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: E9B080
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.792 |
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.761 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.573 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.807 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.590 |
CLV_Separin_Metazoa | 117 | 121 | PF03568 | 0.591 |
CLV_Separin_Metazoa | 205 | 209 | PF03568 | 0.510 |
DEG_SCF_SKP2-CKS1_1 | 70 | 77 | PF00560 | 0.796 |
DOC_ANK_TNKS_1 | 127 | 134 | PF00023 | 0.506 |
DOC_CYCLIN_RxL_1 | 50 | 62 | PF00134 | 0.555 |
DOC_MAPK_MEF2A_6 | 183 | 192 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.506 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.591 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.591 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.773 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 160 | 164 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 37 | 44 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 50 | 57 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.503 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.669 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.375 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.749 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.668 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.508 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.763 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.635 |
LIG_LIR_Gen_1 | 187 | 197 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.613 |
LIG_PDZ_Class_2 | 221 | 226 | PF00595 | 0.651 |
LIG_PDZ_Wminus1_1 | 224 | 226 | PF00595 | 0.689 |
LIG_REV1ctd_RIR_1 | 6 | 15 | PF16727 | 0.629 |
LIG_SH2_CRK | 12 | 16 | PF00017 | 0.622 |
LIG_SH2_NCK_1 | 12 | 16 | PF00017 | 0.622 |
LIG_SH2_PTP2 | 189 | 192 | PF00017 | 0.495 |
LIG_SH2_SRC | 99 | 102 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 12 | 16 | PF00017 | 0.622 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.500 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.699 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.527 |
LIG_UBA3_1 | 56 | 63 | PF00899 | 0.518 |
LIG_WW_3 | 117 | 121 | PF00397 | 0.591 |
MOD_CDK_SPK_2 | 22 | 27 | PF00069 | 0.746 |
MOD_CDK_SPxK_1 | 71 | 77 | PF00069 | 0.798 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.770 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.697 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.709 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.751 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.499 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.765 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.521 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.651 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.793 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.647 |
MOD_GlcNHglycan | 104 | 108 | PF01048 | 0.800 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.734 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.688 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.626 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.617 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.698 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.650 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.665 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.592 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.730 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.668 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.678 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.621 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.592 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.619 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.614 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.571 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.642 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.440 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.529 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.618 |
MOD_NEK2_2 | 184 | 189 | PF00069 | 0.575 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.592 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.497 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.592 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.719 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.563 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.658 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.545 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.733 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.718 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.746 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.738 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.773 |
MOD_SUMO_for_1 | 153 | 156 | PF00179 | 0.719 |
MOD_SUMO_rev_2 | 117 | 127 | PF00179 | 0.730 |
MOD_SUMO_rev_2 | 175 | 185 | PF00179 | 0.481 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.620 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.495 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.601 |
TRG_NLS_MonoExtC_3 | 124 | 130 | PF00514 | 0.722 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P417 | Leptomonas seymouri | 42% | 100% |
A0A3S7X1X0 | Leishmania donovani | 89% | 100% |
A4HGW0 | Leishmania braziliensis | 72% | 100% |
A4I3Z0 | Leishmania infantum | 89% | 100% |
Q4Q805 | Leishmania major | 91% | 100% |