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: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H8A5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 149 | 155 | PF00089 | 0.282 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.353 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.385 |
DEG_APCC_DBOX_1 | 151 | 159 | PF00400 | 0.362 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.328 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.220 |
DOC_CYCLIN_yCln2_LP_2 | 87 | 93 | PF00134 | 0.413 |
DOC_MAPK_gen_1 | 121 | 128 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 121 | 128 | PF00069 | 0.295 |
DOC_PP1_RVXF_1 | 127 | 133 | PF00149 | 0.389 |
DOC_PP1_RVXF_1 | 90 | 97 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.244 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.278 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 152 | 156 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 298 | 306 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 56 | 65 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 98 | 105 | PF00244 | 0.334 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.402 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.535 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.422 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.495 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.484 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.425 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.401 |
LIG_HP1_1 | 151 | 155 | PF01393 | 0.286 |
LIG_LIR_Apic_2 | 34 | 39 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 15 | 24 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 227 | 238 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 342 | 351 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 342 | 346 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.311 |
LIG_PCNA_PIPBox_1 | 312 | 321 | PF02747 | 0.441 |
LIG_PDZ_Class_1 | 366 | 371 | PF00595 | 0.468 |
LIG_Pex14_1 | 156 | 160 | PF04695 | 0.324 |
LIG_Pex14_2 | 128 | 132 | PF04695 | 0.315 |
LIG_Pex14_2 | 32 | 36 | PF04695 | 0.277 |
LIG_REV1ctd_RIR_1 | 94 | 102 | PF16727 | 0.312 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.441 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.439 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.384 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.510 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.325 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.683 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.298 |
LIG_SUMO_SIM_anti_2 | 244 | 250 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 307 | 317 | PF11976 | 0.415 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.337 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.405 |
LIG_WW_1 | 41 | 44 | PF00397 | 0.317 |
MOD_CDK_SPK_2 | 147 | 152 | PF00069 | 0.404 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.312 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.405 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.422 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.495 |
MOD_GlcNHglycan | 270 | 274 | PF01048 | 0.637 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.365 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.542 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.536 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.388 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.554 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.358 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.285 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.295 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.531 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.317 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.464 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.497 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.492 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.328 |
MOD_NEK2_2 | 164 | 169 | PF00069 | 0.468 |
MOD_PKA_1 | 339 | 345 | PF00069 | 0.301 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.379 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.320 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.467 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.450 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.371 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.357 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.426 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.367 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.523 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.413 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.337 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.422 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.508 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.495 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.579 |
TRG_AP2beta_CARGO_1 | 227 | 237 | PF09066 | 0.297 |
TRG_DiLeu_BaEn_1 | 213 | 218 | PF01217 | 0.285 |
TRG_DiLeu_BaEn_1 | 309 | 314 | PF01217 | 0.363 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.501 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.402 |
TRG_NLS_MonoExtN_4 | 282 | 287 | PF00514 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7L5 | Leptomonas seymouri | 68% | 92% |
A0A0S4JE30 | Bodo saltans | 34% | 100% |
A0A0S4JK16 | Bodo saltans | 54% | 85% |
A0A1X0NVQ6 | Trypanosomatidae | 63% | 97% |
A0A1X0P1X9 | Trypanosomatidae | 31% | 100% |
A0A3Q8IFT0 | Leishmania donovani | 28% | 89% |
A0A3R7KWZ0 | Trypanosoma rangeli | 63% | 97% |
A0A3R7KYN0 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WTN3 | Leishmania donovani | 88% | 92% |
A4HIA2 | Leishmania braziliensis | 28% | 89% |
A4HWM5 | Leishmania infantum | 88% | 92% |
A4I5I6 | Leishmania infantum | 28% | 89% |
C9ZXR2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 98% |
E9AQD2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 92% |
E9B0T1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 90% |
Q4Q7E7 | Leishmania major | 28% | 100% |
Q4QF43 | Leishmania major | 88% | 100% |
V5BPI9 | Trypanosoma cruzi | 32% | 100% |
V5BUE5 | Trypanosoma cruzi | 60% | 100% |