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 |
Related structures:
AlphaFold database: A4HGS8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.476 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.434 |
DEG_SPOP_SBC_1 | 183 | 187 | PF00917 | 0.402 |
DOC_CKS1_1 | 263 | 268 | PF01111 | 0.369 |
DOC_CYCLIN_yCln2_LP_2 | 176 | 182 | PF00134 | 0.572 |
DOC_MAPK_gen_1 | 163 | 170 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 202 | 210 | PF00069 | 0.393 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.474 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.440 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.427 |
LIG_APCC_ABBA_1 | 206 | 211 | PF00400 | 0.305 |
LIG_BRCT_BRCA1_1 | 132 | 136 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 54 | 58 | PF00533 | 0.382 |
LIG_Clathr_ClatBox_1 | 142 | 146 | PF01394 | 0.326 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.730 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.384 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.457 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.380 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.539 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.274 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.502 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.438 |
LIG_Integrin_RGD_1 | 67 | 69 | PF01839 | 0.468 |
LIG_LIR_Gen_1 | 55 | 65 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 80 | 85 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.377 |
LIG_Pex14_1 | 14 | 18 | PF04695 | 0.548 |
LIG_Pex14_2 | 252 | 256 | PF04695 | 0.343 |
LIG_REV1ctd_RIR_1 | 266 | 275 | PF16727 | 0.472 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.424 |
LIG_SH3_2 | 172 | 177 | PF14604 | 0.326 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.456 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.609 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.348 |
LIG_SUMO_SIM_anti_2 | 213 | 218 | PF11976 | 0.314 |
LIG_SUMO_SIM_anti_2 | 50 | 55 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 48 | 55 | PF11976 | 0.402 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.527 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.619 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.453 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.385 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.486 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.524 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.276 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.494 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.516 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.628 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.491 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.584 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.407 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.735 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.606 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.485 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.524 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.650 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.547 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.273 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.547 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.272 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.449 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.430 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.502 |
MOD_PK_1 | 285 | 291 | PF00069 | 0.285 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.459 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.462 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.250 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.396 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.450 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.363 |
MOD_Plk_2-3 | 184 | 190 | PF00069 | 0.481 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.399 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.389 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.405 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.382 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.671 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.598 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.379 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.424 |
MOD_SUMO_rev_2 | 166 | 175 | PF00179 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.491 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I496 | Leptomonas seymouri | 47% | 93% |
A0A1X0NQQ5 | Trypanosomatidae | 31% | 96% |
A0A3Q8IER6 | Leishmania donovani | 80% | 99% |
A0A422N9C9 | Trypanosoma rangeli | 36% | 96% |
A4I3V5 | Leishmania infantum | 80% | 99% |
D0A923 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B045 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 99% |
Q4Q840 | Leishmania major | 80% | 100% |
V5D5P4 | Trypanosoma cruzi | 37% | 98% |