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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 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 | 1 |
Related structures:
AlphaFold database: A0A3S5H804
PDB structure(s): 7ane_o
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 528 | 532 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.480 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 15 | 17 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.352 |
CLV_PCSK_PC1ET2_1 | 469 | 471 | PF00082 | 0.392 |
CLV_PCSK_PC7_1 | 566 | 572 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.410 |
DEG_APCC_DBOX_1 | 204 | 212 | PF00400 | 0.377 |
DEG_MDM2_SWIB_1 | 180 | 188 | PF02201 | 0.343 |
DEG_MDM2_SWIB_1 | 328 | 336 | PF02201 | 0.345 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.540 |
DEG_SCF_FBW7_2 | 513 | 520 | PF00400 | 0.423 |
DOC_CKS1_1 | 243 | 248 | PF01111 | 0.412 |
DOC_CKS1_1 | 527 | 532 | PF01111 | 0.479 |
DOC_CYCLIN_RxL_1 | 155 | 167 | PF00134 | 0.383 |
DOC_CYCLIN_RxL_1 | 199 | 212 | PF00134 | 0.385 |
DOC_CYCLIN_RxL_1 | 322 | 331 | PF00134 | 0.350 |
DOC_CYCLIN_RxL_1 | 455 | 466 | PF00134 | 0.410 |
DOC_MAPK_gen_1 | 155 | 163 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 202 | 210 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 288 | 297 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 202 | 210 | PF00069 | 0.386 |
DOC_PP1_RVXF_1 | 157 | 164 | PF00149 | 0.370 |
DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.419 |
DOC_PP1_RVXF_1 | 300 | 307 | PF00149 | 0.332 |
DOC_PP1_RVXF_1 | 32 | 39 | PF00149 | 0.460 |
DOC_PP1_RVXF_1 | 345 | 351 | PF00149 | 0.432 |
DOC_PP1_RVXF_1 | 352 | 358 | PF00149 | 0.381 |
DOC_PP1_RVXF_1 | 541 | 548 | PF00149 | 0.411 |
DOC_PP1_RVXF_1 | 572 | 579 | PF00149 | 0.426 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.365 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.411 |
DOC_SPAK_OSR1_1 | 472 | 476 | PF12202 | 0.384 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.358 |
DOC_USP7_MATH_2 | 18 | 24 | PF00917 | 0.471 |
DOC_USP7_UBL2_3 | 151 | 155 | PF12436 | 0.442 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.446 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.446 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 386 | 394 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 570 | 578 | PF00244 | 0.458 |
LIG_APCC_ABBA_1 | 75 | 80 | PF00400 | 0.406 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.420 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 594 | 598 | PF00533 | 0.515 |
LIG_Clathr_ClatBox_1 | 216 | 220 | PF01394 | 0.473 |
LIG_Clathr_ClatBox_1 | 327 | 331 | PF01394 | 0.352 |
LIG_deltaCOP1_diTrp_1 | 156 | 163 | PF00928 | 0.374 |
LIG_deltaCOP1_diTrp_1 | 318 | 328 | PF00928 | 0.354 |
LIG_deltaCOP1_diTrp_1 | 37 | 44 | PF00928 | 0.565 |
LIG_deltaCOP1_diTrp_1 | 441 | 446 | PF00928 | 0.445 |
LIG_deltaCOP1_diTrp_1 | 497 | 505 | PF00928 | 0.365 |
LIG_deltaCOP1_diTrp_1 | 91 | 99 | PF00928 | 0.358 |
LIG_EH_1 | 96 | 100 | PF12763 | 0.317 |
LIG_eIF4E_1 | 358 | 364 | PF01652 | 0.418 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.407 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.441 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.344 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.503 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.384 |
LIG_FHA_2 | 570 | 576 | PF00498 | 0.430 |
LIG_LIR_Apic_2 | 318 | 324 | PF02991 | 0.374 |
LIG_LIR_Apic_2 | 37 | 41 | PF02991 | 0.532 |
LIG_LIR_Apic_2 | 501 | 507 | PF02991 | 0.354 |
LIG_LIR_Apic_2 | 53 | 57 | PF02991 | 0.318 |
LIG_LIR_Apic_2 | 87 | 93 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 372 | 381 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 497 | 507 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 296 | 300 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 497 | 502 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 556 | 562 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 575 | 581 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 595 | 601 | PF02991 | 0.296 |
LIG_PALB2_WD40_1 | 180 | 188 | PF16756 | 0.343 |
LIG_Pex14_1 | 398 | 402 | PF04695 | 0.362 |
LIG_Pex14_1 | 95 | 99 | PF04695 | 0.332 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.331 |
LIG_Pex14_2 | 328 | 332 | PF04695 | 0.355 |
LIG_PTB_Apo_2 | 179 | 186 | PF02174 | 0.339 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.527 |
LIG_SH2_CRK | 385 | 389 | PF00017 | 0.392 |
LIG_SH2_GRB2like | 375 | 378 | PF00017 | 0.469 |
LIG_SH2_SRC | 375 | 378 | PF00017 | 0.469 |
LIG_SH2_SRC | 522 | 525 | PF00017 | 0.444 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.403 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 375 | 379 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 394 | 398 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 549 | 553 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 534 | 537 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.457 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.494 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.486 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.443 |
LIG_SH3_5 | 530 | 534 | PF00018 | 0.537 |
LIG_SUMO_SIM_anti_2 | 109 | 114 | PF11976 | 0.405 |
LIG_SUMO_SIM_anti_2 | 212 | 218 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 206 | 212 | PF11976 | 0.391 |
LIG_TYR_ITIM | 343 | 348 | PF00017 | 0.519 |
LIG_UBA3_1 | 149 | 155 | PF00899 | 0.416 |
LIG_UBA3_1 | 273 | 279 | PF00899 | 0.376 |
LIG_UBA3_1 | 408 | 415 | PF00899 | 0.500 |
LIG_WRC_WIRS_1 | 51 | 56 | PF05994 | 0.409 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.438 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.457 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.381 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.599 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.425 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.388 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.431 |
MOD_CMANNOS | 59 | 62 | PF00535 | 0.395 |
MOD_Cter_Amidation | 128 | 131 | PF01082 | 0.529 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.357 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.474 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.616 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.410 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.448 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.369 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.529 |
MOD_N-GLC_1 | 437 | 442 | PF02516 | 0.426 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.561 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.600 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.437 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.445 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.363 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.410 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.520 |
MOD_NEK2_2 | 478 | 483 | PF00069 | 0.409 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.410 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.549 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.625 |
MOD_PIKK_1 | 569 | 575 | PF00454 | 0.571 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.396 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.598 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.522 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.440 |
MOD_PKB_1 | 130 | 138 | PF00069 | 0.515 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.354 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.373 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.447 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.473 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.546 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.499 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.420 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.445 |
MOD_SUMO_rev_2 | 198 | 204 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 258 | 265 | PF00179 | 0.442 |
MOD_SUMO_rev_2 | 37 | 43 | PF00179 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 203 | 208 | PF01217 | 0.384 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 470 | 472 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.480 |
TRG_NLS_Bipartite_1 | 235 | 257 | PF00514 | 0.423 |
TRG_NLS_MonoExtC_3 | 252 | 258 | PF00514 | 0.449 |
TRG_NLS_MonoExtC_3 | 534 | 539 | PF00514 | 0.444 |
TRG_NLS_MonoExtN_4 | 128 | 134 | PF00514 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 186 | 190 | PF00026 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3J0 | Leptomonas seymouri | 96% | 100% |
A0A0S4IZR5 | Bodo saltans | 83% | 97% |
A0A1X0P5F3 | Trypanosomatidae | 89% | 100% |
A0A422N423 | Trypanosoma rangeli | 89% | 100% |
A4HN65 | Leishmania braziliensis | 99% | 100% |
A4IBT2 | Leishmania infantum | 100% | 100% |
C9ZYT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 86% | 100% |
E9AFL9 | Leishmania major | 100% | 100% |
E9B6S2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
V5DUK9 | Trypanosoma cruzi | 88% | 100% |