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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 21 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0005737 | cytoplasm | 2 | 2 |
Related structures:
AlphaFold database: A4HEJ1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016874 | ligase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 10 | 14 | PF00656 | 0.557 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.552 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.657 |
CLV_PCSK_PC7_1 | 249 | 255 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.572 |
DOC_MAPK_gen_1 | 241 | 250 | PF00069 | 0.340 |
DOC_PP1_RVXF_1 | 144 | 151 | PF00149 | 0.348 |
DOC_PP1_RVXF_1 | 272 | 279 | PF00149 | 0.294 |
DOC_PP4_FxxP_1 | 200 | 203 | PF00568 | 0.389 |
DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.285 |
LIG_14-3-3_CanoR_1 | 130 | 138 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 26 | 31 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 305 | 311 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.474 |
LIG_Actin_WH2_2 | 297 | 315 | PF00022 | 0.426 |
LIG_eIF4E_1 | 143 | 149 | PF01652 | 0.314 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.420 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.561 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.397 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.533 |
LIG_HCF-1_HBM_1 | 269 | 272 | PF13415 | 0.248 |
LIG_Integrin_isoDGR_2 | 120 | 122 | PF01839 | 0.538 |
LIG_Integrin_RGD_1 | 123 | 125 | PF01839 | 0.674 |
LIG_KLC1_Yacidic_2 | 289 | 294 | PF13176 | 0.205 |
LIG_LIR_Apic_2 | 170 | 174 | PF02991 | 0.428 |
LIG_LIR_Apic_2 | 197 | 203 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 289 | 295 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 187 | 195 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 269 | 278 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 70 | 74 | PF02991 | 0.387 |
LIG_Pex14_1 | 181 | 185 | PF04695 | 0.421 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.312 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.442 |
LIG_SH2_GRB2like | 108 | 111 | PF00017 | 0.343 |
LIG_SH2_GRB2like | 171 | 174 | PF00017 | 0.425 |
LIG_SH2_GRB2like | 97 | 100 | PF00017 | 0.307 |
LIG_SH2_NCK_1 | 189 | 193 | PF00017 | 0.346 |
LIG_SH2_PTP2 | 111 | 114 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 292 | 295 | PF00017 | 0.289 |
LIG_SH2_PTP2 | 36 | 39 | PF00017 | 0.391 |
LIG_SH2_SRC | 189 | 192 | PF00017 | 0.360 |
LIG_SH2_SRC | 292 | 295 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 272 | 276 | PF00017 | 0.298 |
LIG_SH2_STAT3 | 58 | 61 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.201 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.337 |
LIG_SH3_1 | 171 | 177 | PF00018 | 0.317 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.426 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.498 |
LIG_Sin3_3 | 206 | 213 | PF02671 | 0.215 |
LIG_SUMO_SIM_anti_2 | 296 | 302 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.292 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.246 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.491 |
LIG_TYR_ITIM | 109 | 114 | PF00017 | 0.502 |
LIG_TYR_ITIM | 34 | 39 | PF00017 | 0.307 |
LIG_TYR_ITIM | 52 | 57 | PF00017 | 0.368 |
LIG_TYR_ITSM | 185 | 192 | PF00017 | 0.361 |
LIG_UBA3_1 | 300 | 308 | PF00899 | 0.390 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.301 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.485 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.365 |
MOD_CMANNOS | 147 | 150 | PF00535 | 0.464 |
MOD_Cter_Amidation | 120 | 123 | PF01082 | 0.584 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.330 |
MOD_GlcNHglycan | 180 | 184 | PF01048 | 0.498 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.605 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.318 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.369 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.409 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.475 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.439 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.551 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.452 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.347 |
MOD_Plk_2-3 | 191 | 197 | PF00069 | 0.329 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.476 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.399 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.363 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.437 |
MOD_SUMO_for_1 | 175 | 178 | PF00179 | 0.568 |
MOD_SUMO_for_1 | 227 | 230 | PF00179 | 0.437 |
MOD_SUMO_rev_2 | 191 | 200 | PF00179 | 0.441 |
MOD_SUMO_rev_2 | 240 | 248 | PF00179 | 0.533 |
TRG_DiLeu_BaEn_4 | 190 | 196 | PF01217 | 0.273 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.326 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.497 |
TRG_NLS_MonoExtN_4 | 243 | 250 | PF00514 | 0.458 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I309 | Leptomonas seymouri | 61% | 100% |
A0A0N1I7J8 | Leptomonas seymouri | 27% | 84% |
A0A0N1PB04 | Leptomonas seymouri | 28% | 93% |
A0A1X0NR96 | Trypanosomatidae | 28% | 100% |
A0A1X0NR98 | Trypanosomatidae | 25% | 100% |
A0A1X0NY88 | Trypanosomatidae | 37% | 100% |
A0A1X0NYK9 | Trypanosomatidae | 37% | 100% |
A0A3R7KMG1 | Trypanosoma rangeli | 35% | 100% |
A0A3S7WZA9 | Leishmania donovani | 84% | 100% |
A0A3S7X769 | Leishmania donovani | 27% | 100% |
A4HLZ4 | Leishmania braziliensis | 28% | 99% |
A4I1M7 | Leishmania infantum | 84% | 100% |
A4I9C4 | Leishmania infantum | 27% | 90% |
C9ZK72 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A867 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AXR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9B4C3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q4Q3Q2 | Leishmania major | 27% | 90% |
Q4Q9R0 | Leishmania major | 82% | 100% |
V5BF57 | Trypanosoma cruzi | 26% | 100% |
V5DIU8 | Trypanosoma cruzi | 36% | 100% |