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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0019867 | outer membrane | 3 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0001401 | SAM complex | 5 | 1 |
GO:0005742 | mitochondrial outer membrane translocase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0098799 | outer mitochondrial membrane protein complex | 3 | 1 |
Related structures:
AlphaFold database: E9ALP2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006839 | mitochondrial transport | 4 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007005 | mitochondrion organization | 5 | 1 |
GO:0007006 | mitochondrial membrane organization | 5 | 1 |
GO:0007008 | outer mitochondrial membrane organization | 6 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0045040 | protein insertion into mitochondrial outer membrane | 6 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051204 | protein insertion into mitochondrial membrane | 5 | 1 |
GO:0051205 | protein insertion into membrane | 5 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0070585 | protein localization to mitochondrion | 6 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:0090151 | establishment of protein localization to mitochondrial membrane | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.434 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.203 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.462 |
DOC_CYCLIN_RxL_1 | 205 | 212 | PF00134 | 0.412 |
DOC_CYCLIN_yCln2_LP_2 | 20 | 26 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 365 | 371 | PF00134 | 0.425 |
DOC_MAPK_gen_1 | 102 | 109 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 431 | 440 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 89 | 98 | PF00069 | 0.514 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.470 |
DOC_PP2B_PxIxI_1 | 116 | 122 | PF00149 | 0.534 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.491 |
DOC_USP7_UBL2_3 | 169 | 173 | PF12436 | 0.561 |
LIG_14-3-3_CanoR_1 | 130 | 134 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 168 | 175 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 207 | 211 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 235 | 241 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 331 | 337 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 454 | 458 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 67 | 74 | PF00244 | 0.345 |
LIG_Actin_WH2_2 | 385 | 401 | PF00022 | 0.380 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.313 |
LIG_BRCT_BRCA1_1 | 428 | 432 | PF00533 | 0.412 |
LIG_BRCT_BRCA1_1 | 467 | 471 | PF00533 | 0.509 |
LIG_Clathr_ClatBox_1 | 30 | 34 | PF01394 | 0.575 |
LIG_deltaCOP1_diTrp_1 | 342 | 350 | PF00928 | 0.457 |
LIG_EH_1 | 247 | 251 | PF12763 | 0.545 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.490 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.538 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.653 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.510 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.573 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.293 |
LIG_Integrin_isoDGR_2 | 452 | 454 | PF01839 | 0.570 |
LIG_LIR_Gen_1 | 146 | 157 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 278 | 286 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 456 | 466 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.576 |
LIG_LYPXL_S_1 | 309 | 313 | PF13949 | 0.425 |
LIG_PDZ_Class_2 | 468 | 473 | PF00595 | 0.526 |
LIG_Pex14_1 | 467 | 471 | PF04695 | 0.474 |
LIG_Pex14_2 | 367 | 371 | PF04695 | 0.332 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.452 |
LIG_REV1ctd_RIR_1 | 310 | 317 | PF16727 | 0.425 |
LIG_SH2_PTP2 | 137 | 140 | PF00017 | 0.425 |
LIG_SH2_PTP2 | 291 | 294 | PF00017 | 0.416 |
LIG_SH2_SRC | 137 | 140 | PF00017 | 0.425 |
LIG_SH2_STAT3 | 260 | 263 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.416 |
LIG_SH3_1 | 290 | 296 | PF00018 | 0.313 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.313 |
LIG_SUMO_SIM_par_1 | 118 | 124 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 7 | 15 | PF11976 | 0.473 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.568 |
LIG_UBA3_1 | 391 | 399 | PF00899 | 0.376 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.408 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.376 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.411 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.583 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.437 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.381 |
MOD_Cter_Amidation | 166 | 169 | PF01082 | 0.433 |
MOD_Cter_Amidation | 452 | 455 | PF01082 | 0.582 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.548 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.425 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.356 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.556 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.652 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.612 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.449 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.498 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.316 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.127 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.313 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.491 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.484 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.513 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.320 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.651 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.425 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.425 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.304 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.245 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.313 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.313 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.356 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.461 |
MOD_NEK2_2 | 129 | 134 | PF00069 | 0.521 |
MOD_NEK2_2 | 376 | 381 | PF00069 | 0.425 |
MOD_NEK2_2 | 453 | 458 | PF00069 | 0.588 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.534 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.404 |
MOD_PK_1 | 143 | 149 | PF00069 | 0.512 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.410 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.478 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.278 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.496 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.582 |
MOD_PKB_1 | 65 | 73 | PF00069 | 0.492 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.481 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.509 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.399 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.425 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.457 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.324 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.605 |
MOD_SUMO_for_1 | 282 | 285 | PF00179 | 0.392 |
MOD_SUMO_rev_2 | 97 | 103 | PF00179 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.596 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.127 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 64 | 67 | PF00400 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 403 | 407 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1R7 | Leptomonas seymouri | 80% | 100% |
A0A1X0NZZ7 | Trypanosomatidae | 61% | 99% |
A0A3R7L3S8 | Trypanosoma rangeli | 60% | 99% |
A0A3S5H7L5 | Leishmania donovani | 95% | 100% |
A4HIY6 | Leishmania braziliensis | 92% | 100% |
A4I4P0 | Leishmania infantum | 95% | 100% |
C9ZLC7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 99% |
E9AE43 | Leishmania major | 95% | 100% |
Q10478 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
Q5U3I0 | Danio rerio | 26% | 100% |
Q6AXV4 | Rattus norvegicus | 26% | 100% |
Q6P806 | Xenopus tropicalis | 25% | 100% |
Q803G5 | Danio rerio | 25% | 100% |
Q8BGH2 | Mus musculus | 26% | 100% |
Q9Y512 | Homo sapiens | 24% | 100% |
V5D9V3 | Trypanosoma cruzi | 61% | 92% |