Conserved eukaryotic protein, involved in protein trafficking.. Localization: Golgi (by homology)
Intracellular protein trafficking, Integral membrane S linking to the trans Golgi network
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005802 | trans-Golgi network | 4 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
Related structures:
AlphaFold database: A4I4M5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006893 | Golgi to plasma membrane transport | 5 | 1 |
GO:0006895 | Golgi to endosome transport | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0016482 | cytosolic transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0034067 | protein localization to Golgi apparatus | 6 | 1 |
GO:0043001 | Golgi to plasma membrane protein transport | 5 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 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:0051668 | localization within membrane | 3 | 1 |
GO:0061951 | establishment of protein localization to plasma membrane | 5 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0072659 | protein localization to plasma membrane | 5 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:0098876 | vesicle-mediated transport to the plasma membrane | 4 | 1 |
GO:1990778 | protein localization to cell periphery | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.744 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.418 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.404 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.546 |
DEG_APCC_DBOX_1 | 269 | 277 | PF00400 | 0.618 |
DEG_ODPH_VHL_1 | 114 | 125 | PF01847 | 0.726 |
DEG_SPOP_SBC_1 | 291 | 295 | PF00917 | 0.767 |
DOC_CKS1_1 | 76 | 81 | PF01111 | 0.749 |
DOC_CYCLIN_RxL_1 | 214 | 222 | PF00134 | 0.618 |
DOC_CYCLIN_RxL_1 | 31 | 41 | PF00134 | 0.598 |
DOC_MAPK_gen_1 | 216 | 223 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 269 | 278 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 216 | 223 | PF00069 | 0.618 |
DOC_MAPK_NFAT4_5 | 216 | 224 | PF00069 | 0.618 |
DOC_PP4_FxxP_1 | 133 | 136 | PF00568 | 0.673 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.754 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.382 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 7 | 12 | PF00244 | 0.455 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.482 |
LIG_BIR_III_4 | 329 | 333 | PF00653 | 0.791 |
LIG_BIR_III_4 | 338 | 342 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.368 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.704 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.640 |
LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.385 |
LIG_eIF4E_1 | 208 | 214 | PF01652 | 0.546 |
LIG_eIF4E_1 | 228 | 234 | PF01652 | 0.183 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.762 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.679 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.411 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.411 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.757 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.594 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.645 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.714 |
LIG_LIR_Apic_2 | 130 | 136 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 11 | 20 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 124 | 133 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 24 | 35 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.385 |
LIG_MLH1_MIPbox_1 | 23 | 27 | PF16413 | 0.387 |
LIG_NRBOX | 200 | 206 | PF00104 | 0.456 |
LIG_NRBOX | 238 | 244 | PF00104 | 0.430 |
LIG_PCNA_yPIPBox_3 | 193 | 205 | PF02747 | 0.456 |
LIG_REV1ctd_RIR_1 | 123 | 132 | PF16727 | 0.675 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.727 |
LIG_SH2_SRC | 93 | 96 | PF00017 | 0.689 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.428 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.802 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.648 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.705 |
LIG_SUMO_SIM_anti_2 | 97 | 106 | PF11976 | 0.606 |
LIG_SUMO_SIM_par_1 | 356 | 361 | PF11976 | 0.698 |
LIG_TRAF2_1 | 365 | 368 | PF00917 | 0.770 |
LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.411 |
LIG_Vh1_VBS_1 | 92 | 110 | PF01044 | 0.638 |
MOD_CDK_SPK_2 | 75 | 80 | PF00069 | 0.675 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.819 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.685 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.763 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.752 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.724 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.705 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.469 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.516 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.581 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.511 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.754 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.697 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.697 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.632 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.747 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.688 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.746 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.708 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.620 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.198 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.499 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.455 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.584 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.411 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.678 |
MOD_NEK2_2 | 121 | 126 | PF00069 | 0.724 |
MOD_NEK2_2 | 136 | 141 | PF00069 | 0.625 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.779 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.716 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.782 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.779 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.816 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.716 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.707 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.535 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.572 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.404 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.260 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.392 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.721 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.658 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.740 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.747 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.430 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 342 | 345 | PF00400 | 0.762 |
TRG_ER_diLys_1 | 372 | 376 | PF00400 | 0.775 |
TRG_Pf-PMV_PEXEL_1 | 217 | 222 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAN0 | Leptomonas seymouri | 45% | 100% |
A0A3Q8IDS8 | Leishmania donovani | 100% | 100% |
A4HHH5 | Leishmania braziliensis | 69% | 100% |
E9AE23 | Leishmania major | 86% | 94% |
E9ALR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |