Intracellular protein trafficking, Uncharacterized
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) | yes | yes: 6 |
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. | yes | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IJX3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0006886 | intracellular protein transport | 4 | 10 |
GO:0007034 | vacuolar transport | 4 | 10 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0016192 | vesicle-mediated transport | 4 | 10 |
GO:0016197 | endosomal transport | 4 | 10 |
GO:0032509 | endosome transport via multivesicular body sorting pathway | 5 | 10 |
GO:0032511 | late endosome to vacuole transport via multivesicular body sorting pathway | 6 | 10 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0033365 | protein localization to organelle | 5 | 10 |
GO:0043328 | protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway | 5 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0045324 | late endosome to vacuole transport | 5 | 10 |
GO:0046907 | intracellular transport | 3 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0051649 | establishment of localization in cell | 3 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0071985 | multivesicular body sorting pathway | 5 | 10 |
GO:0072594 | establishment of protein localization to organelle | 4 | 10 |
GO:0072665 | protein localization to vacuole | 6 | 10 |
GO:0072666 | establishment of protein localization to vacuole | 5 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0005543 | phospholipid binding | 3 | 10 |
GO:0008289 | lipid binding | 2 | 10 |
GO:0032182 | ubiquitin-like protein binding | 3 | 10 |
GO:0035091 | phosphatidylinositol binding | 4 | 10 |
GO:0043130 | ubiquitin binding | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 214 | 218 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 432 | 436 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 463 | 467 | PF00656 | 0.705 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.805 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.444 |
CLV_PCSK_FUR_1 | 185 | 189 | PF00082 | 0.858 |
CLV_PCSK_FUR_1 | 210 | 214 | PF00082 | 0.784 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.836 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.804 |
CLV_PCSK_PC7_1 | 61 | 67 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.429 |
DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.596 |
DEG_SPOP_SBC_1 | 448 | 452 | PF00917 | 0.781 |
DOC_CKS1_1 | 378 | 383 | PF01111 | 0.825 |
DOC_CKS1_1 | 401 | 406 | PF01111 | 0.702 |
DOC_CYCLIN_RxL_1 | 98 | 106 | PF00134 | 0.508 |
DOC_MAPK_gen_1 | 172 | 180 | PF00069 | 0.696 |
DOC_MAPK_gen_1 | 51 | 59 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 124 | 132 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 172 | 180 | PF00069 | 0.689 |
DOC_MAPK_MEF2A_6 | 268 | 276 | PF00069 | 0.688 |
DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.691 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.851 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.814 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.816 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.843 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.828 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.796 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.837 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.866 |
LIG_14-3-3_CanoR_1 | 228 | 235 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 290 | 299 | PF00244 | 0.675 |
LIG_Actin_WH2_2 | 275 | 292 | PF00022 | 0.614 |
LIG_BH_BH3_1 | 141 | 157 | PF00452 | 0.615 |
LIG_BIR_III_2 | 313 | 317 | PF00653 | 0.823 |
LIG_BIR_III_4 | 466 | 470 | PF00653 | 0.701 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.484 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.585 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.525 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.619 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.825 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.722 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.566 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.442 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.512 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.550 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.618 |
LIG_GBD_Chelix_1 | 215 | 223 | PF00786 | 0.791 |
LIG_HCF-1_HBM_1 | 270 | 273 | PF13415 | 0.631 |
LIG_IBAR_NPY_1 | 20 | 22 | PF08397 | 0.448 |
LIG_LIR_Gen_1 | 270 | 278 | PF02991 | 0.637 |
LIG_LIR_Gen_1 | 38 | 45 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 506 | 512 | PF02991 | 0.743 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 506 | 511 | PF02991 | 0.744 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.469 |
LIG_SH2_GRB2like | 242 | 245 | PF00017 | 0.593 |
LIG_SH2_PTP2 | 273 | 276 | PF00017 | 0.684 |
LIG_SH2_SRC | 22 | 25 | PF00017 | 0.507 |
LIG_SH2_SRC | 39 | 42 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.470 |
LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.543 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.745 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.752 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.880 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.882 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.709 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.789 |
LIG_SH3_3 | 491 | 497 | PF00018 | 0.867 |
LIG_SUMO_SIM_anti_2 | 54 | 61 | PF11976 | 0.578 |
LIG_SUMO_SIM_par_1 | 274 | 280 | PF11976 | 0.609 |
LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.680 |
LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.844 |
LIG_TRAF2_1 | 413 | 416 | PF00917 | 0.808 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.874 |
LIG_TRAF2_2 | 190 | 195 | PF00917 | 0.830 |
LIG_UBA3_1 | 6 | 13 | PF00899 | 0.511 |
LIG_UBA3_1 | 81 | 87 | PF00899 | 0.505 |
LIG_WW_3 | 357 | 361 | PF00397 | 0.868 |
MOD_CDK_SPxxK_3 | 416 | 423 | PF00069 | 0.691 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.693 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.866 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.855 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.547 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.600 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.894 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.857 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.829 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.639 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.599 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.615 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.841 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.793 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.774 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.858 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.813 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.872 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.522 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.641 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.628 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.436 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.737 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.807 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.802 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.904 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.814 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.855 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.709 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.543 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.483 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.598 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.876 |
MOD_N-GLC_2 | 251 | 253 | PF02516 | 0.687 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.493 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.582 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.616 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.552 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.859 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.810 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.795 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.864 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.439 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.541 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.645 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.570 |
MOD_PIKK_1 | 479 | 485 | PF00454 | 0.829 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.449 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.648 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.481 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.692 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.508 |
MOD_Plk_2-3 | 211 | 217 | PF00069 | 0.643 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.478 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.548 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.645 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.548 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.846 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.811 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.458 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.467 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.805 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.788 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.795 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.840 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.867 |
MOD_SUMO_for_1 | 176 | 179 | PF00179 | 0.722 |
MOD_SUMO_for_1 | 301 | 304 | PF00179 | 0.663 |
TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.595 |
TRG_DiLeu_BaEn_2 | 39 | 45 | PF01217 | 0.544 |
TRG_DiLeu_BaEn_4 | 144 | 150 | PF01217 | 0.667 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.642 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.774 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 65 | 69 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB53 | Leptomonas seymouri | 58% | 96% |
A0A0S4JSH6 | Bodo saltans | 34% | 100% |
A0A3R7M014 | Trypanosoma rangeli | 41% | 100% |
A4HQ30 | Leishmania braziliensis | 65% | 99% |
A4IDT6 | Leishmania infantum | 100% | 100% |
E9ATU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |
Q4Q0P8 | Leishmania major | 87% | 100% |
V5BM99 | Trypanosoma cruzi | 40% | 100% |