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: E9ATN3
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0032259 | methylation | 2 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0043414 | macromolecule methylation | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
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:0008276 | protein methyltransferase activity | 3 | 5 |
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:0140096 | catalytic activity, acting on a protein | 2 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.710 |
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 390 | 394 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.769 |
CLV_PCSK_FUR_1 | 458 | 462 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.524 |
CLV_PCSK_PC7_1 | 229 | 235 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.430 |
CLV_Separin_Metazoa | 463 | 467 | PF03568 | 0.424 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.539 |
DOC_ANK_TNKS_1 | 124 | 131 | PF00023 | 0.713 |
DOC_CYCLIN_RxL_1 | 172 | 179 | PF00134 | 0.549 |
DOC_CYCLIN_RxL_1 | 229 | 241 | PF00134 | 0.516 |
DOC_CYCLIN_yCln2_LP_2 | 242 | 248 | PF00134 | 0.370 |
DOC_CYCLIN_yCln2_LP_2 | 368 | 374 | PF00134 | 0.184 |
DOC_MAPK_gen_1 | 436 | 444 | PF00069 | 0.512 |
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 | 0.480 |
DOC_PP2B_PxIxI_1 | 468 | 474 | PF00149 | 0.494 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.702 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.398 |
LIG_14-3-3_CanoR_1 | 290 | 299 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 355 | 363 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 46 | 52 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 56 | 63 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 81 | 91 | PF00244 | 0.751 |
LIG_Actin_WH2_2 | 14 | 31 | PF00022 | 0.589 |
LIG_Actin_WH2_2 | 65 | 82 | PF00022 | 0.692 |
LIG_APCC_ABBA_1 | 495 | 500 | PF00400 | 0.378 |
LIG_BRCT_BRCA1_1 | 251 | 255 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 360 | 364 | PF00533 | 0.328 |
LIG_Clathr_ClatBox_1 | 142 | 146 | PF01394 | 0.447 |
LIG_CtBP_PxDLS_1 | 15 | 19 | PF00389 | 0.604 |
LIG_deltaCOP1_diTrp_1 | 206 | 213 | PF00928 | 0.374 |
LIG_deltaCOP1_diTrp_1 | 274 | 279 | PF00928 | 0.357 |
LIG_EH1_1 | 479 | 487 | PF00400 | 0.514 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.328 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.506 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.526 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.689 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.606 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.453 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.404 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.342 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.568 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.460 |
LIG_Integrin_RGD_1 | 125 | 127 | PF01839 | 0.711 |
LIG_LIR_Gen_1 | 354 | 364 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 412 | 421 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 438 | 449 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 90 | 98 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.683 |
LIG_MYND_1 | 265 | 269 | PF01753 | 0.371 |
LIG_PTB_Apo_2 | 402 | 409 | PF02174 | 0.364 |
LIG_PTB_Phospho_1 | 402 | 408 | PF10480 | 0.362 |
LIG_SH2_CRK | 282 | 286 | PF00017 | 0.246 |
LIG_SH2_CRK | 399 | 403 | PF00017 | 0.505 |
LIG_SH2_PTP2 | 408 | 411 | PF00017 | 0.397 |
LIG_SH2_PTP2 | 414 | 417 | PF00017 | 0.434 |
LIG_SH2_SRC | 248 | 251 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.246 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.581 |
LIG_SH2_STAT3 | 501 | 504 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.682 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.584 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.366 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.435 |
LIG_SUMO_SIM_anti_2 | 138 | 144 | PF11976 | 0.510 |
LIG_SUMO_SIM_anti_2 | 330 | 337 | PF11976 | 0.413 |
LIG_TRAF2_1 | 502 | 505 | PF00917 | 0.576 |
LIG_TRAF2_2 | 373 | 378 | PF00917 | 0.436 |
LIG_TRAF2_2 | 411 | 416 | PF00917 | 0.432 |
LIG_UBA3_1 | 177 | 185 | PF00899 | 0.539 |
LIG_WRC_WIRS_1 | 91 | 96 | PF05994 | 0.462 |
MOD_CDC14_SPxK_1 | 302 | 305 | PF00782 | 0.449 |
MOD_CDC14_SPxK_1 | 352 | 355 | PF00782 | 0.398 |
MOD_CDK_SPK_2 | 168 | 173 | PF00069 | 0.532 |
MOD_CDK_SPxK_1 | 299 | 305 | PF00069 | 0.449 |
MOD_CDK_SPxK_1 | 349 | 355 | PF00069 | 0.398 |
MOD_CDK_SPxxK_3 | 168 | 175 | PF00069 | 0.385 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.584 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.602 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.755 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.566 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.430 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.594 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.325 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.461 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.463 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.704 |
MOD_CMANNOS | 276 | 279 | PF00535 | 0.359 |
MOD_GlcNHglycan | 133 | 137 | PF01048 | 0.760 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.542 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.407 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.641 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.385 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.678 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.651 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.706 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.377 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.552 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.449 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.455 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.688 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.476 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.673 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.567 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.749 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.753 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.690 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.407 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.302 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.624 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.443 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.617 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.720 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.487 |
MOD_PKA_1 | 80 | 86 | PF00069 | 0.482 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.590 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.483 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.475 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.228 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.498 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.660 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.654 |
MOD_PKB_1 | 44 | 52 | PF00069 | 0.531 |
MOD_PKB_1 | 56 | 64 | PF00069 | 0.645 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.594 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.307 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.571 |
MOD_Plk_2-3 | 146 | 152 | PF00069 | 0.670 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.608 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.602 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.446 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.236 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.672 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.525 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.670 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.398 |
MOD_SUMO_rev_2 | 144 | 154 | PF00179 | 0.642 |
TRG_DiLeu_BaLyEn_6 | 262 | 267 | PF01217 | 0.382 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.685 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 457 | 460 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXT0 | Leptomonas seymouri | 56% | 100% |
A0A0S4K087 | Bodo saltans | 49% | 100% |
A0A1X0P0C0 | Trypanosomatidae | 49% | 100% |
A0A3R7N4Z4 | Trypanosoma rangeli | 48% | 100% |
A0A3S7XBK9 | Leishmania donovani | 88% | 100% |
A4HPW6 | Leishmania braziliensis | 72% | 97% |
A4IDM8 | Leishmania infantum | 89% | 100% |
D0A4B4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
Q4Q0W5 | Leishmania major | 87% | 100% |
V5DLL0 | Trypanosoma cruzi | 50% | 100% |