Intracellular protein trafficking, Coatomer delta subunit-like
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: 15 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0030117 | membrane coat | 3 | 12 |
GO:0030120 | vesicle coat | 4 | 12 |
GO:0030126 | COPI vesicle coat | 5 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0098588 | bounding membrane of organelle | 4 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005794 | Golgi apparatus | 5 | 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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A0A3Q8IAE4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0048193 | Golgi vesicle transport | 5 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051645 | Golgi localization | 3 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 462 | 466 | PF00656 | 0.396 |
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.368 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.630 |
CLV_PCSK_FUR_1 | 170 | 174 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.079 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.443 |
DEG_SPOP_SBC_1 | 406 | 410 | PF00917 | 0.371 |
DOC_CYCLIN_RxL_1 | 356 | 367 | PF00134 | 0.348 |
DOC_CYCLIN_yCln2_LP_2 | 489 | 495 | PF00134 | 0.439 |
DOC_MAPK_DCC_7 | 315 | 324 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 325 | 332 | PF00069 | 0.278 |
DOC_MAPK_MEF2A_6 | 423 | 432 | PF00069 | 0.412 |
DOC_PP2B_LxvP_1 | 430 | 433 | PF13499 | 0.383 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.428 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.332 |
LIG_14-3-3_CanoR_1 | 19 | 27 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 390 | 400 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 494 | 503 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 527 | 536 | PF00244 | 0.389 |
LIG_APCC_ABBA_1 | 133 | 138 | PF00400 | 0.448 |
LIG_BH_BH3_1 | 518 | 534 | PF00452 | 0.412 |
LIG_BIR_III_4 | 273 | 277 | PF00653 | 0.641 |
LIG_BRCT_BRCA1_1 | 347 | 351 | PF00533 | 0.278 |
LIG_EH1_1 | 85 | 93 | PF00400 | 0.313 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.501 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.344 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.410 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.293 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.395 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.316 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.375 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.263 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.376 |
LIG_LIR_Apic_2 | 218 | 224 | PF02991 | 0.685 |
LIG_LIR_Gen_1 | 109 | 116 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 446 | 457 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 64 | 71 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 487 | 493 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.325 |
LIG_Pex14_2 | 110 | 114 | PF04695 | 0.319 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.533 |
LIG_SH2_NCK_1 | 415 | 419 | PF00017 | 0.383 |
LIG_SH2_SRC | 50 | 53 | PF00017 | 0.343 |
LIG_SH2_SRC | 60 | 63 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.526 |
LIG_SH2_STAT3 | 58 | 61 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.407 |
LIG_SH3_2 | 424 | 429 | PF14604 | 0.383 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.572 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.278 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.330 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.296 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.362 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.300 |
LIG_SUMO_SIM_anti_2 | 327 | 332 | PF11976 | 0.280 |
LIG_SUMO_SIM_par_1 | 327 | 334 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 67 | 74 | PF11976 | 0.296 |
LIG_TRAF2_1 | 141 | 144 | PF00917 | 0.403 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.404 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.383 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.397 |
LIG_UBA3_1 | 66 | 75 | PF00899 | 0.321 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.633 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.619 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.404 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.303 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.497 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.265 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.375 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.373 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.393 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.383 |
MOD_Cter_Amidation | 122 | 125 | PF01082 | 0.361 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.579 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.627 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.580 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.603 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.265 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.316 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.374 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.270 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.602 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.620 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.334 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.245 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.292 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.531 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.352 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.364 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.310 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.386 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.584 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.383 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.410 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.366 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.222 |
MOD_N-GLC_1 | 468 | 473 | PF02516 | 0.275 |
MOD_N-GLC_1 | 506 | 511 | PF02516 | 0.423 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.581 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.668 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.379 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.393 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.366 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.316 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.611 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.705 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.467 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.294 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.293 |
MOD_PKA_1 | 159 | 165 | PF00069 | 0.547 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.603 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.383 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.366 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.402 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.574 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.355 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.354 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.268 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.364 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.419 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.405 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.306 |
MOD_Plk_2-3 | 106 | 112 | PF00069 | 0.459 |
MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.189 |
MOD_Plk_2-3 | 138 | 144 | PF00069 | 0.422 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.613 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.280 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.383 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.268 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.391 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.332 |
MOD_SUMO_for_1 | 324 | 327 | PF00179 | 0.383 |
TRG_DiLeu_BaEn_1 | 327 | 332 | PF01217 | 0.297 |
TRG_DiLeu_BaEn_1 | 64 | 69 | PF01217 | 0.329 |
TRG_DiLeu_BaEn_4 | 143 | 149 | PF01217 | 0.526 |
TRG_DiLeu_BaLyEn_6 | 35 | 40 | PF01217 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.329 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.312 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 26 | 29 | PF00400 | 0.356 |
TRG_NES_CRM1_1 | 255 | 270 | PF08389 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.356 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I039 | Leptomonas seymouri | 75% | 100% |
A0A0S4KK09 | Bodo saltans | 44% | 100% |
A0A1X0NYY5 | Trypanosomatidae | 52% | 97% |
A0A422N6V7 | Trypanosoma rangeli | 52% | 100% |
A4H8P5 | Leishmania braziliensis | 87% | 100% |
A4HX15 | Leishmania infantum | 100% | 100% |
C9ZVY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AQS9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
P43621 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 98% |
P48444 | Homo sapiens | 31% | 100% |
P49661 | Oryza sativa subsp. japonica | 32% | 100% |
P53619 | Bos taurus | 32% | 100% |
Q09236 | Caenorhabditis elegans | 31% | 100% |
Q0DJ99 | Oryza sativa subsp. japonica | 32% | 100% |
Q0DJA0 | Oryza sativa subsp. japonica | 32% | 100% |
Q4QEP9 | Leishmania major | 97% | 100% |
Q55EZ6 | Dictyostelium discoideum | 31% | 99% |
Q5RA77 | Pongo abelii | 31% | 100% |
Q5XJY5 | Mus musculus | 31% | 100% |
Q5ZL57 | Gallus gallus | 31% | 100% |
Q66H80 | Rattus norvegicus | 31% | 100% |
Q93Y22 | Arabidopsis thaliana | 31% | 100% |
V5BI39 | Trypanosoma cruzi | 51% | 99% |