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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3S7X5S5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.685 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.556 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.483 |
CLV_PCSK_PC7_1 | 238 | 244 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.587 |
DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.698 |
DOC_CYCLIN_RxL_1 | 313 | 324 | PF00134 | 0.511 |
DOC_MAPK_gen_1 | 242 | 251 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 242 | 250 | PF00069 | 0.468 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.674 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 177 | 187 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 216 | 220 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 223 | 232 | PF00244 | 0.655 |
LIG_AP2alpha_1 | 232 | 236 | PF02296 | 0.470 |
LIG_BRCT_BRCA1_1 | 232 | 236 | PF00533 | 0.690 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.809 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.507 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.761 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.699 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.494 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.563 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.540 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.484 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.753 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.716 |
LIG_LIR_Gen_1 | 229 | 236 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.445 |
LIG_Pex14_2 | 232 | 236 | PF04695 | 0.470 |
LIG_PTAP_UEV_1 | 288 | 293 | PF05743 | 0.658 |
LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.704 |
LIG_SH3_1 | 299 | 305 | PF00018 | 0.621 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.698 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.604 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.736 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.593 |
LIG_SUMO_SIM_anti_2 | 122 | 129 | PF11976 | 0.564 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.595 |
LIG_UBA3_1 | 248 | 254 | PF00899 | 0.468 |
LIG_WW_3 | 305 | 309 | PF00397 | 0.589 |
MOD_CDC14_SPxK_1 | 174 | 177 | PF00782 | 0.602 |
MOD_CDK_SPxK_1 | 171 | 177 | PF00069 | 0.602 |
MOD_CDK_SPxK_1 | 293 | 299 | PF00069 | 0.593 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.654 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.696 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.540 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.678 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.751 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.753 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.670 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.595 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.785 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.590 |
MOD_GlcNHglycan | 168 | 172 | PF01048 | 0.770 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.560 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.689 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.753 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.606 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.358 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.453 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.685 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.768 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.712 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.701 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.697 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.725 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.730 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.438 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.694 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.400 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.613 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.782 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.784 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.510 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.450 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.627 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.510 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.758 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.802 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.456 |
MOD_PKB_1 | 223 | 231 | PF00069 | 0.572 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.402 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.642 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.702 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.682 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.803 |
MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.741 |
MOD_Plk_2-3 | 276 | 282 | PF00069 | 0.583 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.402 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.504 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.612 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.556 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.729 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.673 |
TRG_DiLeu_BaLyEn_6 | 86 | 91 | PF01217 | 0.566 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 278 | 282 | PF00026 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Y8 | Leptomonas seymouri | 46% | 99% |
A4HKL6 | Leishmania braziliensis | 67% | 98% |
A4I848 | Leishmania infantum | 100% | 100% |
E9B306 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q550 | Leishmania major | 93% | 100% |