Apparently a divergent chaperone with distant Eukaryotic affinities. Topology is very unclear. Likely non-TM
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HHI9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 125 | 129 | PF00656 | 0.404 |
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.211 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.555 |
CLV_PCSK_FUR_1 | 367 | 371 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.495 |
DEG_APCC_DBOX_1 | 337 | 345 | PF00400 | 0.640 |
DEG_APCC_KENBOX_2 | 304 | 308 | PF00400 | 0.630 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.531 |
DOC_CKS1_1 | 360 | 365 | PF01111 | 0.774 |
DOC_CKS1_1 | 374 | 379 | PF01111 | 0.552 |
DOC_CYCLIN_RxL_1 | 11 | 23 | PF00134 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 281 | 287 | PF00134 | 0.645 |
DOC_MAPK_gen_1 | 265 | 272 | PF00069 | 0.719 |
DOC_PP1_SILK_1 | 338 | 343 | PF00149 | 0.643 |
DOC_PP2B_LxvP_1 | 277 | 280 | PF13499 | 0.723 |
DOC_PP4_FxxP_1 | 176 | 179 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.557 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.233 |
LIG_14-3-3_CanoR_1 | 352 | 357 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 370 | 374 | PF00244 | 0.796 |
LIG_14-3-3_CanoR_1 | 39 | 45 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 9 | 14 | PF00244 | 0.333 |
LIG_ActinCP_TwfCPI_2 | 176 | 185 | PF01115 | 0.503 |
LIG_BIR_III_4 | 46 | 50 | PF00653 | 0.290 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.483 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.714 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.407 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.290 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.684 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.760 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.290 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.499 |
LIG_LIR_Apic_2 | 173 | 179 | PF02991 | 0.424 |
LIG_LIR_Apic_2 | 181 | 187 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 245 | 249 | PF02991 | 0.712 |
LIG_LIR_Apic_2 | 88 | 94 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 59 | 68 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.286 |
LIG_MAD2 | 352 | 360 | PF02301 | 0.806 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.548 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.545 |
LIG_SH2_NCK_1 | 27 | 31 | PF00017 | 0.324 |
LIG_SH2_NCK_1 | 386 | 390 | PF00017 | 0.624 |
LIG_SH2_SRC | 246 | 249 | PF00017 | 0.590 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 380 | 384 | PF00017 | 0.763 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.331 |
LIG_SH2_STAT3 | 251 | 254 | PF00017 | 0.717 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.308 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.795 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.730 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.558 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.422 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.398 |
LIG_WRPW_2 | 177 | 180 | PF00400 | 0.423 |
MOD_CDK_SPK_2 | 373 | 378 | PF00069 | 0.763 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.585 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.623 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.636 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.537 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.425 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.394 |
MOD_Cter_Amidation | 367 | 370 | PF01082 | 0.440 |
MOD_Cter_Amidation | 406 | 409 | PF01082 | 0.440 |
MOD_Cter_Amidation | 70 | 73 | PF01082 | 0.675 |
MOD_DYRK1A_RPxSP_1 | 359 | 363 | PF00069 | 0.774 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.566 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.444 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.469 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.442 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.727 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.505 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.404 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.501 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.367 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.233 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.768 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.789 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.392 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.521 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.600 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.635 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.497 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.507 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.563 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.376 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.558 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.324 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.704 |
MOD_PKA_1 | 369 | 375 | PF00069 | 0.625 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.482 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.302 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.534 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.233 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.627 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.722 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.805 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.488 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.396 |
MOD_PKB_1 | 37 | 45 | PF00069 | 0.391 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.504 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.742 |
MOD_Plk_2-3 | 382 | 388 | PF00069 | 0.802 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.472 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.460 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.478 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.337 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.774 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.552 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.636 |
MOD_SUMO_rev_2 | 26 | 35 | PF00179 | 0.297 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.290 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 17 | 22 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 283 | 288 | PF00026 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P346 | Leptomonas seymouri | 52% | 100% |
A0A1X0NJW8 | Trypanosomatidae | 31% | 100% |
A0A3Q8IEI2 | Leishmania donovani | 73% | 100% |
A0A422P027 | Trypanosoma rangeli | 30% | 100% |
A4I4P7 | Leishmania infantum | 73% | 100% |
E9AE50 | Leishmania major | 74% | 99% |
E9ALN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
V5BN31 | Trypanosoma cruzi | 32% | 100% |