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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AV24
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.741 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.803 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.838 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.528 |
CLV_PCSK_FUR_1 | 336 | 340 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.837 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.837 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.781 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.846 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.813 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.698 |
DEG_APCC_DBOX_1 | 87 | 95 | PF00400 | 0.578 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.705 |
DEG_SCF_FBW7_1 | 294 | 300 | PF00400 | 0.619 |
DOC_CKS1_1 | 294 | 299 | PF01111 | 0.556 |
DOC_CYCLIN_RxL_1 | 233 | 243 | PF00134 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 142 | 148 | PF00134 | 0.555 |
DOC_CYCLIN_yCln2_LP_2 | 383 | 389 | PF00134 | 0.475 |
DOC_MAPK_DCC_7 | 141 | 150 | PF00069 | 0.646 |
DOC_MAPK_MEF2A_6 | 141 | 150 | PF00069 | 0.533 |
DOC_MAPK_RevD_3 | 148 | 164 | PF00069 | 0.629 |
DOC_PP2B_LxvP_1 | 142 | 145 | PF13499 | 0.554 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.698 |
DOC_PP2B_LxvP_1 | 383 | 386 | PF13499 | 0.637 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.806 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.735 |
DOC_USP7_UBL2_3 | 402 | 406 | PF12436 | 0.823 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 224 | 232 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 267 | 277 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 306 | 314 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 403 | 409 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.619 |
LIG_Actin_WH2_2 | 196 | 212 | PF00022 | 0.513 |
LIG_Clathr_ClatBox_1 | 68 | 72 | PF01394 | 0.630 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.481 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.624 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.788 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.496 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.426 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.678 |
LIG_LIR_Gen_1 | 154 | 162 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 366 | 376 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 366 | 371 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 418 | 422 | PF02991 | 0.552 |
LIG_PCNA_yPIPBox_3 | 406 | 420 | PF02747 | 0.718 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.602 |
LIG_SH3_2 | 294 | 299 | PF14604 | 0.556 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.589 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.541 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.742 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.557 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.634 |
LIG_TRAF2_1 | 36 | 39 | PF00917 | 0.541 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.540 |
LIG_TYR_ITIM | 115 | 120 | PF00017 | 0.651 |
LIG_WW_3 | 160 | 164 | PF00397 | 0.657 |
LIG_WW_3 | 179 | 183 | PF00397 | 0.416 |
LIG_WW_3 | 296 | 300 | PF00397 | 0.558 |
MOD_CDK_SPK_2 | 331 | 336 | PF00069 | 0.640 |
MOD_CDK_SPxK_1 | 293 | 299 | PF00069 | 0.558 |
MOD_CDK_SPxxK_3 | 247 | 254 | PF00069 | 0.633 |
MOD_CDK_SPxxK_3 | 331 | 338 | PF00069 | 0.532 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.554 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.480 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.570 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.803 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.734 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.676 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.673 |
MOD_Cter_Amidation | 265 | 268 | PF01082 | 0.551 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.477 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.503 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.826 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.783 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.588 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.602 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.534 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.842 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.764 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.713 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.758 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.616 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.801 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.725 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.833 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.831 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.701 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.555 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.671 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.602 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.665 |
MOD_LATS_1 | 90 | 96 | PF00433 | 0.692 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.774 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.595 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.612 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.812 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.491 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.589 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.849 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.803 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.576 |
MOD_PKA_1 | 267 | 273 | PF00069 | 0.719 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.726 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.738 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.732 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.552 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.577 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.596 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.653 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.588 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.748 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.737 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.714 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.704 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.642 |
MOD_SUMO_rev_2 | 185 | 191 | PF00179 | 0.597 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.637 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.796 |
TRG_ER_diArg_1 | 52 | 54 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.522 |
TRG_NLS_MonoExtC_3 | 428 | 433 | PF00514 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0U2 | Leptomonas seymouri | 44% | 100% |
A0A3S7WWD6 | Leishmania donovani | 87% | 100% |
A4HBQ4 | Leishmania braziliensis | 77% | 100% |
A4HZ56 | Leishmania infantum | 87% | 100% |
Q4QCF8 | Leishmania major | 86% | 100% |