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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: Q4QJF5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.675 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.425 |
CLV_PCSK_FUR_1 | 290 | 294 | PF00082 | 0.702 |
CLV_PCSK_FUR_1 | 328 | 332 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.848 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.848 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.839 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.693 |
CLV_Separin_Metazoa | 315 | 319 | PF03568 | 0.683 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.691 |
DEG_Kelch_Keap1_1 | 74 | 79 | PF01344 | 0.488 |
DEG_SPOP_SBC_1 | 34 | 38 | PF00917 | 0.456 |
DOC_CYCLIN_RxL_1 | 289 | 301 | PF00134 | 0.692 |
DOC_CYCLIN_yCln2_LP_2 | 225 | 231 | PF00134 | 0.779 |
DOC_MAPK_gen_1 | 289 | 297 | PF00069 | 0.695 |
DOC_MAPK_MEF2A_6 | 26 | 33 | PF00069 | 0.473 |
DOC_PP1_RVXF_1 | 291 | 298 | PF00149 | 0.691 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.821 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.677 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.819 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.437 |
LIG_14-3-3_CanoR_1 | 208 | 215 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 244 | 253 | PF00244 | 0.848 |
LIG_14-3-3_CanoR_1 | 41 | 45 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 80 | 90 | PF00244 | 0.466 |
LIG_Actin_WH2_2 | 57 | 75 | PF00022 | 0.441 |
LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.551 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.473 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.749 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.470 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.837 |
LIG_GBD_Chelix_1 | 113 | 121 | PF00786 | 0.684 |
LIG_LIR_Gen_1 | 27 | 35 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.471 |
LIG_MYND_1 | 236 | 240 | PF01753 | 0.680 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.417 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.511 |
LIG_SH2_GRB2like | 305 | 308 | PF00017 | 0.668 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.470 |
LIG_SH3_1 | 233 | 239 | PF00018 | 0.623 |
LIG_SH3_2 | 239 | 244 | PF14604 | 0.682 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.679 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.827 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.790 |
LIG_SUMO_SIM_par_1 | 173 | 180 | PF11976 | 0.587 |
LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.469 |
LIG_WW_2 | 236 | 239 | PF00397 | 0.619 |
MOD_CDK_SPK_2 | 251 | 256 | PF00069 | 0.779 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.580 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.820 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.711 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.757 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.716 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.851 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.596 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.474 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.779 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.653 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.465 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.459 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.423 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.720 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.710 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.805 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.447 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.454 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.474 |
MOD_PKA_1 | 80 | 86 | PF00069 | 0.482 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.741 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.458 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.482 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.722 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.426 |
MOD_Plk_2-3 | 143 | 149 | PF00069 | 0.549 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.780 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.461 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.467 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.819 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.754 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.432 |
MOD_SUMO_for_1 | 283 | 286 | PF00179 | 0.574 |
TRG_DiLeu_BaLyEn_6 | 51 | 56 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.443 |
TRG_NLS_Bipartite_1 | 311 | 329 | PF00514 | 0.695 |
TRG_Pf-PMV_PEXEL_1 | 296 | 300 | PF00026 | 0.685 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5I0 | Leishmania donovani | 90% | 100% |
A4HSG9 | Leishmania infantum | 90% | 100% |
E9AKF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |