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: A0A3Q8IDK6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 167 | 171 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.457 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 337 | 339 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.744 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.557 |
DEG_APCC_DBOX_1 | 85 | 93 | PF00400 | 0.577 |
DEG_COP1_1 | 108 | 117 | PF00400 | 0.709 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.733 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.670 |
DOC_CYCLIN_RxL_1 | 196 | 205 | PF00134 | 0.707 |
DOC_CYCLIN_yCln2_LP_2 | 320 | 326 | PF00134 | 0.775 |
DOC_MAPK_gen_1 | 65 | 73 | PF00069 | 0.623 |
DOC_PP1_RVXF_1 | 75 | 82 | PF00149 | 0.539 |
DOC_PP1_RVXF_1 | 88 | 95 | PF00149 | 0.620 |
DOC_PP2B_LxvP_1 | 211 | 214 | PF13499 | 0.586 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.536 |
DOC_PP4_FxxP_1 | 94 | 97 | PF00568 | 0.698 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.665 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 236 | 241 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 345 | 349 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 370 | 374 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 86 | 90 | PF00244 | 0.567 |
LIG_Actin_WH2_1 | 345 | 363 | PF00022 | 0.703 |
LIG_Actin_WH2_2 | 146 | 162 | PF00022 | 0.624 |
LIG_Clathr_ClatBox_1 | 248 | 252 | PF01394 | 0.611 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.683 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.647 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.612 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.457 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.686 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.625 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.647 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.645 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.543 |
LIG_LIR_Apic_2 | 258 | 262 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 185 | 194 | PF02991 | 0.746 |
LIG_LIR_Gen_1 | 353 | 360 | PF02991 | 0.713 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.756 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 321 | 325 | PF02991 | 0.740 |
LIG_LIR_Nem_3 | 353 | 357 | PF02991 | 0.717 |
LIG_PAM2_1 | 200 | 212 | PF00658 | 0.640 |
LIG_RPA_C_Fungi | 63 | 75 | PF08784 | 0.593 |
LIG_SH2_CRK | 198 | 202 | PF00017 | 0.684 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.739 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.725 |
LIG_SH2_STAT3 | 23 | 26 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.495 |
LIG_SH3_1 | 95 | 101 | PF00018 | 0.523 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.736 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.514 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.508 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.700 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.622 |
LIG_SUMO_SIM_par_1 | 264 | 271 | PF11976 | 0.530 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.631 |
LIG_TRAF2_1 | 353 | 356 | PF00917 | 0.734 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.669 |
LIG_TRFH_1 | 209 | 213 | PF08558 | 0.667 |
LIG_TYR_ITIM | 352 | 357 | PF00017 | 0.691 |
MOD_CDK_SPxxK_3 | 338 | 345 | PF00069 | 0.802 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.678 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.697 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.550 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.599 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.746 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.736 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.742 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.547 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.671 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.767 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.554 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.675 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.619 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.653 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.633 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.827 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.771 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.693 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.770 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.691 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.605 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.805 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.639 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.745 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.751 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.584 |
MOD_PK_1 | 236 | 242 | PF00069 | 0.503 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.567 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.732 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.672 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.568 |
MOD_PKB_1 | 338 | 346 | PF00069 | 0.721 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.579 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.451 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.591 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.591 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.546 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.534 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.440 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.771 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.736 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.798 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.717 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.576 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.538 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.624 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.801 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.543 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.618 |
MOD_SUMO_for_1 | 336 | 339 | PF00179 | 0.699 |
MOD_SUMO_rev_2 | 355 | 363 | PF00179 | 0.724 |
TRG_DiLeu_BaEn_1 | 146 | 151 | PF01217 | 0.582 |
TRG_DiLeu_BaEn_4 | 355 | 361 | PF01217 | 0.723 |
TRG_DiLeu_BaEn_4 | 84 | 90 | PF01217 | 0.666 |
TRG_DiLeu_BaLyEn_6 | 196 | 201 | PF01217 | 0.624 |
TRG_DiLeu_BaLyEn_6 | 28 | 33 | PF01217 | 0.566 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.688 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.743 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.732 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.746 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 31 | 35 | PF00026 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 57 | 62 | PF00026 | 0.666 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P503 | Leptomonas seymouri | 39% | 94% |
A4HEN2 | Leishmania braziliensis | 71% | 100% |
A4I1W0 | Leishmania infantum | 100% | 100% |
E9AY05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q9G8 | Leishmania major | 88% | 99% |