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: A0A3S5H580
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.798 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.625 |
CLV_PCSK_FUR_1 | 149 | 153 | PF00082 | 0.760 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.798 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 182 | 184 | PF00082 | 0.702 |
CLV_PCSK_PC7_1 | 178 | 184 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.736 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.814 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.682 |
DEG_APCC_KENBOX_2 | 66 | 70 | PF00400 | 0.641 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.717 |
DEG_SCF_FBW7_1 | 188 | 193 | PF00400 | 0.749 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 404 | 414 | PF00069 | 0.629 |
DOC_MAPK_gen_1 | 420 | 426 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 197 | 205 | PF00069 | 0.721 |
DOC_PP2B_PxIxI_1 | 200 | 206 | PF00149 | 0.717 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.619 |
DOC_USP7_MATH_2 | 190 | 196 | PF00917 | 0.578 |
DOC_USP7_UBL2_3 | 67 | 71 | PF12436 | 0.639 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.798 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.648 |
LIG_14-3-3_CanoR_1 | 353 | 357 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.691 |
LIG_Actin_WH2_2 | 213 | 228 | PF00022 | 0.727 |
LIG_Actin_WH2_2 | 389 | 406 | PF00022 | 0.618 |
LIG_BIR_III_2 | 21 | 25 | PF00653 | 0.695 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.579 |
LIG_eIF4E_1 | 115 | 121 | PF01652 | 0.670 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.675 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.598 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.545 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.529 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.658 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.830 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.643 |
LIG_GBD_Chelix_1 | 281 | 289 | PF00786 | 0.563 |
LIG_HCF-1_HBM_1 | 212 | 215 | PF13415 | 0.598 |
LIG_LIR_Gen_1 | 110 | 121 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.774 |
LIG_LIR_Nem_3 | 413 | 417 | PF02991 | 0.453 |
LIG_SH2_CRK | 328 | 332 | PF00017 | 0.471 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.734 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.654 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.592 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.725 |
LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.679 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.754 |
LIG_TYR_ITIM | 81 | 86 | PF00017 | 0.581 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.760 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.679 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.656 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.663 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.553 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.689 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.765 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.726 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.639 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.747 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.747 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.777 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.782 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.623 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.403 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.700 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.687 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.747 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.780 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.699 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.768 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.719 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.620 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.707 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.376 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.707 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.654 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.781 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.683 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.447 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.588 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.528 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.600 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.610 |
MOD_PKA_1 | 28 | 34 | PF00069 | 0.639 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.711 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.744 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.679 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.639 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.686 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.621 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.718 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.737 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.683 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.705 |
MOD_PKB_1 | 59 | 67 | PF00069 | 0.676 |
MOD_Plk_2-3 | 252 | 258 | PF00069 | 0.690 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.674 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.582 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.499 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.630 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.697 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.802 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.640 |
TRG_DiLeu_BaEn_4 | 211 | 217 | PF01217 | 0.636 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.598 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.679 |
TRG_DiLeu_BaLyEn_6 | 326 | 331 | PF01217 | 0.573 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.560 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.819 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.806 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.616 |
TRG_ER_FFAT_2 | 169 | 177 | PF00635 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 9 | 13 | PF00026 | 0.679 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVL6 | Leptomonas seymouri | 35% | 100% |
A4H3T5 | Leishmania braziliensis | 61% | 100% |
A4HS10 | Leishmania infantum | 99% | 100% |
E9ACP7 | Leishmania major | 89% | 100% |
E9AJZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |