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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005741 | mitochondrial outer membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0019867 | outer membrane | 3 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0031968 | organelle outer membrane | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B5A2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.375 |
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 60 | 64 | PF00656 | 0.663 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.444 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.430 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.649 |
DOC_CDC14_PxL_1 | 231 | 239 | PF14671 | 0.426 |
DOC_MAPK_DCC_7 | 302 | 312 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 364 | 374 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 80 | 91 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 283 | 290 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 85 | 93 | PF00069 | 0.562 |
DOC_PP2B_LxvP_1 | 145 | 148 | PF13499 | 0.359 |
DOC_PP4_FxxP_1 | 113 | 116 | PF00568 | 0.325 |
DOC_SPAK_OSR1_1 | 417 | 421 | PF12202 | 0.433 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.399 |
DOC_USP7_UBL2_3 | 332 | 336 | PF12436 | 0.430 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.377 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 172 | 176 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 283 | 289 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 392 | 399 | PF00244 | 0.401 |
LIG_Actin_WH2_2 | 270 | 285 | PF00022 | 0.364 |
LIG_Actin_WH2_2 | 354 | 369 | PF00022 | 0.404 |
LIG_eIF4E_1 | 242 | 248 | PF01652 | 0.289 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.367 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.381 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.693 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.537 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.461 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.792 |
LIG_GBD_Chelix_1 | 69 | 77 | PF00786 | 0.305 |
LIG_Integrin_isoDGR_2 | 354 | 356 | PF01839 | 0.322 |
LIG_LIR_Gen_1 | 181 | 191 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 348 | 352 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.416 |
LIG_PDZ_Class_1 | 431 | 436 | PF00595 | 0.343 |
LIG_Pex14_2 | 341 | 345 | PF04695 | 0.432 |
LIG_PTB_Apo_2 | 236 | 243 | PF02174 | 0.389 |
LIG_PTB_Phospho_1 | 236 | 242 | PF10480 | 0.391 |
LIG_REV1ctd_RIR_1 | 338 | 348 | PF16727 | 0.388 |
LIG_SH2_GRB2like | 267 | 270 | PF00017 | 0.294 |
LIG_SH2_PTP2 | 359 | 362 | PF00017 | 0.400 |
LIG_SH2_SRC | 267 | 270 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.469 |
LIG_SH2_STAT3 | 347 | 350 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.651 |
LIG_SH3_1 | 359 | 365 | PF00018 | 0.425 |
LIG_SH3_2 | 362 | 367 | PF14604 | 0.439 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.359 |
LIG_SUMO_SIM_par_1 | 142 | 150 | PF11976 | 0.347 |
LIG_TRAF2_1 | 368 | 371 | PF00917 | 0.269 |
LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.514 |
LIG_UBA3_1 | 226 | 233 | PF00899 | 0.452 |
LIG_WRC_WIRS_1 | 337 | 342 | PF05994 | 0.335 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.705 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.387 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.468 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.370 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.431 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.640 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.427 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.491 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.382 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.510 |
MOD_GlcNHglycan | 164 | 168 | PF01048 | 0.561 |
MOD_GlcNHglycan | 331 | 335 | PF01048 | 0.478 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.482 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.448 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.406 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.536 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.615 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.524 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.326 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.554 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.337 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.484 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.477 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.434 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.297 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.713 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.755 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.470 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.349 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.337 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.578 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.432 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.428 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.386 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.697 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.527 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.490 |
MOD_Plk_2-3 | 171 | 177 | PF00069 | 0.432 |
MOD_Plk_2-3 | 382 | 388 | PF00069 | 0.507 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.508 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.337 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.541 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.544 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.538 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.472 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.347 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.378 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.390 |
MOD_SUMO_for_1 | 178 | 181 | PF00179 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.341 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.468 |
TRG_ER_diLys_1 | 431 | 436 | PF00400 | 0.391 |
TRG_NES_CRM1_1 | 196 | 211 | PF08389 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 224 | 229 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 24 | 29 | PF00026 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 417 | 421 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 81 | 86 | PF00026 | 0.534 |
TRG_PTS1 | 433 | 436 | PF00515 | 0.362 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1E1 | Leptomonas seymouri | 65% | 92% |
A0A0S4INK9 | Bodo saltans | 44% | 99% |
A0A1X0PAR0 | Trypanosomatidae | 60% | 100% |
A0A3S7X876 | Leishmania donovani | 92% | 100% |
A0A422NNH0 | Trypanosoma rangeli | 60% | 87% |
A4HB32 | Leishmania braziliensis | 85% | 100% |
A4IAN7 | Leishmania infantum | 92% | 100% |
C9ZM15 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
Q4Q2N1 | Leishmania major | 93% | 100% |
V5DLX6 | Trypanosoma cruzi | 61% | 100% |