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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9B1H7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 44 | 48 | PF00656 | 0.629 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.626 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.410 |
CLV_PCSK_PC7_1 | 131 | 137 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.393 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.600 |
DOC_CKS1_1 | 229 | 234 | PF01111 | 0.340 |
DOC_PP1_RVXF_1 | 165 | 172 | PF00149 | 0.418 |
DOC_PP1_RVXF_1 | 28 | 34 | PF00149 | 0.465 |
DOC_PP2B_LxvP_1 | 220 | 223 | PF13499 | 0.547 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.625 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.372 |
LIG_14-3-3_CanoR_1 | 135 | 144 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 225 | 232 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 268 | 273 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 62 | 70 | PF00244 | 0.560 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.560 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.581 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.532 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.571 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.585 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.506 |
LIG_LIR_Apic_2 | 138 | 144 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 178 | 186 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.492 |
LIG_NRBOX | 179 | 185 | PF00104 | 0.298 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.360 |
LIG_SH2_GRB2like | 125 | 128 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.385 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.400 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.722 |
LIG_SUMO_SIM_par_1 | 268 | 273 | PF11976 | 0.464 |
LIG_TRAF2_1 | 150 | 153 | PF00917 | 0.590 |
LIG_WW_3 | 222 | 226 | PF00397 | 0.356 |
MOD_CDK_SPK_2 | 228 | 233 | PF00069 | 0.411 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.425 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.556 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.626 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.575 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.540 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.581 |
MOD_Cter_Amidation | 106 | 109 | PF01082 | 0.361 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.466 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.436 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.435 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.378 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.716 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.667 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.545 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.384 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.397 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.514 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.502 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.564 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.539 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.622 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.396 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.591 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.462 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.534 |
MOD_OFUCOSY | 253 | 258 | PF10250 | 0.558 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.369 |
MOD_PK_1 | 268 | 274 | PF00069 | 0.421 |
MOD_PKA_1 | 135 | 141 | PF00069 | 0.514 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.562 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.634 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.675 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.378 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.565 |
MOD_PKB_1 | 62 | 70 | PF00069 | 0.515 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.607 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.372 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.244 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.466 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.761 |
TRG_Pf-PMV_PEXEL_1 | 245 | 250 | PF00026 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P346 | Leptomonas seymouri | 27% | 79% |
A0A0N1I1W6 | Leptomonas seymouri | 40% | 97% |
A0A1X0NJW8 | Trypanosomatidae | 24% | 92% |
A0A3Q8IEI2 | Leishmania donovani | 28% | 74% |
A0A422P027 | Trypanosoma rangeli | 28% | 97% |
A4I4P7 | Leishmania infantum | 28% | 74% |
E9ALN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q4Q6N7 | Leishmania major | 79% | 100% |
V5BN31 | Trypanosoma cruzi | 26% | 96% |