | 224 | 228 | PF04695 | 0.438 |
LIG_Pex14_1 | 536 | 540 | PF04695 | 0.551 |
LIG_PTB_Apo_2 | 407 | 414 | PF02174 | 0.522 |
LIG_PTB_Phospho_1 | 407 | 413 | PF10480 | 0.491 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.522 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.508 |
LIG_SH2_CRK | 485 | 489 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 115 | 119 | PF00017 | 0.568 |
LIG_SH2_NCK_1 | 228 | 232 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 476 | 480 | PF00017 | 0.459 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.447 |
LIG_SH2_SRC | 281 | 284 | PF00017 | 0.447 |
LIG_SH2_SRC | 369 | 372 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.289 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.544 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.458 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.438 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.563 |
LIG_SUMO_SIM_par_1 | 89 | 94 | PF11976 | 0.380 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.455 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.441 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.452 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.476 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.499 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.512 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.604 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.423 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.580 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.580 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.322 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.325 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.301 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.289 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.272 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.257 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.394 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.512 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.599 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.496 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.457 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.538 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.583 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.500 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.462 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.365 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.633 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.492 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.280 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.520 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.430 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.398 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.524 |
MOD_PK_1 | 474 | 480 | PF00069 | 0.409 |
MOD_PKA_1 | 138 | 144 | PF00069 | 0.427 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.438 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.506 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.492 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.577 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.387 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.483 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.445 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.577 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.469 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.422 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.469 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.292 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.480 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.496 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.438 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.418 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.513 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.726 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.542 |
MOD_SUMO_rev_2 | 291 | 297 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_4 | 463 | 469 | PF01217 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 86 | 91 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.468 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 532 | 534 | PF00400 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.280 |
TRG_Pf-PMV_PEXEL_1 | 40 | 44 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM8 | Leptomonas seymouri | 51% | 71% |
A0A1X0NJ79 | Trypanosomatidae | 39% | 95% |
A0A3S7X4A8 | Leishmania donovani | 92% | 100% |
A4HJ86 | Leishmania braziliensis | 77% | 71% |
A4I6N0 | Leishmania infantum | 92% | 100% |
C9ZM67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 88% |
E9B1Q3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5BPH7 | Trypanosoma cruzi | 40% | 86% |