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 | no | yes: 7, no: 5 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4H7B4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 223 | 227 | PF00656 | 0.338 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.418 |
CLV_PCSK_FUR_1 | 18 | 22 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.380 |
DOC_MAPK_gen_1 | 18 | 27 | PF00069 | 0.539 |
DOC_MAPK_JIP1_4 | 21 | 27 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 18 | 27 | PF00069 | 0.539 |
DOC_PP4_FxxP_1 | 172 | 175 | PF00568 | 0.301 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.438 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.245 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.275 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.259 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.428 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.302 |
LIG_14-3-3_CanoR_1 | 145 | 153 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.411 |
LIG_ActinCP_TwfCPI_2 | 54 | 63 | PF01115 | 0.384 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.605 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.301 |
LIG_EH1_1 | 291 | 299 | PF00400 | 0.290 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.355 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.263 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.597 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.319 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.309 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.338 |
LIG_GBD_Chelix_1 | 27 | 35 | PF00786 | 0.299 |
LIG_IRF3_LxIS_1 | 153 | 160 | PF10401 | 0.301 |
LIG_LIR_Apic_2 | 52 | 57 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 100 | 108 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 239 | 244 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 286 | 297 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 134 | 138 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.296 |
LIG_NRBOX | 30 | 36 | PF00104 | 0.367 |
LIG_Pex14_1 | 288 | 292 | PF04695 | 0.387 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.301 |
LIG_Pex14_2 | 189 | 193 | PF04695 | 0.329 |
LIG_Rb_LxCxE_1 | 65 | 82 | PF01857 | 0.252 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.331 |
LIG_SH2_PTP2 | 47 | 50 | PF00017 | 0.293 |
LIG_SH2_SRC | 47 | 50 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 103 | 107 | PF00017 | 0.211 |
LIG_SH2_STAT3 | 183 | 186 | PF00017 | 0.324 |
LIG_SH2_STAT3 | 275 | 278 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.365 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.301 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.307 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.621 |
LIG_SUMO_SIM_par_1 | 21 | 26 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.343 |
LIG_TRAF2_1 | 327 | 330 | PF00917 | 0.717 |
LIG_TRFH_1 | 171 | 175 | PF08558 | 0.211 |
LIG_Vh1_VBS_1 | 291 | 309 | PF01044 | 0.222 |
LIG_WRC_WIRS_1 | 51 | 56 | PF05994 | 0.377 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.350 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.716 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.814 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.662 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.531 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.487 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.656 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.668 |
MOD_GlcNHglycan | 58 | 62 | PF01048 | 0.622 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.290 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.350 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.400 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.448 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.747 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.727 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.749 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.501 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.681 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.598 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.256 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.301 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.434 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.716 |
MOD_NEK2_2 | 178 | 183 | PF00069 | 0.231 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.287 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.409 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.748 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.679 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.361 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.297 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.633 |
MOD_PKB_1 | 19 | 27 | PF00069 | 0.411 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.329 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.621 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.636 |
MOD_Plk_2-3 | 220 | 226 | PF00069 | 0.301 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.354 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.255 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.275 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.343 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.721 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.386 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.302 |
MOD_SUMO_rev_2 | 220 | 230 | PF00179 | 0.287 |
MOD_SUMO_rev_2 | 325 | 334 | PF00179 | 0.648 |
TRG_DiLeu_BaLyEn_6 | 111 | 116 | PF01217 | 0.211 |
TRG_DiLeu_BaLyEn_6 | 64 | 69 | PF01217 | 0.245 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.416 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.627 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY91 | Leptomonas seymouri | 34% | 100% |
A0A0N1PG18 | Leptomonas seymouri | 47% | 94% |
A0A3S5H587 | Leishmania donovani | 34% | 100% |
A0A3S5H6P8 | Leishmania donovani | 69% | 100% |
A4H3U3 | Leishmania braziliensis | 33% | 100% |
A4HS17 | Leishmania infantum | 34% | 100% |
A4HVQ9 | Leishmania infantum | 69% | 100% |
E9AK04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9APF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4QG23 | Leishmania major | 67% | 100% |
Q9XZY2 | Leishmania major | 34% | 100% |