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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8ID79
Term | Name | Level | Count |
---|---|---|---|
GO:0000041 | transition metal ion transport | 7 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0006816 | calcium ion transport | 7 | 1 |
GO:0006828 | manganese ion transport | 8 | 1 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030001 | metal ion transport | 6 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0032468 | Golgi calcium ion homeostasis | 8 | 1 |
GO:0032472 | Golgi calcium ion transport | 8 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055074 | calcium ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0070588 | calcium ion transmembrane transport | 6 | 1 |
GO:0071421 | manganese ion transmembrane transport | 6 | 1 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0005384 | manganese ion transmembrane transporter activity | 7 | 1 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 1 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 1 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 1 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 1 |
GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 206 | 212 | PF00089 | 0.263 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.418 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.207 |
DEG_APCC_DBOX_1 | 144 | 152 | PF00400 | 0.501 |
DEG_APCC_DBOX_1 | 166 | 174 | PF00400 | 0.207 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.667 |
DOC_CYCLIN_yCln2_LP_2 | 147 | 153 | PF00134 | 0.320 |
DOC_MAPK_DCC_7 | 143 | 153 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 142 | 153 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 39 | 47 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 39 | 47 | PF00069 | 0.420 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.591 |
DOC_USP7_MATH_2 | 125 | 131 | PF00917 | 0.692 |
LIG_14-3-3_CanoR_1 | 209 | 213 | PF00244 | 0.439 |
LIG_14-3-3_CterR_2 | 247 | 252 | PF00244 | 0.431 |
LIG_EH1_1 | 29 | 37 | PF00400 | 0.407 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.216 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.483 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.438 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.433 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.566 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.242 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.242 |
LIG_IBAR_NPY_1 | 180 | 182 | PF08397 | 0.221 |
LIG_PCNA_PIPBox_1 | 225 | 234 | PF02747 | 0.265 |
LIG_Pex14_2 | 156 | 160 | PF04695 | 0.274 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 93 | 97 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.692 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.374 |
LIG_SH3_1 | 119 | 125 | PF00018 | 0.690 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.690 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.672 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.260 |
LIG_SUMO_SIM_par_1 | 149 | 154 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 18 | 24 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 227 | 233 | PF11976 | 0.265 |
LIG_TYR_ITIM | 91 | 96 | PF00017 | 0.504 |
LIG_UBA3_1 | 35 | 42 | PF00899 | 0.422 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.608 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.437 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.424 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.608 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.242 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.453 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.429 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.242 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.608 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.210 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.207 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.465 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.685 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.242 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.260 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.407 |
MOD_NEK2_2 | 41 | 46 | PF00069 | 0.407 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.207 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.263 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.501 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.207 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.451 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.407 |
MOD_Plk_2-3 | 103 | 109 | PF00069 | 0.616 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.460 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.264 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.242 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.420 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.433 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.181 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.540 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMD2 | Leptomonas seymouri | 80% | 98% |
A0A0S4KKH4 | Bodo saltans | 71% | 100% |
A0A1X0P7U1 | Trypanosomatidae | 68% | 97% |
A0A422P389 | Trypanosoma rangeli | 70% | 100% |
A2YXC7 | Oryza sativa subsp. indica | 46% | 90% |
A2ZE50 | Oryza sativa subsp. indica | 46% | 90% |
A4H9Y9 | Leishmania braziliensis | 88% | 100% |
A4HY53 | Leishmania infantum | 100% | 100% |
B8AAM2 | Oryza sativa subsp. indica | 36% | 74% |
B9G125 | Oryza sativa subsp. japonica | 41% | 100% |
E9ARY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
P38301 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 90% |
P52875 | Mus musculus | 44% | 78% |
P52876 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 43% | 100% |
Q10320 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 88% |
Q2R2Z4 | Oryza sativa subsp. japonica | 36% | 73% |
Q2R4J1 | Oryza sativa subsp. japonica | 46% | 90% |
Q4QDJ0 | Leishmania major | 97% | 100% |
Q4V899 | Rattus norvegicus | 44% | 78% |
Q5NAY7 | Oryza sativa subsp. japonica | 36% | 74% |
Q6ZIB9 | Oryza sativa subsp. japonica | 46% | 89% |
Q93Y38 | Arabidopsis thaliana | 45% | 86% |
Q94AX5 | Arabidopsis thaliana | 36% | 68% |
Q9C6M1 | Arabidopsis thaliana | 40% | 100% |
Q9HC07 | Homo sapiens | 44% | 78% |
Q9P7Q0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 96% |
Q9SX28 | Arabidopsis thaliana | 39% | 100% |
Q9T0H9 | Arabidopsis thaliana | 37% | 70% |
V5BBV0 | Trypanosoma cruzi | 63% | 100% |