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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AQ11
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0003676 | nucleic acid binding | 3 | 5 |
GO:0003723 | RNA binding | 4 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
GO:0003729 | mRNA binding | 5 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.592 |
CLV_PCSK_FUR_1 | 107 | 111 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.491 |
DOC_CKS1_1 | 98 | 103 | PF01111 | 0.768 |
DOC_CYCLIN_yCln2_LP_2 | 95 | 101 | PF00134 | 0.594 |
DOC_MAPK_gen_1 | 107 | 117 | PF00069 | 0.604 |
DOC_MAPK_MEF2A_6 | 109 | 117 | PF00069 | 0.619 |
DOC_PP2B_LxvP_1 | 172 | 175 | PF13499 | 0.672 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.576 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 109 | 114 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 187 | 197 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 86 | 95 | PF00244 | 0.496 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.673 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.542 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.660 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.615 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.595 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.687 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.705 |
LIG_IBAR_NPY_1 | 203 | 205 | PF08397 | 0.589 |
LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.680 |
LIG_LIR_Apic_2 | 147 | 151 | PF02991 | 0.679 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.698 |
LIG_PCNA_yPIPBox_3 | 156 | 164 | PF02747 | 0.467 |
LIG_REV1ctd_RIR_1 | 20 | 29 | PF16727 | 0.444 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.674 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.677 |
LIG_SH2_NCK_1 | 143 | 147 | PF00017 | 0.609 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.699 |
LIG_SH3_1 | 148 | 154 | PF00018 | 0.444 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.650 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.444 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.741 |
LIG_SUMO_SIM_par_1 | 111 | 116 | PF11976 | 0.614 |
MOD_CDK_SPxxK_3 | 100 | 107 | PF00069 | 0.683 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.635 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.614 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.730 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.704 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.691 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.705 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.652 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.630 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.714 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.458 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.740 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.596 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.625 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.618 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.616 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.714 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.691 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.569 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.498 |
MOD_NEK2_2 | 131 | 136 | PF00069 | 0.420 |
MOD_OFUCOSY | 186 | 192 | PF10250 | 0.629 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.695 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.672 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.496 |
MOD_PKA_1 | 109 | 115 | PF00069 | 0.693 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.693 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.635 |
MOD_PKB_1 | 107 | 115 | PF00069 | 0.697 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.613 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.419 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.609 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.642 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.705 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.740 |
MOD_SUMO_rev_2 | 41 | 51 | PF00179 | 0.578 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.614 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3Y1 | Leptomonas seymouri | 69% | 100% |
A0A1X0NV29 | Trypanosomatidae | 43% | 100% |
A0A3S7WT90 | Leishmania donovani | 87% | 100% |
A0A422NSB0 | Trypanosoma rangeli | 38% | 100% |
A4H7Y4 | Leishmania braziliensis | 81% | 100% |
A4HWB1 | Leishmania infantum | 87% | 100% |
C9ZNU9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4QFH0 | Leishmania major | 87% | 100% |