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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q4J3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.472 |
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.596 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.641 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.645 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.664 |
CLV_PCSK_PC7_1 | 193 | 199 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.759 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.666 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.672 |
DEG_SPOP_SBC_1 | 22 | 26 | PF00917 | 0.607 |
DOC_AGCK_PIF_1 | 125 | 130 | PF00069 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 147 | 153 | PF00134 | 0.428 |
DOC_CYCLIN_yCln2_LP_2 | 171 | 177 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 193 | 202 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 209 | 216 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 196 | 204 | PF00069 | 0.523 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.683 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.340 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.698 |
LIG_14-3-3_CanoR_1 | 120 | 124 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 316 | 326 | PF00244 | 0.347 |
LIG_APCC_ABBA_1 | 186 | 191 | PF00400 | 0.456 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.344 |
LIG_BRCT_BRCA1_1 | 266 | 270 | PF00533 | 0.327 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.634 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.339 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.377 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.509 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.621 |
LIG_LIR_Apic_2 | 129 | 135 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 122 | 132 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.402 |
LIG_Pex14_1 | 304 | 308 | PF04695 | 0.366 |
LIG_Pex14_2 | 128 | 132 | PF04695 | 0.369 |
LIG_Pex14_2 | 234 | 238 | PF04695 | 0.561 |
LIG_Pex14_2 | 270 | 274 | PF04695 | 0.436 |
LIG_PTB_Apo_2 | 262 | 269 | PF02174 | 0.476 |
LIG_REV1ctd_RIR_1 | 184 | 194 | PF16727 | 0.453 |
LIG_SH2_NCK_1 | 287 | 291 | PF00017 | 0.448 |
LIG_SH2_NCK_1 | 295 | 299 | PF00017 | 0.421 |
LIG_SH2_SRC | 310 | 313 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 295 | 299 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.375 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.501 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.603 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.692 |
LIG_SUMO_SIM_par_1 | 113 | 118 | PF11976 | 0.595 |
LIG_SUMO_SIM_par_1 | 63 | 69 | PF11976 | 0.665 |
LIG_UBA3_1 | 285 | 294 | PF00899 | 0.291 |
LIG_UBA3_1 | 330 | 339 | PF00899 | 0.549 |
LIG_UBA3_1 | 4 | 13 | PF00899 | 0.665 |
LIG_WRC_WIRS_1 | 125 | 130 | PF05994 | 0.344 |
LIG_WRC_WIRS_1 | 330 | 335 | PF05994 | 0.419 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.633 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.513 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.621 |
MOD_Cter_Amidation | 194 | 197 | PF01082 | 0.665 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.490 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.414 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.380 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.399 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.698 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.668 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.370 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.538 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.515 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.572 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.688 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.520 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.591 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.518 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.498 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.561 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.627 |
MOD_NEK2_2 | 344 | 349 | PF00069 | 0.603 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.647 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.490 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.735 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.609 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.411 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.716 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.765 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.588 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.356 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.333 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.402 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.569 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.626 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.722 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.339 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.498 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.633 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.583 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.702 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.647 |
TRG_ER_FFAT_2 | 267 | 278 | PF00635 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 283 | 288 | PF00026 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA32 | Leptomonas seymouri | 68% | 100% |
A0A0S4JM85 | Bodo saltans | 28% | 100% |
A0A3Q8IGN8 | Leishmania donovani | 95% | 100% |
A0A3S5IR52 | Trypanosoma rangeli | 30% | 100% |
A4HL63 | Leishmania braziliensis | 82% | 100% |
E9AHM7 | Leishmania infantum | 95% | 100% |
E9B3K6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BB92 | Trypanosoma cruzi | 33% | 100% |