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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IDM8
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0032259 | methylation | 2 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0043414 | macromolecule methylation | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0008276 | protein methyltransferase activity | 3 | 4 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.725 |
CLV_C14_Caspase3-7 | 390 | 394 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.776 |
CLV_PCSK_FUR_1 | 458 | 462 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.529 |
CLV_PCSK_PC7_1 | 229 | 235 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.523 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.539 |
DEG_SCF_TRCP1_1 | 60 | 66 | PF00400 | 0.610 |
DOC_ANK_TNKS_1 | 124 | 131 | PF00023 | 0.727 |
DOC_CYCLIN_RxL_1 | 172 | 179 | PF00134 | 0.567 |
DOC_CYCLIN_RxL_1 | 229 | 241 | PF00134 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 242 | 248 | PF00134 | 0.368 |
DOC_MAPK_gen_1 | 436 | 444 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 488 | 497 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 466 | 475 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 490 | 499 | PF00069 | 0.478 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.713 |
DOC_PP2B_PxIxI_1 | 468 | 474 | PF00149 | 0.493 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.344 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 290 | 299 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 355 | 363 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 46 | 52 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 56 | 63 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 81 | 91 | PF00244 | 0.753 |
LIG_Actin_WH2_2 | 14 | 31 | PF00022 | 0.625 |
LIG_Actin_WH2_2 | 65 | 82 | PF00022 | 0.620 |
LIG_APCC_ABBA_1 | 495 | 500 | PF00400 | 0.371 |
LIG_BRCT_BRCA1_1 | 251 | 255 | PF00533 | 0.497 |
LIG_BRCT_BRCA1_1 | 360 | 364 | PF00533 | 0.476 |
LIG_CtBP_PxDLS_1 | 15 | 19 | PF00389 | 0.639 |
LIG_deltaCOP1_diTrp_1 | 206 | 213 | PF00928 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 274 | 279 | PF00928 | 0.376 |
LIG_EH1_1 | 479 | 487 | PF00400 | 0.512 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.476 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.503 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.519 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.674 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.633 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.530 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.563 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.452 |
LIG_Integrin_RGD_1 | 125 | 127 | PF01839 | 0.728 |
LIG_LIR_Gen_1 | 361 | 372 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 438 | 449 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 90 | 98 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.671 |
LIG_MYND_1 | 265 | 269 | PF01753 | 0.370 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.647 |
LIG_PTB_Apo_2 | 402 | 409 | PF02174 | 0.361 |
LIG_PTB_Phospho_1 | 402 | 408 | PF10480 | 0.360 |
LIG_SH2_CRK | 399 | 403 | PF00017 | 0.502 |
LIG_SH2_NCK_1 | 91 | 95 | PF00017 | 0.551 |
LIG_SH2_PTP2 | 408 | 411 | PF00017 | 0.393 |
LIG_SH2_PTP2 | 414 | 417 | PF00017 | 0.426 |
LIG_SH2_SRC | 248 | 251 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.502 |
LIG_SH2_STAT3 | 501 | 504 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.530 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.580 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.363 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.431 |
LIG_SUMO_SIM_anti_2 | 139 | 144 | PF11976 | 0.492 |
LIG_SUMO_SIM_anti_2 | 330 | 337 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 14 | 20 | PF11976 | 0.699 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.390 |
LIG_TRAF2_1 | 502 | 505 | PF00917 | 0.582 |
LIG_UBA3_1 | 177 | 185 | PF00899 | 0.540 |
MOD_CDC14_SPxK_1 | 302 | 305 | PF00782 | 0.526 |
MOD_CDC14_SPxK_1 | 352 | 355 | PF00782 | 0.525 |
MOD_CDK_SPK_2 | 168 | 173 | PF00069 | 0.554 |
MOD_CDK_SPxK_1 | 299 | 305 | PF00069 | 0.578 |
MOD_CDK_SPxK_1 | 349 | 355 | PF00069 | 0.525 |
MOD_CDK_SPxxK_3 | 168 | 175 | PF00069 | 0.407 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.581 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.762 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.665 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.745 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.582 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.451 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.603 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.326 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.571 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.456 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.710 |
MOD_CMANNOS | 276 | 279 | PF00535 | 0.373 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.332 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.383 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.517 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.621 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.687 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.682 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.653 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.720 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.399 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.639 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.562 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.566 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.668 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.468 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.651 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.324 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.748 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.698 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.445 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.588 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.667 |
MOD_NEK2_2 | 387 | 392 | PF00069 | 0.531 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.492 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.553 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.599 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.563 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.581 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.404 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.487 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.647 |
MOD_PKB_1 | 56 | 64 | PF00069 | 0.625 |
MOD_Plk_2-3 | 129 | 135 | PF00069 | 0.639 |
MOD_Plk_2-3 | 146 | 152 | PF00069 | 0.697 |
MOD_Plk_2-3 | 221 | 227 | PF00069 | 0.564 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.600 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.601 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.445 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.652 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.546 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.669 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.525 |
MOD_SUMO_rev_2 | 144 | 154 | PF00179 | 0.660 |
TRG_DiLeu_BaLyEn_6 | 262 | 267 | PF01217 | 0.382 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.667 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 457 | 460 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXT0 | Leptomonas seymouri | 56% | 100% |
A0A0S4K087 | Bodo saltans | 47% | 100% |
A0A1X0P0C0 | Trypanosomatidae | 47% | 100% |
A0A3R7N4Z4 | Trypanosoma rangeli | 53% | 100% |
A0A3S7XBK9 | Leishmania donovani | 100% | 100% |
A4HPW6 | Leishmania braziliensis | 72% | 97% |
D0A4B4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9ATN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q0W5 | Leishmania major | 93% | 100% |
V5DLL0 | Trypanosoma cruzi | 51% | 100% |