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: 12 |
NetGPI | no | yes: 0, no: 12 |
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: A4HNZ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.648 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.171 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.541 |
DEG_APCC_DBOX_1 | 348 | 356 | PF00400 | 0.282 |
DEG_SPOP_SBC_1 | 148 | 152 | PF00917 | 0.537 |
DOC_ANK_TNKS_1 | 212 | 219 | PF00023 | 0.574 |
DOC_CKS1_1 | 46 | 51 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 359 | 366 | PF00134 | 0.226 |
DOC_MAPK_gen_1 | 64 | 72 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 532 | 541 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 64 | 72 | PF00069 | 0.455 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.450 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.513 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 222 | 227 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 391 | 400 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 481 | 487 | PF00244 | 0.374 |
LIG_Actin_WH2_2 | 467 | 483 | PF00022 | 0.351 |
LIG_Clathr_ClatBox_1 | 123 | 127 | PF01394 | 0.452 |
LIG_deltaCOP1_diTrp_1 | 250 | 256 | PF00928 | 0.395 |
LIG_EH1_1 | 487 | 495 | PF00400 | 0.494 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.608 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.773 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.399 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.379 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.281 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.400 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.438 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.511 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.200 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.460 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.322 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.580 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.496 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.433 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.532 |
LIG_Integrin_RGD_1 | 179 | 181 | PF01839 | 0.431 |
LIG_LIR_Gen_1 | 246 | 257 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 366 | 375 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 415 | 423 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 425 | 432 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 86 | 97 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.379 |
LIG_LYPXL_S_1 | 396 | 400 | PF13949 | 0.483 |
LIG_LYPXL_yS_3 | 397 | 400 | PF13949 | 0.287 |
LIG_NRBOX | 488 | 494 | PF00104 | 0.424 |
LIG_PCNA_PIPBox_1 | 226 | 235 | PF02747 | 0.293 |
LIG_Pex14_1 | 253 | 257 | PF04695 | 0.389 |
LIG_Pex14_2 | 249 | 253 | PF04695 | 0.386 |
LIG_Pex14_2 | 412 | 416 | PF04695 | 0.347 |
LIG_Rb_LxCxE_1 | 88 | 103 | PF01857 | 0.554 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.353 |
LIG_SH2_STAT3 | 166 | 169 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.309 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.353 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.401 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.740 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.648 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.503 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.391 |
LIG_SUMO_SIM_anti_2 | 121 | 127 | PF11976 | 0.412 |
LIG_SUMO_SIM_anti_2 | 225 | 231 | PF11976 | 0.490 |
LIG_SUMO_SIM_anti_2 | 470 | 475 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 121 | 127 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 350 | 357 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 83 | 88 | PF11976 | 0.348 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.614 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.524 |
LIG_TRAF2_1 | 93 | 96 | PF00917 | 0.479 |
LIG_TYR_ITIM | 87 | 92 | PF00017 | 0.410 |
LIG_UBA3_1 | 226 | 231 | PF00899 | 0.469 |
LIG_UBA3_1 | 440 | 447 | PF00899 | 0.453 |
LIG_UBA3_1 | 492 | 501 | PF00899 | 0.432 |
LIG_WRC_WIRS_1 | 56 | 61 | PF05994 | 0.517 |
MOD_CDK_SPxK_1 | 100 | 106 | PF00069 | 0.434 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.740 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.529 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.427 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.507 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.313 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.547 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.402 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.391 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.443 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.481 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.518 |
MOD_CMANNOS | 253 | 256 | PF00535 | 0.393 |
MOD_GlcNHglycan | 155 | 159 | PF01048 | 0.714 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.500 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.733 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.486 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.482 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.524 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.540 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.375 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.467 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.544 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.508 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.394 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.213 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.445 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.720 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.563 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.442 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.369 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.411 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.407 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.360 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.416 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.440 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.510 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.447 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.329 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.337 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.497 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.470 |
MOD_PKB_1 | 18 | 26 | PF00069 | 0.512 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.706 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.541 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.472 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.305 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.509 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.214 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.431 |
MOD_Plk_2-3 | 245 | 251 | PF00069 | 0.546 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.554 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.407 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.403 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.482 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.479 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.402 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.403 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.338 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.441 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.513 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.471 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.748 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.473 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.411 |
MOD_SUMO_for_1 | 290 | 293 | PF00179 | 0.352 |
TRG_DiLeu_BaEn_1 | 119 | 124 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_1 | 201 | 206 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_3 | 425 | 431 | PF01217 | 0.297 |
TRG_DiLeu_BaEn_4 | 95 | 101 | PF01217 | 0.538 |
TRG_DiLeu_LyEn_5 | 95 | 100 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 421 | 424 | PF00400 | 0.312 |
TRG_NES_CRM1_1 | 344 | 356 | PF08389 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 349 | 353 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 362 | 366 | PF00026 | 0.216 |
TRG_Pf-PMV_PEXEL_1 | 429 | 433 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1E7 | Leptomonas seymouri | 67% | 98% |
A0A0S4JC36 | Bodo saltans | 39% | 100% |
A0A1X0P7Z1 | Trypanosomatidae | 44% | 100% |
A0A3Q8IIW2 | Leishmania donovani | 79% | 100% |
A0A422MZU5 | Trypanosoma rangeli | 47% | 100% |
A4HNZ7 | Leishmania braziliensis | 99% | 100% |
A4ICJ8 | Leishmania infantum | 79% | 91% |
D0A2X3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ASQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 88% |
Q4Q1T8 | Leishmania major | 79% | 100% |
V5BU60 | Trypanosoma cruzi | 46% | 100% |