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: A4HWC2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.757 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.665 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 181 | 183 | PF00082 | 0.747 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.521 |
DEG_APCC_DBOX_1 | 9 | 17 | PF00400 | 0.582 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.685 |
DEG_SCF_FBW7_1 | 153 | 159 | PF00400 | 0.617 |
DOC_CKS1_1 | 153 | 158 | PF01111 | 0.618 |
DOC_CYCLIN_RxL_1 | 119 | 130 | PF00134 | 0.382 |
DOC_CYCLIN_yCln2_LP_2 | 49 | 55 | PF00134 | 0.552 |
DOC_MAPK_DCC_7 | 91 | 101 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 91 | 99 | PF00069 | 0.554 |
DOC_PP1_RVXF_1 | 120 | 127 | PF00149 | 0.441 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.529 |
DOC_PP4_FxxP_1 | 107 | 110 | PF00568 | 0.601 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.624 |
DOC_WD40_RPTOR_TOS_1 | 30 | 35 | PF00400 | 0.497 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 10 | 14 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 182 | 187 | PF00244 | 0.763 |
LIG_Actin_WH2_2 | 25 | 43 | PF00022 | 0.593 |
LIG_Actin_WH2_2 | 64 | 79 | PF00022 | 0.527 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.498 |
LIG_LIR_Apic_2 | 104 | 110 | PF02991 | 0.609 |
LIG_LIR_Apic_2 | 148 | 153 | PF02991 | 0.624 |
LIG_LIR_Gen_1 | 12 | 20 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 202 | 212 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 12 | 17 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.650 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.606 |
LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.573 |
LIG_SH3_1 | 150 | 156 | PF00018 | 0.604 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.625 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.351 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.552 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.521 |
LIG_SUMO_SIM_par_1 | 97 | 104 | PF11976 | 0.547 |
LIG_TYR_ITIM | 203 | 208 | PF00017 | 0.594 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.632 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.577 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.583 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.631 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.472 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.352 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.460 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.735 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.635 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.566 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.618 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.745 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.541 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.440 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.713 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.474 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.521 |
MOD_NEK2_2 | 167 | 172 | PF00069 | 0.550 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.497 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.733 |
MOD_PKA_1 | 180 | 186 | PF00069 | 0.696 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.490 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.585 |
MOD_PKB_1 | 180 | 188 | PF00069 | 0.735 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.705 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.493 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.613 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.712 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.593 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.483 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.559 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.613 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.581 |
MOD_SUMO_rev_2 | 87 | 93 | PF00179 | 0.592 |
TRG_DiLeu_BaEn_1 | 199 | 204 | PF01217 | 0.562 |
TRG_DiLeu_BaEn_4 | 18 | 24 | PF01217 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 119 | 124 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.667 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.588 |
TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.394 |
TRG_NLS_MonoExtC_3 | 179 | 184 | PF00514 | 0.702 |
TRG_NLS_MonoExtN_4 | 180 | 185 | PF00514 | 0.743 |
TRG_Pf-PMV_PEXEL_1 | 122 | 127 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF0 | Leptomonas seymouri | 47% | 100% |
A0A1X0NTQ5 | Trypanosomatidae | 25% | 83% |
A0A3Q8IA55 | Leishmania donovani | 100% | 100% |
A4H7Z4 | Leishmania braziliensis | 70% | 100% |
C9ZNV4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 85% |
E9AQ22 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QFF9 | Leishmania major | 93% | 100% |
V5DCR1 | Trypanosoma cruzi | 28% | 82% |