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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0031201 | SNARE 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:0098796 | membrane protein complex | 2 | 1 |
Related structures:
AlphaFold database: E9ANH6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 10 |
GO:0016192 | vesicle-mediated transport | 4 | 10 |
GO:0048193 | Golgi vesicle transport | 5 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005484 | SNAP receptor activity | 3 | 10 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 10 |
GO:0060090 | molecular adaptor activity | 1 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 238 | 244 | PF00089 | 0.368 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.304 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.280 |
CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.264 |
DEG_APCC_DBOX_1 | 133 | 141 | PF00400 | 0.614 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.655 |
DEG_SPOP_SBC_1 | 159 | 163 | PF00917 | 0.672 |
DOC_CYCLIN_RxL_1 | 172 | 182 | PF00134 | 0.447 |
DOC_CYCLIN_RxL_1 | 224 | 234 | PF00134 | 0.449 |
DOC_CYCLIN_RxL_1 | 255 | 266 | PF00134 | 0.389 |
DOC_MAPK_gen_1 | 224 | 232 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 23 | 31 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 55 | 65 | PF00069 | 0.635 |
DOC_MAPK_MEF2A_6 | 181 | 188 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 235 | 242 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 25 | 33 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 58 | 67 | PF00069 | 0.504 |
DOC_MAPK_NFAT4_5 | 235 | 243 | PF00069 | 0.473 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.473 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.746 |
LIG_14-3-3_CanoR_1 | 181 | 187 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 224 | 230 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 241 | 249 | PF00244 | 0.236 |
LIG_Actin_WH2_2 | 123 | 140 | PF00022 | 0.628 |
LIG_Actin_WH2_2 | 225 | 243 | PF00022 | 0.449 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.653 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.654 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.666 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.465 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.629 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.657 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.700 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.535 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.659 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.408 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.547 |
LIG_LIR_Gen_1 | 265 | 274 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.487 |
LIG_NRBOX | 173 | 179 | PF00104 | 0.449 |
LIG_PCNA_yPIPBox_3 | 220 | 230 | PF02747 | 0.448 |
LIG_PDZ_Class_3 | 269 | 274 | PF00595 | 0.418 |
LIG_SH2_CRK | 92 | 96 | PF00017 | 0.522 |
LIG_SH2_PTP2 | 268 | 271 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.386 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.761 |
LIG_SUMO_SIM_par_1 | 182 | 187 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 228 | 234 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.475 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.635 |
MOD_CDC14_SPxK_1 | 20 | 23 | PF00782 | 0.555 |
MOD_CDK_SPxK_1 | 17 | 23 | PF00069 | 0.567 |
MOD_CDK_SPxxK_3 | 101 | 108 | PF00069 | 0.682 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.714 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.695 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.492 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.381 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.593 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.740 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.692 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.513 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.402 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.559 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.507 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.489 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.413 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.565 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.780 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.716 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.686 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.398 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.419 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.448 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.469 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.724 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.465 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.467 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.455 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.201 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.581 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.654 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.583 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.287 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.427 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.741 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.723 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.748 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.740 |
MOD_SUMO_rev_2 | 182 | 191 | PF00179 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.180 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1V7 | Leptomonas seymouri | 59% | 100% |
A0A1X0NV60 | Trypanosomatidae | 42% | 100% |
A0A3S5ISC5 | Trypanosoma rangeli | 39% | 100% |
A0A3S7WRJ0 | Leishmania donovani | 90% | 100% |
A4H9S8 | Leishmania braziliensis | 81% | 100% |
A4HUU1 | Leishmania infantum | 90% | 100% |
Q4QH50 | Leishmania major | 91% | 100% |
V5BBG4 | Trypanosoma cruzi | 44% | 100% |