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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9AFM7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008474 | palmitoyl-(protein) hydrolase activity | 3 | 2 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016790 | thiolester hydrolase activity | 4 | 2 |
GO:0098599 | palmitoyl hydrolase activity | 3 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 125 | 129 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.710 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.332 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.214 |
DEG_APCC_DBOX_1 | 270 | 278 | PF00400 | 0.562 |
DOC_CYCLIN_RxL_1 | 291 | 301 | PF00134 | 0.631 |
DOC_CYCLIN_RxL_1 | 353 | 362 | PF00134 | 0.643 |
DOC_MAPK_DCC_7 | 310 | 318 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 219 | 227 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 245 | 255 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 307 | 317 | PF00069 | 0.560 |
DOC_MAPK_JIP1_4 | 294 | 300 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 280 | 288 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 307 | 315 | PF00069 | 0.526 |
DOC_PP1_RVXF_1 | 297 | 303 | PF00149 | 0.551 |
DOC_PP1_RVXF_1 | 354 | 361 | PF00149 | 0.567 |
DOC_PP2B_LxvP_1 | 350 | 353 | PF13499 | 0.670 |
DOC_PP2B_LxvP_1 | 59 | 62 | PF13499 | 0.649 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.812 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.703 |
DOC_USP7_UBL2_3 | 336 | 340 | PF12436 | 0.614 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 299 | 303 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 66 | 75 | PF00244 | 0.581 |
LIG_Actin_WH2_2 | 286 | 301 | PF00022 | 0.556 |
LIG_Actin_WH2_2 | 327 | 345 | PF00022 | 0.638 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.394 |
LIG_BIR_III_4 | 121 | 125 | PF00653 | 0.753 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.586 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.598 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.654 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.610 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.606 |
LIG_G3BP_FGDF_1 | 1 | 6 | PF02136 | 0.298 |
LIG_IRF3_LxIS_1 | 295 | 301 | PF10401 | 0.632 |
LIG_LIR_Apic_2 | 212 | 218 | PF02991 | 0.516 |
LIG_LIR_Apic_2 | 290 | 295 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 151 | 157 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.150 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.482 |
LIG_LYPXL_yS_3 | 42 | 45 | PF13949 | 0.670 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.413 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.562 |
LIG_SH2_PTP2 | 292 | 295 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.616 |
LIG_SH2_STAT3 | 213 | 216 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 32 | 35 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.523 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.793 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.506 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.547 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.597 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.577 |
LIG_SUMO_SIM_anti_2 | 223 | 231 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 201 | 206 | PF11976 | 0.589 |
LIG_TRFH_1 | 80 | 84 | PF08558 | 0.588 |
LIG_TYR_ITIM | 40 | 45 | PF00017 | 0.680 |
LIG_WRC_WIRS_1 | 149 | 154 | PF05994 | 0.629 |
LIG_WRC_WIRS_1 | 3 | 8 | PF05994 | 0.407 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.675 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.530 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.407 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.570 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.548 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.594 |
MOD_Cter_Amidation | 246 | 249 | PF01082 | 0.219 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.563 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.546 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.460 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.460 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.339 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.400 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.302 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.420 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.432 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.485 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.498 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.665 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.739 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.672 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.648 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.288 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.493 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.501 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.729 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.790 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.598 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.482 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.615 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.487 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.420 |
MOD_NEK2_2 | 234 | 239 | PF00069 | 0.586 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.534 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.604 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.695 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.633 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.482 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.660 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.736 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.577 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.402 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.339 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.670 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 356 | 361 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK32 | Leptomonas seymouri | 61% | 96% |
A0A1X0P675 | Trypanosomatidae | 43% | 100% |
A0A3Q8IMT8 | Leishmania donovani | 94% | 100% |
A0A3R7NFR6 | Trypanosoma rangeli | 44% | 100% |
A4HN72 | Leishmania braziliensis | 83% | 100% |
A4IBU0 | Leishmania infantum | 94% | 100% |
C9ZYS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B6T0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BXX8 | Trypanosoma cruzi | 43% | 100% |