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: A0A3S7WPQ1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.613 |
CLV_PCSK_FUR_1 | 297 | 301 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.348 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.428 |
DEG_APCC_DBOX_1 | 211 | 219 | PF00400 | 0.583 |
DEG_APCC_DBOX_1 | 76 | 84 | PF00400 | 0.343 |
DEG_SPOP_SBC_1 | 168 | 172 | PF00917 | 0.463 |
DOC_CKS1_1 | 177 | 182 | PF01111 | 0.635 |
DOC_CYCLIN_RxL_1 | 74 | 84 | PF00134 | 0.353 |
DOC_MAPK_gen_1 | 102 | 112 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 149 | 157 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 296 | 306 | PF00069 | 0.607 |
DOC_MAPK_gen_1 | 53 | 62 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 105 | 114 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 297 | 306 | PF00069 | 0.587 |
DOC_PP1_RVXF_1 | 130 | 136 | PF00149 | 0.405 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.710 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 118 | 122 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 225 | 235 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 299 | 305 | PF00244 | 0.599 |
LIG_Actin_WH2_2 | 103 | 120 | PF00022 | 0.473 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.478 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.380 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.499 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.571 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.616 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.696 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.560 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.433 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.360 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.506 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.617 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.640 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.343 |
LIG_NRBOX | 85 | 91 | PF00104 | 0.432 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.532 |
LIG_SH3_2 | 307 | 312 | PF14604 | 0.615 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.739 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.612 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.803 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.625 |
LIG_SH3_CIN85_PxpxPR_1 | 180 | 185 | PF14604 | 0.555 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.610 |
LIG_SxIP_EBH_1 | 225 | 238 | PF03271 | 0.625 |
LIG_UBA3_1 | 288 | 296 | PF00899 | 0.573 |
MOD_CDC14_SPxK_1 | 293 | 296 | PF00782 | 0.577 |
MOD_CDC14_SPxK_1 | 309 | 312 | PF00782 | 0.619 |
MOD_CDK_SPxK_1 | 290 | 296 | PF00069 | 0.574 |
MOD_CDK_SPxK_1 | 306 | 312 | PF00069 | 0.614 |
MOD_CDK_SPxxK_3 | 178 | 185 | PF00069 | 0.552 |
MOD_CDK_SPxxK_3 | 290 | 297 | PF00069 | 0.577 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.612 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.766 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.636 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.422 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.444 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.598 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.562 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.343 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.568 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.582 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.395 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.648 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.367 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.481 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.728 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.556 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.646 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.639 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.605 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.646 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.392 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.544 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.528 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.392 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.442 |
MOD_PKA_1 | 197 | 203 | PF00069 | 0.552 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.478 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.672 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.536 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.468 |
MOD_PKB_1 | 240 | 248 | PF00069 | 0.590 |
MOD_PKB_1 | 298 | 306 | PF00069 | 0.670 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.544 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.598 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.697 |
MOD_Plk_2-3 | 22 | 28 | PF00069 | 0.476 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.460 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.529 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.388 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.636 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.602 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.680 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.517 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.693 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.504 |
MOD_SUMO_rev_2 | 193 | 200 | PF00179 | 0.691 |
TRG_DiLeu_BaEn_1 | 57 | 62 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.372 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.602 |
TRG_NLS_Bipartite_1 | 225 | 243 | PF00514 | 0.633 |
TRG_NLS_MonoCore_2 | 238 | 243 | PF00514 | 0.651 |
TRG_NLS_MonoCore_2 | 295 | 300 | PF00514 | 0.585 |
TRG_NLS_MonoExtC_3 | 238 | 244 | PF00514 | 0.652 |
TRG_NLS_MonoExtC_3 | 295 | 300 | PF00514 | 0.595 |
TRG_NLS_MonoExtN_4 | 294 | 300 | PF00514 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 300 | 305 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZD5 | Leptomonas seymouri | 40% | 100% |
A4H4U7 | Leishmania braziliensis | 73% | 100% |
A4HT26 | Leishmania infantum | 100% | 100% |
E9AL14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QIU0 | Leishmania major | 90% | 100% |