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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HNY2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.674 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.516 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.519 |
DEG_SCF_FBW7_1 | 7 | 13 | PF00400 | 0.520 |
DEG_SPOP_SBC_1 | 105 | 109 | PF00917 | 0.526 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.835 |
DOC_CKS1_1 | 7 | 12 | PF01111 | 0.572 |
DOC_CYCLIN_RxL_1 | 285 | 294 | PF00134 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 320 | 326 | PF00134 | 0.520 |
DOC_MAPK_gen_1 | 240 | 250 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 243 | 250 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 6 | 14 | PF00069 | 0.520 |
DOC_MAPK_RevD_3 | 281 | 296 | PF00069 | 0.560 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.810 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.794 |
LIG_14-3-3_CanoR_1 | 173 | 177 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 261 | 270 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 288 | 293 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 41 | 51 | PF00244 | 0.645 |
LIG_Actin_WH2_2 | 157 | 175 | PF00022 | 0.460 |
LIG_APCC_ABBA_1 | 81 | 86 | PF00400 | 0.530 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.765 |
LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.584 |
LIG_deltaCOP1_diTrp_1 | 330 | 337 | PF00928 | 0.525 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.554 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.697 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.526 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.410 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.505 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.508 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.539 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.574 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.548 |
LIG_IRF3_LxIS_1 | 168 | 175 | PF10401 | 0.441 |
LIG_IRF3_LxIS_1 | 8 | 15 | PF10401 | 0.519 |
LIG_LIR_Gen_1 | 158 | 168 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 169 | 176 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 9 | 18 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 9 | 14 | PF02991 | 0.687 |
LIG_MYND_3 | 82 | 86 | PF01753 | 0.529 |
LIG_Pex14_2 | 277 | 281 | PF04695 | 0.549 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.715 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.518 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.795 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.543 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.569 |
LIG_SUMO_SIM_anti_2 | 78 | 83 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 246 | 251 | PF11976 | 0.512 |
LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.497 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.519 |
LIG_WW_3 | 285 | 289 | PF00397 | 0.549 |
MOD_CDK_SPK_2 | 238 | 243 | PF00069 | 0.542 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.721 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.727 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.562 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.526 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.513 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.523 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.582 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.636 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.546 |
MOD_DYRK1A_RPxSP_1 | 6 | 10 | PF00069 | 0.516 |
MOD_GlcNHglycan | 148 | 152 | PF01048 | 0.591 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.749 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.649 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.834 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.759 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.547 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.505 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.498 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.678 |
MOD_LATS_1 | 219 | 225 | PF00433 | 0.442 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.784 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.566 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.717 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.527 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.700 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.534 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.470 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.477 |
MOD_NEK2_2 | 44 | 49 | PF00069 | 0.545 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.533 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.766 |
MOD_PK_1 | 221 | 227 | PF00069 | 0.458 |
MOD_PK_1 | 77 | 83 | PF00069 | 0.525 |
MOD_PKA_1 | 261 | 267 | PF00069 | 0.521 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.535 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.452 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.521 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.597 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.731 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.742 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.458 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.518 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.525 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.672 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.746 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.542 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.526 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.567 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.590 |
MOD_SUMO_rev_2 | 249 | 259 | PF00179 | 0.501 |
TRG_DiLeu_BaEn_1 | 92 | 97 | PF01217 | 0.529 |
TRG_DiLeu_BaEn_2 | 217 | 223 | PF01217 | 0.703 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.715 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.760 |
TRG_ER_diArg_1 | 202 | 204 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 288 | 293 | PF00026 | 0.567 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAI1 | Leishmania donovani | 53% | 69% |
A4ICL2 | Leishmania infantum | 53% | 69% |
E9ASP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 68% |
Q4Q1V4 | Leishmania major | 51% | 69% |