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:0005739 | mitochondrion | 5 | 1 |
GO:0017087 | mitochondrial processing peptidase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 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:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: E9B4A1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006839 | mitochondrial transport | 4 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0030150 | protein import into mitochondrial matrix | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0065002 | intracellular protein transmembrane transport | 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:0071806 | protein transmembrane transport | 3 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 1 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004175 | endopeptidase activity | 4 | 2 |
GO:0004222 | metalloendopeptidase activity | 5 | 2 |
GO:0008233 | peptidase activity | 3 | 2 |
GO:0008237 | metallopeptidase activity | 4 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.334 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.298 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.521 |
DEG_SCF_FBW7_1 | 420 | 425 | PF00400 | 0.490 |
DEG_SPOP_SBC_1 | 232 | 236 | PF00917 | 0.250 |
DOC_CKS1_1 | 195 | 200 | PF01111 | 0.286 |
DOC_CYCLIN_yCln2_LP_2 | 169 | 175 | PF00134 | 0.424 |
DOC_MAPK_MEF2A_6 | 275 | 284 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 378 | 386 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 98 | 107 | PF00069 | 0.337 |
DOC_PP1_RVXF_1 | 219 | 225 | PF00149 | 0.280 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.332 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.395 |
DOC_USP7_UBL2_3 | 271 | 275 | PF12436 | 0.258 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.297 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 143 | 147 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 193 | 198 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 75 | 81 | PF00244 | 0.465 |
LIG_Actin_WH2_2 | 463 | 480 | PF00022 | 0.385 |
LIG_APCC_ABBA_1 | 451 | 456 | PF00400 | 0.304 |
LIG_BRCT_BRCA1_1 | 152 | 156 | PF00533 | 0.380 |
LIG_eIF4E_1 | 344 | 350 | PF01652 | 0.258 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.474 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.415 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.472 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.231 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.337 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.324 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.578 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.405 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.277 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.388 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.336 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.369 |
LIG_LIR_Gen_1 | 153 | 162 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 186 | 195 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 296 | 304 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 408 | 418 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 462 | 470 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 473 | 482 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 450 | 454 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 462 | 466 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.395 |
LIG_PDZ_Class_1 | 478 | 483 | PF00595 | 0.487 |
LIG_SH2_CRK | 297 | 301 | PF00017 | 0.303 |
LIG_SH2_CRK | 463 | 467 | PF00017 | 0.435 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 195 | 199 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 297 | 301 | PF00017 | 0.153 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.501 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.384 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.310 |
LIG_SUMO_SIM_anti_2 | 102 | 107 | PF11976 | 0.339 |
LIG_SUMO_SIM_anti_2 | 114 | 120 | PF11976 | 0.313 |
LIG_SUMO_SIM_anti_2 | 392 | 400 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 392 | 400 | PF11976 | 0.388 |
LIG_TRAF2_1 | 421 | 424 | PF00917 | 0.495 |
LIG_UBA3_1 | 154 | 161 | PF00899 | 0.458 |
LIG_UBA3_1 | 45 | 52 | PF00899 | 0.316 |
MOD_CDK_SPxK_1 | 194 | 200 | PF00069 | 0.286 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.488 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.361 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.419 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.258 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.453 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.342 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.523 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.277 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.298 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.401 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.365 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.525 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.416 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.267 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.291 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.326 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.455 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.454 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.391 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.422 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.392 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.399 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.265 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.314 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.263 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.406 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.371 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.465 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.465 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.485 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.354 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.322 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.238 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.512 |
MOD_N-GLC_1 | 477 | 482 | PF02516 | 0.478 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.445 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.646 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.459 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.269 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.334 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.270 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.486 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.557 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.390 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.356 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.425 |
MOD_PKA_1 | 193 | 199 | PF00069 | 0.334 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.451 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.437 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.363 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.510 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.370 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.355 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.306 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.260 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.517 |
MOD_Plk_2-3 | 181 | 187 | PF00069 | 0.302 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.538 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.447 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.380 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.261 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.346 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.563 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.286 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.297 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.488 |
MOD_SUMO_for_1 | 51 | 54 | PF00179 | 0.394 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.334 |
TRG_NES_CRM1_1 | 114 | 128 | PF08389 | 0.373 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDS4 | Leptomonas seymouri | 77% | 100% |
A0A1X0NSX1 | Trypanosomatidae | 65% | 100% |
A0A3Q8IMP0 | Leishmania donovani | 95% | 100% |
A0A422N4E4 | Trypanosoma rangeli | 64% | 100% |
A0A422N9N5 | Trypanosoma rangeli | 22% | 99% |
A4HLX2 | Leishmania braziliensis | 90% | 100% |
A4HMG0 | Leishmania braziliensis | 20% | 99% |
A4I9A1 | Leishmania infantum | 95% | 100% |
C9ZJC5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
O04308 | Arabidopsis thaliana | 25% | 97% |
O75439 | Homo sapiens | 25% | 99% |
O86835 | Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) | 21% | 100% |
O94745 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 96% |
P10507 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 20% | 100% |
P11914 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P20069 | Rattus norvegicus | 26% | 92% |
P22695 | Homo sapiens | 22% | 100% |
P23004 | Bos taurus | 22% | 100% |
P29677 | Solanum tuberosum | 27% | 96% |
P31800 | Bos taurus | 21% | 100% |
P31930 | Homo sapiens | 21% | 100% |
P32551 | Rattus norvegicus | 22% | 100% |
P43264 | Euglena gracilis | 23% | 98% |
P97997 | Blastocladiella emersonii | 27% | 100% |
Q03346 | Rattus norvegicus | 24% | 99% |
Q04805 | Bacillus subtilis (strain 168) | 22% | 100% |
Q0P5M8 | Bos taurus | 27% | 92% |
Q10713 | Homo sapiens | 26% | 92% |
Q23295 | Caenorhabditis elegans | 23% | 100% |
Q3SZ71 | Bos taurus | 24% | 99% |
Q42290 | Arabidopsis thaliana | 21% | 91% |
Q4Q3S5 | Leishmania major | 94% | 100% |
Q4UML9 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 20% | 100% |
Q4W6B5 | Dictyostelium discoideum | 22% | 100% |
Q54F93 | Dictyostelium discoideum | 24% | 100% |
Q5R513 | Pongo abelii | 26% | 92% |
Q5REK3 | Pongo abelii | 24% | 99% |
Q95XN2 | Caenorhabditis elegans | 25% | 94% |
Q9CXT8 | Mus musculus | 24% | 99% |
Q9CZ13 | Mus musculus | 20% | 100% |
Q9DB77 | Mus musculus | 21% | 100% |
Q9DC61 | Mus musculus | 25% | 92% |
Q9P7X1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 100% |
Q9ZU25 | Arabidopsis thaliana | 25% | 96% |
V5BIM6 | Trypanosoma cruzi | 64% | 100% |