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: 3 |
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:0000814 | ESCRT II complex | 3 | 11 |
GO:0010008 | endosome membrane | 5 | 11 |
GO:0012506 | vesicle membrane | 4 | 11 |
GO:0016020 | membrane | 2 | 11 |
GO:0030659 | cytoplasmic vesicle membrane | 5 | 11 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0031902 | late endosome membrane | 6 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0036452 | ESCRT complex | 2 | 11 |
GO:0098588 | bounding membrane of organelle | 4 | 11 |
GO:0098796 | membrane protein complex | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HA31
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0006886 | intracellular protein transport | 4 | 11 |
GO:0007034 | vacuolar transport | 4 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0016192 | vesicle-mediated transport | 4 | 11 |
GO:0016197 | endosomal transport | 4 | 11 |
GO:0032509 | endosome transport via multivesicular body sorting pathway | 5 | 11 |
GO:0032511 | late endosome to vacuole transport via multivesicular body sorting pathway | 6 | 11 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0033365 | protein localization to organelle | 5 | 11 |
GO:0043328 | protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway | 5 | 11 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0045324 | late endosome to vacuole transport | 5 | 11 |
GO:0046907 | intracellular transport | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0051649 | establishment of localization in cell | 3 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0071985 | multivesicular body sorting pathway | 5 | 11 |
GO:0072594 | establishment of protein localization to organelle | 4 | 11 |
GO:0072665 | protein localization to vacuole | 6 | 11 |
GO:0072666 | establishment of protein localization to vacuole | 5 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0005543 | phospholipid binding | 3 | 11 |
GO:0008289 | lipid binding | 2 | 11 |
GO:0032182 | ubiquitin-like protein binding | 3 | 11 |
GO:0032266 | phosphatidylinositol-3-phosphate binding | 6 | 11 |
GO:0035091 | phosphatidylinositol binding | 4 | 11 |
GO:0043130 | ubiquitin binding | 4 | 11 |
GO:1901981 | phosphatidylinositol phosphate binding | 5 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.338 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.181 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.181 |
CLV_Separin_Metazoa | 66 | 70 | PF03568 | 0.538 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.561 |
DEG_SPOP_SBC_1 | 164 | 168 | PF00917 | 0.620 |
DEG_SPOP_SBC_1 | 170 | 174 | PF00917 | 0.572 |
DOC_CKS1_1 | 146 | 151 | PF01111 | 0.494 |
DOC_CYCLIN_RxL_1 | 410 | 420 | PF00134 | 0.381 |
DOC_CYCLIN_yCln2_LP_2 | 146 | 152 | PF00134 | 0.495 |
DOC_CYCLIN_yCln2_LP_2 | 316 | 322 | PF00134 | 0.538 |
DOC_CYCLIN_yCln2_LP_2 | 61 | 67 | PF00134 | 0.561 |
DOC_MAPK_DCC_7 | 312 | 322 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 271 | 280 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 34 | 44 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 413 | 423 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 271 | 280 | PF00069 | 0.538 |
DOC_PP1_RVXF_1 | 411 | 418 | PF00149 | 0.381 |
DOC_PP1_RVXF_1 | 98 | 104 | PF00149 | 0.485 |
DOC_PP2B_LxvP_1 | 61 | 64 | PF13499 | 0.472 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.381 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 401 | 409 | PF00244 | 0.534 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.561 |
LIG_BRCT_BRCA1_1 | 77 | 81 | PF00533 | 0.561 |
LIG_CtBP_PxDLS_1 | 64 | 68 | PF00389 | 0.561 |
LIG_eIF4E_1 | 338 | 344 | PF01652 | 0.381 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.434 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.715 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.451 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.437 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.538 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.458 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.510 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.489 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.487 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.561 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.515 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.490 |
LIG_GBD_Chelix_1 | 276 | 284 | PF00786 | 0.202 |
LIG_GBD_Chelix_1 | 433 | 441 | PF00786 | 0.272 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 290 | 301 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 336 | 344 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 460 | 466 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 460 | 464 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.536 |
LIG_NRBOX | 339 | 345 | PF00104 | 0.381 |
LIG_NRBOX | 361 | 367 | PF00104 | 0.468 |
LIG_NRBOX | 437 | 443 | PF00104 | 0.381 |
LIG_PDZ_Class_2 | 461 | 466 | PF00595 | 0.392 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.299 |
LIG_RPA_C_Fungi | 348 | 360 | PF08784 | 0.456 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.423 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.423 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 459 | 463 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.405 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.658 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.311 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.322 |
LIG_SH3_CIN85_PxpxPR_1 | 176 | 181 | PF14604 | 0.584 |
LIG_SUMO_SIM_anti_2 | 318 | 324 | PF11976 | 0.456 |
LIG_SUMO_SIM_anti_2 | 339 | 345 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 436 | 442 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 339 | 345 | PF11976 | 0.423 |
LIG_UBA3_1 | 304 | 310 | PF00899 | 0.300 |
LIG_UBA3_1 | 437 | 444 | PF00899 | 0.423 |
MOD_CDK_SPK_2 | 83 | 88 | PF00069 | 0.256 |
MOD_CDK_SPxxK_3 | 394 | 401 | PF00069 | 0.203 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.530 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.777 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.423 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.395 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.307 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.421 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.368 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.368 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.380 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.203 |
MOD_Cter_Amidation | 345 | 348 | PF01082 | 0.423 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.707 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.665 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.334 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.363 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.269 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.334 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.319 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.299 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.561 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.780 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.715 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.205 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.370 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.270 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.256 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.367 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.399 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.325 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.418 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.203 |
MOD_N-GLC_2 | 324 | 326 | PF02516 | 0.400 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.354 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.331 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.527 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.213 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.291 |
MOD_PK_1 | 246 | 252 | PF00069 | 0.359 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.456 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.325 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.300 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.384 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.447 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.456 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.201 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.434 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.265 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.362 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.315 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.331 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.355 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.614 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.749 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.639 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.354 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.374 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.318 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.222 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.360 |
MOD_SUMO_rev_2 | 117 | 123 | PF00179 | 0.286 |
MOD_SUMO_rev_2 | 412 | 418 | PF00179 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.314 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.423 |
TRG_NES_CRM1_1 | 414 | 425 | PF08389 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3P0 | Leptomonas seymouri | 66% | 100% |
A0A1X0P698 | Trypanosomatidae | 43% | 100% |
A0A3R7M0G6 | Trypanosoma rangeli | 41% | 100% |
A0A3S7WVL4 | Leishmania donovani | 77% | 100% |
A4HY94 | Leishmania infantum | 77% | 100% |
A5PK00 | Bos taurus | 26% | 100% |
D0A0M8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AS26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
P0C0A2 | Rattus norvegicus | 27% | 100% |
Q4QDE7 | Leishmania major | 75% | 96% |
Q6DDF4 | Xenopus laevis | 26% | 100% |
Q7ZVK4 | Danio rerio | 26% | 100% |
Q86VN1 | Homo sapiens | 27% | 100% |
Q91XD6 | Mus musculus | 27% | 100% |
Q9VU87 | Drosophila melanogaster | 24% | 100% |
V5AMS4 | Trypanosoma cruzi | 42% | 100% |