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: E9AL14
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.684 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.714 |
CLV_PCSK_FUR_1 | 299 | 303 | PF00082 | 0.805 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.743 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.555 |
CLV_Separin_Metazoa | 215 | 219 | PF03568 | 0.506 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.513 |
DEG_APCC_DBOX_1 | 213 | 221 | PF00400 | 0.690 |
DEG_APCC_DBOX_1 | 76 | 84 | PF00400 | 0.429 |
DOC_ANK_TNKS_1 | 168 | 175 | PF00023 | 0.440 |
DOC_CKS1_1 | 181 | 186 | PF01111 | 0.715 |
DOC_CYCLIN_RxL_1 | 74 | 81 | PF00134 | 0.452 |
DOC_MAPK_gen_1 | 102 | 112 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 149 | 157 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 298 | 308 | PF00069 | 0.651 |
DOC_MAPK_MEF2A_6 | 105 | 114 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 299 | 308 | PF00069 | 0.685 |
DOC_PP1_RVXF_1 | 130 | 136 | PF00149 | 0.486 |
DOC_PP1_RVXF_1 | 216 | 223 | PF00149 | 0.606 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.675 |
DOC_USP7_UBL2_3 | 196 | 200 | PF12436 | 0.507 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 100 | 107 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 118 | 122 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.699 |
LIG_Actin_WH2_2 | 103 | 120 | PF00022 | 0.586 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.560 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.416 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.592 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.737 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.811 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.582 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.342 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.583 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.734 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.709 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.611 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.432 |
LIG_Integrin_RGD_1 | 244 | 246 | PF01839 | 0.485 |
LIG_NRBOX | 85 | 91 | PF00104 | 0.536 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.578 |
LIG_SH3_2 | 309 | 314 | PF14604 | 0.704 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.440 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.803 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.645 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.803 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.722 |
LIG_SUMO_SIM_par_1 | 289 | 295 | PF11976 | 0.684 |
LIG_SUMO_SIM_par_1 | 81 | 88 | PF11976 | 0.325 |
LIG_SxIP_EBH_1 | 227 | 240 | PF03271 | 0.744 |
LIG_UBA3_1 | 290 | 298 | PF00899 | 0.676 |
MOD_CDC14_SPxK_1 | 295 | 298 | PF00782 | 0.676 |
MOD_CDC14_SPxK_1 | 311 | 314 | PF00782 | 0.708 |
MOD_CDK_SPxK_1 | 292 | 298 | PF00069 | 0.676 |
MOD_CDK_SPxK_1 | 308 | 314 | PF00069 | 0.703 |
MOD_CDK_SPxxK_3 | 292 | 299 | PF00069 | 0.678 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.652 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.644 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.810 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.629 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.495 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.487 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.727 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.692 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.630 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.431 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.656 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.672 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.649 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.789 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.551 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.665 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.456 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.585 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.657 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.799 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.709 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.615 |
MOD_LATS_1 | 300 | 306 | PF00433 | 0.520 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.737 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.534 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.479 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.644 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.609 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.592 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.449 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.511 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.581 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.724 |
MOD_PKB_1 | 98 | 106 | PF00069 | 0.609 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.652 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.812 |
MOD_Plk_2-3 | 22 | 28 | PF00069 | 0.552 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.566 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.602 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.469 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.711 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.674 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.787 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.555 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.703 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.607 |
MOD_SUMO_rev_2 | 195 | 202 | PF00179 | 0.798 |
TRG_DiLeu_BaEn_1 | 57 | 62 | PF01217 | 0.591 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.457 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.700 |
TRG_NLS_Bipartite_1 | 227 | 245 | PF00514 | 0.751 |
TRG_NLS_MonoCore_2 | 240 | 245 | PF00514 | 0.768 |
TRG_NLS_MonoExtC_3 | 240 | 246 | PF00514 | 0.772 |
TRG_NLS_MonoExtC_3 | 297 | 302 | PF00514 | 0.693 |
TRG_NLS_MonoExtN_4 | 296 | 302 | PF00514 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 289 | 294 | PF00026 | 0.702 |
TRG_Pf-PMV_PEXEL_1 | 302 | 307 | PF00026 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZD5 | Leptomonas seymouri | 40% | 100% |
A0A3S7WPQ1 | Leishmania donovani | 86% | 100% |
A4H4U7 | Leishmania braziliensis | 74% | 99% |
A4HT26 | Leishmania infantum | 87% | 100% |
Q4QIU0 | Leishmania major | 88% | 99% |