A signal-anchored protein probably with an extra re-entrant loop. Localization: ER (by homology)
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4HN72
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008474 | palmitoyl-(protein) hydrolase activity | 3 | 1 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016790 | thiolester hydrolase activity | 4 | 1 |
GO:0098599 | palmitoyl hydrolase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 125 | 129 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.634 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.283 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.295 |
CLV_PCSK_PC7_1 | 244 | 250 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.313 |
DEG_APCC_DBOX_1 | 270 | 278 | PF00400 | 0.530 |
DOC_ANK_TNKS_1 | 116 | 123 | PF00023 | 0.704 |
DOC_CYCLIN_RxL_1 | 291 | 301 | PF00134 | 0.509 |
DOC_CYCLIN_RxL_1 | 353 | 362 | PF00134 | 0.521 |
DOC_MAPK_DCC_7 | 310 | 318 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 219 | 227 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 248 | 255 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 307 | 317 | PF00069 | 0.521 |
DOC_MAPK_JIP1_4 | 294 | 300 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 307 | 315 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 297 | 303 | PF00149 | 0.537 |
DOC_PP1_RVXF_1 | 354 | 361 | PF00149 | 0.520 |
DOC_PP2B_LxvP_1 | 350 | 353 | PF13499 | 0.631 |
DOC_PP2B_LxvP_1 | 59 | 62 | PF13499 | 0.604 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.672 |
DOC_USP7_UBL2_3 | 336 | 340 | PF12436 | 0.565 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.736 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 299 | 303 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 66 | 75 | PF00244 | 0.538 |
LIG_Actin_WH2_2 | 286 | 301 | PF00022 | 0.509 |
LIG_Actin_WH2_2 | 327 | 345 | PF00022 | 0.600 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.348 |
LIG_BIR_III_4 | 100 | 104 | PF00653 | 0.589 |
LIG_DLG_GKlike_1 | 141 | 149 | PF00625 | 0.532 |
LIG_DLG_GKlike_1 | 280 | 288 | PF00625 | 0.373 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.578 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.463 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.619 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.635 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.548 |
LIG_Integrin_isoDGR_2 | 346 | 348 | PF01839 | 0.303 |
LIG_IRF3_LxIS_1 | 295 | 301 | PF10401 | 0.507 |
LIG_LIR_Apic_2 | 212 | 218 | PF02991 | 0.491 |
LIG_LIR_Apic_2 | 290 | 295 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 151 | 157 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.145 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.441 |
LIG_LYPXL_yS_3 | 42 | 45 | PF13949 | 0.641 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.255 |
LIG_PAM2_1 | 280 | 292 | PF00658 | 0.427 |
LIG_PCNA_PIPBox_1 | 375 | 384 | PF02747 | 0.491 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.356 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.534 |
LIG_SH2_PTP2 | 292 | 295 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.579 |
LIG_SH2_STAT3 | 32 | 35 | PF00017 | 0.532 |
LIG_SH2_STAT3 | 41 | 44 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.527 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.475 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.503 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.572 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 223 | 231 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 201 | 206 | PF11976 | 0.463 |
LIG_TRAF2_1 | 377 | 380 | PF00917 | 0.418 |
LIG_TRFH_1 | 80 | 84 | PF08558 | 0.554 |
LIG_TYR_ITIM | 40 | 45 | PF00017 | 0.558 |
LIG_WRC_WIRS_1 | 149 | 154 | PF05994 | 0.509 |
LIG_WRC_WIRS_1 | 27 | 32 | PF05994 | 0.347 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.684 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.628 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.499 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.479 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.492 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.662 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.655 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.513 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.427 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.330 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.294 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.241 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.387 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.316 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.382 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.714 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.695 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.635 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.493 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.795 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.479 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.596 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.633 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.224 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.439 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.504 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.438 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.350 |
MOD_NEK2_2 | 234 | 239 | PF00069 | 0.463 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.491 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.558 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.500 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.469 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.606 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.425 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.555 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.342 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.572 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.734 |
TRG_DiLeu_BaLyEn_6 | 35 | 40 | PF01217 | 0.582 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.641 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 356 | 361 | PF00026 | 0.316 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK32 | Leptomonas seymouri | 61% | 96% |
A0A0S4J610 | Bodo saltans | 38% | 100% |
A0A1X0P675 | Trypanosomatidae | 42% | 100% |
A0A3Q8IMT8 | Leishmania donovani | 83% | 100% |
A0A3R7NFR6 | Trypanosoma rangeli | 43% | 100% |
A4IBU0 | Leishmania infantum | 83% | 100% |
C9ZYS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AFM7 | Leishmania major | 83% | 100% |
E9B6T0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
V5BXX8 | Trypanosoma cruzi | 44% | 100% |