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: A4HMY2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.794 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.815 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.773 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.665 |
CLV_PCSK_FUR_1 | 351 | 355 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.836 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.773 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.836 |
CLV_PCSK_PC1ET2_1 | 258 | 260 | PF00082 | 0.522 |
CLV_PCSK_PC7_1 | 222 | 228 | PF00082 | 0.831 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.777 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.527 |
DEG_APCC_DBOX_1 | 95 | 103 | PF00400 | 0.587 |
DEG_Kelch_Keap1_1 | 271 | 276 | PF01344 | 0.539 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.562 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.697 |
DOC_CYCLIN_RxL_1 | 84 | 95 | PF00134 | 0.671 |
DOC_MAPK_gen_1 | 182 | 190 | PF00069 | 0.667 |
DOC_MAPK_gen_1 | 240 | 250 | PF00069 | 0.818 |
DOC_PP1_RVXF_1 | 85 | 92 | PF00149 | 0.579 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.793 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.583 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.777 |
LIG_14-3-3_CanoR_1 | 103 | 113 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 18 | 26 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 182 | 190 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 30 | 37 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 351 | 360 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.776 |
LIG_14-3-3_CanoR_1 | 47 | 57 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.565 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.616 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.404 |
LIG_deltaCOP1_diTrp_1 | 301 | 311 | PF00928 | 0.671 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.476 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.772 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.526 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.772 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.677 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.733 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.617 |
LIG_LIR_Gen_1 | 125 | 134 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.549 |
LIG_Pex14_2 | 128 | 132 | PF04695 | 0.565 |
LIG_RPA_C_Fungi | 82 | 94 | PF08784 | 0.634 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.538 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.772 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.683 |
LIG_SH2_NCK_1 | 124 | 128 | PF00017 | 0.425 |
LIG_SH2_SRC | 124 | 127 | PF00017 | 0.431 |
LIG_SUMO_SIM_par_1 | 116 | 122 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 195 | 203 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 209 | 216 | PF11976 | 0.645 |
LIG_TYR_ITIM | 358 | 363 | PF00017 | 0.590 |
LIG_WW_3 | 237 | 241 | PF00397 | 0.551 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.739 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.743 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.661 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.688 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.709 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.539 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.609 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.775 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.727 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.662 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.604 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.513 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.737 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.589 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.775 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.478 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.732 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.721 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.751 |
MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.651 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.590 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.650 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.777 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.748 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.583 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.658 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.547 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.714 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.661 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.692 |
MOD_PK_1 | 105 | 111 | PF00069 | 0.702 |
MOD_PK_1 | 244 | 250 | PF00069 | 0.548 |
MOD_PKA_1 | 182 | 188 | PF00069 | 0.775 |
MOD_PKA_1 | 226 | 232 | PF00069 | 0.570 |
MOD_PKA_1 | 352 | 358 | PF00069 | 0.787 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.574 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.613 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.647 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.775 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.653 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.519 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.695 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.574 |
MOD_PKB_1 | 103 | 111 | PF00069 | 0.708 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.650 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.647 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.512 |
MOD_Plk_2-3 | 151 | 157 | PF00069 | 0.468 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.671 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.515 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.627 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.779 |
MOD_SUMO_rev_2 | 146 | 155 | PF00179 | 0.739 |
MOD_SUMO_rev_2 | 203 | 210 | PF00179 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 336 | 341 | PF01217 | 0.775 |
TRG_DiLeu_BaLyEn_6 | 359 | 364 | PF01217 | 0.685 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.772 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.692 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.776 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.671 |
TRG_NES_CRM1_1 | 65 | 78 | PF08389 | 0.488 |
TRG_NLS_Bipartite_1 | 226 | 244 | PF00514 | 0.560 |
TRG_NLS_MonoExtC_3 | 239 | 244 | PF00514 | 0.550 |
TRG_NLS_MonoExtN_4 | 238 | 244 | PF00514 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 362 | 367 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5S0 | Leptomonas seymouri | 42% | 73% |
A0A3S7X9K7 | Leishmania donovani | 72% | 74% |
A4IBK6 | Leishmania infantum | 72% | 74% |
E9AFD9 | Leishmania major | 73% | 100% |
E9B6J4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 74% |