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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9B4C5
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016311 | dephosphorylation | 5 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0016791 | phosphatase activity | 5 | 9 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.312 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.162 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.384 |
CLV_PCSK_FUR_1 | 7 | 11 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.460 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.316 |
DOC_ANK_TNKS_1 | 9 | 16 | PF00023 | 0.316 |
DOC_CYCLIN_RxL_1 | 250 | 258 | PF00134 | 0.186 |
DOC_MAPK_gen_1 | 236 | 244 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 126 | 134 | PF00069 | 0.246 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.279 |
LIG_14-3-3_CanoR_1 | 79 | 83 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 87 | 91 | PF00244 | 0.328 |
LIG_CtBP_PxDLS_1 | 91 | 95 | PF00389 | 0.433 |
LIG_eIF4E_1 | 166 | 172 | PF01652 | 0.312 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.365 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.338 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.312 |
LIG_LIR_Gen_1 | 182 | 190 | PF02991 | 0.207 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 188 | 192 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.306 |
LIG_NRBOX | 167 | 173 | PF00104 | 0.316 |
LIG_Pex14_1 | 36 | 40 | PF04695 | 0.259 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.277 |
LIG_SH2_PTP2 | 166 | 169 | PF00017 | 0.370 |
LIG_SH2_SRC | 220 | 223 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.370 |
LIG_SUMO_SIM_par_1 | 167 | 173 | PF11976 | 0.312 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.372 |
LIG_UBA3_1 | 135 | 143 | PF00899 | 0.316 |
LIG_WRC_WIRS_1 | 186 | 191 | PF05994 | 0.162 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.460 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.387 |
MOD_GlcNHglycan | 74 | 78 | PF01048 | 0.409 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.355 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.232 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.453 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.316 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.368 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.316 |
MOD_NEK2_2 | 212 | 217 | PF00069 | 0.318 |
MOD_PKA_1 | 78 | 84 | PF00069 | 0.316 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.405 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.328 |
MOD_Plk_2-3 | 203 | 209 | PF00069 | 0.246 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.313 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.387 |
MOD_SUMO_rev_2 | 103 | 110 | PF00179 | 0.169 |
MOD_SUMO_rev_2 | 173 | 181 | PF00179 | 0.259 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.203 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.382 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.417 |
TRG_NES_CRM1_1 | 247 | 258 | PF08389 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 253 | 258 | PF00026 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4V5 | Leptomonas seymouri | 27% | 100% |
A0A0N1HYX0 | Leptomonas seymouri | 49% | 100% |
A0A0N1PC37 | Leptomonas seymouri | 53% | 100% |
A0A0N1PFC3 | Leptomonas seymouri | 36% | 100% |
A0A3S7WWX6 | Leishmania donovani | 28% | 100% |
A0A3S7X743 | Leishmania donovani | 86% | 100% |
A4HZQ2 | Leishmania infantum | 29% | 100% |
A4I9C5 | Leishmania infantum | 86% | 100% |
E9AVK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P40289 | Cupriavidus necator (strain ATCC 17699 / DSM 428 / KCTC 22496 / NCIMB 10442 / H16 / Stanier 337) | 28% | 95% |
Q4Q3Q1 | Leishmania major | 90% | 100% |
Q4QBX1 | Leishmania major | 27% | 100% |