Publication identifier(s): 26167471
Might belong to a Kinetoplastid-specific lectin domain protein family. Experiments of homologues indicate them to localize to ER (PMID: 26167471). Highly expanded in the Trypanosoma genus, while relatively limited in Leishmaniids.. Localization: ER (experimental)
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: 10 |
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 | yes | yes: 7, no: 6 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A0A3S5H6P8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.316 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.443 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.434 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 3 | 9 | PF00134 | 0.496 |
DOC_MAPK_gen_1 | 16 | 25 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 16 | 25 | PF00069 | 0.473 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.269 |
DOC_PP4_FxxP_1 | 394 | 397 | PF00568 | 0.676 |
DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.372 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.236 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.396 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.236 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 143 | 151 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 202 | 207 | PF00244 | 0.244 |
LIG_14-3-3_CanoR_1 | 334 | 339 | PF00244 | 0.691 |
LIG_ActinCP_TwfCPI_2 | 52 | 61 | PF01115 | 0.343 |
LIG_BIR_III_2 | 109 | 113 | PF00653 | 0.236 |
LIG_BRCT_BRCA1_1 | 203 | 207 | PF00533 | 0.269 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.369 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.313 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.366 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.287 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.307 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.316 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.627 |
LIG_GBD_Chelix_1 | 25 | 33 | PF00786 | 0.537 |
LIG_IRF3_LxIS_1 | 151 | 158 | PF10401 | 0.269 |
LIG_LIR_Apic_2 | 393 | 397 | PF02991 | 0.827 |
LIG_LIR_Apic_2 | 51 | 55 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 98 | 106 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.281 |
LIG_NRBOX | 28 | 34 | PF00104 | 0.425 |
LIG_Pex14_1 | 286 | 290 | PF04695 | 0.360 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.269 |
LIG_Pex14_2 | 187 | 191 | PF04695 | 0.308 |
LIG_Rb_LxCxE_1 | 63 | 80 | PF01857 | 0.231 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.757 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.345 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.276 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.273 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.496 |
LIG_SUMO_SIM_anti_2 | 24 | 29 | PF11976 | 0.554 |
LIG_SUMO_SIM_anti_2 | 292 | 298 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 19 | 24 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.436 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.688 |
LIG_WRC_WIRS_1 | 49 | 54 | PF05994 | 0.333 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.329 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.697 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.811 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.693 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.646 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.492 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.410 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.635 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.504 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.618 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.535 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.352 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.311 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.329 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.374 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.375 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.326 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.759 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.699 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.745 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.469 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.646 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.664 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.556 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.510 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.269 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.247 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.382 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.556 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.275 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.702 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.627 |
MOD_NEK2_2 | 404 | 409 | PF00069 | 0.641 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.258 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.370 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.456 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.762 |
MOD_PKA_1 | 413 | 419 | PF00069 | 0.661 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.341 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.266 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.328 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.741 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.308 |
MOD_Plk_2-3 | 218 | 224 | PF00069 | 0.269 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.287 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.255 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.265 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.422 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.700 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.704 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.640 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.236 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.367 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.650 |
MOD_SUMO_rev_2 | 218 | 228 | PF00179 | 0.258 |
MOD_SUMO_rev_2 | 407 | 416 | PF00179 | 0.629 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.406 |
TRG_NES_CRM1_1 | 359 | 371 | PF08389 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY91 | Leptomonas seymouri | 36% | 100% |
A0A0N1PG18 | Leptomonas seymouri | 49% | 94% |
A0A1X0NVE8 | Trypanosomatidae | 23% | 100% |
A0A3S5H587 | Leishmania donovani | 35% | 100% |
A4H3U3 | Leishmania braziliensis | 35% | 100% |
A4H7B4 | Leishmania braziliensis | 69% | 100% |
A4HS17 | Leishmania infantum | 35% | 100% |
A4HVQ9 | Leishmania infantum | 100% | 100% |
E9AK04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9APF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4QG23 | Leishmania major | 87% | 100% |
Q9XZY2 | Leishmania major | 35% | 100% |