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: A4HS10
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.539 |
CLV_PCSK_FUR_1 | 149 | 153 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 182 | 184 | PF00082 | 0.602 |
CLV_PCSK_PC7_1 | 178 | 184 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.681 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.534 |
DEG_APCC_KENBOX_2 | 66 | 70 | PF00400 | 0.506 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.618 |
DEG_SCF_FBW7_1 | 188 | 193 | PF00400 | 0.647 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 404 | 414 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 420 | 426 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 197 | 205 | PF00069 | 0.629 |
DOC_PP2B_PxIxI_1 | 200 | 206 | PF00149 | 0.628 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.527 |
DOC_USP7_UBL2_3 | 67 | 71 | PF12436 | 0.502 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 353 | 357 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.589 |
LIG_Actin_WH2_2 | 213 | 228 | PF00022 | 0.621 |
LIG_Actin_WH2_2 | 389 | 406 | PF00022 | 0.464 |
LIG_BIR_III_2 | 21 | 25 | PF00653 | 0.586 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.519 |
LIG_eIF4E_1 | 115 | 121 | PF01652 | 0.544 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.568 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.560 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.427 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.407 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.574 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.692 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.584 |
LIG_GBD_Chelix_1 | 281 | 289 | PF00786 | 0.443 |
LIG_HCF-1_HBM_1 | 212 | 215 | PF13415 | 0.541 |
LIG_LIR_Gen_1 | 110 | 121 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 413 | 417 | PF02991 | 0.339 |
LIG_SH2_CRK | 328 | 332 | PF00017 | 0.357 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.533 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.444 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.614 |
LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.572 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.651 |
LIG_TYR_ITIM | 81 | 86 | PF00017 | 0.474 |
MOD_CDK_SPK_2 | 192 | 197 | PF00069 | 0.531 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.679 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.635 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.540 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.533 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.435 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.582 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.667 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.608 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.503 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.736 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.699 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.653 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.622 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.551 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.362 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.591 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.655 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.612 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.752 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.577 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.673 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.574 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.483 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.609 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.353 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.584 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.519 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.581 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.395 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.479 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.424 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.526 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.562 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.600 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.628 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.607 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.615 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.567 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.483 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.602 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.602 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.570 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.642 |
MOD_PKB_1 | 59 | 67 | PF00069 | 0.530 |
MOD_Plk_2-3 | 252 | 258 | PF00069 | 0.576 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.572 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.462 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.388 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.475 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.577 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.711 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.523 |
TRG_DiLeu_BaEn_4 | 211 | 217 | PF01217 | 0.566 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 326 | 331 | PF01217 | 0.422 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.506 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.537 |
TRG_ER_FFAT_2 | 169 | 177 | PF00635 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 9 | 13 | PF00026 | 0.602 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVL6 | Leptomonas seymouri | 35% | 100% |
A0A3S5H580 | Leishmania donovani | 99% | 100% |
A4H3T5 | Leishmania braziliensis | 60% | 100% |
E9ACP7 | Leishmania major | 89% | 100% |
E9AJZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |