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: E9AT29
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.654 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.561 |
DEG_APCC_DBOX_1 | 201 | 209 | PF00400 | 0.523 |
DOC_CYCLIN_RxL_1 | 199 | 209 | PF00134 | 0.521 |
DOC_CYCLIN_RxL_1 | 290 | 302 | PF00134 | 0.634 |
DOC_CYCLIN_RxL_1 | 339 | 348 | PF00134 | 0.599 |
DOC_CYCLIN_yCln2_LP_2 | 187 | 193 | PF00134 | 0.685 |
DOC_CYCLIN_yCln2_LP_2 | 59 | 65 | PF00134 | 0.505 |
DOC_MAPK_DCC_7 | 188 | 198 | PF00069 | 0.649 |
DOC_MAPK_gen_1 | 88 | 97 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 91 | 99 | PF00069 | 0.374 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.701 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.426 |
DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.478 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.553 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.432 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 148 | 152 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 9 | 17 | PF00244 | 0.390 |
LIG_CtBP_PxDLS_1 | 315 | 319 | PF00389 | 0.535 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.412 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.370 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.548 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.511 |
LIG_LIR_Apic_2 | 26 | 31 | PF02991 | 0.355 |
LIG_LIR_Apic_2 | 322 | 328 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 15 | 25 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 37 | 45 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 75 | 86 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.364 |
LIG_NRP_CendR_1 | 349 | 350 | PF00754 | 0.633 |
LIG_Pex14_2 | 24 | 28 | PF04695 | 0.457 |
LIG_Pex14_2 | 39 | 43 | PF04695 | 0.408 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 102 | 105 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 266 | 269 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.404 |
LIG_SH3_1 | 108 | 114 | PF00018 | 0.620 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.701 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.635 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.634 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.505 |
LIG_SUMO_SIM_par_1 | 194 | 199 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 68 | 76 | PF11976 | 0.462 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.665 |
LIG_WRC_WIRS_1 | 90 | 95 | PF05994 | 0.347 |
LIG_WW_3 | 137 | 141 | PF00397 | 0.503 |
MOD_CDK_SPxxK_3 | 289 | 296 | PF00069 | 0.596 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.647 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.520 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.312 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.671 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.492 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.491 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.508 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.406 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.499 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.416 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.712 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.714 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.634 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.688 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.715 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.464 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.584 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.516 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.625 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.385 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.644 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.630 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.704 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.653 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.496 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.504 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.370 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.601 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.473 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.673 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.649 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.633 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.528 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.601 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.424 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.384 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.386 |
MOD_NEK2_2 | 320 | 325 | PF00069 | 0.547 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.472 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.634 |
MOD_PKA_1 | 256 | 262 | PF00069 | 0.579 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.634 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.492 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.500 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.579 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.481 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.508 |
MOD_Plk_2-3 | 32 | 38 | PF00069 | 0.433 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.652 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.576 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.386 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.689 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.592 |
MOD_SUMO_rev_2 | 245 | 252 | PF00179 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 199 | 204 | PF01217 | 0.592 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.605 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.507 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.598 |
TRG_NES_CRM1_1 | 19 | 32 | PF08389 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 343 | 348 | PF00026 | 0.607 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y4 | Leptomonas seymouri | 47% | 100% |
A0A3S7XB07 | Leishmania donovani | 90% | 100% |
A4HPB8 | Leishmania braziliensis | 79% | 100% |
A4ICF8 | Leishmania infantum | 90% | 100% |
Q4Q1G9 | Leishmania major | 90% | 100% |