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: A4H7Y4
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0003723 | RNA binding | 4 | 6 |
GO:0003729 | mRNA binding | 5 | 5 |
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:0097159 | organic cyclic compound binding | 2 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.596 |
CLV_PCSK_FUR_1 | 106 | 110 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.398 |
DOC_CKS1_1 | 97 | 102 | PF01111 | 0.739 |
DOC_MAPK_gen_1 | 106 | 116 | PF00069 | 0.597 |
DOC_MAPK_MEF2A_6 | 108 | 116 | PF00069 | 0.615 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.688 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.686 |
LIG_14-3-3_CanoR_1 | 108 | 113 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 186 | 196 | PF00244 | 0.596 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.672 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.654 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.681 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.595 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.662 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.689 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.729 |
LIG_IBAR_NPY_1 | 202 | 204 | PF08397 | 0.583 |
LIG_LIR_Apic_2 | 123 | 129 | PF02991 | 0.692 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.727 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.498 |
LIG_REV1ctd_RIR_1 | 20 | 29 | PF16727 | 0.444 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.697 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.676 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.606 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.701 |
LIG_SH2_STAT3 | 159 | 162 | PF00017 | 0.692 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.692 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.649 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.717 |
LIG_SUMO_SIM_anti_2 | 69 | 75 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 110 | 115 | PF11976 | 0.614 |
LIG_TYR_ITIM | 145 | 150 | PF00017 | 0.474 |
MOD_CDK_SPxxK_3 | 99 | 106 | PF00069 | 0.658 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.558 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.695 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.681 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.693 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.621 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.520 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.607 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.746 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.541 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.736 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.563 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.611 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.606 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.744 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.609 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.482 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.587 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.552 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.563 |
MOD_OFUCOSY | 185 | 191 | PF10250 | 0.613 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.481 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.694 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.654 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.605 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.690 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.690 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.618 |
MOD_PKB_1 | 106 | 114 | PF00069 | 0.690 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.481 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.607 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.532 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.662 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.736 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.713 |
MOD_SUMO_rev_2 | 41 | 51 | PF00179 | 0.655 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.695 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.639 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3Y1 | Leptomonas seymouri | 68% | 99% |
A0A1X0NV29 | Trypanosomatidae | 43% | 100% |
A0A3S7WT90 | Leishmania donovani | 82% | 100% |
A0A422NSB0 | Trypanosoma rangeli | 39% | 100% |
A4HWB1 | Leishmania infantum | 82% | 100% |
C9ZNU9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AQ11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QFH0 | Leishmania major | 81% | 100% |