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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9AVP2
Term | Name | Level | Count |
---|---|---|---|
GO:0006473 | protein acetylation | 6 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 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:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 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 | 8 |
GO:0008080 | N-acetyltransferase activity | 6 | 8 |
GO:0016407 | acetyltransferase activity | 5 | 8 |
GO:0016410 | N-acyltransferase activity | 5 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016746 | acyltransferase activity | 3 | 8 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.601 |
CLV_PCSK_FUR_1 | 403 | 407 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.705 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.533 |
DEG_ODPH_VHL_1 | 317 | 329 | PF01847 | 0.487 |
DOC_CDC14_PxL_1 | 49 | 57 | PF14671 | 0.385 |
DOC_CKS1_1 | 310 | 315 | PF01111 | 0.521 |
DOC_CYCLIN_RxL_1 | 219 | 228 | PF00134 | 0.571 |
DOC_CYCLIN_yCln2_LP_2 | 103 | 109 | PF00134 | 0.465 |
DOC_MAPK_gen_1 | 385 | 395 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 321 | 329 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 376 | 382 | PF00149 | 0.380 |
DOC_PP2B_LxvP_1 | 103 | 106 | PF13499 | 0.464 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.609 |
DOC_PP4_FxxP_1 | 33 | 36 | PF00568 | 0.393 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.508 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 202 | 211 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 345 | 349 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 422 | 428 | PF00244 | 0.453 |
LIG_APCC_ABBA_1 | 381 | 386 | PF00400 | 0.391 |
LIG_APCC_ABBA_1 | 387 | 392 | PF00400 | 0.349 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.507 |
LIG_Clathr_ClatBox_1 | 263 | 267 | PF01394 | 0.487 |
LIG_CSL_BTD_1 | 233 | 236 | PF09270 | 0.451 |
LIG_EH1_1 | 322 | 330 | PF00400 | 0.507 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.692 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.507 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.501 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.454 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.532 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.359 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.632 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.470 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.450 |
LIG_HCF-1_HBM_1 | 40 | 43 | PF13415 | 0.371 |
LIG_LIR_Apic_2 | 168 | 173 | PF02991 | 0.653 |
LIG_LIR_Apic_2 | 30 | 36 | PF02991 | 0.416 |
LIG_LIR_Apic_2 | 472 | 477 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 100 | 109 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 254 | 263 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.300 |
LIG_MYND_1 | 53 | 57 | PF01753 | 0.434 |
LIG_MYND_3 | 149 | 153 | PF01753 | 0.595 |
LIG_RPA_C_Fungi | 332 | 344 | PF08784 | 0.311 |
LIG_SH2_PTP2 | 255 | 258 | PF00017 | 0.343 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.653 |
LIG_SH2_SRC | 43 | 46 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.428 |
LIG_SH3_1 | 54 | 60 | PF00018 | 0.435 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.531 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.381 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.802 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.484 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.499 |
LIG_SUMO_SIM_anti_2 | 324 | 329 | PF11976 | 0.362 |
LIG_SUMO_SIM_anti_2 | 48 | 53 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 75 | 85 | PF11976 | 0.475 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.600 |
LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.416 |
LIG_WRC_WIRS_1 | 167 | 172 | PF05994 | 0.609 |
LIG_WW_3 | 197 | 201 | PF00397 | 0.468 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.533 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.580 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.643 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.711 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.448 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.350 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.600 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.590 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.229 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.468 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.437 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.587 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.548 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.569 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.334 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.212 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.723 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.632 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.630 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.604 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.591 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.348 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.284 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.814 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.446 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.406 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.482 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.544 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.595 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.378 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.311 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.544 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.601 |
MOD_NEK2_2 | 423 | 428 | PF00069 | 0.438 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.663 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.194 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.325 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.642 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.657 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.537 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.623 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.258 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.527 |
MOD_PKB_1 | 200 | 208 | PF00069 | 0.600 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.630 |
MOD_Plk_2-3 | 270 | 276 | PF00069 | 0.194 |
MOD_Plk_2-3 | 78 | 84 | PF00069 | 0.445 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.532 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.587 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.462 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.395 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.560 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.419 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.345 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.699 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.357 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.255 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.411 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.632 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.637 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.553 |
TRG_DiLeu_LyEn_5 | 5 | 10 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.343 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 397 | 402 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4Y0 | Leptomonas seymouri | 41% | 100% |
A0A3S7WX61 | Leishmania donovani | 86% | 100% |
A4HCA5 | Leishmania braziliensis | 69% | 100% |
A4HZT7 | Leishmania infantum | 86% | 100% |
Q4QBT7 | Leishmania major | 84% | 100% |
V5BR45 | Trypanosoma cruzi | 32% | 100% |