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: 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 | yes | yes: 7, no: 0 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A4H7B5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.202 |
CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.641 |
CLV_MEL_PAP_1 | 301 | 307 | PF00089 | 0.466 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.531 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 439 | 441 | PF00082 | 0.452 |
CLV_PCSK_PC7_1 | 440 | 446 | PF00082 | 0.536 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.552 |
DEG_SPOP_SBC_1 | 390 | 394 | PF00917 | 0.608 |
DOC_CYCLIN_yClb3_PxF_3 | 233 | 241 | PF00134 | 0.414 |
DOC_MAPK_gen_1 | 289 | 298 | PF00069 | 0.699 |
DOC_MAPK_MEF2A_6 | 2 | 11 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 289 | 298 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 250 | 257 | PF00149 | 0.390 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.267 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 235 | 245 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 440 | 444 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 449 | 458 | PF00244 | 0.824 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.202 |
LIG_BIR_III_4 | 179 | 183 | PF00653 | 0.202 |
LIG_BIR_III_4 | 67 | 71 | PF00653 | 0.304 |
LIG_BRCT_BRCA1_1 | 451 | 455 | PF00533 | 0.726 |
LIG_EH1_1 | 264 | 272 | PF00400 | 0.241 |
LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.259 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.654 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.334 |
LIG_GBD_Chelix_1 | 268 | 276 | PF00786 | 0.210 |
LIG_LIR_Gen_1 | 149 | 156 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 220 | 231 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 259 | 270 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 452 | 463 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.726 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.501 |
LIG_NRBOX | 29 | 35 | PF00104 | 0.319 |
LIG_PDZ_Class_2 | 468 | 473 | PF00595 | 0.703 |
LIG_Pex14_1 | 133 | 137 | PF04695 | 0.300 |
LIG_Pex14_1 | 152 | 156 | PF04695 | 0.171 |
LIG_Pex14_1 | 261 | 265 | PF04695 | 0.340 |
LIG_Pex14_2 | 247 | 251 | PF04695 | 0.471 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.710 |
LIG_SH2_GRB2like | 377 | 380 | PF00017 | 0.616 |
LIG_SH2_NCK_1 | 323 | 327 | PF00017 | 0.710 |
LIG_SH2_NCK_1 | 44 | 48 | PF00017 | 0.281 |
LIG_SH2_SRC | 377 | 380 | PF00017 | 0.653 |
LIG_SH2_SRC | 385 | 388 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.357 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.288 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.259 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.423 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.595 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.684 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.659 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.724 |
LIG_SUMO_SIM_par_1 | 11 | 17 | PF11976 | 0.537 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.631 |
LIG_TRAF2_1 | 343 | 346 | PF00917 | 0.760 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.747 |
LIG_TRAF2_2 | 360 | 365 | PF00917 | 0.718 |
LIG_UBA3_1 | 30 | 39 | PF00899 | 0.422 |
LIG_Vh1_VBS_1 | 7 | 25 | PF01044 | 0.427 |
LIG_WRC_WIRS_1 | 193 | 198 | PF05994 | 0.202 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.202 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.673 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.415 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.844 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.233 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.203 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.314 |
MOD_Cter_Amidation | 181 | 184 | PF01082 | 0.402 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.457 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.451 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.549 |
MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.444 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.630 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.615 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.584 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.285 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.251 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.223 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.473 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.663 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.438 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.755 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.755 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.778 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.286 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.322 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.288 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.429 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.537 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.392 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.648 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.621 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.370 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.221 |
MOD_NEK2_2 | 284 | 289 | PF00069 | 0.477 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.300 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.451 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.739 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.668 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.659 |
MOD_PIKK_1 | 449 | 455 | PF00454 | 0.728 |
MOD_PKA_1 | 439 | 445 | PF00069 | 0.738 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.632 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.776 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.202 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.314 |
MOD_PKB_1 | 447 | 455 | PF00069 | 0.724 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.318 |
MOD_Plk_2-3 | 139 | 145 | PF00069 | 0.202 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.349 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.378 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.645 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.409 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.308 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.267 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.684 |
MOD_SUMO_for_1 | 290 | 293 | PF00179 | 0.631 |
MOD_SUMO_rev_2 | 170 | 178 | PF00179 | 0.202 |
TRG_DiLeu_BaEn_3 | 292 | 298 | PF01217 | 0.558 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.241 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.733 |
TRG_Pf-PMV_PEXEL_1 | 449 | 453 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2I6 | Leptomonas seymouri | 45% | 100% |
A0A0N1I9Y8 | Leptomonas seymouri | 28% | 100% |
A0A3S7WSM6 | Leishmania donovani | 67% | 100% |
A4HVR0 | Leishmania infantum | 67% | 100% |
E9APF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4QG22 | Leishmania major | 67% | 100% |