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: Q4QFX6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.813 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.689 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.839 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 207 | 209 | PF00082 | 0.633 |
CLV_PCSK_PC7_1 | 255 | 261 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.602 |
CLV_Separin_Metazoa | 116 | 120 | PF03568 | 0.527 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.536 |
DOC_CYCLIN_yCln2_LP_2 | 329 | 335 | PF00134 | 0.558 |
DOC_CYCLIN_yCln2_LP_2 | 61 | 67 | PF00134 | 0.521 |
DOC_MAPK_gen_1 | 162 | 172 | PF00069 | 0.738 |
DOC_MAPK_gen_1 | 197 | 203 | PF00069 | 0.658 |
DOC_MAPK_gen_1 | 34 | 43 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 163 | 172 | PF00069 | 0.735 |
DOC_MAPK_MEF2A_6 | 368 | 375 | PF00069 | 0.573 |
DOC_MAPK_NFAT4_5 | 368 | 376 | PF00069 | 0.577 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.532 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.837 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.818 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.643 |
DOC_USP7_UBL2_3 | 144 | 148 | PF12436 | 0.746 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 106 | 110 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 223 | 231 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 259 | 267 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.828 |
LIG_14-3-3_CanoR_1 | 361 | 371 | PF00244 | 0.647 |
LIG_Actin_WH2_2 | 103 | 121 | PF00022 | 0.582 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.663 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.764 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.704 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.745 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.783 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.732 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.655 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.732 |
LIG_LIR_Apic_2 | 289 | 295 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 102 | 110 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 18 | 29 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 213 | 220 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 30 | 38 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 82 | 90 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.623 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.542 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.524 |
LIG_SH3_1 | 162 | 168 | PF00018 | 0.741 |
LIG_SH3_1 | 292 | 298 | PF00018 | 0.543 |
LIG_SH3_2 | 295 | 300 | PF14604 | 0.631 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.755 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.602 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.707 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.702 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.631 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.474 |
LIG_SH3_4 | 146 | 153 | PF00018 | 0.747 |
LIG_TRAF2_1 | 266 | 269 | PF00917 | 0.712 |
MOD_CDC14_SPxK_1 | 297 | 300 | PF00782 | 0.556 |
MOD_CDK_SPxK_1 | 294 | 300 | PF00069 | 0.548 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.585 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.726 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.712 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.685 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.802 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.634 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.550 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.778 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.593 |
MOD_Cter_Amidation | 122 | 125 | PF01082 | 0.532 |
MOD_DYRK1A_RPxSP_1 | 276 | 280 | PF00069 | 0.748 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.792 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.609 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.774 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.782 |
MOD_GlcNHglycan | 325 | 329 | PF01048 | 0.676 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.662 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.651 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.482 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.713 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.710 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.692 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.816 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.840 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.621 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.479 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.612 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.706 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.630 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.663 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.705 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.786 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.724 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.544 |
MOD_NEK2_2 | 312 | 317 | PF00069 | 0.818 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.638 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.666 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.798 |
MOD_PKA_1 | 259 | 265 | PF00069 | 0.636 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.606 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.632 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.758 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.656 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.717 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.543 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.612 |
MOD_PKB_1 | 259 | 267 | PF00069 | 0.726 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.478 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.795 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.602 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.606 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.398 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.788 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.555 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.716 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.653 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.813 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.691 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 281 | 286 | PF01217 | 0.710 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.777 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.608 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.829 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 348 | 352 | PF00026 | 0.676 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB18 | Leptomonas seymouri | 50% | 97% |
A0A3S7WSS6 | Leishmania donovani | 94% | 100% |
A4H7H0 | Leishmania braziliensis | 73% | 100% |
A4HVV1 | Leishmania infantum | 94% | 100% |
E9APK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |