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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9AE50
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.347 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.329 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.700 |
DEG_SPOP_SBC_1 | 334 | 338 | PF00917 | 0.590 |
DOC_ANK_TNKS_1 | 140 | 147 | PF00023 | 0.663 |
DOC_CKS1_1 | 361 | 366 | PF01111 | 0.552 |
DOC_CKS1_1 | 375 | 380 | PF01111 | 0.335 |
DOC_CYCLIN_RxL_1 | 11 | 23 | PF00134 | 0.536 |
DOC_MAPK_gen_1 | 264 | 273 | PF00069 | 0.716 |
DOC_PP2B_LxvP_1 | 278 | 281 | PF13499 | 0.722 |
DOC_PP4_FxxP_1 | 177 | 180 | PF00568 | 0.596 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.738 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.338 |
LIG_14-3-3_CanoR_1 | 332 | 341 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 353 | 358 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 371 | 375 | PF00244 | 0.589 |
LIG_ActinCP_TwfCPI_2 | 177 | 186 | PF01115 | 0.689 |
LIG_BIR_III_4 | 46 | 50 | PF00653 | 0.472 |
LIG_BRCT_BRCA1_1 | 156 | 160 | PF00533 | 0.653 |
LIG_EH_1 | 186 | 190 | PF12763 | 0.592 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.682 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.589 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.485 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.507 |
LIG_LIR_Apic_2 | 174 | 180 | PF02991 | 0.597 |
LIG_LIR_Apic_2 | 183 | 188 | PF02991 | 0.696 |
LIG_LIR_Apic_2 | 244 | 250 | PF02991 | 0.672 |
LIG_LIR_Apic_2 | 88 | 94 | PF02991 | 0.720 |
LIG_LIR_Gen_1 | 111 | 120 | PF02991 | 0.650 |
LIG_LIR_Gen_1 | 251 | 260 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.467 |
LIG_MAD2 | 353 | 361 | PF02301 | 0.705 |
LIG_PDZ_Class_3 | 390 | 395 | PF00595 | 0.469 |
LIG_Pex14_1 | 109 | 113 | PF04695 | 0.680 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.731 |
LIG_Pex14_2 | 189 | 193 | PF04695 | 0.552 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.672 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.628 |
LIG_SH2_NCK_1 | 27 | 31 | PF00017 | 0.496 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.744 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.526 |
LIG_SH2_STAT3 | 252 | 255 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.648 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.503 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.489 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.478 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.346 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.615 |
LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.602 |
LIG_WRPW_2 | 178 | 181 | PF00400 | 0.597 |
MOD_CDK_SPK_2 | 374 | 379 | PF00069 | 0.501 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.786 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.712 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.688 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.602 |
MOD_Cter_Amidation | 70 | 73 | PF01082 | 0.468 |
MOD_DYRK1A_RPxSP_1 | 360 | 364 | PF00069 | 0.564 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.353 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.398 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.570 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.525 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.427 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.505 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.695 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.536 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.689 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.418 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.446 |
MOD_N-GLC_2 | 121 | 123 | PF02516 | 0.485 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.694 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.517 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.585 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.714 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.528 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.655 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.691 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.658 |
MOD_PKA_1 | 264 | 270 | PF00069 | 0.665 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.687 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.714 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.626 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.547 |
MOD_PKB_1 | 37 | 45 | PF00069 | 0.539 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.688 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.512 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.662 |
MOD_Plk_2-3 | 383 | 389 | PF00069 | 0.523 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.686 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.617 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.564 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.543 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.336 |
MOD_SUMO_rev_2 | 149 | 158 | PF00179 | 0.635 |
MOD_SUMO_rev_2 | 26 | 35 | PF00179 | 0.558 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.648 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.472 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 284 | 288 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P346 | Leptomonas seymouri | 55% | 100% |
A0A0N1I1W6 | Leptomonas seymouri | 29% | 100% |
A0A1X0NJW8 | Trypanosomatidae | 32% | 100% |
A0A3Q8IEI2 | Leishmania donovani | 94% | 100% |
A0A422P027 | Trypanosoma rangeli | 32% | 100% |
A4HHI9 | Leishmania braziliensis | 74% | 96% |
A4I4P7 | Leishmania infantum | 94% | 100% |
E9ALN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q6N7 | Leishmania major | 29% | 100% |
V5BN31 | Trypanosoma cruzi | 32% | 100% |