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) | yes | yes: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
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: 13 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: A0A3Q8I9P0
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 14 |
GO:0005509 | calcium ion binding | 5 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043169 | cation binding | 3 | 14 |
GO:0046872 | metal ion binding | 4 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 147 | 151 | PF00656 | 0.389 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.367 |
CLV_PCSK_FUR_1 | 183 | 187 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.521 |
DOC_CKS1_1 | 33 | 38 | PF01111 | 0.856 |
DOC_MAPK_gen_1 | 183 | 191 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 213 | 221 | PF00069 | 0.566 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.507 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.705 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.619 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.607 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.607 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.415 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.365 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.576 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.828 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.425 |
LIG_LIR_Apic_2 | 16 | 21 | PF02991 | 0.804 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 171 | 181 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 220 | 231 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.499 |
LIG_PCNA_yPIPBox_3 | 64 | 76 | PF02747 | 0.500 |
LIG_PDZ_Class_1 | 229 | 234 | PF00595 | 0.455 |
LIG_PTB_Apo_2 | 5 | 12 | PF02174 | 0.732 |
LIG_PTB_Phospho_1 | 5 | 11 | PF10480 | 0.729 |
LIG_Rb_pABgroove_1 | 109 | 117 | PF01858 | 0.352 |
LIG_SH2_CRK | 11 | 15 | PF00017 | 0.743 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.732 |
LIG_SH2_NCK_1 | 11 | 15 | PF00017 | 0.852 |
LIG_SH2_PTP2 | 194 | 197 | PF00017 | 0.380 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.759 |
LIG_SH2_STAT3 | 39 | 42 | PF00017 | 0.763 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.731 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.365 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.799 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.681 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.655 |
LIG_UBA3_1 | 111 | 117 | PF00899 | 0.485 |
LIG_WRC_WIRS_1 | 223 | 228 | PF05994 | 0.547 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.389 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.435 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.458 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.509 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.384 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.453 |
MOD_GlcNHglycan | 146 | 150 | PF01048 | 0.417 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.359 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.827 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.717 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.415 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.417 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.362 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.365 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.526 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.384 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.774 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.473 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.500 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.400 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.845 |
MOD_PKA_1 | 144 | 150 | PF00069 | 0.465 |
MOD_PKA_1 | 185 | 191 | PF00069 | 0.371 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.362 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.381 |
MOD_PKB_1 | 143 | 151 | PF00069 | 0.379 |
MOD_PKB_1 | 183 | 191 | PF00069 | 0.430 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.348 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.411 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.407 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.423 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.527 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.704 |
MOD_SUMO_rev_2 | 122 | 131 | PF00179 | 0.348 |
TRG_DiLeu_BaEn_2 | 195 | 201 | PF01217 | 0.407 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.365 |
TRG_ER_diArg_1 | 142 | 145 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P882 | Leptomonas seymouri | 74% | 100% |
A0A0N0P8K6 | Leptomonas seymouri | 45% | 100% |
A0A0S4INC8 | Bodo saltans | 25% | 100% |
A0A0S4JBG2 | Bodo saltans | 56% | 82% |
A0A1X0NJH7 | Trypanosomatidae | 52% | 96% |
A0A3Q8IW81 | Leishmania donovani | 31% | 100% |
A0A422P491 | Trypanosoma rangeli | 42% | 96% |
A4H7C7 | Leishmania braziliensis | 80% | 100% |
A4HPN5 | Leishmania braziliensis | 31% | 100% |
A4HVS3 | Leishmania infantum | 100% | 100% |
A4ID29 | Leishmania infantum | 31% | 100% |
C9ZML6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9APG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
E9APH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
G3V7W1 | Rattus norvegicus | 34% | 100% |
O75340 | Homo sapiens | 34% | 100% |
P05434 | Chlamydomonas reinhardtii | 24% | 100% |
P12815 | Mus musculus | 34% | 100% |
P25070 | Arabidopsis thaliana | 24% | 100% |
P25071 | Arabidopsis thaliana | 28% | 72% |
P53238 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 70% |
Q0JC44 | Oryza sativa subsp. japonica | 24% | 94% |
Q12798 | Homo sapiens | 25% | 100% |
Q24956 | Giardia intestinalis | 25% | 100% |
Q2QY10 | Oryza sativa subsp. japonica | 30% | 80% |
Q2R1Z5 | Oryza sativa subsp. japonica | 22% | 100% |
Q4Q148 | Leishmania major | 31% | 100% |
Q4QG08 | Leishmania major | 97% | 100% |
Q4QG09 | Leishmania major | 53% | 100% |
Q5PQ53 | Xenopus laevis | 28% | 83% |
Q641Z8 | Rattus norvegicus | 29% | 83% |
Q6DC93 | Danio rerio | 30% | 87% |
Q8BFY6 | Mus musculus | 29% | 85% |
Q8VC88 | Mus musculus | 27% | 100% |
Q8W4L0 | Arabidopsis thaliana | 30% | 70% |
Q94743 | Schistosoma japonicum | 35% | 100% |
Q9FYE4 | Arabidopsis thaliana | 28% | 66% |
Q9LX27 | Arabidopsis thaliana | 22% | 100% |
Q9UBV8 | Homo sapiens | 28% | 82% |
Q9ZQH1 | Arabidopsis thaliana | 25% | 100% |
V5BM44 | Trypanosoma cruzi | 45% | 100% |