Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 12 |
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:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ARF8
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0032781 | positive regulation of ATP-dependent activity | 4 | 1 |
GO:0043462 | regulation of ATP-dependent activity | 3 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001671 | ATPase activator activity | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0031072 | heat shock protein binding | 3 | 12 |
GO:0051087 | protein-folding chaperone binding | 3 | 12 |
GO:0051879 | Hsp90 protein binding | 4 | 12 |
GO:0098772 | molecular function regulator activity | 1 | 12 |
GO:0140677 | molecular function activator activity | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.449 |
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.252 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.278 |
DOC_PP2B_LxvP_1 | 179 | 182 | PF13499 | 0.572 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.747 |
DOC_USP7_UBL2_3 | 90 | 94 | PF12436 | 0.447 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 149 | 153 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 262 | 266 | PF00244 | 0.504 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.545 |
LIG_deltaCOP1_diTrp_1 | 331 | 338 | PF00928 | 0.452 |
LIG_EVH1_1 | 179 | 183 | PF00568 | 0.618 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.557 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.467 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.488 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.482 |
LIG_LIR_Gen_1 | 158 | 167 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 234 | 242 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 271 | 282 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 58 | 67 | PF02991 | 0.541 |
LIG_LIR_LC3C_4 | 298 | 301 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.541 |
LIG_Pex14_1 | 333 | 337 | PF04695 | 0.452 |
LIG_Pex14_2 | 160 | 164 | PF04695 | 0.452 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.425 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.517 |
LIG_SH2_PTP2 | 274 | 277 | PF00017 | 0.513 |
LIG_SH2_SRC | 124 | 127 | PF00017 | 0.513 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.425 |
LIG_SH2_SRC | 274 | 277 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 347 | 351 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.452 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.602 |
LIG_SUMO_SIM_anti_2 | 298 | 303 | PF11976 | 0.524 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.513 |
LIG_TYR_ITIM | 59 | 64 | PF00017 | 0.538 |
LIG_WRC_WIRS_1 | 156 | 161 | PF05994 | 0.488 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.661 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.400 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.759 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.714 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.628 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.473 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.450 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.538 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.457 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.741 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.725 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.468 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.463 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.671 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.689 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.591 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.300 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.326 |
MOD_GlcNHglycan | 69 | 73 | PF01048 | 0.252 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.724 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.632 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.553 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.539 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.456 |
MOD_LATS_1 | 37 | 43 | PF00433 | 0.549 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.526 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.541 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.466 |
MOD_NEK2_2 | 148 | 153 | PF00069 | 0.538 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.461 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.538 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.557 |
MOD_PK_1 | 39 | 45 | PF00069 | 0.557 |
MOD_PKA_1 | 203 | 209 | PF00069 | 0.754 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.535 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.484 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.519 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.418 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.444 |
MOD_Plk_2-3 | 155 | 161 | PF00069 | 0.528 |
MOD_Plk_2-3 | 325 | 331 | PF00069 | 0.530 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.538 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.538 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.469 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.504 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.370 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.547 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.674 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.538 |
MOD_SUMO_for_1 | 305 | 308 | PF00179 | 0.479 |
MOD_SUMO_for_1 | 62 | 65 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 114 | 123 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 196 | 206 | PF00179 | 0.761 |
MOD_SUMO_rev_2 | 251 | 259 | PF00179 | 0.538 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.452 |
TRG_NES_CRM1_1 | 54 | 66 | PF08389 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 30 | 34 | PF00026 | 0.263 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2A4 | Leptomonas seymouri | 70% | 99% |
A0A0S4JAT2 | Bodo saltans | 49% | 100% |
A0A1X0P6W4 | Trypanosomatidae | 57% | 100% |
A0A3R7MY48 | Trypanosoma rangeli | 53% | 100% |
A0A3S7WUS5 | Leishmania donovani | 92% | 100% |
A4H9C6 | Leishmania braziliensis | 84% | 100% |
A4HXP7 | Leishmania infantum | 92% | 100% |
A6QQC0 | Bos taurus | 27% | 100% |
D0A023 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
O95433 | Homo sapiens | 30% | 100% |
Q12449 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
Q4QE21 | Leishmania major | 93% | 100% |
Q55DB6 | Dictyostelium discoideum | 28% | 92% |
Q8BK64 | Mus musculus | 29% | 100% |
Q8N9S3 | Mus musculus | 28% | 100% |
Q9P782 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
V5B6E4 | Trypanosoma cruzi | 55% | 100% |