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 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 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 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X4A8
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: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:0032259 | methylation | 2 | 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 | 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:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.589 |
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 297 | 301 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 352 | 356 | PF00656 | 0.585 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.633 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.377 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.319 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.664 |
DOC_CYCLIN_RxL_1 | 188 | 199 | PF00134 | 0.518 |
DOC_CYCLIN_RxL_1 | 319 | 326 | PF00134 | 0.553 |
DOC_MAPK_DCC_7 | 327 | 336 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 327 | 336 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 76 | 86 | PF00069 | 0.544 |
DOC_MAPK_HePTP_8 | 324 | 336 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 327 | 336 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 80 | 88 | PF00069 | 0.532 |
DOC_MAPK_RevD_3 | 63 | 77 | PF00069 | 0.536 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.530 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.586 |
DOC_USP7_UBL2_3 | 76 | 80 | PF12436 | 0.516 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 327 | 332 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 66 | 74 | PF00244 | 0.494 |
LIG_Actin_WH2_2 | 50 | 68 | PF00022 | 0.519 |
LIG_BIR_III_4 | 25 | 29 | PF00653 | 0.643 |
LIG_BIR_III_4 | 355 | 359 | PF00653 | 0.589 |
LIG_eIF4E_1 | 173 | 179 | PF01652 | 0.513 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.552 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.496 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.560 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.589 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.405 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.551 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.523 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.471 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.542 |
LIG_Integrin_RGD_1 | 437 | 439 | PF01839 | 0.296 |
LIG_Integrin_RGD_1 | 81 | 83 | PF01839 | 0.343 |
LIG_LIR_Gen_1 | 102 | 112 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 127 | 135 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 18 | 29 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 449 | 458 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.406 |
LIG_LYPXL_S_1 | 172 | 176 | PF13949 | 0.313 |
LIG_LYPXL_yS_3 | 173 | 176 | PF13949 | 0.513 |
LIG_NRBOX | 320 | 326 | PF00104 | 0.480 |
LIG_Pex14_1 | 224 | 228 | PF04695 | 0.490 |
LIG_Pex14_1 | 536 | 540 | PF04695 | 0.608 |
LIG_PTB_Apo_2 | 407 | 414 | PF02174 | 0.561 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.561 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.549 |
LIG_SH2_CRK | 485 | 489 | PF00017 | 0.539 |
LIG_SH2_NCK_1 | 115 | 119 | PF00017 | 0.588 |
LIG_SH2_NCK_1 | 228 | 232 | PF00017 | 0.561 |
LIG_SH2_NCK_1 | 476 | 480 | PF00017 | 0.521 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.527 |
LIG_SH2_SRC | 281 | 284 | PF00017 | 0.527 |
LIG_SH2_SRC | 369 | 372 | PF00017 | 0.589 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.589 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.358 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.571 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.510 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.490 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.585 |
MOD_CDC14_SPxK_1 | 434 | 437 | PF00782 | 0.449 |
MOD_CDK_SPxK_1 | 431 | 437 | PF00069 | 0.449 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.507 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.535 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.536 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.565 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.553 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.766 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.415 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.526 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.471 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.588 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.644 |
MOD_Cter_Amidation | 277 | 280 | PF01082 | 0.376 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.344 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.330 |
MOD_GlcNHglycan | 266 | 270 | PF01048 | 0.311 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.337 |
MOD_GlcNHglycan | 300 | 304 | PF01048 | 0.324 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.334 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.355 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.295 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.780 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.342 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.583 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.602 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.527 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.561 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.589 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.496 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.539 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.444 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.769 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.598 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.507 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.327 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.330 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.589 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.496 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.474 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.561 |
MOD_PK_1 | 474 | 480 | PF00069 | 0.486 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.482 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.614 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.529 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.645 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.449 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.456 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.449 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.533 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.507 |
MOD_Plk_2-3 | 186 | 192 | PF00069 | 0.471 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.645 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.458 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.488 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.494 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.520 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.356 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.572 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.609 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.490 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.577 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.589 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.581 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.757 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.574 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.548 |
TRG_DiLeu_BaEn_4 | 463 | 469 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.561 |
TRG_DiLeu_BaLyEn_6 | 86 | 91 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.589 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 532 | 534 | PF00400 | 0.672 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 40 | 44 | PF00026 | 0.553 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM8 | Leptomonas seymouri | 52% | 71% |
A0A1X0NJ79 | Trypanosomatidae | 38% | 95% |
A4HJ86 | Leishmania braziliensis | 77% | 100% |
A4I6N0 | Leishmania infantum | 99% | 100% |
C9ZM67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 88% |
E9B1Q3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q6F7 | Leishmania major | 92% | 100% |
V5BPH7 | Trypanosoma cruzi | 40% | 86% |