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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HGQ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 398 | 402 | PF00656 | 0.724 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.398 |
CLV_C14_Caspase3-7 | 548 | 552 | PF00656 | 0.465 |
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.506 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.377 |
CLV_PCSK_PC1ET2_1 | 514 | 516 | PF00082 | 0.502 |
CLV_PCSK_PC7_1 | 286 | 292 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.255 |
DEG_APCC_DBOX_1 | 3 | 11 | PF00400 | 0.358 |
DEG_COP1_1 | 119 | 129 | PF00400 | 0.514 |
DOC_CKS1_1 | 387 | 392 | PF01111 | 0.488 |
DOC_CYCLIN_RxL_1 | 512 | 520 | PF00134 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 234 | 240 | PF00134 | 0.402 |
DOC_CYCLIN_yCln2_LP_2 | 387 | 393 | PF00134 | 0.567 |
DOC_MAPK_DCC_7 | 231 | 240 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 514 | 521 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 338 | 347 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 4 | 11 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 514 | 521 | PF00069 | 0.481 |
DOC_MAPK_NFAT4_5 | 338 | 346 | PF00069 | 0.249 |
DOC_MAPK_NFAT4_5 | 514 | 522 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 445 | 452 | PF00149 | 0.446 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.564 |
DOC_USP7_UBL2_3 | 200 | 204 | PF12436 | 0.343 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 183 | 189 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 264 | 271 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 371 | 377 | PF00244 | 0.607 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.368 |
LIG_Actin_WH2_2 | 532 | 548 | PF00022 | 0.369 |
LIG_BIR_III_4 | 478 | 482 | PF00653 | 0.442 |
LIG_BIR_III_4 | 89 | 93 | PF00653 | 0.588 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.251 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.340 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.509 |
LIG_BRCT_BRCA1_1 | 447 | 451 | PF00533 | 0.542 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.487 |
LIG_Clathr_ClatBox_1 | 342 | 346 | PF01394 | 0.318 |
LIG_CSL_BTD_1 | 387 | 390 | PF09270 | 0.499 |
LIG_deltaCOP1_diTrp_1 | 134 | 140 | PF00928 | 0.470 |
LIG_eIF4E_1 | 336 | 342 | PF01652 | 0.282 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.631 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.364 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.280 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.435 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.478 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.475 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.490 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.745 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.475 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.438 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.790 |
LIG_GBD_Chelix_1 | 339 | 347 | PF00786 | 0.381 |
LIG_LIR_Apic_2 | 160 | 166 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 115 | 125 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.489 |
LIG_LYPXL_yS_3 | 336 | 339 | PF13949 | 0.317 |
LIG_NRBOX | 338 | 344 | PF00104 | 0.462 |
LIG_Pex14_2 | 140 | 144 | PF04695 | 0.349 |
LIG_Pex14_2 | 451 | 455 | PF04695 | 0.433 |
LIG_REV1ctd_RIR_1 | 449 | 457 | PF16727 | 0.424 |
LIG_REV1ctd_RIR_1 | 49 | 57 | PF16727 | 0.356 |
LIG_SH2_CRK | 495 | 499 | PF00017 | 0.546 |
LIG_SH2_SRC | 54 | 57 | PF00017 | 0.374 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 78 | 82 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.512 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.485 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.408 |
LIG_SUMO_SIM_anti_2 | 344 | 353 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 341 | 346 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 389 | 394 | PF11976 | 0.375 |
LIG_TRAF2_1 | 437 | 440 | PF00917 | 0.780 |
LIG_TRAF2_1 | 74 | 77 | PF00917 | 0.602 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.440 |
MOD_CDK_SPxxK_3 | 238 | 245 | PF00069 | 0.445 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.428 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.523 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.516 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.342 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.586 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.652 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.306 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.442 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.425 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.425 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.541 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.544 |
MOD_CMANNOS | 385 | 388 | PF00535 | 0.467 |
MOD_Cter_Amidation | 14 | 17 | PF01082 | 0.620 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.537 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.567 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.483 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.531 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.483 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.499 |
MOD_GlcNHglycan | 32 | 37 | PF01048 | 0.597 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.537 |
MOD_GlcNHglycan | 396 | 400 | PF01048 | 0.482 |
MOD_GlcNHglycan | 405 | 409 | PF01048 | 0.491 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.692 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.383 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.581 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.395 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.736 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.715 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.412 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.604 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.334 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.477 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.631 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.369 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.659 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.404 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.495 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.381 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.460 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.359 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.442 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.521 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.476 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.579 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.365 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.348 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.500 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.500 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.501 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.628 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.468 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.266 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.503 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.522 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.363 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.430 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.461 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.598 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.333 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.420 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.481 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.393 |
MOD_Plk_2-3 | 431 | 437 | PF00069 | 0.718 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.389 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.484 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.294 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.396 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.538 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.382 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.576 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.449 |
TRG_DiLeu_BaEn_1 | 177 | 182 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_1 | 293 | 298 | PF01217 | 0.400 |
TRG_DiLeu_BaEn_1 | 501 | 506 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_2 | 531 | 537 | PF01217 | 0.370 |
TRG_DiLeu_BaLyEn_6 | 387 | 392 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 290 | 292 | PF00400 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 515 | 520 | PF00026 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL93 | Leptomonas seymouri | 57% | 100% |
A0A1X0NQS9 | Trypanosomatidae | 34% | 100% |
A0A3S7X1P6 | Leishmania donovani | 76% | 100% |
A0A422NBH7 | Trypanosoma rangeli | 37% | 100% |
A4I3S9 | Leishmania infantum | 77% | 100% |
D0A878 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B021 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q865 | Leishmania major | 79% | 99% |
V5DCT5 | Trypanosoma cruzi | 36% | 100% |