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:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9AD18
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 2 |
GO:0006458 | 'de novo' protein folding | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0042026 | protein refolding | 3 | 2 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 2 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 2 |
GO:0061077 | chaperone-mediated protein folding | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0051082 | unfolded protein binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 167 | 171 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 201 | 205 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.236 |
CLV_PCSK_FUR_1 | 206 | 210 | PF00082 | 0.427 |
CLV_PCSK_FUR_1 | 70 | 74 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.236 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.288 |
CLV_PCSK_PC7_1 | 209 | 215 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.208 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.555 |
DOC_PP4_FxxP_1 | 252 | 255 | PF00568 | 0.683 |
DOC_SPAK_OSR1_1 | 209 | 213 | PF12202 | 0.673 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.590 |
DOC_USP7_UBL2_3 | 33 | 37 | PF12436 | 0.400 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 176 | 182 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 209 | 213 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 214 | 220 | PF00244 | 0.592 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.705 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.665 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.670 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.266 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.595 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.606 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.504 |
LIG_LIR_Apic_2 | 249 | 255 | PF02991 | 0.684 |
LIG_LIR_Gen_1 | 16 | 25 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 289 | 299 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 61 | 71 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.417 |
LIG_NRBOX | 286 | 292 | PF00104 | 0.327 |
LIG_PCNA_yPIPBox_3 | 14 | 24 | PF02747 | 0.465 |
LIG_Pex14_2 | 130 | 134 | PF04695 | 0.490 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.586 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.377 |
LIG_SH2_CRK | 64 | 68 | PF00017 | 0.400 |
LIG_SH2_NCK_1 | 64 | 68 | PF00017 | 0.442 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.667 |
LIG_SH2_STAT3 | 76 | 79 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.623 |
LIG_SUMO_SIM_anti_2 | 307 | 313 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 283 | 289 | PF11976 | 0.379 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.515 |
LIG_WRPW_2 | 175 | 178 | PF00400 | 0.591 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.649 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.638 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.576 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.623 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.526 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.652 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.400 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.400 |
MOD_Cter_Amidation | 206 | 209 | PF01082 | 0.430 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.432 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.204 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.297 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.420 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.650 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.555 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.668 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.611 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.622 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.212 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.473 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.388 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.407 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.706 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.577 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.274 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.591 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.698 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.467 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.619 |
MOD_PK_1 | 56 | 62 | PF00069 | 0.457 |
MOD_PKA_1 | 208 | 214 | PF00069 | 0.655 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.603 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.588 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.630 |
MOD_Plk_2-3 | 198 | 204 | PF00069 | 0.590 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.233 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.234 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.467 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.616 |
MOD_SUMO_rev_2 | 26 | 35 | PF00179 | 0.400 |
TRG_DiLeu_BaEn_4 | 147 | 153 | PF01217 | 0.570 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.669 |
TRG_NES_CRM1_1 | 127 | 140 | PF08389 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.380 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD75 | Leptomonas seymouri | 77% | 85% |
A0A0S4JV26 | Bodo saltans | 41% | 87% |
A0A1X0P3X0 | Trypanosomatidae | 54% | 88% |
A0A3S5IRT6 | Trypanosoma rangeli | 52% | 85% |
A0A3S7X0F2 | Leishmania donovani | 95% | 67% |
A4HFG5 | Leishmania braziliensis | 83% | 85% |
A4I2M7 | Leishmania infantum | 95% | 85% |
B7KEJ8 | Gloeothece citriformis (strain PCC 7424) | 30% | 86% |
D0A5P1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 87% |
E9AYU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 85% |
V5BN28 | Trypanosoma cruzi | 51% | 78% |