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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AXD4
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016791 | phosphatase activity | 5 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.730 |
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.349 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.222 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.509 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.509 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.530 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 274 | 283 | PF00134 | 0.546 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.557 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 184 | 193 | PF00244 | 0.614 |
LIG_APCC_ABBA_1 | 302 | 307 | PF00400 | 0.546 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.617 |
LIG_BRCT_BRCA1_1 | 212 | 216 | PF00533 | 0.733 |
LIG_Clathr_ClatBox_1 | 309 | 313 | PF01394 | 0.546 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.438 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.560 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.546 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.718 |
LIG_GBD_Chelix_1 | 237 | 245 | PF00786 | 0.346 |
LIG_LIR_Gen_1 | 299 | 309 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.588 |
LIG_LYPXL_yS_3 | 251 | 254 | PF13949 | 0.546 |
LIG_NRBOX | 241 | 247 | PF00104 | 0.546 |
LIG_PDZ_Class_2 | 321 | 326 | PF00595 | 0.575 |
LIG_Pex14_2 | 301 | 305 | PF04695 | 0.504 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.466 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.790 |
LIG_SH2_NCK_1 | 80 | 84 | PF00017 | 0.713 |
LIG_SH2_SRC | 134 | 137 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.790 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.680 |
LIG_SUMO_SIM_par_1 | 251 | 256 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 278 | 285 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 306 | 313 | PF11976 | 0.619 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.648 |
MOD_CDC14_SPxK_1 | 191 | 194 | PF00782 | 0.490 |
MOD_CDK_SPxK_1 | 188 | 194 | PF00069 | 0.493 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.663 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.706 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.516 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.580 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.748 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.392 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.546 |
MOD_Cter_Amidation | 316 | 319 | PF01082 | 0.538 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.690 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.805 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.313 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.492 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.796 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.779 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.652 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.692 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.585 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.733 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.728 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.772 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.706 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.346 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.528 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.524 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.471 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.484 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.644 |
MOD_PKA_1 | 318 | 324 | PF00069 | 0.509 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.509 |
MOD_Plk_2-3 | 308 | 314 | PF00069 | 0.619 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.546 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.546 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.509 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.532 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.707 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.678 |
MOD_SUMO_for_1 | 113 | 116 | PF00179 | 0.746 |
MOD_SUMO_rev_2 | 222 | 227 | PF00179 | 0.753 |
TRG_DiLeu_BaEn_4 | 307 | 313 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 249 | 254 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.790 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 175 | 179 | PF00026 | 0.649 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKW7 | Leptomonas seymouri | 57% | 87% |
A0A3S7WYV2 | Leishmania donovani | 90% | 96% |
A4HEG1 | Leishmania braziliensis | 78% | 100% |
A4I198 | Leishmania infantum | 89% | 96% |
Q4QA38 | Leishmania major | 86% | 100% |