A tail-anchored chaperone, with homology to ER-associated (secreted) heat shock proteins (plant ERDJ3). However, this subfamily appears to be oriented towards the cytoplasm.
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 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9B2I2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.521 |
CLV_PCSK_FUR_1 | 3 | 7 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.243 |
CLV_Separin_Metazoa | 227 | 231 | PF03568 | 0.537 |
DEG_APCC_KENBOX_2 | 91 | 95 | PF00400 | 0.504 |
DOC_AGCK_PIF_1 | 296 | 301 | PF00069 | 0.510 |
DOC_CKS1_1 | 33 | 38 | PF01111 | 0.555 |
DOC_MAPK_gen_1 | 153 | 163 | PF00069 | 0.523 |
DOC_MAPK_gen_1 | 291 | 299 | PF00069 | 0.368 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.451 |
DOC_USP7_UBL2_3 | 191 | 195 | PF12436 | 0.653 |
DOC_USP7_UBL2_3 | 211 | 215 | PF12436 | 0.405 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.547 |
LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 194 | 200 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 210 | 214 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 231 | 241 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 262 | 270 | PF00244 | 0.505 |
LIG_14-3-3_CterR_2 | 311 | 316 | PF00244 | 0.425 |
LIG_Actin_WH2_2 | 195 | 212 | PF00022 | 0.517 |
LIG_Actin_WH2_2 | 214 | 232 | PF00022 | 0.504 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.448 |
LIG_deltaCOP1_diTrp_1 | 206 | 213 | PF00928 | 0.509 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.417 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.545 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.652 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.438 |
LIG_IBAR_NPY_1 | 40 | 42 | PF08397 | 0.437 |
LIG_LIR_Gen_1 | 258 | 268 | PF02991 | 0.514 |
LIG_LIR_LC3C_4 | 64 | 67 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.452 |
LIG_Pex14_1 | 295 | 299 | PF04695 | 0.372 |
LIG_REV1ctd_RIR_1 | 190 | 199 | PF16727 | 0.537 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.501 |
LIG_SH3_1 | 30 | 36 | PF00018 | 0.537 |
LIG_SH3_1 | 68 | 74 | PF00018 | 0.480 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.578 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.477 |
LIG_SUMO_SIM_anti_2 | 285 | 291 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 43 | 48 | PF11976 | 0.462 |
LIG_TYR_ITIM | 86 | 91 | PF00017 | 0.491 |
LIG_WRC_WIRS_1 | 245 | 250 | PF05994 | 0.516 |
MOD_CDK_SPxxK_3 | 32 | 39 | PF00069 | 0.551 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.549 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.664 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.548 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.537 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.593 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.506 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.394 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.396 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.374 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.560 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.507 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.531 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.438 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.609 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.589 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.547 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.488 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.557 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.340 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.448 |
MOD_NEK2_2 | 105 | 110 | PF00069 | 0.639 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.539 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.485 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.483 |
MOD_PKA_1 | 137 | 143 | PF00069 | 0.615 |
MOD_PKA_1 | 230 | 236 | PF00069 | 0.681 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.616 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.638 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.540 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.520 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.684 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.507 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.620 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.514 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.446 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.468 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.515 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.374 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.549 |
TRG_DiLeu_BaEn_2 | 276 | 282 | PF01217 | 0.504 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.724 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 156 | 160 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 273 | 277 | PF00026 | 0.303 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I888 | Leptomonas seymouri | 83% | 100% |
A0A0S4KIH6 | Bodo saltans | 61% | 98% |
A0A1X0NV04 | Trypanosomatidae | 63% | 100% |
A0A3R7NF81 | Trypanosoma rangeli | 60% | 100% |
A0A3S7X5A0 | Leishmania donovani | 96% | 100% |
A4HK40 | Leishmania braziliensis | 92% | 100% |
A4I7M3 | Leishmania infantum | 96% | 100% |
D0A9S5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
Q4Q5M4 | Leishmania major | 95% | 100% |
V5AQU3 | Trypanosoma cruzi | 61% | 100% |