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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q7X3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.618 |
CLV_PCSK_FUR_1 | 55 | 59 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.671 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.696 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.533 |
DEG_APCC_DBOX_1 | 207 | 215 | PF00400 | 0.627 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.557 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.654 |
DEG_SCF_FBW7_1 | 362 | 369 | PF00400 | 0.578 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 180 | 184 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 189 | 193 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 299 | 305 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 66 | 72 | PF00244 | 0.589 |
LIG_Actin_WH2_2 | 102 | 120 | PF00022 | 0.621 |
LIG_Actin_WH2_2 | 214 | 230 | PF00022 | 0.562 |
LIG_APCC_ABBA_1 | 214 | 219 | PF00400 | 0.565 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.686 |
LIG_BIR_III_2 | 219 | 223 | PF00653 | 0.560 |
LIG_BIR_III_4 | 357 | 361 | PF00653 | 0.677 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.525 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.502 |
LIG_Clathr_ClatBox_1 | 146 | 150 | PF01394 | 0.510 |
LIG_Clathr_ClatBox_1 | 172 | 176 | PF01394 | 0.567 |
LIG_deltaCOP1_diTrp_1 | 200 | 210 | PF00928 | 0.632 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.570 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.488 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.638 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.605 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.547 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.618 |
LIG_LIR_Gen_1 | 142 | 151 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 2 | 13 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 233 | 242 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 322 | 328 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 69 | 78 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 142 | 146 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 233 | 237 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 303 | 307 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.566 |
LIG_RPA_C_Fungi | 46 | 58 | PF08784 | 0.705 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.482 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.553 |
LIG_SH2_NCK_1 | 187 | 191 | PF00017 | 0.562 |
LIG_SH2_NCK_1 | 293 | 297 | PF00017 | 0.642 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.603 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.685 |
LIG_SH2_STAP1 | 78 | 82 | PF00017 | 0.630 |
LIG_SH2_STAT3 | 317 | 320 | PF00017 | 0.522 |
LIG_SH2_STAT3 | 34 | 37 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.534 |
LIG_SH3_1 | 118 | 124 | PF00018 | 0.668 |
LIG_SH3_2 | 121 | 126 | PF14604 | 0.713 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.653 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.742 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 129 | 136 | PF11976 | 0.654 |
LIG_SUMO_SIM_par_1 | 145 | 150 | PF11976 | 0.516 |
LIG_TYR_ITIM | 291 | 296 | PF00017 | 0.622 |
LIG_UBA3_1 | 146 | 152 | PF00899 | 0.482 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.513 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.436 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.616 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.610 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.538 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.651 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.705 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.551 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.615 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.603 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.389 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.647 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.605 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.685 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.595 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.702 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.578 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.448 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.655 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.613 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.693 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.486 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.603 |
MOD_NEK2_2 | 161 | 166 | PF00069 | 0.518 |
MOD_NEK2_2 | 67 | 72 | PF00069 | 0.424 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.563 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.555 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.564 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.573 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.555 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.584 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.606 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.520 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.619 |
MOD_Plk_2-3 | 263 | 269 | PF00069 | 0.596 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.506 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.502 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.643 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.585 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.807 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.641 |
MOD_SUMO_rev_2 | 145 | 154 | PF00179 | 0.520 |
TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.525 |
TRG_DiLeu_BaEn_2 | 149 | 155 | PF01217 | 0.602 |
TRG_DiLeu_BaEn_2 | 205 | 211 | PF01217 | 0.422 |
TRG_DiLeu_BaEn_2 | 305 | 311 | PF01217 | 0.631 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.691 |
TRG_NLS_Bipartite_1 | 98 | 119 | PF00514 | 0.553 |
TRG_NLS_MonoExtN_4 | 112 | 119 | PF00514 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5J9 | Leptomonas seymouri | 48% | 100% |
A0A3S7X1Y7 | Leishmania donovani | 92% | 100% |
A4HGZ2 | Leishmania braziliensis | 72% | 93% |
A4I424 | Leishmania infantum | 91% | 100% |
E9B0B1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5B930 | Trypanosoma cruzi | 24% | 100% |