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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q6S6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.762 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.550 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.753 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.623 |
DOC_CKS1_1 | 288 | 293 | PF01111 | 0.749 |
DOC_CKS1_1 | 294 | 299 | PF01111 | 0.639 |
DOC_CYCLIN_yCln2_LP_2 | 294 | 300 | PF00134 | 0.739 |
DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 77 | 85 | PF00069 | 0.583 |
DOC_PP2B_LxvP_1 | 66 | 69 | PF13499 | 0.725 |
DOC_PP4_FxxP_1 | 156 | 159 | PF00568 | 0.717 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.613 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.733 |
DOC_PP4_FxxP_1 | 244 | 247 | PF00568 | 0.795 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.734 |
DOC_USP7_MATH_2 | 159 | 165 | PF00917 | 0.789 |
DOC_USP7_UBL2_3 | 218 | 222 | PF12436 | 0.742 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.751 |
LIG_14-3-3_CanoR_1 | 226 | 230 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 24 | 31 | PF00244 | 0.666 |
LIG_Actin_WH2_2 | 210 | 228 | PF00022 | 0.537 |
LIG_APCC_ABBA_1 | 196 | 201 | PF00400 | 0.622 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.780 |
LIG_deltaCOP1_diTrp_1 | 201 | 211 | PF00928 | 0.744 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.693 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.692 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.678 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.692 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.688 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.666 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.560 |
LIG_LIR_Apic_2 | 153 | 159 | PF02991 | 0.722 |
LIG_LIR_Apic_2 | 209 | 214 | PF02991 | 0.725 |
LIG_LIR_Apic_2 | 241 | 247 | PF02991 | 0.783 |
LIG_LIR_Gen_1 | 167 | 178 | PF02991 | 0.767 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.758 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.692 |
LIG_NRBOX | 80 | 86 | PF00104 | 0.615 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.688 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.623 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.757 |
LIG_SH2_NCK_1 | 233 | 237 | PF00017 | 0.705 |
LIG_SH2_NCK_1 | 320 | 324 | PF00017 | 0.645 |
LIG_SH2_NCK_1 | 345 | 349 | PF00017 | 0.751 |
LIG_SH2_NCK_1 | 7 | 11 | PF00017 | 0.652 |
LIG_SH2_SRC | 345 | 348 | PF00017 | 0.730 |
LIG_SH2_SRC | 7 | 10 | PF00017 | 0.653 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.746 |
LIG_SH2_STAT3 | 307 | 310 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.690 |
LIG_SH3_1 | 360 | 366 | PF00018 | 0.700 |
LIG_SH3_2 | 62 | 67 | PF14604 | 0.791 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.755 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.677 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.671 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.746 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.727 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.702 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.607 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.648 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.726 |
LIG_SH3_4 | 106 | 113 | PF00018 | 0.718 |
LIG_SH3_4 | 218 | 225 | PF00018 | 0.773 |
LIG_SUMO_SIM_anti_2 | 25 | 32 | PF11976 | 0.673 |
LIG_SUMO_SIM_par_1 | 44 | 50 | PF11976 | 0.530 |
LIG_TRAF2_1 | 93 | 96 | PF00917 | 0.773 |
MOD_CDK_SPK_2 | 217 | 222 | PF00069 | 0.775 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.768 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.619 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.646 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.602 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.758 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.677 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.557 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.777 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.705 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.789 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.691 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.743 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.745 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.729 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.642 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.772 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.661 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.680 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.640 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.669 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.616 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.692 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.699 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.716 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.680 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.591 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.734 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.661 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.690 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.735 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.713 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.629 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.746 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.678 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.721 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.642 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.702 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.667 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.691 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.720 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.694 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.790 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.667 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.628 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.710 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.503 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.749 |
MOD_SUMO_rev_2 | 152 | 162 | PF00179 | 0.676 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGN6 | Leptomonas seymouri | 55% | 98% |
A0A3Q8IEJ9 | Leishmania donovani | 94% | 100% |
A0A422NME0 | Trypanosoma rangeli | 26% | 99% |
A4HIU8 | Leishmania braziliensis | 76% | 100% |
A4I653 | Leishmania infantum | 94% | 100% |
C9ZRH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 96% |
E9B1D6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BX10 | Trypanosoma cruzi | 25% | 99% |