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). Extensively duplicated gene family.. 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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 16 |
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: 11, no: 2 |
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: E9B6F8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.374 |
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.558 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.681 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.444 |
DEG_COP1_1 | 111 | 121 | PF00400 | 0.428 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.622 |
DEG_SCF_FBW7_2 | 294 | 301 | PF00400 | 0.656 |
DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.477 |
DOC_CKS1_1 | 48 | 53 | PF01111 | 0.461 |
DOC_MAPK_DCC_7 | 300 | 310 | PF00069 | 0.634 |
DOC_PP1_RVXF_1 | 259 | 266 | PF00149 | 0.491 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.696 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.544 |
LIG_APCC_ABBA_1 | 232 | 237 | PF00400 | 0.407 |
LIG_APCC_ABBAyCdc20_2 | 231 | 237 | PF00400 | 0.412 |
LIG_BRCT_BRCA1_1 | 237 | 241 | PF00533 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 262 | 271 | PF00928 | 0.424 |
LIG_EH1_1 | 273 | 281 | PF00400 | 0.368 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.576 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.448 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.394 |
LIG_GBD_Chelix_1 | 286 | 294 | PF00786 | 0.381 |
LIG_IRF3_LxIS_1 | 272 | 278 | PF10401 | 0.235 |
LIG_LIR_Gen_1 | 120 | 128 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 22 | 30 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 268 | 279 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 316 | 322 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 316 | 321 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.494 |
LIG_LYPXL_S_1 | 170 | 174 | PF13949 | 0.649 |
LIG_LYPXL_yS_3 | 171 | 174 | PF13949 | 0.450 |
LIG_NRBOX | 25 | 31 | PF00104 | 0.555 |
LIG_PCNA_PIPBox_1 | 161 | 170 | PF02747 | 0.453 |
LIG_Pex14_1 | 20 | 24 | PF04695 | 0.535 |
LIG_Pex14_1 | 270 | 274 | PF04695 | 0.364 |
LIG_Pex14_2 | 143 | 147 | PF04695 | 0.510 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.433 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.462 |
LIG_SH2_GRB2like | 318 | 321 | PF00017 | 0.765 |
LIG_SH2_NCK_1 | 48 | 52 | PF00017 | 0.533 |
LIG_SH2_PTP2 | 244 | 247 | PF00017 | 0.443 |
LIG_SH2_PTP2 | 318 | 321 | PF00017 | 0.687 |
LIG_SH2_SRC | 244 | 247 | PF00017 | 0.464 |
LIG_SH2_SRC | 318 | 321 | PF00017 | 0.736 |
LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.535 |
LIG_SH2_STAT3 | 56 | 59 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.741 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.522 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.537 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.772 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.715 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.661 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.235 |
LIG_SUMO_SIM_par_1 | 148 | 155 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 306 | 312 | PF11976 | 0.613 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.661 |
LIG_TRFH_1 | 168 | 172 | PF08558 | 0.441 |
LIG_TYR_ITIM | 242 | 247 | PF00017 | 0.595 |
LIG_TYR_ITIM | 289 | 294 | PF00017 | 0.433 |
LIG_WRC_WIRS_1 | 118 | 123 | PF05994 | 0.439 |
MOD_CDK_SPK_2 | 352 | 357 | PF00069 | 0.630 |
MOD_CDK_SPxK_1 | 294 | 300 | PF00069 | 0.652 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.484 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.510 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.472 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.452 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.730 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.709 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.640 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.649 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.703 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.522 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.579 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.731 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.541 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.523 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.445 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.471 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.535 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.663 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.602 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.570 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.510 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.497 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.486 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.235 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.614 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.422 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.483 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.547 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.552 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.453 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.476 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.759 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.505 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.434 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.445 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.407 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.437 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.494 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.691 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.495 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.552 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.461 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.652 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.659 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.544 |
MOD_SUMO_rev_2 | 392 | 401 | PF00179 | 0.672 |
TRG_DiLeu_BaEn_2 | 236 | 242 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.799 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2I6 | Leptomonas seymouri | 33% | 85% |
A0A0N1I9Y8 | Leptomonas seymouri | 37% | 100% |
A0A1X0NK39 | Trypanosomatidae | 25% | 100% |
A0A1X0NVE8 | Trypanosomatidae | 22% | 100% |
A0A3S7WSM6 | Leishmania donovani | 34% | 86% |
A0A3S7X9E7 | Leishmania donovani | 90% | 100% |
A4HMU5 | Leishmania braziliensis | 75% | 99% |
A4HVR0 | Leishmania infantum | 34% | 86% |
E9AFA3 | Leishmania major | 88% | 100% |
E9AHW4 | Leishmania infantum | 91% | 100% |
E9APF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 86% |
Q4QG22 | Leishmania major | 30% | 100% |